Good-Risk Group of Patients With Myeloma Saw Better Outcomes – Cancer Therapy Advisor

Researchers have used deep whole-genome sequencing (WGS) to identify genomic markers of a good-risk group of patients with multiple myeloma with prolonged survival. Specifically, patients found to have a low genomic scar score and chromosome 9 gain had superior outcomes.

In the study, researchers analyzed WGS data from a 2009 study from 183 patients with newly diagnosed myeloma who had been treated with lenalidomide, bortezomib, and dexamethasone alone or in combination with autologous stem cell transplant. These data were then integrated with clinical data.

The researchers calculated a genomic scar score (GSS) using allele-specific copy-number alterations. Patients with a total score of 5 or less were considered to have a low GSS.

On average, WGS identified 7343 single nucleotide variants, 235 small insertions, and 376 deletions per patient. Significant variations in mutational load were found, with hyperdiploid myeloma having the lowest and t(14;16) myeloma having the highest load (P =.004).

In all, patients with a low GSS had significantly longer median progression-free survival and overall survival than other patients. The researchers identified a genomically defined subgroup of patients accounting for about 17% of patients with low DNA damage (a low genomic scar score with chromosome 9 gain) and a superior outcome. These patients had 100% overall survival at 69 months.

Other characteristics of this subgroup included lower mutational load with significant contribution from age-related mutations and NRAS mutation. Specifically, patients with low GSS and chromosome 9 gain had significantly lower mutational load compared with other groups (P =.0002).

Interestingly, the superior outcome group identified here was independent of traditional clinical risk factors, such as ISS, response to treatment, and achievement of [minimal residual disease] negativity, the researchers wrote. Importantly, our study shows that, in addition to traditional risk markers, we can use genomic markers such as low GSS and gain9 to identify true low-risk groups.

Reference

Samur MK, Samur AA, Fulciniti M, et al. Genome-wide somatic alterations in multiple myeloma reveal a superior outcome group [published online July 20, 2020]. J Clin Oncol. doi: 10.1200/jco.20.00461

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Good-Risk Group of Patients With Myeloma Saw Better Outcomes - Cancer Therapy Advisor

‘Year of Preparations for the Next Fifty Years’ will contribute to country’s development process – Emirates News Agency

ABU DHABI, 3rd August, 2020 (WAM) -- In 2020, the UAEs achievements, most notably the launch of the Hope Probe to Mars and the operation of Unit 1 of the Barakah Nuclear Power Plant, have proven that the "Year of Preparations for the Next Fifty Years" will significantly contribute to the countrys development process.

Despite the difficult circumstances facing the world caused by the coronavirus, COVID-19, pandemic, the UAE has succeeded in turning challenges into opportunities for innovation and development, which is reflected in its approach to limiting the spread of the virus through a range of creative measures, such as developing technology to discover the virus using lasers that generate results in a record time, using stem cell therapy for patients, and participating in global efforts to find a vaccine.

In 2020, the UAEs achievements reflect the national ambitions and wisdom of its leadership. The Hope Probe project involved nearly 200 Emirati engineers and researchers, who worked hard for six years to fulfil the UAE's dream to reach the Red Planet.

The Barakah Nuclear Power Plant also highlights the UAEs efforts to build the capacities of national cadres in this sector. Nearly 244 employees work for the Federal Authority for Nuclear Regulation, FANR, with 67 percent being Emiratis, of which 45 percent are in leading and managerial positions. Women also account for over 40 percent of the Authoritys employees.

Once all four units of the plant are commercially operating, the UAE's Barakah Nuclear Energy Plant will produce up to 25 percent of the country's electricity requirements while in parallel preventing the release of 21 million tons of carbon emissions each year.

On the level of combating COVID-19, Emirati national cadres and institutions joined the front line since the first day to discover the first case in the country, and contributed to achieving milestones at the global level.

In May, a patent was granted by the Ministry of Economy for the development of an innovative and promising treatment for COVID-19 infections using stem cells. The treatment was developed by a team of doctors and researchers at the Abu Dhabi Stem Cell Center, ADSCC, and involves extracting stem cells from the patients own blood and reintroducing them after activating them.

QuantLase Imaging Lab, the medical-research arm of the Abu Dhabi Stock Exchange-listed International Holdings Company, IHC, announced that it has developed novel equipment which enables for much faster mass screenings, with test results available in seconds and allowing testing on a wider scale.

