Understanding CAR T-Cell Therapy Utilization Patterns Among the Community Oncology Setting – Targeted Oncology

Thirty-nine percent of oncologists working in the community setting refer 2 out of 5 patients to receive chimeric antigen receptor (CAR) T-cell therapy at hospitals, according to data from a surveydisseminated by Cardinal Health Specialty Solutions.1

The research also showed that a decent portion of oncologists (27%), do not refer or administer CAR T-cell therapy at all, and a small proportion, 6%, perform in-office infusions. The survey raises questions about how to improve CAR T-cell availability for patients treated at community clinics. The recommendation born from the survey was to align stakeholders to address the concerns of the oncology population

In an interview with Targeted Oncology, Bruce Feinberg, DO, vice president, chief medical officer Cardinal Health Specialty Solutions, discussed the use of CAR T-cell therapy in the community oncology setting, the challenges oncologist face, and the next wave of innovation to improve CAR T-cell administration for patients.

TARGETED ONCOLOGY: Can you discuss CAR T-cell therapies that are FDA-approved in hematologic malignancies? How have these therapies impacted treatment?

Feinberg: The story of CAR T goes back a little before the drugs were approved. The recognition that our view of cancer in general was thinking of cancer as an invader. The way we thought about bacteria or viruses so that they were the enemy that we are going to then destroy.The recognition that changed all that was rather than thinking about cancer as the external alien enemy, because cancer was created by cells, and they are human cells that are transforming, should we be thinking about how to then look at the problem a little bit differently and see it as a failure of the host, as opposed to the invader.The story really begins as we think about empowering the immune system. The first aspects of that go back to the 1980s with interferons, interleukins, and tumor-infiltrating lymphocytes, and that was the first round.

The second way begins as we started to now think about the mid-2000 teams with the immune checkpoint inhibitors and start to look at manipulating T cells. The T-cell manipulation that begins with CART is not stopping with CAR T. It is going to be developing into bispecific antibodies, and natural killer cells that are then manipulated, so we are going to be seeing a rapid expansion of this host empowerment, how we really trigger the immune system to do its job, and then control this process, which really is a process of self as opposed to the external enemy.

Now that we have CAR T cells, what are the key challenges community oncologists facewith giving this treatment to patients?

The good news regarding these challenges is that we have had these challenges before. I mentioned that we think back in the early first phase of empowering the immune system with treatments like interleukin-2, we have the same kind of problem intensive treatment performed in hospital patients in ICU environments. We have also had that same world-specific to hematologic malignancies when we think about transplant, initially allogeneic transplant and then with autologous transplant, but similarly intensive complex programs, and multi-step approaches to patient care often done in tertiary care academic environments. There has been a background that really helps this field move forward quickly, based on that prior experience.

But the barriers that we have witnessed are those barriers we have seen before. Having an educated community workforce of healthcare providers who are knowledgeable about these treatments, an academic, tertiary care environment, where they remove all the barriers to those patient referrals, and hopefully patients who understand to some degree that complexity of the program will be willing to undergo consent for those procedures. Each of those barriers exist, but each of those barriers has been seen before, and we can rely on past experiences to help guide us forward.

Cardinal Health conducted a survey around in-office infusion and referrals for CAR T-cell therapy. How did community oncologists respond?

The research has been focused on both understanding physician perceptions. Are these therapies ready for primetime? Do they adopt and support these therapies? If they do support and adopt, what are the barriers to being able to refer patients for these treatments? Then lastly, what are the outcomes of these patients by getting into the chart itself and understanding the outcomes of patients? We have done all that in recent years, and some of that work was just recently presented at iSPOR.

At iSPOR, particularly regarding diffuse large B-cell lymphoma, there were 2 observational research studies that were done. One looked at the feasibility of being able to use that electronic health record in the community oncologist office to be able to understand the full journey of the patient who undergoes CAR T therapy, and can it understandthe scope and quality of the data that is housed within that medical record?

The second aspect of it was understanding. Could you be able to assess outcomes from the data within that medical record? So,2 parallel studies that were done specifically in diffuse large B-cell lymphoma, and also studies that have been done trying to look at new areas like multiple myeloma and understanding what physicians' perceptions about another hematologic malignancyin which there will be CAR T therapy available.

How do you interpret the findings from this survey?

For the community oncologist's electronic health record as a data source for conducting research on patients who are undergoing CAR T and other therapies, what we found is that the data source was rich and robust. For almost every major benchmark, in terms of the patient journey for CAR T,prior therapy, the timing of that prior therapy, the nature of that prior therapy, the referral to the tertiary center for consideration for CAR T, the actual evaluation for CAR T, the pheresis procedure, the site of the lympho-depletion procedure, chemotherapy, the actual administration of CAR T, the subsequent adverse event tracking, and the ER visits and hospitalizations, as well as the return to the community oncology clinic, all of that data was available within the community oncologist health record. That is a treasure trove of data that we can use as we start to expand the CAR T arsenal to understand the patient experience with CAR T in the real-world setting.

As we know, patients and clinical trials are often not representative of what is happening in real-world patients and clinical trials. First, less than 3% of adults with cancer participate in oncologic clinical trials, and those that do are healthier, they are less diverse, they are younger, they often are more health literate, and they have a higher socioeconomic status. That lack of representation becomes a problem that we start to extrapolate to all comers. Understanding what is happening in the real world to these patients is critical, and our data demonstrates that using the community oncologists to abstract the records is giving us that data that is necessary to understand the patient's experience. That is1 key outcome is that in the feasibility study, we saw as a strong positive for a new data source that can evaluate the real-world experience of patients undergoing CAR T-cell therapy.

The second outcome is that based on the feasibility of that data, could we find interesting details and insights about those patients being treated?We saw some interesting patterns of care that seemed to be geographically different. The timing of referrals and the nature of the CAR T-cell treatmentwere different as we looked across the major geographic regions of the country. Trying to understand that is going to be critical as the research continues, so are these trends and patterns related to Centers of Excellence and the KOLs, who often speak from those centers of excellence within a region?

