Dr. Flowers on Efforts to Improve Frontline Treatment in DLBCL – OncLive

Christopher Flowers, MD, discusses efforts to improve the frontline standard of care in diffuse large B-cell lymphoma.

Christopher Flowers, MD,department chair, Department of Lymphoma/Myeloma, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, discusses efforts to improve the frontline standard of care in diffuse large B-cell lymphoma (DLBCL).

The frontline standard of care therapy has not changed significantly over the past 20 years in DLBCL, Flowers says. In the early 2000s, it was observed that the addition of rituximab to standard CHOP (R-CHOP) therapy improved survival for elderly patients with DLBCL compared with CHOP alone, Flowers explains.

Although several research efforts have attempted to improve upon frontline R-CHOP, no survival advantages have been demonstrated, Flowers says. For example, randomized phase 3 trials evaluating intensified treatment approaches, stem cell transplantation, and the addition of novel agents, including bortezomib (Velcade), lenalidomide (Revlimid), and ibrutinib (Imbruvica), have been reported without demonstrating improvement vs R-CHOP in most patients with DLBCL, Flowers concludes.

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Dr. Flowers on Efforts to Improve Frontline Treatment in DLBCL - OncLive

Future Directions in the Treatment of Polycythemia Vera – OncLive

A thought leader in hematologic malignancies provides key insights into the future of treatment for polycythemia vera by considering the potential role of treatment sequencing or combination therapy.

EP. 1 : Myeloproliferative Neoplasms: Diagnosing Polycythemia Vera

EP. 2 : Risk Stratification and Treatment Considerations in PV

EP. 3 : PV Treatment Options and Dosing

EP. 4 : The JAK2 Pathway in Polycythemia Vera

EP. 5 : Ruxolitinib in PV: The RESPONSE Trial

EP. 6 : Ruxolitinib in PV: The RESPONSE-2 Trial

EP. 7 : Future Directions in the Treatment of Polycythemia Vera

Jamile Shammo, MD, FASCP, FACP: We now have optionsfor patients who have polycythemiavera [PV]. I know that other options may be available in the future for patients who have this entity. I think that its a good thing that we should be able to offer our patients multiple options.Clearly, patients whohavehad issues with enlarged spleen arent able to tolerate hydroxyurea, and people who had heavy burden with phlebotomy may not be able to tolerate phlebotomy,soruxolitinib presents a very good option for the treatment of their disease.For patients who are interested in having children in a few months, thismay represent a good option for them to achieve that goal.For patients who dont have that possibility or who had failedall ofthe abovetreatments, we will have clinical trials so that we can offer them novel agents that would have the potential for controlling their disease moving forward.

It would be important to see what the clinical trials would bring. I would think that combination therapies may be most helpful in more advanced disease entities like myelofibrosis where you can justify the risk of combination therapy because its a much more aggressive disease than it would be the case with PV.Perhaps you could consider that in advanced PV, or maybe you could consider this in patients with PV and multiple mutations.Ithas tobe considered in a certain group of patients. I dont know that I would necessarily consider combination therapy in all-comers with PV. Ithas tobe thought of in a rational fashion.

We need to understand this group of patients better on a molecular level.We know a lot about the landscape of their molecular profiles, but we know less about how to treat that. We know less about the landscape of people who relapseafter a particular treatmentand how to address thatparticular treatment, for example. We probably need to know more about how to utilize transplant in that setting.Theres a lot to be learned about how to use this.

Of course, there is also awhole slew of JAK[Janus kinase]inhibitors that may have various properties as well. It isinteresting to think about utilizing them pre-and post-transplant. Thereare a whole slew of biological agents that could be combined with JAK inhibitors to see how we can make the most out of that combination. We can learnhowthey canbe explored either alone or in combination with stem cell transplantation.Theres a lot that needs to be done, but all thathas tobe done in the context of a clinical trial.It probably starts with understanding more about the disease biology,taking it to some type of a clinical trial, andkeeping our eyes opentoget an observation to translate that into some type of conclusion that may be beneficial to patients.

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FDA Grants Priority Review to Genentech’s Tecentriq as Adjuvant Treatment for Certain People With Early Non-small Cell Lung Cancer – Business Wire

SOUTH SAN FRANCISCO, Calif.--(BUSINESS WIRE)--Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY), today announced that the U.S. Food and Drug Administration (FDA) has accepted the companys supplemental Biologics License Application (sBLA) and granted Priority Review for Tecentriq (atezolizumab) as adjuvant treatment following surgery and platinum-based chemotherapy for people with non-small cell lung cancer (NSCLC) whose tumors express PD-L11%, as determined by an FDA-approved test. The FDA is reviewing the application under the Real-Time Oncology Review pilot program, which aims to explore a more efficient review process to ensure safe and effective treatments are available to patients as early as possible. The FDA is expected to make a decision on approval by December 1, 2021.

New treatment options are urgently needed in early-stage non-small cell lung cancer to help the nearly 50% of people who currently experience a recurrence following surgery, said Levi Garraway, M.D., Ph.D., chief medical officer and head of Global Product Development. Tecentriq is the first cancer immunotherapy to show a clinically meaningful benefit in the adjuvant lung cancer setting, and were working closely with the FDA to bring this significant advancement to patients as quickly as possible.