The technology will reinforce the UAEs position as a hub of research and innovation, as scientists around the world scramble to devise a faster method of testing for patients suspected to have been infected with the coronavirus and potentially identifying carriers before they become infectious.

The first World Health Organisation, WHO, enlisted global clinical Phase III trial of Sinopharm CNBGs inactivated vaccine to combat COVID-19 started in Abu Dhabi.

The worlds first Phase III trial is the result of a cooperation partnership between Abu Dhabi based G42 Healthcare, currently at the forefront of the battle against COVID-19 in the UAE, and Sinopharm CNBG, the worlds sixth-largest vaccine manufacturer, ranked 169th on the Fortune Global 500 list of 2018.

The trials are being operated by health practitioners from Abu Dhabi Health Services, SEHA, who are providing facilities at five of their clinics in Abu Dhabi and Al Ain in addition to a mobile clinic to ensure the trials are readily accessible to volunteers participating in the programme.

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'Year of Preparations for the Next Fifty Years' will contribute to country's development process - Emirates News Agency

Stem Cell Therapy Market Latest Trends, Development, Revenue, Demand And Forecast To 2022 – Market Research Correspondent

Stem Cell Therapy Market is worth USD 11.99 billion in 2016 and is expected to reach USD 60.94 billion by 2022, growing at a CAGR of 31.1% from 2016 to 2022.

The global stem cell therapy market report offers in-depth analysis of the market size (revenue), market share, major market segments, different geographic regions, forecast for the next five years, key market players, and premium industry trends. It also focuses on the key drivers, restraints, opportunities and challenges in the stem cell therapy market.

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KEY BENEFITS OF THE REPORT: Deeper understanding of the strategies adopted by the key players in this market to stay competitive Granular analysis about the growth map of the market during the next five years Comprehensive analysis of the key market players and their market share

KEY PREMIUM INDUSTRY INSIGHTS: The increasing government initiatives and funding from various organizations, the increased spending on research and development, rapid technological advancement in genomics, and the rising awareness about the stem cell therapy are some of the factors fuelling the growth of the stem cell therapy market.

Other factors, such as the robust product pipelines and increasing approval of the new clinical trials are fuelling the growth of the stem cell therapy market further. However, improper infrastructure, insufficient storage systems, and ethical problems are the major restraints for the stem cell therapy market.

MARKET SEGMENTATION: This report analyzes the stem cell therapy market by the following segments:

Stem Cell Therapy Market, by Treatments Allogeneic Stem Cell Therapy Autologous Stem Cell Therapy Stem Cell Therapy Market, by Applications Oncology Central Nervous System Diseases Eye Diseases Musculoskeletal Diseases Wound & Injuries Metabolic Disorders Cardiovascular Disorders Immune System Disorders Stem Cell Therapy Market, by End-users Hospitals Ambulatory Surgical Centers

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KEY MARKET PLAYERS: Key players in the stem cell therapy market include:

Vericel Corporation. Stem Cells, Inc. Mesoblast, Ltd. Gamida Cell Osiris Therapeutics, Inc. Chiesi Farmaceutici S.p.A ReNeuron Group, plc

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FDA-approved treatment puts rare cancer with skin manifestations on the map – Dermatology Times

A small group of scientists and clinicians are trying to build awareness of this cancer, and how to diagnose and treat it. While this rare and aggressive hematologic malignancy hasnt had a standardized therapeutic approach in the past, that is also changing. The FDA approved tagraxofusp (Elzonris, Stemline) in 2019 as the first medication indicated to treat BPDCN, according to a drug review published June 24, 2020 in the journal Expert Review of Anticancer Therapy.1

Progress aside, theres still a long way to go in creating awareness among dermatologists, primary care physicians, emergency department providers and pediatricians all of whom are most likely to encounter people with possible BPDCN, says Naveen Pemmaraju,M.D., associate professor in the department of leukemia at The University of Texas MD Anderson Cancer Center. Dr. Pemmaraju is senior author on the recent Expert Review of Anticancer Therapy paper, and he led the pivotal study published in April 2019 in the New England Journal of Medicine that led to the FDAs approval of tagraxofusp for the treatment of BPDCN.2

Having the clinical trial is great, but now that the drug is commercially available there was a call for what are the practical considerations for Tagraxofusp in BPDCN? Dr. Pemmaraju says. Thats why we wrote this paper.