Memorial Sloan Kettering often influences what happens in the Mid Atlantic, MD Anderson influences what happens in the South and the Southwest, and a center like UCLA influenceswhat's happens on the West Coast. As the Centers of Excellence have an influence, are we going to see differences in patterns of care in these different regions? Then, what were the outcome differences between those patterns of care?

Can you provide background on your study of CAR T-cell utilization patterns for relapsed/refractory diffuse large B-cell lymphoma in the US-based community hematologists/oncologists?

It has been almost 7 years since we first started to evaluate and publish on the broader world of empowering the host through immunologic therapies in the treatment of cancer. Our CAR T work now is 5 years, there have been a half dozen publications, similar tothe ones that we are talking about now, over the course of the past 5 years. We are trending that rate of adoption, that perceptions of physicians, the perceived barriers they find, and we are not just doing that assessment of physicians in the community, but we are also gathering experts from the major tertiary care centers to understand what they are perceiving as barriers and a general sense that CAR T therapy currently is under-utilized for those reasons and those barriers. What we find is there are still problems. The patients undergoing CAR T therapy have advanced disease, and are not clinically stable. The current timeline for CAR T, which can take 6 weeks from point of referral to point of CAR T-cell administration, often is problematic because of that patient instability.

Then, there are a host of new therapies which entered the armamentarium of treating physicians, which are making it confusing as to which is the appropriate second-line, third-line treatment. Recent data from ZUMA-7 [NCT03391466]trial has demonstrated that CAR T is a more effective therapythan autologous stem cell transplant as the first salvage treatment. That also adds a dynamic so that when we are doing this research, it can't be viewed as static. We have to be viewing it as a need for recurrent evaluations, as therapy indications change, and as new therapies come alive. Part of the basis for this research is really to be able to constantly trend what's happening in the field of newer therapies and how physicians perceive those new therapies and what are the outcomes of the patients. They're referring for those therapies. That was the focus of the work we've recently have done in diffuse large B-cell lymphoma.

Based on these 2 studies, how do you think the challenges that oncologists are experiencing with CAR T cells are impacting patient care?

I think overall, it is a good story. I think all physicians who treat cancer, particularly patients who have refractory or relapsed disease, for whom cure has been elusive, are looking for new therapeutic options. CAR T came with a tremendous amount of enthusiasm and excitement, but also with some concern about itstoxicity. Now, we are seeing second- and third-generation CAR T therapies, we're seeing expanded indications for earlier line of treatment. I think that excitement continues, and I think reservations are decreasing.

I think communication between tertiary care centers and community oncologists is improving, and we're getting closer to that point where patients will not have to leave home and leave their communities for this treatment, but we are not there yet.We are still testing and trying to understand what it will take for community physicians to participate in this aspect of care. I think that is going to be the next wave of innovation, and it will be operational innovation, rather than just drug development innovation, on how we can get these therapies to be done closer to the time of need.

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Understanding CAR T-Cell Therapy Utilization Patterns Among the Community Oncology Setting - Targeted Oncology

Tafasitamab Plus Lenalidomide Superior to Standard Therapies in Key Subgroups of High-Risk R/R DLBCL – Cancer Network

Subgroup analysis of the RE-MIND trial support use of tafasitamab plus lenalidomide to treat high-risk diffuse large B-cell lymphoma.

A subgroup analysis of the observational RE-MIND2 study (NCT04697160) in patients with stem cell transplantineligible high-risk diffuse large B-cell lymphoma (DLBCL) suggests improved overall survival (OS) with tafasitamab (Monjuvi) plus lenalidomide (Revlimid) treatment vs selected systemic therapies, according to data presented at the 2022 American Society of Clinical Oncology (ASCO) Annual Meeting.1

Using matched cohorts of patients in subgroups based on the number of extranodal sites and presence or absence of elevated lactate dehydrogenase (LDH) level, the hazard ratio for OS suggests a trend toward favoring tafasitamab plus lenalidomide in each matched analysis set overall, and in most patient subgroups, said lead investigator Grzegorz S. Nowakowski, MD, of the Division of Hematology at the Mayo Clinic in Rochester, Minnesota.

In each subgroup examined, there was a trend favoring enhanced OS with tafasitamab plus lenalidomide when compared with systemic therapies pooled, rituximab [Rituxan] plus lenalidomide [Revlimid; R2], and polatuzumab [Polivy] plus bendamustine and rituximab [pola-BR].1

For the tafasitamab plus lenalidomide versus systemic therapies pooled matched cohort comparison, median OS was:

For the tafasitamab plus lenalidomide versus pola-BR matched cohort comparison, median OS was:

For the tafasitamab plus lenalidomide vs R2 matched cohort comparison, median OS was:

For the tafasitamab plus lenalidomide versus CD19-directed CAR-T cell therapy matched cohort comparison, median OS was:

The observed trend of shorter OS duration of CAR-T cells versus tafasitamab plus lenalidomide in high-risk patients warrants further investigation, said Dr. Nowakowski. We note that analyses between tafasitamb and comparator therapies are not powered for statistical comparison. Small sample size resulted in wide confidence intervals; therefore, those results must be interpreted with caution.

RE-MIND2 compared patient outcomes from the phase 2 L-MIND study (NCT02399085)2 with those from closely matched real-world cohorts, including patients treated with other systemic therapies for DLBCL pooled in a single cohort and cohorts comprising patients treated with common regimens.

Patients from L-MIND were closely matched with patients from 4 RE-MIND2 cohorts using estimated propensity score based one-to-one nearest neighbor matching balanced for up to 9 baseline covariates according to clinical relevance and other available patient records.

A total of 3454 patients were enrolled in RE-MIND2 from 200 study sites. The 1:1 matching methodology resulted in 76 pairs for tafasitamab plus lenalidomide versus systemic therapies pooled, 24 pairs versus pola-BR, 33 pairs versus R2, and 37 pairs versus CAR T-cell therapy.

The differences in cohort sizes reflects availability of baseline covariate data in hospital databases for therapies of interest, Nowakowski said.

Despite small sample sizes, these results may aid in contextualizing therapy options for treating patients with R/R DBCL, Nowakowski concluded.

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Tafasitamab Plus Lenalidomide Superior to Standard Therapies in Key Subgroups of High-Risk R/R DLBCL - Cancer Network

Eagles Club will host Hengeveld benefit | News – nwestiowa.com

REGIONALA benefit will be held Saturday at the Sheldon Eagles Club for a Hartley man facing a second bout with cancer at the age of 26.