This application is based on disease-free survival (DFS) results from an interim analysis of the Phase III IMpower010 study, the first and only Phase III study of a cancer immunotherapy to demonstrate positive results in the adjuvant lung cancer setting. The study showed that treatment with Tecentriq following surgery and platinum-based chemotherapy reduced the risk of disease recurrence or death (DFS) by 34% (hazard ratio [HR]=0.66, 95% CI: 0.50-0.88) in people with Stage II-IIIA NSCLC whose tumors express PD-L11%, compared with best supportive care (BSC). In this population, median DFS was not yet reached for Tecentriq compared with 35.3 months for BSC. Follow-up on the IMpower010 trial will continue with planned analyses of DFS in the overall intent-to-treat (ITT) population, including Stage IB patients, which at the time of analysis did not cross the threshold, and overall survival (OS) data, which were immature at the time of interim analysis. Safety data for Tecentriq were consistent with its known safety profile and no new safety signals were identified. Results from the IMpower010 trial were presented at the 2021 ASCO Annual Meeting.

About the IMpower010 study

IMpower010 is a Phase III, global, multicenter, open-label, randomized study evaluating the efficacy and safety of Tecentriq compared with BSC, in participants with Stage IB-IIIA NSCLC (UICC 7th edition), following surgical resection and up to 4 cycles of adjuvant cisplatin-based chemotherapy. The study randomized 1,005 people with a ratio of 1:1 to receive either Tecentriq (up to 16 cycles) or BSC. The primary endpoint is investigator-determined DFS in the PD-L1-positive Stage II-IIIA, all randomized Stage II-IIIA and ITT Stage IB-IIIA populations. Key secondary endpoints include OS in the overall study population, ITT Stage IB-IIIA NSCLC.

About lung cancer

According to the American Cancer Society, it is estimated that more than 235,000 Americans will be diagnosed with lung cancer in 2021, and NSCLC accounts for 80-85% of all lung cancers. Today, about half of all people with early lung cancer still experience a cancer recurrence following surgery, but treating lung cancer early, before it has spread, may help prevent the disease from returning and provide people with the best opportunity for a cure.

About Tecentriq (atezolizumab)

Tecentriq is a monoclonal antibody designed to bind with a protein called PD-L1. Tecentriq is designed to bind to PD-L1 expressed on tumor cells and tumor-infiltrating immune cells, blocking its interactions with both PD-1 and B7.1 receptors. By inhibiting PD-L1, Tecentriq may enable the re-activation of T cells. Tecentriq may also affect normal cells.

Tecentriq U.S. Indications

Tecentriq is a prescription medicine used to treat adults with:

A type of lung cancer called non-small cell lung cancer (NSCLC).

A type of lung cancer called small cell lung cancer (SCLC).

It is not known if Tecentriq is safe and effective in children.

Important Safety Information

What is the most important information about Tecentriq?

Tecentriq can cause the immune system to attack normal organs and tissues in any area of the body and can affect the way they work. These problems can sometimes become severe or life threatening and can lead to death. Patients can have more than one of these problems at the same time. These problems may happen anytime during their treatment or even after their treatment has ended.

Patients should call or see their healthcare provider right away if they develop any new or worse signs or symptoms, including:

Lung problems

Intestinal problems

Liver problems

Hormone gland problems

Kidney problems

Skin problems

Problems can also happen in other organs.

These are not all of the signs and symptoms of immune system problems that can happen with Tecentriq. Patients should call or see their healthcare provider right away for any new or worse signs or symptoms, including:

Infusion reactions that can sometimes be severe or life-threatening. Signs and symptoms of infusion reactions may include:

Complications, including graft-versus-host disease (GVHD), in people who have received a bone marrow (stem cell) transplant that uses donor stem cells (allogeneic). These complications can be serious and can lead to death. These complications may happen if patients undergo transplantation either before or after being treated with Tecentriq. A healthcare provider will monitor for these complications.

Getting medical treatment right away may help keep these problems from becoming more serious. A healthcare provider will check patients for these problems during their treatment with Tecentriq. A healthcare provider may treat patients with corticosteroid or hormone replacement medicines. A healthcare provider may also need to delay or completely stop treatment with Tecentriq if patients have severe side effects.

Before receiving Tecentriq, patients should tell their healthcare provider about all of their medical conditions, including if they:

Patients should tell their healthcare provider about all the medicines they take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.

The most common side effects of Tecentriq when used alone include:

The most common side effects of Tecentriq when used in lung cancer with other anti-cancer medicines include:

Tecentriq may cause fertility problems in females, which may affect the ability to have children. Patients should talk to their healthcare provider if they have concerns about fertility.

These are not all the possible side effects of Tecentriq. Patients should ask their healthcare provider or pharmacist for more information about the benefits and side effects of Tecentriq.

Report side effects to the FDA at 1-800-FDA-1088 or http://www.fda.gov/medwatch.

Report side effects to Genentech at 1-888-835-2555.

Please see http://www.Tecentriq.com for full Prescribing Information and additional Important Safety Information.