Dermatologists, take noteDr. Pemmaraju points to three stand-out practical considerations for providers.

One is that most people in medicine have yet to even hear about the disease, he says. When people on the frontlines see skin lesions, the only way theyre going to know whether its BPDCN is with a biopsy. Tissue is the issue, as they say. If something looks irregular, abnormal and if its clinically indicated to do a biopsy, do a biopsy. A lot of these patients get mistaken for other diseases, infections, other cancers. So, I think the biopsy is important.

The need for expert review goes along with the first practical consideration.

CD123 (interleukin-3 receptor alpha unit) is overexpressed in 100% of BPDCN patients. But thats not the only way to differentiate this cancer on biopsy. CD123, CD4, CD56 as the golden triad of BPDCN, according to Dr. Pemmaraju.

Now we know there are other markers, TCL1, TCF 4, CD303 and others. When you put together these three to six markers, it helps you distinguish BPDCN, which is extraordinarily rare compared to the more common cancers like acute myeloid leukemia (AML), cutis, cutaneous t-cell lymphoma. Obviously, this differentiates completely from skin infections and all these other noncancer entities, Dr. Pemmaraju says.

The second practical consideration is that, although rare diseases commonly have limited-to-no treatment options, a therapy for BPDCN exists and more are being investigated. Studies suggest that BPDCN incidence is as low as 0.44% of all hematologic cancers and 0.7% of cutaneous lymphomas, according to the paper. Despite the low numbers, BPDCN treatment is available with tagraxofusp. Researchers are also conducting multiple clinical trials for BPDCN drugs in development, including the B-cell lymphoma-2 (BCL-2) inhibitor, venetoclax, and a chimeric antigen receptor (CAR) T-cell therapy.

The third consideration: The significance of dermatologists and dermatopathologists roles in BPDCN diagnosis.

As we educate our fellow hematologists/oncologists, we must continue to educate dermatologists, many of whom are going to see this disease for the very first time in the clinic before anybody else. I believe BPDCN will soon appear on dermatology and derm-path board exams, Dr. Pemmaraju says.

BPDCN skin lesions usually present as dark and purplish and can be maculopapular.

I would say clinically there is a somewhat distinct look, although I would add the caveat that these lesions act heterogeneously, he says.

Focusing on TagraxofuspResearchers reported that tagraxofusp, aCD123-directed cytotox, demonstrated efficacy in BPDCN patients along with an overall manageable safety profile, according to the NEJM study.

A historically deadly disease, BPDCNs median overall survival after chemotherapy had been 8 to 14 months, according to Dr. Pemmaraju. Hematopoietic stem cell transplant might prolong survival in patients healthy enough to have the stem cell transplant.

Among the 29 previously untreated patients, the survival rates of 59% at 18 months and 52% at 24 months rates that were influenced by the number of patients who went into remission after tagraxofusp therapy and could thus undergo hematopoietic stem-cell transplantation represent an improvement over rates in historically published data. We also observed a 67% overall response rate among previously treated patients. Notably, we report a meaningful survival with tagraxofusp among patients with relapsed or refractory disease (median overall survival, 8.5 months), Dr. Pemmaraju and colleagues report in the NEJM.

Interestingly, patients skin lesions went away rapidly in the vast majority of people treated with tagraxofusp, according to Dr. Pemmaraju.

Capillary leak syndrome emerged as the most drug-associated serious adverse, manifested by edema, tachycardia, hypoalbuminemia and hypotension.

There also is the issue of drug resistance. Researchers have found, in vivo, that resistance to tagraxofusp in cell lines is associated with decreased DPH1 expression and azacitadine might reverse tagraxofusp resistance.

More research is needed to study how combining tagraxofusp with other targeted therapies may improve outcomes. Research also is needed to study tagraxofusp use in pediatric patients. The FDAs approval is for tagraxofusp is as first-line therapy for BPDCN for adults and children ages 2 years and older. But only a small number of pediatric patients have been treated so far, the authors report.

DisclosureMD Anderson funded the study. Dr. Pemmaraju has received research funding/clinical trials support from Affymetrix, SagerStrong Foundation, Novaris, Stemline, Samus, AbbVie, Cellectis, Daiichi Sankyo, and Plexxikon.

References

1. Lee SS, Mccue D, Pemmaraju N. Tagraxofusp as treatment for patients with blastic plasmacytoid dendritic cell neoplasm. Expert Rev Anticancer Ther. 2020;:1-8.