Branden Hengeveld was diagnosed in February of 2021 with Hodgkin lymphoma and went through six months of chemotherapy. After this treatment, he was given the all-clear in August.

In December, he had a follow-up scan, and the doctors noticed some concerning things. They did a biopsy, but it came back negative. Hengeveld went back for another scan in March and enlarged lymph nodes prompted another biopsy which this time came back positive for Hodgkin lymphoma.

When it was discovered, the cancer already was between stages 2 and 3.

Hengeveld has started doing chemotherapy treatment again in Sioux Falls, SD, to shrink his cancer and then at the end of June, he will be headed to Mayo Clinic in Rochester, MN, for around six weeks.

Six to eight weeks is the usual, but they said just prepare for a 100-day stay, he said.

Hengeveld will be undergoing a stem cell transplant treatment at Mayo. The treatment consists of three weeks of tests, then six days of strong chemotherapy followed by the stem cell transplant which will take three weeks of recovery.

He will have to stay in Rochester during the entire process.

Funds raised by Saturdays benefit will go toward travel, rent and any other expenses for Hengeveld during his treatment.

Hengeveld grew up in Sanborn and lives in Hartley. He has worked for the last few years at Den Hartog Industries in Hospers, where he became friends with Vanessa Harig who is hosting the event.

Pretty much everyone at Den Hartog knows Branden, Harig said. Hes a very great guy and is always very happy and bubbly. It is going to be hard when he is away in Rochester.

Hengevelds father and brother knew they wanted to hold a benefit for him but were unsure how to organize it, so they sought out Harigs assistance.

Me being crazy like I am, said, Yea, I can organize a benefit, Harig said.

She is no stranger to organizing events and helping others. Harig is the director of the Awakening Grace Foundation in Orange City, which helps those who have lost a child during pregnancy or infancy.

Although she has a lot going on, Harig felt up to the task and the cause worthy.

A lot of people get caught off guard when the realize how young Branden is and that he has already had cancer twice, she said. Hes fighting hard and doing everything he can.

Despite all that has happened, Hengeveld remains positive.

Its been a process for sure, he said. But Ive met a lot of people and made some good friends throughout it.

Hengeveld has a GoFundMe page as well as a Facebook page where he posts updates.

Saturdays fundraising event will consist of a spaghetti supper with garlic bread and homemade desserts starting at 5 p.m. until it is gone as well as a silent auction 5-7 p.m. There also will be a raffle for a Traeger smoker grill which will be drawn for at 7:30 p.m. Tickets for the raffle are $20 each and 100 tickets will be sold. Participants need not be present to win.

Text Vanessa Harig at 712-344-2149 to enter the raffle or for any questions.

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Eagles Club will host Hengeveld benefit | News - nwestiowa.com

The Oncology Institute set to join the Russell 2000 and Russell 3000 Indexes – StreetInsider.com

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CERRITOS, Calif., June 07, 2022 (GLOBE NEWSWIRE) -- The Oncology Institute, Inc. (NASDAQ: TOI), one of the largest value-based oncology groups in the United States, today announced thatit will join the Russell 2000 and Russell 3000 Indexes after the 2022 Russell indexes annual reconstitution, effective after the US market opens on June 27, according to a preliminary list of additions posted June 3.

Annual Russell indexes reconstitution captures the 4,000 largest US stocks as of May 6, ranking them by total market capitalization. Membership in the US all-cap Russell 3000 Index, which remains in place for one year, means automatic inclusion in the large-cap Russell 1000 Index or small-cap Russell 2000 Index and the appropriate growth and value style indexes. FTSE Russell determines membership for its Russell indexes primarily by objective, market-capitalization rankings, and style attributes.

We are excited to be joining the Russell indexes as this represents another important milestone since becoming a public company in November of 2021, said Brad Hively, CEO of TOI. As we grow our business and execute our strategic objectives, we look forward to educating key stakeholders about TOIs innovative oncology care and our continued progress.

Russell indexes are widely used by investment managers and institutional investors for index funds and as benchmarks for active investment strategies. Approximately $12 trillion in assets are benchmarked against Russells US indexes. Russell indexes are part of FTSE Russell, a leading global index provider.

For more information on the Russell 3000 Index and the Russell indexes reconstitution, go to the Russell Reconstitution section on the FTSE Russell website.

About The Oncology Institute, Inc.

Founded in 2007, TOI is advancing oncology by delivering highly specialized, value-based cancer care in the community setting. TOI offers cutting-edge, evidence-based cancer care to a population of approximately 1.5 million patients including clinical trials, stem cell transplants, transfusions, and other care delivery models traditionally associated with the most advanced care delivery organizations. With 80+ employed clinicians and more than 600 teammates in over 50 clinic locations and growing, TOI is changing oncology for the better. For more information visitwww.theoncologyinstitute.com.

Contacts

Media

The Oncology Institute Julie Korinke [emailprotected](562) 735-3226 x 88806

Revive Michael Petrone [emailprotected](615) 760-4542

Investors

Solebury Trout Maria Lycouris [emailprotected]

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The Foundation of Hope and Innovation Partners with Venice Family Clinic to Provide Free Mammograms – GlobeNewswire

CERRITOS, Calif., May 24, 2022 (GLOBE NEWSWIRE) -- The Foundation of Hope and Innovation, a charity supported by The Oncology Institute, Inc. (NASDAQ: TOI), announced a $40,000 donation to Venice Family Clinic to fund mammography services to women in Los Angeles. The donation will fund 10 free mammography days throughout greater Los Angeles.

The Foundation of Hope and Innovation selected Venice Family Clinic to be the first grant recipient of 2022 because of its 50-year history of providing primary care, specialty care, dental care, and mental health services to their community. Venice Family Clinics services align closely with The Foundation of Hope and Innovations founding principles: advance treatment options for patients and fill the gaps in healthcare delivery, including early detection of cancer and mental health support for patients.