About Genentech in cancer immunotherapy

Genentech has been developing medicines to redefine treatment in oncology for more than 35 years, and today, realizing the full potential of cancer immunotherapy is a major area of focus. With more than 20 immunotherapy molecules in development, Genentech is investigating the potential benefits of immunotherapy alone, and in combination with various chemotherapies, targeted therapies and other immunotherapies with the goal of providing each person with a treatment tailored to harness their own unique immune system.

In addition to Genentechs approved PD-L1 checkpoint inhibitor, the companys broad cancer immunotherapy pipeline includes other checkpoint inhibitors, individualized neoantigen therapies and T cell bispecific antibodies. For more information visit http://www.gene.com/cancer-immunotherapy.

About Genentech in lung cancer

Lung cancer is a major area of focus and investment for Genentech, and we are committed to developing new approaches, medicines and tests that can help people with this deadly disease. Our goal is to provide an effective treatment option for every person diagnosed with lung cancer. We currently have five approved medicines to treat certain kinds of lung cancer and more than 10 medicines being developed to target the most common genetic drivers of lung cancer or to boost the immune system to combat the disease.

About Genentech

Founded more than 40 years ago, Genentech is a leading biotechnology company that discovers, develops, manufactures and commercializes medicines to treat patients with serious and life-threatening medical conditions. The company, a member of the Roche Group, has headquarters in South San Francisco, California. For additional information about the company, please visit http://www.gene.com.

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FDA Grants Priority Review to Genentech's Tecentriq as Adjuvant Treatment for Certain People With Early Non-small Cell Lung Cancer - Business Wire

Cellino Appoints Industry Pioneer Robert J. Palay to the Board – Business Wire

CAMBRIDGE, Mass.--(BUSINESS WIRE)--Cellino, a personalized regenerative medicine company developing an AI-guided laser editing platform for autologous cell-based therapies, today announced the appointment of industry pioneer Robert J. Palay, J.D., M.B.A., to the Cellino Board of Directors.

Mr. Palay is one of the pioneers of the induced pluripotent stem cell (iPSC) industry. He was Founder, Chairman of the Board, and Chief Executive Officer of Cellular Dynamic International (NASDAQ: ICEL), one of the first companies to harness IPSCs and their derivatives for use in drug discovery and therapeutics. CDI was acquired by FujiFilm for $307M in 2015. Prior to Cellular Dynamic International, he was a co-founder and Chairman of the Board of NimbleGen Systems, a early adopter of light directed synthesis for manufacturing genomic micro-arrays. NGS was acquired by Roche in 2007 for $272.5M. He was previously a Fellow at Harvards Advanced Leadership Initiative where he focused on emerging biothreats.

"We are pleased to welcome Robert to the Cellino Board," said Nabiha Saklayen, Ph.D, CEO & Co-Founder, Cellino. "Roberts deep experience in pioneering the light-directed synthesis and iPSC industries will be invaluable to Cellino as we grow our business at that unique interface and pursue our mission to serve patients."

"I am thrilled to join the Cellino Board," said Robert J. Palay. "Cellinos platform is the future of the stem cell industry. They have the unique ability to bring laser precision and artificial intelligence to the manufacture of IPSCs and their derivative cells. Their innovation offers a clear path to dramatic improvements in the quality and quantity of manufactured human cells, while simultaneously dramatically reducing cost. No one else has technology offering such a robust and powerful platform."

Mr. Palay was also a co-founder and Chairman of the Board of Genetic Assemblies, a synthetic biology company, which was acquired by Codon Devices in 2006. Mr. Palay is currently Chairman of Tactics II Equity LLC, a life science investment and advisory firm. He is currently a member of the board of directors of the Center for Strategic Risks and a founder of the Alliance to End Biological Threats. Mr. Palay received a J.D. and M.B.A. from Northwestern University, and an A.B. from Harvard College.

About Cellino

Cellino is an autologous regenerative medicine company developing an AI-guided single-cell laser editing platform for cell-based therapies. The company has developed a scalable platform that automates and standardizes autologous stem cell production, accelerating the development of life-saving medicines for patients. Cellino is based in Cambridge, MA. For additional information, please visit http://www.cellinobio.com.

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Cellino Appoints Industry Pioneer Robert J. Palay to the Board - Business Wire

Tachyon and AbCellera Collaborate to Develop Novel Antibody Therapeutic Targeting TGF- Superfamily Member for the Treatment of Cancer – Yahoo Finance

LEFTY1, a secreted dual inhibitor of the NODAL/SMAD2 and BMP7/SMAD5 pathway, is implicated in driving cancer stem cell biology and unregulated tumor cell growth

HOUSTON & VANCOUVER, British Columbia, August 03, 2021--(BUSINESS WIRE)--Tachyon Therapeutics, Inc. (Tachyon), a research and development focused biotechnology company, and AbCellera (Nasdaq: ABCL), a technology company with a centralized operating system for next-generation antibody discovery, today announced a collaboration to facilitate the discovery and development of a therapeutic antibody targeting LEFTY1, a member of the transforming growth factor (TGF-) superfamily and validated extracellular drug target expressed in advanced cancers. Under the terms of the agreement, AbCellera is eligible to receive milestone payments and royalties on products that are derived from its antibody discovery platform. In addition, AbCellera has the option to invest in preclinical and clinical development in exchange for an increased share of product sales.