2. Pemmaraju N, Lane AA, Sweet KL, et al. Tagraxofusp in Blastic Plasmacytoid Dendritic-Cell Neoplasm. N Engl J Med. 2019;380(17):1628-1637.

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FDA-approved treatment puts rare cancer with skin manifestations on the map - Dermatology Times

Stem Cell Assay Market To 2026: Growth Analysis By Manufacturers, Regions, Types And Applications – Research Newspaper

The Stem Cell Assay Market report includes overview, which interprets value chain structure, industrial environment, regional analysis, applications, market size, and forecast. This is a latest report, covering the current COVID-19 impact on the market. The pandemic of Coronavirus (COVID-19) has affected every aspect of life globally. This has brought along several changes in market conditions. The rapidly changing market scenario and initial and future assessment of the impact is covered in the report. The report provides an overall analysis of the market based on types, applications, regions, and for the forecast period from 2020 to 2026. It also offers investment opportunities and probable threats in the market based on an intelligent analysis.

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More on the language of immunity – Cosmos

This continues the process from last week (the I essay) of introducing terms that will be encountered as we engage with the complexities of immunity. Ive bolded a few words and phrases that, while some may be commonplace, will be used in an unfamiliar context. Repertoire is in that category.

Repertoire is mainly owned by the entertainment and performance cultures. The repertoires of: an opera singer or solo instrumentalist; amazing strokes from a top tennis player; tricky moves by a spin bowler; and the playlist that defines the repertoires of both actors and a theatrical company like Bell Shakespeare or the fictional Good Companions in JB Priestleys novel. What were discussing here is a diversity of selected repertoires, with that selection being made first by the performers on the basis of their specific abilities and interests, then by those who care to engage by listening, buying tickets and attending an event as part of their target audience. The audience for, say, the latest Opera Australia production of Don Giovanni at Sydney Opera House will, though there may be some crossover, be largely different from that enjoying live music at a Kings Cross night club.

Immunologists use repertoire in discussing the extraordinary diversity of the adaptive immune system (See Immuno and the Red and the white essays) that has evolved to limit the damage caused by pathogens as different as measles virus and malaria. When it comes to any individual infection, what we are talking about is, in fact, three quite distinct repertoires that incorporate a diversity of highly specific recognition molecules, or receptors, expressed on three very distinct categories of immune white blood cells (WBCs) that do very different jobs in protecting us. Each cell, or lymphocyte (the terms are interchangeable here), within these populations of immune performers expresses only one highly specific receptor that, with its feet anchored firmly in the outer membrane of the cell, is made up of two protein chains. At the outer tip of these molecules, we find individually unique but enormously varied structural motifs (styles?) that bind to one or other target induced by the infectious process, in this case by SARS-CoV-2.

Taking the human performer analogy, it is these targets (we call them antigens in immunology) that are the audience selecting a high-performance repertoire from the enormous pool of possible candidates that live within each and every one of us, just as the nine billion or so human beings on our planet are the precursor pool for the top musicians and sports people selected by target audiences. Fans pay money to see them because they have great regard, or affinity for what they do. The central principle of specific immunity is that high affinity binding of an individual cell surface receptor to a particular target antigen leads to its incorporation in a selected response repertoire.

The three categories of immune lymphocytes that concern us here are the B cells, the CD4+ helper T cells and the CD8+ killer T cells. The B refers to a weird organ in birds called the Bursa of Fabricius where nave, or precursor, B cells first develop and start to express their surface receptors, the B cell receptors (BCRs). Mammals like us dont have that bursa (which has nothing to do with bursitis,) but we think that the same type of process goes on in our bone marrow (BM).

The T refers to the thymus, the organ in the neck that is large in children and gets smaller (involutes) as we age. BM stem cells travel to the thymus via the blood, where they multiply, differentiate and express the T cell receptors (TCRs) that direct the attention of the CD4+ T helpers and CD8+ T killers. After exiting the thymus into the blood, these nave T cell pools provide the narrow, antigen-selected repertoires that coalesce after infection or vaccination.

The CD of CD4 and CD8 is short for cluster of differentiation and is just part of a classification scheme for molecules on the surface of immune cells. Currently, there are 371 members in this molecular club some of which are differentially expressed on the surface of antigen-selected immune T cells (and B cells) as they multiply, then go down different functional pathways. These CD activation markers allow us to characterise distinct CD4+ and CD8+ T cell subsets.