Early detection of cancer is critically important to ensure prompt treatment and optimal outcomes, shared Dr. Daniel Virnich, Board President for The Foundation of Hope and Innovation. By partnering with a well-respected non-profit healthcare provider like Venice Family Clinic, we can ensure that more people have access to affordable cancer screening services and timely cancer treatment.

Venice Family Clinic provides high-quality, comprehensive health care to families and individuals who might otherwise go without the care they need. With 17 locations serving nearly 45,000 patients, Venice Family Clinic increases access to quality healthcare for Angelinos in need and helps ensure more people have access to early cancer screenings.

The generous donation by The Foundation of Hope and Innovation will ensure 200 patients access mammograms they may not have otherwise been able to access, added Rigoberto Garcia, Director of Health Education at Venice Family Clinic. We are thrilled to be able to extend these services to more patients.

About The Foundation of Hope and InnovationThe Foundation of Hope and Innovation believes that every patient, and their family, deserves access to high quality care and support services. They are committed to filling gaps in healthcare delivery, including early detection and mental health support. For more information visit http://www.foundationofhopeandinnovation.org.

About The Oncology Institute, Inc.Founded in 2007, The Oncology Institute of Hope and Innovation (TOI) is advancing oncology by delivering highly specialized, value-based cancer care in the community setting. TOI offers cutting-edge, evidence-based cancer care to a population of approximately 1.5 million patients including clinical trials, stem cell transplants, transfusions, and other care delivery models traditionally associated with the most advanced care delivery organizations. With 80+ employed clinicians and more than 600 teammates in 50 clinic locations and growing, TOI is changing oncology for the better. For more information visit http://www.theoncologyinstitute.com.

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The Foundation of Hope and Innovation Partners with Venice Family Clinic to Provide Free Mammograms - GlobeNewswire

The path to least resistance: How our researchers are outsmarting cancers survival skills – Cancer Research UK News

Breast cancer cells Credit: NCI

Drug resistance is one of biomedicines biggest threats, standing in the way of cures for all manner of viruses, infections and diseases, including cancer. But our scientists across the country are working hard to tackle it.

After a shock breast cancer diagnosis in January 2021 at the age of 48, doctor and mother Tina* underwent six months of chemotherapy, which for many people with early-diagnosed breast cancer can be curative. But a test following treatment confirmed the presence of residual cancer cells. Cells that had somehow survived the treatment onslaught. Cells that indicate the cancer could return. When I was told that my treatment hadnt been entirely successful, I initially felt very upset, Tina recalls. Id had a difficult time through chemo, needing multiple blood transfusions and experiencing multiple delays in treatment due to low blood counts. To then be told that there seemed to be residual disease due to chemo resistance was very hard to hear.

To be told after treatment that there seemed to be residual disease due to chemo resistance was very hard to hear Tina, breast cancer patient

Despite the huge progress weve made in breast cancer survival which has doubled in the UK over the past 40 years Tinas is a reality for many women with triple negative breast cancer, a subtype that can be harder to treat. For these women, when cancer does recur its more difficult to get on top of, explains Cancer Research UK clinician scientist Dr Sheeba Irshad. Dr Irshad is part of a growing cohort across our institutes and centres who are working to expose and exploit the mechanisms that allow some cancer cells to resist treatment (from chemotherapy to targeted treatments and even immunotherapies), lay dormant and then re-emerge later, when theyre harder to eradicate.

Drug resistance is a major reason why cancer regrows after treatment, so its also a significant contributor to people not surviving their disease, confirms Professor Dan Tennant, a Cancer Research UK biochemist at the University of Birmingham. Hes setting his sights on hypoxia a low-oxygen state in cells that occurs in most solid cancers and is a leading cause of drug resistance. Like all cells, cancer cells need oxygen to survive and multiply. When oxygen is scarce, theyre forced to adapt, finding compensatory ways to complete fundamental processes. Whats left is a cancer cell with a markedly different metabolism than a cancer cell with a normal oxygen supply. And one that stands out to someone like Professor Tennant, whos investigating how cancer cells survive such hostile conditions.

I dont think its a coincidence that, for example, glioblastoma an aggressive brain tumour is one of the most hypoxic tumour types and also incredibly resistant to treatments, he reasons. Given that hypoxic cells are some of the most drug-resistant cells within a tumour, by targeting them, we can directly alleviate resistance. And because the rest of the body has a normal oxygen supply, going after just the hypoxic cancer cells means patients should experience fewer negative side effects. Thinking about long-term therapy and a persons quality of life, thats a huge bonus, he adds.

Earlier this year, Professor Tennants team landed on a promising drug target. By feeding hypoxic cells nutrients such as sugars and watching how they use them compared to cancer cells with normal oxygen levels, they identified an enzyme that plays a critical role in hypoxic cells. When they removed the enzyme from cancer cells in mice, it caused the hypoxic tumour cells to die.

Despite this focus on the most fundamental elements of biology, Professor Tennant and his team are making steady progress toward the clinic not least because just 50 metres away, Cancer Research UK neurosurgeon Professor Colin Watts is collecting tissue samples from volunteer patients and passing them to the team so they can check their lab-based models against the real thing. The data generated on each side quickens the pace of progress. As Professor Tennant explains, Now, when we take our discovery science and try to translate it into new therapies, it has a better chance of working.

Its an attitude shared by Professor Stephen Tait at the Cancer Research UK Beatson Institute in Glasgow, whos also eager to use our vast clinical network to translate lab discoveries swiftly. He and his team are examining what happens when treatments do their job well but cause harmful unintended consequences. They found that when chemotherapy successfully kills a cancer cell, the dying cell can emit a protein that acts as a protector to neighbouring cancer cells, shrouding them from chemotherapy and allowing them to emerge unscathed. Professor Tait now hopes to test this by combining chemotherapy with a drug to inhibit this protein.

Its promising work, but perhaps more exciting is some of the teams earlier research, which is now flying towards the clinic thanks to an alliance set up by Cancer Research UK. Its based on their discovery that by blocking a class of proteins called caspases before a cancer cell is killed, the dying cell releases signals to the immune system. In normal circumstances, the immune system ignores cell death if it didnt, it would constantly be responding to the billions of cells that die within us each day. But with the immune system alerted, any leftover cancer cells can be ambushed and killed. Professor Tait is modest about the discovery: Like a lot of things in research, if you just stay alert, you see exciting stuff going on, he says. But their findings could lead to a new class of treatments that combine the strength of chemotherapy with the bodys perceptive immune response.