"At Tachyon, we are focused on innovation, precision, science, and speed to develop first-in-class therapeutics against significant new drug targets in cancer biology," said Frank Perabo, M.D., Ph.D., Chief Executive Officer of Tachyon. "AbCellera has consistently demonstrated these four qualities as they accelerate the discovery of first-in-class therapeutic antibodies for novel biology. We look forward to working with their team to target LEFTY1, a major signaling regulator of the TGF- superfamily, and unlock a new pathway to treat advanced cancers."

Members of the TGF- superfamily control numerous cellular functions, including proliferation, apoptosis, differentiation, epithelial-mesenchymal transition, adhesion, and migration. Because of their ubiquitous and regulatory roles in both normal and cancer cell biology, TGF- superfamily members, such as LEFTY1 are highly sought after, yet challenging drug targets. Research led by Tachyons scientific founder, Michael F. Clarke, Ph.D., who was the first to identify and characterize cancer stem cells in solid tumors, revealed that LEFTY1 suppresses NODAL/SMAD2 and BMP7/SMAD5 pathways to promote long-term proliferation of normal and malignant mammary epithelial cells.1 As a secreted extracellular protein, LEFTY1 represents an important target to control SMAD-dependent signals that promote the long-term growth and self-renewal of cancer stem cells.

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"Our collaboration with Tachyon represents an opportunity to expedite the translation of breakthrough research of a novel and significant cancer drug target into a first-in-class antibody therapeutic for patients with advanced cancers and limited treatment options," said Carl Hansen, Ph.D., CEO of AbCellera. "This collaboration exemplifies innovative deal structures that align our interest with our partners and provides AbCellera with optionality to deepen our participation in the success of the antibodies we discover. We are excited to partner with Tachyon to pursue a previously unexplored mechanism and develop therapies that we anticipate will impact cancer treatment."

1. Zabala, et al., LEFTY1 Is a Dual-SMAD Inhibitor that Promotes Mammary Progenitor Growth and Tumorigenesis. Cell Stem Cell. 2020.

About Tachyon Therapeutics Inc.

Tachyon Therapeutics, Inc. is a R&D focused biotechnology company developing novel, first-in-class therapeutics for the treatment of advanced cancers. Tachyon operates with a dedicated internal core development team and a virtual external network of expertise to achieve one goal advance development of promising drug targets with speed and innovation, without compromising the quality or integrity of science. For more information, please visit http://www.tachyontx.com.

About AbCellera Biologics Inc.

AbCellera is a technology company that searches, decodes, and analyzes natural immune systems to find antibodies that its partners can develop into drugs to prevent and treat disease. AbCellera partners with drug developers of all sizes, from large pharmaceutical to small biotechnology companies, empowering them to move quickly, reduce cost, and tackle the toughest problems in drug development. For more information, please visit http://www.abcellera.com.

AbCellera Forward-looking Statements

This press release contains forward-looking statements, including statements made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. The forward-looking statements are based on managements beliefs and assumptions and on information currently available to management. All statements contained in this release other than statements of historical fact are forward-looking statements, including statements regarding our ability to develop, commercialize and achieve market acceptance of our current and planned products and services, our research and development efforts, and other matters regarding our business strategies, use of capital, results of operations and financial position, and plans and objectives for future operations.

In some cases, you can identify forward-looking statements by the words "may," "will," "could," "would," "should," "expect," "intend," "plan," "anticipate," "believe," "estimate," "predict," "project," "potential," "continue," "ongoing" or the negative of these terms or other comparable terminology, although not all forward-looking statements contain these words. These statements involve risks, uncertainties and other factors that may cause actual results, levels of activity, performance, or achievements to be materially different from the information expressed or implied by these forward-looking statements. These risks, uncertainties and other factors are described under "Risk Factors," "Management's Discussion and Analysis of Financial Condition and Results of Operations" and elsewhere in the documents we file with the Securities and Exchange Commission from time to time. We caution you that forward-looking statements are based on a combination of facts and factors currently known by us and our projections of the future, about which we cannot be certain. As a result, the forward-looking statements may not prove to be accurate. The forward-looking statements in this press release represent our views as of the date hereof. We undertake no obligation to update any forward-looking statements for any reason, except as required by law.

Source: AbCellera Biologics Inc.

View source version on businesswire.com: https://www.businesswire.com/news/home/20210803005352/en/

Contacts

Tachyon Inquiries Frank Perabo, M.D., Ph.D., Chief Executive Officer; ir@tachyontx.com, +1 (832) 952-0829

AbCellera Inquiries Media: Jessica Yingling, Ph.D., media@abcellera.com, +1 (236) 521-6774 Business Development: Neil Berkley, bd@abcellera.com, +1 (604) 559-9005 Investor Relations: Melanie Solomon, ir@abcellera.com, +1 (778) 729-9116

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Tachyon and AbCellera Collaborate to Develop Novel Antibody Therapeutic Targeting TGF- Superfamily Member for the Treatment of Cancer - Yahoo Finance

Sophomore saves sister’s life with stem cell donation – University of Miami

After a live-saving transplant to overcome leukemia, Sophia Nealon teamed up with her sister to create Bye, Bye, Bad Blood, a creative childrens tale that aims to teach young cancer patients about their diagnosis and prepare them and their families for what is to come.