The BCRs on naive B cells are an early form of the immunoglobulin (Ig), or antibody molecules that we met last week. By the time the Igs are being secreted by the B cell descendants, the large protein factory plasma cells, the BCRs will have been refined and changed by a process called affinity maturation that is unique for the B cell/plasma cell lineage and does not happen for the T cells. More of that later.

The CD4+ T helpers are, if you use the performer analogy, the agents and promotors of immunity. The CD8+ T killers are the assassins, the killers within that sounds a bit dangerous, but they are very important. Enough for now!

This article is the latest in theSetting it Straightseries written by Laureate ProfessorPeter Dohertyfrom Australias University of Melbourne and Doherty Institute to explain aspects of the evolving COVID-19 pandemic. You can read them allhere.

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More on the language of immunity - Cosmos

Stem Cell Treatment Seen to Safely Aid Speech in ALS Patients in… – ALS News Today

Stem cells collected from a patients bone marrow and infused into the spinal fluid safely improved speaking abilities after 28 daysfor most of the 12 adults with amyotrophic lateral sclerosis (ALS) evaluated in a small study.

Its researchers recommend further investigation of this approach in treatingspeech difficultiesin ALS, a common and early symptom of this neurological disease that is known as dysarthria.

The study, Articulation recovery in ALS patients after lineage negative adjuvant cell therapy preliminary report, was published in the International Journal of Medical Sciences.

Current treatments for speech disorders in ALS, which is marked by the deterioration of nerve cells that control voluntary muscle movement (motor neurons), are medicines to ease muscle weakness, tongue twitching, and excess salivation, as well as speech therapy support.

Despite widespread use of these approaches, treatments that address speech problems in ALS are still limited.

The administration of stem cells isolated from a patient then used as a treatment in that same person (autologous) may help to trigger the release of neurological growth factors, called neurotrophic factors, provide support for motor neurons, and slow disease progression.

Researchers atPomeranian Medical University in Poland conducted an open-label, Phase 1 clinical trial (NCT02193893) in 12 ALS patients, four women and eight men, between the ages of 21 and 65.

Bone marrow was collected from each person, and stem cells then isolated to include only lineage-negative cells (LIN-). These are immature stem cells and progenitor cells that have not yet become functioning blood cells.

The LIN- cells were returned to each patient via an infusion into the cerebrospinal fluid (CSF, the liquid that surrounds the brain and spinal cord) of the lumbar vertebrae of the lower spine.

Before the procedure, and 28 days after, patients were evaluated for speech using the Frenchay Dysarthria Assessment (FDA), a standardized test that relies on a nine-point rating scale, measuring oral structure, function, and speech.

CSF was collected to measure levels of various neurotrophic factors and pro-inflammatory proteins, both before cell infusion and 28 days later.

Two particular factors nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF) were tested in patients blood on the day of the infusion, and three and seven days later, and again at three months.

Of note, neurotrophicfactors are signaling molecules that play an important role in the survival and growth of nerve cells.

Based on their FDA scores, patients were divided into two groups: group 1 was composed of eight patients who improved in five or more speech measures; the four patients in group 2 did not show such improvement.

Patients in group 1 were older (average age of 55.8), and had a shorter disease duration (average of 2.6 years), the researchers noted.

Compared to baseline (study start) measurements, seven out of the eight group 1 patients had marked improvements in phonation time the time a person can say a vowel. Lip performance was enhanced in six people in group 1, and palate functioning and voice loudness improved in five of these patients.

Improvements were found in about 54% of the analyzed speech functions among group 1 patients, and 35% of those in group 2.

It is noteworthy that tongue mobility was the only articulatory function that did not improve in all 12 patients, the researchers wrote.

No significant pre- and post-treatment differences were seen in pro-inflammatory proteins in the CSF of either group. However, one such protein, called C3, was almost two times higher in group 2 patients at the studys start.

At 28 days after the procedure, lower levels of the inflammation marker C-reactive protein in the CSF, particularly in group 1 patients, were found.

Baseline concentrations of the neurotrophic factor BDNF and ofplatelet-derived growth factor alpha (PDGF-AA) were higher in group 1 patients compared with group 2. At 28 days post-treatment, however, group 1 patients showed a significant decrease in concentrations of BDNF, PDGF-AA, andangiopoietin 2 (ANGP-2), and a downward trend in VEGF-A. No significant differences were found among those in group 2.