Back in Birmingham, Cancer Research UK cell biologist Dr Clare Davies is also making clinically relevant fundamental discoveries. Shes studying breast cancer stem cells, which initiate breast tumours. These cells are inherently chemo-resistant because they can repair the DNA damage that chemotherapy induces, she explains. They manage to do this because they have enhanced genes and mechanisms that control DNA repair pathways. These cells also multiply slower than other cancer cells, and because chemotherapy actively targets rapidly dividing cells, they face less bombardment.

We often think that science is a slow burn, but this shows it can really fly when people invest the time and money Dr Clare Davies

Developing drugs that specifically target the pathways enhanced in cancer stem cells would provide a new way to tackle chemo-resistant breast cancer. And Dr Davies and her team have identified an enzyme that they believe helps keep cancer stem cells alive by increasing these pathways. If we can inhibit this enzyme while also delivering chemotherapy, we can block the repair mechanisms and push the cancer stem cell over the edge, she explains, suggesting that we could cut cancer recurrence off at the source. Cancer is clever. It evolves, she says. We must understand the mechanisms underlying this evolution by studying cancer stem cells.

Dr Davies is now working with a pharmaceutical company to progress this work to patients through a clinical trial. We often think that science is a slow burn, but this shows it can really fly when people invest the time and money.

While these steps forward are cause for enthusiasm, they must also be met by innovation and resource in the clinic. Thats why Dr Irshad is leading a clinical trial platform named PHOENIX, which aims to accelerate the drug development pipeline for hard-to-treat breast cancers. Biopsies taken before and after treatment help the team understand the chemo-resistant disease in each individual patient and monitor the efficacy of specific drugs. These short-term efficacy trials allow us to design better trials with a higher likelihood of success, Dr Irshad explains.

Its then that the progress made in breast cancer survival really begins to count. Were lucky in breast cancer care that if secondary cancer is likely, we do have options for our patients, she adds. We can be proactive and that really matters.

With so many advances in drug discovery over the past few decades from improving chemotherapy and radiotherapy, to delivering targeted treatments and immunotherapies drug resistance deals a cruel blow. Only by bridging the biomedical and clinical worlds, and working in partnership with health systems and philanthropic partners, can we create the infrastructure and funding required to support our researchers and clinicians as they strive to remain one step ahead and ensure people like Tina arent left in limbo, waiting to be told whether their cancer has returned.

Researcher images from top to bottom: Dr Sheeba Irshad, Professor Dan Tennant, Professor Stephen Tait, Dr Clare Davies

I found out I had breast cancer on Wednesday 13 January, 2021. I remember the day well.

When I was told that my treatment hadnt been entirely successful, I initially felt very upset. Id had a difficult time through chemo, needing multiple blood transfusions and experiencing multiple delays in treatment due to low blood counts. To then be told that there seemed to be residual disease due to chemo resistance was very hard to hear.

From the outset, my hospital team have been fantastic. The oncologists always had a positive approach. As a mother of young children, I felt that this was essential. And when Dr Irshad told me that I would be entered into the trial, I felt hopeful and grateful that it was possible.

Its incredibly important that researchers like Dr Irshad continue vital research in this area. I never thought I would get breast cancer. I have become friends with a lot of women with breast cancer since my diagnosis. Were all so different. I would give anything to know what caused it. Im hoping that, with research, not only will we find treatments but also causes. I have a daughter and would not want her to go through what I have been through. Currently, Im doing really well. I have returned to work fully and lead a normal life. Lots of good things have happened as a result of my diagnosis. Ive realised how many people care for me and my family and I now lead a healthier lifestyle.

*Name has been changed at the request of the contributor.

Were tremendously grateful for funding weve received from supporters including Gonzalo and Maria Garca, Garfield Weston Foundation, Denise Leffman Trust and Mike Jackson, which has helped facilitate the work featured in this article.

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The path to least resistance: How our researchers are outsmarting cancers survival skills - Cancer Research UK News

Stem Cell Concentration System Market Research Report Contains Key Players, Industry Overview, Supply Chain, Analysis And Forecast To 2021- 2026 The…

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Stem Cell Concentration System Market Research Report Contains Key Players, Industry Overview, Supply Chain, Analysis And Forecast To 2021- 2026 The...

NEW HEMATOLOGY CHIEF AND DIRECTOR OF THE WESLEY CENTER FOR IMMUNOTHERAPY NAMED FOR UNIVERSITY HOSPITALS SEIDMAN CANCER CENTER – 69News WFMZ-TV

CLEVELAND, May 25, 2022 /PRNewswire/ -- One of America's top cancer doctors with a national and international reputation for cancer research will lead the new Wesley Center for Immunotherapy at University Hospitals Seidman Cancer Center as well as the Division of Hematology.

Koen van Besien, MD, PhD, comes to UH Seidman Cancer Center from New York-Presbyterian Hospital, where he has been Director of the Stem Cell Transplant Program and an attending physician. He is also a Professor of Medicine at Weill Cornell Medical College in New York City.

Dr. van Besien will lead the Wesley Center for Immunotherapy at UH Seidman Cancer Center, a cellular therapy facility that generates CAR-T, NK cell and other cellular-based therapies. Physician-scientists engage in groundbreaking research and bring new, life-extending immunotherapy treatments to patients. UH experts are creating cells for treatment in just eight days - an innovation that allows UH Seidman Cancer Center physicians to deliver life-enhancing therapy more quickly than previously possible.

With an established reputation for clinical research and care, Dr. van Besien has made numerous contributions to the field of cellular therapy and stem cell transplantation. Most recently, he has focused on methods to extend the use of transplantation to more patients in need. His group has recently reported the first successful transplant for a patient with HIV and leukemia using a haplo-cord graft - a unique procedure developed by his team. The patient remains free of HIV and leukemia more than four years after transplant.

Dr. van Besien is Editor in Chief of the Journal of Leukemia and Lymphoma and a member of the editorial review boards of the journals Bone Marrow Transplantation and Biology of Blood and Marrow Transplantation. His NIH-supported research has been published in more than 300 peer-reviewed papers.