For Sophia Nealon, saving her sisters life was by far the easiest decision she has ever made.

It took a simple swab from me and our entire family to see who had the highest DNA match percentage, said the Osprey, Florida, resident who studies chemistry at the University of Miami. l was a 100 percent match to be my sisters bone marrow transplant donor.

When the family traveled to New York City for a younger sisters birthday, it became obvious to them that something was wrong because Kassandra Nealon got sick again. Once back home in Florida, she went to see a doctor and the family got the devastating news. Kassandra Nealon, Sophias older sister and recipient of the life-saving stem cell transplant, was diagnosed with Acute T-Cell Lymphoblastic Leukemia at 23 years old, after becoming repeatedly ill with flu-type symptoms in late 2019.

They told her that she had two liters of fluid on her lungs, which was making regular tasks exhausting, said Nealon. Her doctors originally thought it was lymphoma but after testing her blood count, they shared with us that it was actually a type of leukemia. It was a big shock to everyone.

Following the diagnosis, the day-to-day routine of the Nealon family underwent a drastic change, as Kassandra Nealons appointments were located miles away in Tampa. Then the world entered a global pandemic. During this time, Nealon enrolled in her first semester as a University of Miami student, opting to complete the semester remotely.

My mom was the only one allowed at my sisters appointments, so it took a lot of coordination, but we figured out a system that worked for uslike staying in Airbnbs for some weekends and utilizing FaceTime to be with her during her chemo and radiation appointments, she said.

The type of cancer Nealons sister had is commonly diagnosed in young children and is rare in adults. After so many visits to various doctors offices, Kassandra Nealon noticed that there werent many books explaining the specific cancer that is faced mostly by adolescents.

Motivated by her friends and family, Kassandra Nealon felt compelled to create Bye, Bye, Bad Blood, a childrens book that lightheartedly explains the cancer to children and their families. Kassandra Nealon looked to none other than her sister, who draws as a hobby, to illustrate the book.

We decided to sell and market the book through Amazon because it would allow us to make the most profit, said Nealon, who had no prior knowledge about self-publishing a book.

That profit margin was important to Nealon and her sister because 100 percent of it goes directly to the Leukemia and Lymphoma Society,the largest voluntary health organization dedicated to fighting blood cancer in the world.

You dont know who youre helping out and how much you can change someones life with your donation, said Nealon, who also encourages the campus community to sign up with BeTheMatch.com to become a stem cell transplant donor. Becoming a donor is super easy and takes seconds of your time.

Nealons sister is now in remission. While promoting her book, she is determined to finish her medical school applicationsa process that was abruptly stopped as she battled cancer.

Those interested in donating a book to a childrens cancer treatment center or purchasing the book can visit byebyebadblood.com.

To learn more about stem cell transplants at Sylvester Comprehensive Cancer Center, visithttps://umiamihealth.org/en/sylvester-comprehensive-cancer-center/treatments-and-services/hematologic-(blood)-cancers-/bone-marrow-and-stem-cell-transplant.

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Sophomore saves sister's life with stem cell donation - University of Miami

Myelodysplastic Syndrome Treatment Options – Healthline

Your bone marrow produces immature blood cells, also called stem cells. These then develop into one of three types of mature blood cells:

If you have MDS, not all of these stem cells mature. As a result, immature cells can remain in the bone marrow or die. You will have lower levels of mature blood cells in your bloodstream.

A reduced mature blood cell count is a condition known as cytopenia, and its a main characteristic of MDS. A blood test known as a complete blood count (CBC) is one of the first diagnostic tests your doctor will order if they suspect you have MDS.

Removing bone marrow samples through aspiration and biopsy can also help your doctor better understand the nature of your blood marrow disorder. Once your doctor has diagnosed and treated your MDS, these tests can also show how well your bone marrow is responding to treatment.

You will often have a healthcare team if you have this type of disorder, which may include:

The team will develop a treatment plan thats partially based on the type of MDS you have. The World Health Organization (WHO) identifies six main types of MDS.

Your treatment plan may also be based on the prognostic score (outlook for survival) of the disease. MDS is different from most forms of cancer, which are grouped in stages and grades, because its scored on several factors, including:

Before you start MDS treatment, you might also consider your:

Next, well discuss each of the main treatment options for this group of diseases.

Supportive therapy is meant to treat MDS symptoms and prevent complications, rather than treat the underlying disorder itself. Supportive therapy is often used alongside other treatments.

Examples of supportive therapy include:

Lenalidomide is a type of medication called an immunomodulatory agent. Your doctor may suggest this oral medication if you have MDS and a certain genetic change known as an isolated del(5q) chromosome abnormality.

Lenalidomide helps boost red blood cell production in your bone marrow. Its designed to reduce your dependence on blood transfusions.