Growth factors are signaling molecules that, among other things, arecapable of stimulating cell proliferation and differentiation.

It remains unclear why, in parallel with the improvement of articulation, a statistically significant decrease in neurotrophins concentration was observed, the researchers wrote.

BDNF blood levels in both groups reached were highest two to three days after the infusion, then steadily decreased. The nerve growth factor (NGF) followed a similar pattern in group 2 patients. No difference in the levels of BDNF and NGF were found between these groups.

The outcomes of the LIN- cell application in ALS treatment of articulatory organs are promising, the researchers wrote, and proved to be both safe and feasible.

A short-lasting trophic effect of autologous LIN- administration could encourage repeated [cell] application in order to sustain their beneficial effects, however this approach needs further investigation, they added.

Steve holds a PhD in Biochemistry from the Faculty of Medicine at the University of Toronto, Canada. He worked as a medical scientist for 18 years, within both industry and academia, where his research focused on the discovery of new medicines to treat inflammatory disorders and infectious diseases. Steve recently stepped away from the lab and into science communications, where hes helping make medical science information more accessible for everyone.

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Ana holds a PhD in Immunology from the University of Lisbon and worked as a postdoctoral researcher at Instituto de Medicina Molecular (iMM) in Lisbon, Portugal. She graduated with a BSc in Genetics from the University of Newcastle and received a Masters in Biomolecular Archaeology from the University of Manchester, England. After leaving the lab to pursue a career in Science Communication, she served as the Director of Science Communication at iMM.

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Stem Cell Treatment Seen to Safely Aid Speech in ALS Patients in... - ALS News Today

Study Evaluates Diagnostic Value of the Karius Test for Pneumonia in Immunocompromised Patients – OncoZine

Immunocompromised patients are generally at high risk of Invasive Fungal Infections (IFI), potentially leading to diseases like pneumonia, an infection in the lungs which can be caused by a fungus, bacteria, or viral infection.

Pneumonia is a major cause of morbidity and mortality in these individuals and this may especially be the case in patients with hematological malignancies undergoing remission-induction chemotherapy for acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS) and recipients of allogeneic hematopoietic stem cell transplants (HSCT).[1]

Although new treatment options have become available to treat patients with cancer and hematological malignancies, Invasive Fungal Infections remain a major concern due to the increased potential of morbidity and mortality in these patient populations.

The effects of novel anti-cancer agents Although a growing number of new immune-modulating drugs has shown to advance the treatment of patients with cancer, some of these agents have also attribute to the increase of risk for Invasive Fungal Infections. This increased risk may especially be seen in patients treated with tyrosine kinase inhibitors (TKI), in particular inhibitors of Bruton tyrosine kinase (BTK) mammalian target of rapamycin (mTOR) Janus kinase (JAK) and phosphatidylinositol 3 kinases (PI3K) delta.[1]

Inhibition of immune checkpoints, such as programmed cell death protein 1 (PD1) or cytotoxic T lymphocyte-associated protein 4 (CTLA4) may show a wide-ranging of mostly immune-related adverse events. Subsequent immunosuppression, primarily including corticosteroids, may, in turn, result in the development of opportunistic infections including fungi, requiring optimizing the management of immune-related adverse events.[1]

Diagnostic failure Immunocompromised patients can be infected by a broad range of potential pathogens. However, in many cases, diagnostic testing fails to identify a microbial etiology for lower respiratory illness even with bronchoalveolar lavage (BAL).

Studies have shown that culture methods, PCR, and antigen testing on BAL samples only yields a positive result of 30-67% of the time. In addition, Idiopathic Pulmonary Syndrome (IPS), a non-infectious pulmonary complication of transplants, can have many overlapping symptoms with infectious pneumonia. Treatment for IPS is the administration of steroids which can exacerbate infections. As a result, there is a major unmet medical need for better diagnostics to aid in the management of immunocompromised patients with pneumonia.

Clinical evaluation Karius, a life sciences company focused on generating genomic insights for infectious diseases, has developed a microbial cell-free plasma next-generation sequencing test for pathogen detection capable of detecting >1,000 organisms. The test is performed in a CLIA-certified/CAP-accredited laboratory with results typically provided within one day from sample receipt.