Dr. van Besien completed medical school and clinical training at College ND de la Paix in Namur and the University of Leuven, both in Belgium. He holds a PhD from the University of Maastricht in the Netherlands. He completed his hematology/oncology fellowship at Indiana University and in Bruges, Belgium. Dr. van Besien has served on the faculty of MD Anderson Cancer Center in Houston. He also directed transplant programs at the University of Illinois for four years and at the University of Chicago for a decade.

He is fluent in five languages: English, Dutch, German, Spanish and French.

Dr. van Besien joins UH Seidman Cancer Center on July 15.

About University Hospitals Seidman Cancer Center/Cleveland, Ohio

UH Seidman Cancer Center is the only freestanding cancer hospital in Northeast Ohio, where all clinicians and staff are dedicated to the prevention, diagnosis and treatment of cancer while researching new and innovative treatment options through clinical trials. Nationally ranked cancer care is also available to patients through the 11-county region at 16 community-based locations. Our UH Seidman specialists make up 14 cancer-specific teams focused on determining integrated care plans tailored to patient's needs. UH Seidman Cancer Center is part of the National Cancer Institute (NCI)-designated Case Comprehensive Cancer Center at Case Western Reserve University, one of 52 comprehensive cancer centers in the country. Patients have access to advanced treatment options, ranging from a pioneering stem cell transplant program founded more than 40 years ago and a wide range of immunotherapy to the first and only proton therapy center in northern Ohio for adults and children. Go to UHhospitals.org/Seidman for more information.

About University Hospitals / Cleveland, Ohio Founded in 1866, University Hospitals serves the needs of patients through an integrated network of 23 hospitals (including five joint ventures), more than 50 health centers and outpatient facilities, and over 200 physician offices in 16 counties throughout northern Ohio. The system's flagship quaternary care, academic medical center, University Hospitals Cleveland Medical Center, is affiliated with Case Western Reserve University School of Medicine, Northeast Ohio Medical University, Oxford University and the Technion Israel Institute of Technology. The main campus also includes the UH Rainbow Babies & Children's Hospital, ranked among the top children's hospitals in the nation; UH MacDonald Women's Hospital, Ohio's only hospital for women; and UH Seidman Cancer Center, part of the NCI-designated Case Comprehensive Cancer Center. UH is home to some of the most prestigious clinical and research programs in the nation, with more than 3,000 active clinical trials and research studies underway. UH Cleveland Medical Center is perennially among the highest performers in national ranking surveys, including "America's Best Hospitals" from U.S. News & World Report. UH is also home to 19 Clinical Care Delivery and Research Institutes. UH is one of the largest employers in Northeast Ohio with more than 30,000 employees. Follow UH on LinkedIn, Facebook and Twitter. For more information, visit UHhospitals.org.

This news release was issued on behalf of Newswise(TM). For more information, visit http://www.newswise.com.

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SOURCE University Hospitals Cleveland Medical Center

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NEW HEMATOLOGY CHIEF AND DIRECTOR OF THE WESLEY CENTER FOR IMMUNOTHERAPY NAMED FOR UNIVERSITY HOSPITALS SEIDMAN CANCER CENTER - 69News WFMZ-TV

UAE powerhouse VPS Healthcare launches Burjeel Holdings to scale the next generation of its growth – PR Newswire

"Burjeel Holdings enables us to consolidate our healthcare offerings under one platform to create an integrated ecosystem, which will continue our vision to offer end-to-end health solutions under a single window. As we embark on our expansion journey, the platform will provide the foundation to scale up operations in new geographies in the GCC and beyond. It will also enable us to take strategic corporate actions needed to drive our future growth," said Dr. Shamsheer Vayalil, Chairman and Managing Director, VPS Healthcare. "We are proud to launch this exciting next phase of growth on the sidelines of the World Economic Forum Annual Meeting in Davos as a representation of our vision to explore, expand, and grow our capabilities."

Burjeel Holdings will operate nearly 60 assets catering to all socio-economic segments across a range of brands, including Burjeel Hospitals, Medeor Hospital, LLH Hospital, Lifecare Hospital, and Tajmeel. Its flagship facility, Burjeel Medical City, is the largest private hospital in the UAE and the only ESMO-accredited center. In addition to having renowned world-class centers of excellence, Burjeel Holdings consolidates the largest diagnostic network in the UAE and the largest comprehensive cancer center in the nation. Burjeel Holdings will be instrumental in continuing VPS Healthcare's mission of delivering quality and inclusive medical care to people around the world.

Connecting care, scale, and community to benefit refugees from Ukraine

Dr. Shamsheer began his entrepreneurial career with a vision to ensure healthcare equity. In his journey towards fulfilling this vision, he has also focused on outreach through humanitarian efforts. Alongside the launch of Burjeel Holdings, Dr. Shamsheer, a highly regarded philanthropist, announced a commitment of 50 pediatric stem cell transplantations to support Ukraine as well as additional support on behalf of those who join the pledge of support at Burjeel House in Davos.

Dr. Shamsheer and VPS Healthcare have been at the forefront of many humanitarian initiatives over the last 15 years. In 2018, VPS Healthcare enabled the treatment of Yemeni war victims at its hospitals in India. The organization offered the '100 Free Heart Surgeries' initiative for those in need as a tribute to the late H.H. Sheikh Zayed bin Sultan Al Nahyan.

"I am pleased to announce our commitment of support for those affected by the conflict in Ukraine. This contribution is being made toward the important task of rebuilding a strong community in the war-torn region. We have seen that children, especially those undergoing cancer treatment, are suffering the most in this very unfortunate conflict. Burjeel Holdings will look to provide them with the care they desperately need," said Dr. Shamsheer.

VPS Healthcare announced the launch of Burjeel Holdings and its commitment to supporting the Ukrainian refugees at the Burjeel House on the sidelines of the World Economic Forum Annual Meeting in Davos. The Burjeel House will convene intentional, collaborative dialogues on topics like catalyzing equitable health training, and advancing medical innovation.