Experts in a 2017 research review called it an excellent option for MDS patients with low or intermediate disease risk. Potential side effects include:

Antithymocyte globulin is in a large group of drugs known as immunosuppressants that weaken the bodys immune response. Organ transplant recipients usually take them to help prevent rejection of the new organ. You may take antithymocyte globulin to keep your immune system from attacking stem cells in your bone marrow.

Immunosuppressant therapy may be appropriate for you if you have lower-risk MDS and havent had effective results with ESAs and transfusions. You might also try it if you have one or more autoimmune diseases.

One 2018 study found that antithymocyte globulin was effective in about 50 percent of the MDS cases studied.

Certain chemotherapy drugs, known as hypomethylating agents, activate specific genes in your stem cells to help them mature. Two examples of these agents are azacitidine and decitabine. These drugs are used when your doctor determines there is a serious risk for leukemia, which is a serious potential complication of MDS.

Chemotherapy can help improve blood cell counts, sometimes to the point where you no longer need transfusions, and reduce your risk of leukemia. Potential side effects include:

Other chemotherapy drugs may be given with the goal of killing atypical stem cells and allowing more of your healthy cells to mature.

While high-dose chemotherapy drugs can be very effective at sending MDS into remission, the side effects can be severe. You could experience a serious drop in white blood cells, and later, a greater risk of infections developing and progressing quickly.

A stem cell transplant involves removing some of your bone marrow, usually from the pelvic bone, and replacing it with bone marrow that produces healthy blood cells.

The procedure is usually reserved for more serious cases of MDS. Stem cell transplant is the closest treatment option to a cure, but its an invasive and challenging therapy. Because of this, stem cell transplant is limited to people who are considered healthy enough for both the procedure and the recovery process.

Doctors often use chemotherapy drugs with stem cell transplant to treat MDS. Together, they help support the growth of healthy blood cells to replace unhealthy or atypical cells.

While transplants are often very effective at achieving disease remission, particularly in certain patients, the Aplastic Anemia and MDS International Foundation says that a majority of MDS patients will see their condition return over time.

MDS can affect anyone at any age but generally affects adults ages 70 and older. According to the American Cancer Society (ACS), about 10,000 people are diagnosed with MDS in the United States per year.

Disease outcomes vary considerably. Its difficult to predict someones outcome because people respond differently to treatment.

ACS survival statistics range from a median survival of 8.8 years for people with a very low risk score to less than 1 year for MDS patients with a very high risk score.

These survival rates are based on data that includes years before treatments like chemotherapy were available. Its important to remember that researchers are continuing to develop new treatments that may improve disease outcomes.

You may have no symptoms early on or if you have mild MDS. However, for most people with the disease, anemia (low red blood cell counts) and symptoms such as chronic fatigue and shortness of breath are common.

If you have low white blood cell counts, the risk of serious infection may always be present. Low platelet counts can lead to easy bruising and bleeding complications.

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Gold River Productions, Inc. (GRPS) Appoints Michael Berkowitz to spearhead the Rejuvenation Division with StemSpa – Yahoo Finance

Palm Coast, FL, Aug. 04, 2021 (GLOBE NEWSWIRE) -- After months of careful consideration, Gold River Productions, Inc. (OTC Pink: GRPS) (GRPS) opens its Rejuvenation Division and to welcome Michael Berkowitz as the newest member to the Gold River Team. His extensive background in the transformative field of cell-based therapy provides a significant pathway for sustainable revenue and directly compliments our new herbal formulations. With the coupling of our current product line and the considerable advances in stem cell therapeutic development, our direction brings viable attractive options to those suffering from an expansive range of degenerative conditions.

According to Fortune Business Insights, the global stem cells market is projected to grow from $11.90 billion in 2021 to $27.65 billion in 2028 at a CAGR of 12.8%. The factors contributing to the growth include increasing demand for biologics, technological advancement in pluripotential cell therapeutics, and a rising focus on the development of personalized medicines. The growing prevalence of chronic diseases worldwide is anticipated to boost demand through 2028.

As resourcing options are realized, the company intends to bring physical presence to these dynamic and unique options by offering a number of primary free-standing facilities to supply and educate our rapidly growing physician network.

Commenting as the newest member of the team, I am humbled by the support and dedication of Dr. Goulding and his associates at GRPS. Dr. Goulding shares my vision. Ive personally witnessed the effects that stem cells can have with appropriate administration and dosing in over 5000 cases, says Mr. Berkowitz, who will head the Rejuvenation Division of the GRPS subsidiary StemSpa. Ive worked with a number of universities and FDA approved manufacturers in recording and reporting data. Weve been involved in studies including M.S., joint issues, PTSD, and cancer. Im eager for the opportunity to continue and expand this with GRPS.

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Berkowitz continued, What intrigues me most about Dr. Bond and Dr. Goulding is how their products work in concert with pluripotential cells, and our InflammaplexTM formulation will serve as a foundation of support for the cells. Furthermore, almost anyone seeking relief will require adjunctive anti-inflammatory products for their pain and underlying issues. Empowering doctors with these unique adjuvants and giving their patients access to more preferable choices will be a game-changer.