To understand the increased risk and to improve the timely diagnosis of pneumonia in immunocompromised adult patients, including those with hematological cancers, Karius, in collaboration withDuke Clinical Research Institute, has launched a multicenter, prospective study designed to evaluate the diagnostic value of the Karius Test.

The test developed by Karius is a non-invasive liquid biopsy, based on next-generation sequencing of microbial cell-free DNA that can rapidly detect over 1,000 bacteria, DNA viruses, fungi, and parasites. The test helps clinicians make rapid, treatment decisions and is currently being used by over 100 hospitals nationwide by mapping each patients microbial landscape from a single blood draw.

Diagnostic yield Given the medical need, the clinical evaluation will compare the diagnostic yield of the Karius Test to standard testing methods used to diagnose infectious causes of pneumonia in immunocompromised patients including those with hematological cancers.

Patients with suppressed immune systems are especially vulnerable to life-threatening pneumonia due to their decreased ability to fight infections. Standard methods to diagnose pneumonia can be invasive, time-consuming, often requiring weeks to months for a result, and in some cases inconclusive, failing to identify the pathogen causing the infection.

The PICKUP study (NCT04047719) will investigate the additive diagnostic value of the Karius Test in the diagnosis of pneumonia in these patients and its impact on clinical decision-making in this specific population. In addition, the Karius Test will be used to serially monitor pathogen levels during treatment to examine the association between microbial load and pneumonia progression.

The ability to diagnose invasive life-threatening infections in immunocompromised patients has been one of the most challenging areas in clinical infectious disease practice, noted Mickey Kertesz, Chief Executive Office of Karius.

We are enthusiastic to be collaborating with a number of leading cancer centers for this study and anticipate that the Karius Test will demonstrate a higher diagnostic yield than traditional invasive testing methods, Kertesz added

Unknown causative pathogen Often in pneumonia, the causative pathogen is unknown or can be challenging to diagnose despite extensive diagnostic testing, explained Stephen P. Bergin, M.D., Assistant Professor of Pulmonary and Critical Care Medicine at Duke University Health System and lead investigator for the PICKUP study.

Accurate and timely pathogen identification is particularly critical for immunocompromised patients who are susceptible to life-threatening infections from a much broader array of pathogens. We look forward to exploring the potential value of a non-invasive tool capable of rapidly diagnosing respiratory infections in this vulnerable population, Bergin concluded.

Overcoming limitations Previous studies have demonstrated the ability of the Karius Test to overcome many of these limitations to diagnose the cause of pneumonia and enable targeted treatment.

The PICKUP study will include approximately 200 patients from up to 10 centers in the United States, including Duke University Health, University of Pittsburgh Medical Center, Fred Hutchinson Cancer Research Center, The University of Texas MD Anderson Cancer Center, City of Hope, Tulane Cancer Center and Tulane Medical Center and The University of California, San Francisco Medical Center.

Clinical trials Pneumonia in the ImmunoCompromised Use of the Karius Test for the Detection of Undiagnosed Pathogens (PICKUP) NCT04047719

Reference [1] Mellinghoff SC, Panse J, Alakel N, et al. Primary prophylaxis of invasive fungal infections in patients with hematological malignancies: 2017 update of the recommendations of the Infectious Diseases Working Party (AGIHO) of the German Society for Haematology and Medical Oncology (DGHO). Ann Hematol. 2018;97(2):197-207. doi:10.1007/s00277-017-3196-2

Featured image: Karius laboratory. Photo courtesy: 2020 Karius. Used with permission.

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Study Evaluates Diagnostic Value of the Karius Test for Pneumonia in Immunocompromised Patients - OncoZine

Incyte/Morphosys take on CAR-Ts with $198,000 per year antibody – – pharmaphorum

Incyte and Morphosys Monjuvi antibody therapy has been approved for certain patients with lymphoma, as the companies hope to provide a more convenient alternative to expensive and cumbersome CAR-T therapy.

At the beginning of the year Incyte paid $750m to Morphosys for the CD-19 targeting antibody, which has been approved in combination with BMS Revlimid (lenalidomide) for adults with relapsed or refractory diffuse large B-cell lymphoma not otherwise specified.

The indication also covers DLBCL arising from low grade lymphoma and patients not eligible for autologous stem cell transplant.