Contact: M Unnikrishnan [emailprotected]

SOURCE Burjeel Holdings

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UAE powerhouse VPS Healthcare launches Burjeel Holdings to scale the next generation of its growth - PR Newswire

Cord Stem Cell Banking Market Trends Global Industry Analysis, Top Manufacturers, Growth, Opportunities & Forecast to 2028 The Daily Vale – The…

Global Cord Stem Cell Banking Marketsurvey report has been generated with the systematic gathering and evaluation of market information for industry which is presented in a form that explains various facts and figures to the business. This market research report contains a thorough analysis of the market and numerous related factors that range from market drivers, market restraints, market segmentation, opportunities, challenges, and market revenues to competitive analysis. It lends a hand to companies to take decisive actions to deal with threats in niche markets. A brilliant team of analysts, experts, statisticians, forecasters and economists has worked rigorously to generate an advanced and all-inclusive research market report.A research report is a professional and in-depth market report that focuses on primary and secondary drivers, market share, possible sales volume, leading segments and geographical analysis of A industry. It shows that the rise in market value is generally attributed to the rising growth of the application industries and the subsequent rise in demand of applications. This market analysis report gives an examination of various segments that are relied upon to witness the quickest growth amid the approximate forecast frame. The competitive landscape section of the A global business report brings into light a clear insight about the market share analysis of major industry players.

Thecord stem cell banking marketis expected to gain market growth in the forecast period of 2021 to 2028. Data Bridge Market Research analyses the market to grow at a CAGR of 22.2% in the above-mentioned forecast period. Increase in the number of parents storing their childs cord blood drives the cord stem cell banking market.

Get Sample Copy (Including Full TOC, List of Tables & Figures, and Chart) @https://www.databridgemarketresearch.com/request-a-sample/?dbmr=Global-Cord-Stem-Cell-Banking-Market

TOP KEY PLAYERS ofGlobal Clinical Trials MarketCord Stem Cell Banking Market

CBR Systems, Inc

Cordlife

Cells4Life Group LLP

Cryo-Cell International, Inc.

Cryo-Save AG

Lifecell

StemCyte India Therapeutics Pvt. Ltd

Viacord

SMART CELLS PLUS.

Cryoviva India

Global Cord Blood Corporation

National Cord Blood Program

Vita 34, ReeLabs Pvt. Ltd.

Regrow Biosciences Pvt. Ltd.

ACROBiosystems.

Americord Registry LLC.

New York Blood Center

Maze Cord Blood

GoodCell.

AABB

Stem Cell Cryobank

New England Cryogenic Center, Inc.

Market Scenario ofGlobal Clinical Trials MarketCord Stem Cell Banking Market

Cord stem cells banking is defined as the storing of the cord blood cell contained in the umbilical cord and placenta of a newborn child. This cord blood contains the stem cells which can be used in future to treat disease such as leukemia, thalassemia, autoimmune diseases, and inherited metabolic disorders, and few others.

Increased acceptance of stem cell therapeutics is the vital factor escalating the market growth, also rise in the new applications of stem cells indiseasetreatment, rise in the spending on the management of chronic diseases, rise in the growth in awareness about stem cell therapeutics and increase in the mergers and acquisitions by prominent players are the major factors among others driving the cord stem cell banking market. Moreover, rise in the technological advancements and modernization in the healthcare devices and risingresearch and developmentactivities in the healthcare sector will further create new opportunities for cord stem cell banking market in the forecasted period of 2021-2028.

However, high operating cost of stem cell therapeutics and lack of awareness in many developing economies are the major factors among others which will obstruct the market growth, and will further challenge the growth of cord stem cell banking market in the forecast period mentioned above.

The cord stem cell banking market report provides details of new recent developments, trade regulations, import export analysis, production analysis, value chain optimization, market share, impact of domestic and localised market players, analyses opportunities in terms of emerging revenue pockets, changes in market regulations, strategic market growth analysis, market size, category market growths, application niches and dominance, product approvals, product launches, geographic expansions, technological innovations in the market. To gain more info on the cord stem cell banking market contact Data Bridge Market Research for anAnalyst Brief, our team will help you take an informed market decision to achieve market growth.

Cord Stem Cell Banking MarketScope and Market Size

The cord stem cell banking market is segmented on the basis of storage type, product type, service type, source and indication. The growth amongst these segments will help you analyse meagre growth segments in the industries, and provide the users with valuable market overview and market insights to help them in making strategic decisions for identification of core market applications.

On the basis ofstorage type, the cord stem cell banking market is segmented into private banks, hybrid banks and public banks.

Based onproduct type, the cord stem cell banking market is segmented into cord blood, cord blood and cord tissue.

Based on service type, the cord stem cell banking market is segmented into collection & transportation, processing, analysis and storage.

Based on source, the cord stem cell banking market is segmented into umbilical cord blood, bone marrow, peripheral blood stem and menstrual blood

The cord stem cell banking market is also segmented on the basis of role of administration into cerebral palsy, thalassemia, leukemia, diabetes and autism.

This Report Answers the Following Questions:

What are the most significant market trends, challenges, and opportunities? How many segments will the market consist of? Which region is expected to dominate the market in terms of revenue? Which segment is likely to lead in terms of share in the coming years? What are the new strategies adopted by key players to strengthen their position?

Benefits of Purchasing of this Market Research Reports:

Customer Satisfaction:Our team of experts assists you with all your research needs and optimizes your reports. Analyst Support: Before or after purchasing the report, ask a professional analyst to address your questions. Assured Quality: Focuses on accuracy and quality of reports. Incomparable Skills: Analysts provide in-depth insights into reports.

To Gain More Insights into the Market Analysis, Browse Summary of the Research [emailprotected]https://www.databridgemarketresearch.com/reports/global-cord-stem-cell-banking-market

This Market Research Report Highlights:

Assessment of the market Premium Insights Competitive Landscape COVID Impact Analysis Historic Data, Estimates and Forecast Company Profiles Global and Regional Dynamics

Scope of Report:

Cord Stem Cell Banking Market survey report range from latest trends, market segmentation, new market entry, industry forecasting, target market analysis, future directions, opportunity identification, strategic analysis, insights to innovation. This report explains several market factors such as market estimates and forecasts, entry strategies, opportunity analysis, market positioning, competitive landscape, product positioning, market assessment and viability studies. Market drivers, market restraints, opportunities and challenges are also evaluated in this report under market overview which gives helpful insights to businesses for taking right moves. A market document is bestowed with full loyalty to provide the best service and recommendations.