Continuing, he stated, We are in negotiations to construct stand-alone facilities in strategic locations to establish StemSpa, which will serve as centers of excellence in the United States and offshore. We will begin with approximately 1000 doctors thanks to the relationship built between GRPS, heliosDx, and CEO Ashley Sweat of Rushnet (OTC Pink: RSHN). Im very excited to have doctors in this continuously expanding group utilize our inflammatory-reducing product line and have our technology at their fingertips. This will offer an amazing alternative to their patients as well as help us develop broad data collection and deliver data that these biologics are not only effective, but in the right hands and with the right techniques, possess endless possibilities to those suffering.

We are excited to have Mr. Berkowitz on board, says Richard Goulding, M.D., Chairman of the Board of GRPS. Mr. Berkowitz has been involved with over 5000 cases utilizing biologics and pluripotential cells and has a great deal of experience not only procuring appropriate cells, but in targeting specific concerns. The amount of video footage and anecdotal evidence is quite compelling. Theres a tremendous fit here, and the possibilities are exciting. Furthermore, we suspect that, with the proper base of nutrient support, we are optimizing the conditions for obtaining maximum efficacy with these techniques. We intend to be an industry leader for proper technique, procurement, and nutritional support in this complex field.

About Gold River Productions, Inc. Dedicated to changing peoples lives, Gold River is a groundbreaking company aiming at improving quality of life and longevity. Our diverse products and interests include nutraceuticals, CBD, land, education and more. With a unique staff of talented physicians, cultivators, and CBD experts, we are poised to tackle different disease states at an unprecedented level. Utilizing years of experience in herbals, rare cannabinoids, traditional and non-traditional methods of patient care, we are in the unique position to utilize CBD and herbals in the most effective ways possible. Emphasis on what already works, then augmenting effective formulas with high-quality cannabinoids in therapeutic levels, can achieve unprecedented symptom control in a myriad of disease states.

This document contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, which are subject to a number of risks and uncertainties, many of which are outside Gold Rivers control. These include but are not limited to the impact of competitors products, services and pricing; product demand; market acceptance; new product development; reliance on key strategic alliances; the regulatory environment; fluctuations in operating results; and other risks which are detailed from time to time in the Companys filings with the Securities and Exchange Commission and/or OTC Markets. Gold River Productions disclaims any obligation to update or alter its forward-looking statements whether as a result of new information, subsequent events or otherwise.

CONTACT: Gold River Productions, Inc. info@grpsinc.com http://www.GRPSInc.com

About heliosDx: heliosDX is a National Clinical Reference Laboratory offering High-Complexity Urine Drug Testing (UDT), Behavioral Drug Testing, Allergy Droplet Cards, Oral Fluids, Infectious Disease (PCR), and NGS Genetic Testing. We are contracted in 44 of the lower 48 states and looking to expand our reach and capabilities. Always staying ahead of the curve, by continually investing in our infrastructure with the most efficient scientific proven instruments, and latest cutting-edge software for patient and physician satisfaction. This allows heliosDX to provide physicians fast and accurate reporting meeting and exceeding industry benchmarks. We excel in patient and client care through physician designed panels that aid in testing compliance and reporting education.

Contact: Ashley Sweat asweat@heliosdx.com http://www.heliosdx.com (Under Development) @dx_helios

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Gold River Productions, Inc. (GRPS) Appoints Michael Berkowitz to spearhead the Rejuvenation Division with StemSpa - Yahoo Finance

Colin Jackson health: Im in constant pain Athlete to undergo stem cell therapy to help – Express

Colin Ray Jackson, CBE, 54, is a Welsh former sprinter and hurdling Olympic silver medal champion. Colins world record for his 60 metres hurdles stood for an incredible 27 years. As with most athletes of his calibre, Colin suffers with ongoing injuries from his sports days and will be undergoing a treatment to reduce the pain which Mike Tyson recently underwent too.

In recent years, stem cell therapy has been hailed as a miracle cure for many conditions, from wrinkles to spinal repair.

A stem cell is an immature, basic cell that has not yet developed to become, say, a skin cell or a muscle cell or a nerve cell.

There are different types of stem cells that the body can use for different purposes.

There is evidence that stem cell treatments work by triggering damaged tissues in the body to repair themselves, often referred to as regenerative therapy.

In animal studies, stem cell treatments have shown promise for various diseases, including heart disease, Parkinsons disease and muscular dystrophy.

A study undertaken by Dr Timothy McGuine found that 34 percent of athletes involved in the one-year study were more likely to report a history of knee and hip injuries.

Additionally, he found that specialised athletes, such as those competing in the Olympic games, were twice as likely to sustain a gradual onset or repetitive use injuries than athletes who did not specialise.

Dr McGuine also found that these athletes who find themselves competing year-round, stressing the same muscles and movements, and predisposed to the symptoms of burnout are at higher risk of long-term injuries.

Many doctors and athletes use stem cell therapy to treat sports injuries, such as Achilles tendinopathy or damaged knee ligaments, said Sports Health.

The site continued: While increasing in popularity, stem cell therapy is not considered standard practice by sports medicine doctors and not covered by most insurance companies.