Monjuvi (tafasitamab) targets the CD-19, a protein on the surface of B-cells that is also targeted by Amgens bispecific antibody Blincyto (blinatumomab) for acute lymphoblastic leukaemia (ALL), as well as two CAR-T therapies Novartis Kymriah (tisagenlecleucel) and Gileads Yescarta (axicabtagene ciloleucel) that are already approved for DLBCL and other B-cell cancers.

Under the agreement with Morphosys the companies will co-market the drugs in the US, while Incyte has exclusive rights outside the US.

The deal with Morphosys could see Incyte pay up to $1.1 billion should certain targets be achieved.

Xencor, which developed the drug before licensing it to Morphosys in 2010, will receive a $25 million milestone payment and a royalty on worldwide net sales.

Before any rebates or discounts Monjuvis wholesale price will average $16,500 per month in the first year of therapy, followed by an average of $13,000 per month in subsequent years because of a decrease in the required number of doses per cycle.

At around $198,000 for the first year this is pricey but may work out as less expensive than CAR-Ts from Novartis and Gilead, depending on how long patients stay on treatment.

CAR-Ts cost $373,000 in adult DLBCL for a single shot of the cell therapy.

CAR-Ts can be highly effective, producing a complete response in about a third of patients, but are made by harvesting a patients own cells and modifying them to fight cancer a lengthy process that might not appeal to all patients.

There are also dangerous side-effects with CAR-Ts, where doctors often have to manage cytokine storms where the immune system goes into overdrive and begins to attack a patients own body.

The FDA approval of Monjuvi was based on data from the MorphoSys-sponsored phase 2 L-MIND study, an open label, multicentre, single arm trial of Monjuvi in combination with lenalidomide as a treatment for adult patients with relapsed or refractory DLBCL.

Results from the study showed an overall response rate of 55%, including a complete response rate of 37% and a partial response rate of 18%.

Warnings and precautions for Monjuvi included infusion-related reactions, serious or severe myelosuppression (including neutropenia (50%), thrombocytopenia (18%), and anemia (7%)), infections (73%) and embryo-foetal toxicity. Neutropenia led to treatment discontinuation in 3.7% of patients.

This accelerated approval may depend on further confirmatory data from larger trials.

Updated to include pricing information

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Incyte/Morphosys take on CAR-Ts with $198,000 per year antibody - - pharmaphorum

Crowdfunding to the rescue for this cancer patient – Telangana Today

New Delhi: Cancer takes innumerable lives each year, and so does the unavailability of cancer treatment due to lack of funds. 33-year-old Nushafreen Palsetia, a software engineer based in Mumbai, was recently diagnosed with a very aggressive form of cancer. Despite a relapse, what helped was life-saving support pouring from over 1,700 donors.

Nushafreen was first diagnosed with Non-Hodgkin Lymphoma in April 2019. After a year of enduring aggressive treatment, she tried to get back to her normal life and work. Unfortunately, Non-Hodgkin Lymphoma, Diffuse Large B Cell Lymphoma (DLBCL), cancer relapsed in her liver in May 2020 which was an unexpected major shock, leaving her and all of her family overwhelmed.

Doctors planned to perform an autologous (her own stem cells) bone marrow transplant in India after the chemotherapy but further tests showed involvement of the bone marrow as well. Hence, her treating doctor recommended the modern CAR-T Cell therapy treatment, available only in the USA, UK, Israel, and a few European countries.

Nushafreens family found Israel as the most affordable option as compared to all other countries offering the treatment. They reached out to Sheba Medical Centre in Israel which estimated the medical expenses as 200,000 USD (approximately Rs 1.5 crore). The treatment will require Nushafreen to be hospitalized for a month or more for the response to treatment and immediate follow up.

As Nushafreens family couldnt afford the high medical expenses, an ImpactGuru crowdfunding campaign was initiated. In two weeks, Nushafreens ImpactGuru.com Page has raised over Rs 1 crore from 1750 donors. The platform raises money online for medical expenses via crowdfunding such as cancer, transplants, and accidents.

According to the co-founder and CEO of the healthcare crowdfunding platform, Piyush Jain, Crowdfunding is driven by a culture of generosity, it allows people to raise money quickly in a hassle free manner without any payback liability. This is a new record for our platform with a single patients family being able to raise more than Rs 1 crore. We hope Nushafreen recovers soon and more patients come forward to utilize our platform in their time of need to get the best available treatment for critical illnesses.

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Crowdfunding to the rescue for this cancer patient - Telangana Today