A portion of the central issues canvassed in the report are: -Investigation of contenders -Whats Next -Market Data Forecast -Opportunity and Risks Assessment -Market Dynamics and Trends

Report Coverage- -It offers an all-encompassing business sector evaluation that remembers data for various market portions like innovation, arts, stage application, and others. -It incorporates an itemized investigation of the COVID-19 pandemics effect available. -It features different procedures taken on by significant market players to get development. -It features the most recent industry advancements. -It features market development surveyed by various topographical areas

Complete Report Details with Table of Content and [emailprotected]https://www.databridgemarketresearch.com/toc/?dbmr=Global-Cord-Stem-Cell-Banking-Market

Cord Stem Cell Banking MarketCountry Level Analysis

The cord stem cell banking market is analysed and market size insights and trends are provided by country, storage type, product type, service type, source and indication as referenced above.

The countries covered in the cord stem cell banking market report are U.S., Canada and Mexico in North America, Germany, France, U.K., Netherlands, Switzerland, Belgium, Russia, Italy, Spain, Turkey, Rest of Europe in Europe, China, Japan, India, South Korea, Singapore, Malaysia, Australia, Thailand, Indonesia, Philippines, Rest of Asia-Pacific (APAC) in the Asia-Pacific (APAC), Saudi Arabia, U.A.E, South Africa, Egypt, Israel, Rest of Middle East and Africa (MEA) as a part of Middle East and Africa (MEA), Brazil, Argentina and Rest of South America as part of South America.

North America dominates the cord stem cell banking market due to rise in the presence of major market participants in the US, ongoing approval of stem cell lines for disease treatment, and increasing awareness among citizens in this region. Asia-Pacific is the expected region in terms of growth in cord stem cell banking market due to rise in the older population along with as surge in prevalence of chronic diseases, and rising per capita healthcare expenditure in this region.

The country section of the cord stem cell banking market report also provides individual market impacting factors and changes in regulation in the market domestically that impacts the current and future trends of the market. Data points such as consumption volumes, production sites and volumes, import export analysis, price trend analysis, cost of raw materials, down-stream and upstream value chain analysis are some of the major pointers used to forecast the market scenario for individual countries. Also, presence and availability of global brands and their challenges faced due to large or scarce competition from local and domestic brands, impact of domestic tariffs and trade routes are considered while providing forecast analysis of the country data.

Healthcare Infrastructure growth Installed base and New Technology Penetration

The cord stem cell banking market also provides you with detailed market analysis for every country growth in healthcare expenditure for capital equipments, installed base of different kind of products for cord stem cell banking market, impact of technology using life line curves and changes in healthcare regulatory scenarios and their impact on the cord stem cell banking market. The data is available for historic period 2010 to 2019.

Competitive Landscape and Cord Stem Cell Banking MarketShare Analysis

The cord stem cell banking market competitive landscape provides details by competitor. Details included are company overview, company financials, revenue generated, market potential, investment in research and development, new market initiatives, global presence, production sites and facilities, production capacities, company strengths and weaknesses, product launch, product width and breadth, application dominance. The above data points provided are only related to the companies focus related to cord stem cell banking market.

Benefits of Purchasing this Market Research Reports:

Customer Satisfaction: Our team of experts assists you with all your research needs and optimizes your reports. Analyst Support: Before or after purchasing the report, ask a professional analyst to address your questions. Assured Quality:Focuses on accuracy and quality of reports. Incomparable Skills: Analysts provide in-depth insights into reports.

Global Cord Stem Cell Banking Marketbusiness report is a meticulous analysis of the existing scenario of the market, which covers several market dynamics. Competent data and brilliant forecasting techniques used in this market report are synonymous with accuracy and correctness. The report endows with the plentiful insights and business solutions that will support staying ahead of the competition. The most accurate way to forecast what the future holds is to understand the trend today and hence this report has been structured by chewing over numerous fragments of the present and upcoming market scenario. The world-class market research report is framed with the most excellent and sophisticated tools of collecting, recording, estimating, and analyzing market data..

The various aspects of A market survey report range from the latest trends, market segmentation, new market entry, industry forecasting, target market analysis, future directions, opportunity identification, strategic analysis, insights to innovation. This report explains several market factors such as market estimates and forecasts, entry strategies, opportunity analysis, market positioning, competitive landscape, product positioning, market assessment, and viability studies. Market drivers, market restraints, opportunities, and challenges are also evaluated in this report under market overview which gives helpful insights to businesses for taking right moves.

Key Highlights of Report: -Overview of key market forces propelling and restraining market growth -Offers a clear understanding of the competitive landscape and key product segments -An analysis of strategies of major competitors -Detailed analyses of industry trends -A well-defined technological growth map with an impact-analysis -Provides profiles of major competitors of the market. -Details of their operations, product and services. -Recent developments and key financial metrics.

Key Insights in the report: -Historical and current market size and projection up to 2029 -Market trends impacting the growth of the global taste modulators market -Analyze and forecast the taste modulators market on the basis of, application and type. -Trends of key regional and country-level markets for processes, derivative, and application -Company profiling of key players which includes business operations, product and services, geographic presence, recent developments and key financial analysis

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Data Bridge Market Research is a versatile market research and consulting firm with over 500 analysts working in different industries. We have catered more than 40% of the fortune 500 companies globally and have a network of more than 5000+ clientele around the globe. Our coverage of industries include Medical Devices, Pharmaceuticals, Biotechnology, Semiconductors, Machinery, Information and Communication Technology, Automobiles and Automotive, Chemical and Material, Packaging, Food and Beverages, Cosmetics, Specialty Chemicals, Fast Moving Consumer Goods, Robotics, among many others. We provide a variety of services such as market verified industry reports, technology trend analysis, Formative market research, strategic consulting, vendor analysis, production and demand analysis, consumer impact studies among many others.

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Cord Stem Cell Banking Market Trends Global Industry Analysis, Top Manufacturers, Growth, Opportunities & Forecast to 2028 The Daily Vale - The...