The process of collecting stem cells is often called harvesting. Physicians usually harvest stem cells from the patients fat, blood, or bone marrow.

Many physicians who use stem cell therapy hypothesize that, when placed into a certain environment, stem cells can transform to meet a certain need.

Other sports stars who underwent stem cell therapy for long-term injuries included Cristiano Ronaldo, Rafael Nadal and most recently Mike Tyson.

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Colin Jackson health: Im in constant pain Athlete to undergo stem cell therapy to help - Express

The Basics of MDS: Diagnosis and Staging – Curetoday.com

Myelodysplastic syndromes, known commonly as MDS, are a group of bone marrow diseases characterized by bone marrow failure, or an inadequate production of blood counts called cytopenia.

In a presentation at the CURE Educated Patient Leukemia Summit, Dr. Rami Komrokji, section head for Leukemia and MDS and Vice Chair of the Department of Malignant Hematology at Moffit Cancer Center, gave a run down on the diagnosis and staging process for MDS.

Diagnosing MDS

Komrokji explained that the myelo- prefix means bone marrow, and -dysplasia means abnormal-looking cells. When a patient has cytopenia, they may experience certain symptoms.

If patient is anemic, they will have shortness of breath, fatigue, palpitations, said Komrokji in an interview with CURE. If they have low platelets, they will have bleeding tendency, bruising. If they have low white blood cell counts, they will have maybe infections. So usually, either some of those symptoms will prompt blood testing, or on routine physical exam, the patients are found to have low blood counts. So that's usually the initial step.

Doctors will usually look into nutritional deficiencies such as B12, folate and ferritin, said Komrokji. Eventually, the patients will get a bone marrow aspirate and biopsy to diagnose their disease, which includes several parts.

There is the morphologic part, which means the pathologists are looking at the cells under a microscope, explained Komrokji. And then there is also some genetic testing. We look at cytogenetics nowadays, we look at gene mutations. So we put all of this information together to make the diagnosis.

The hematopathologist must see dysplasia, increased myeloblasts (immature cells known as blasts within the bone marrow) or certain cytogenetic abnormalities to make their diagnosis, Komrokji said.

Sometimes the diagnosis is straightforward, but sometimes it could be challenging, he added. It truly depends on an experienced hematopathologist to make the diagnosis.

Staging and Risk Stratification

Once a patient receives an MDS diagnosis, their doctor will go over risk stratification, or understanding what the risk of their disease is, which is what they consider staging, Komrokji said.

Now in MDS, its not like a lung cancer or colon cancer, he said. The disease does not spread around. The staging is based on the blood counts, on the percentage of those myeloblasts or immature cells (and) the chromosomal makeup of the cells. And nowadays, we sometimes also incorporate the presence of gene mis-happenings as well. So we get a lump score to estimate the risk.

Doctors typically use the International Prognostic Scoring System (IPSS) to categorize patients into one of five categories very low, low, intermediate, high and very high. The risk is the impact on survival and whether the disease will transform to leukemia, Komrokji explained. The disease risk must be known in order to tailor the patients treatment to them.

I always advise patients to see a specialized center in MDS, because obviously, those are not that common diseases, he said. A community oncologist could see a few (cases) per year, while an experienced center like in our place, we see like 15 to 20 per week.

Gene Mutations

Komrokji said that understanding gene mutations is an evolving field that is slowly becoming routine.

I advise all patients to inquire if theyve gotten genetic testing or not, he said. This sort of testing will help them understand any abnormalities. Doctors can look at a patients individual gene levels and detect for mutations, of which at least one was identified in 90% of patients with MDS.

Understanding the patients mutation(s) helps them tell whether there is a clonal hematopoiesis or mis-happening that occurred. It can also impact prognosis and allow them to further understand the disease risk.

And finally, some of them are targetable or important to follow through the treatment, said Komrokji. So patients should probably definitely have a genetic testing done. And sometimes after a treatment failure, we repeat it because we see other mutations that we could target with new drugs.

What Causes MDS?

In most cases, the cause of a patients MDS diagnosis is unknown.

We think it's phenomena of senescence or aging of those stem cells in the bone marrow that produces the blood, said Komrokji. Obviously, the process is very complicated. We have billions and billions of cells divide billions of times a day. So you know, as those cells age, mistakes can happen in them.

In most cases, he said, the mis-happenings which lead to the disease are random and at no fault of the patient. It is extremely rare for MDS to be inherited through familial genes.

There are, however, several known risk factors of MDS. If someone has history of another form of cancer and has received chemotherapy or radiation therapy, they may have possible stem cell damage and can develop MDS this is called therapy-related MDS. There has also been association of the disease with benzene exposure, chemical exposure and radiation exposure. Patients who have connective tissue diseases such as rheumatoid arthritis and lupus are at a slightly higher risk of getting MDS due to inflammation in the body and certain medications used to treat those diseases.

I would say there's a lot of better understanding of the disease in the past several years, of genetic mutation testing and incorporating them in practice, Komrokji said. And I think, you know, there are a lot of new treatments on the horizon for patients; there are several clinical trials in advanced phase.

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The Basics of MDS: Diagnosis and Staging - Curetoday.com