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BMT survivor study finds significant breast cancer risk in young women who received total body irradiation – The Mix

Women who had total body irradiation to prepare for blood or marrow transplantation before age 30 had a 4.5-fold increase in their risk of developing breast cancer later in life.

Smita Bhatia, M.D.A new study examining long-term outcomes of blood or marrow transplantation (BMT) found that patients who received total body irradiation (TBI) at age 30 or younger had a 4.5-fold increase in their risk of developing breast cancer later in life compared with the general population. The research, published in the Journal of Clinical Oncology on July 16, 2020, also found increased risk of breast cancer among women exposed to alkylating agents and anthracyclines as part of BMT.

Women who received TBI were at a 1.5-fold higher risk of breast cancer when compared with the general population overall and at a 4.5-fold higher risk when the exposure occurred at age 30 years or younger, the authors write. Women who were exposed to TBI before age 30 had a 13.9 percent risk of being diagnosed with breast cancer by age 50, they found. By comparison, the average American woman has a 2.38 percent risk of being diagnosed with breast cancer at age 50, according to the American Cancer Society.

As a result of this study, we will be recommending that those transplanted at ages less than 30 years with TBI receive screening with mammography and breast MRI for early detection of breast cancer, said Smita Bhatia, M.D., senior author of the study and director of the Institute for Cancer Outcomes and Survivorship and a senior scientist in the ONeal Comprehensive Cancer Center at the University of Alabama at Birmingham.

"We plan to further study how different aspects of TBI dose and delivery technique are related to secondary cancers, said Andrew McDonald, M.D., assistant professor in the Department of Radiation Oncology and first author of the study. Our long-term goal is to improvetreatment techniques for future patients undergoing BMT as part of their cancer care."

This research was based on the BMT Survivor Study, which is enrolling more than 10,000 patients from the UAB, City of Hope and the University of Minnesota medical centers who underwent transplantation between 1974 and 2014 and survived for at least two years. Survival rates after BMT have been improving at the rate of 10 percent per decade, Bhatia said. But these BMT survivors are uniquely vulnerable to long-term health problems, she said.

Some 23,000 patients received BMT in the United States in 2018, according to the latest figures from the Center for International Blood & Marrow Transplant Research. These are mainly patients with blood cancers such as leukemia, myeloma or lymphoma that are progressing or who have a high risk of relapse. Total body irradiation and chemotherapeutic exposures such as alkylating agents and anthracyclines are used to prepare the patient for BMT.

About 50 percent of [BMT] transplant patients overall receive total body irradiation, including a higher proportion of those patients who are younger, Bhatia said. The decision whether or not to use TBI as part of BMT is based on the primary cancer that is being treated and the type of transplant that is performed, she noted. TBI is used more often among those who receive transplants from their siblings or unrelated donors known as allogeneic transplant as compared to when they receive transplants from their own stem cells, known as autologous transplant.

Bhatias institute is particularly interested in identifying predictive traits of cancer survivors at higher risk for long-term problems that could enable health care providers to tailor screenings and other interventions to these populations.

One under-studied outcome in BMT survivors is the magnitude of risk of breast cancer among women treated with TBI across all ages, Bhatia said. Early detection is known to improve breast-cancer outcomes and data on the women at highest risk to develop radiation-related breast cancer would allow health providers to screen these women at earlier ages.

Women who had a history of breast cancer before BMT, chest radiation before BMT or a mastectomy before BMT were not included in the study cohort. The researchers studied a total of 1,464 female BMT survivors 788 who had allogeneic transplants and 676 who had autologous transplants. TBI was used in 46 percent (660) of these patients. The median length of follow-up was 9.3 years. The most common diagnoses were acute myeloid leukemia or myelodysplastic syndrome (27.5 percent), non-Hodgkin lymphoma (23.3 percent), plasma cell dyscrasias (18 percent), and chronic myelogenous leukemia (10.3 percent).

Thirty-seven of the women developed breast cancer during the study period 19 of the women who had allogeneic transplants and 18 who had autologous transplants. The women developed breast cancer at a median of 9.1 years after BMT. Breast cancers, inclusive of ductal carcinoma in situ, were identified from the completed BMTSS survey.

"To our knowledge, this is the first report of an increased risk of subsequent breast cancer after TBI among female autologous BMT survivors, the authors write. The observation that exposure to alkylating agents and anthracyclines is associated with an increased risk of subsequent breast cancer has been noted in long-term outcomes studies of childhood cancer survivors; however, to our knowledge, this is the first report of this association among BMT survivors.

The researchers did not observe a relationship between TBI dose and the risk of subsequent breast cancer in this study, they write. But the distribution of TBI doses used for the women included in this study was narrow, and additional research is needed to determine if a dose-response relationship between TBI and subsequent breast cancer exists.

In addition to McDonald and Bhatia, other authors of Total Body Irradiation and Risk of Breast Cancer After Blood or Marrow Transplantation: A Blood or Marrow Transplantation Survivor Study Report, include Yanjun Chen, Jessica Wu, Lindsey Hageman, Liton Francisco, Michelle Kung, Emily Ness, Wendy Landier, Ph.D., Kevin Battles, and Donna Salzman, M.D., of UAB; F. Lennie Wong, Ph.D., Saro H. Armenian, D.O., and Stephen J. Forman, M.D., of City of Hope; and Daniel J. Weisdorf, M.D., and Mukta Arora, M.D., of the University of Minnesota.

The work was supported in part by grants from the National Cancer Institute (R01 CA078938 and U01 CA213140) and the Leukemia Lymphoma Society (R650216).

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BMT survivor study finds significant breast cancer risk in young women who received total body irradiation - The Mix

Personalized Cell Therapies Market Trends, Outlook, and Opportunity Analysis up to 2021 focuses on major key players PCT Cell Therapy Services, LLC…

The latest fundamental insights on Personalized Cell Therapies Market with COVID-19 Industry Impact, Forecast Development Scope, and Growth Prospects 2021-2026 is released by PBI. Every market driver, Personalized Cell Therapies marketing channel, growth-driving segments, risk analysis & mitigation is given in this report. The dynamic effects on worldwide Personalized Cell Therapies economies and crucial primary & secondary data sources offered in this study. The Personalized Cell Therapies Industry competitive landscape, regional analysis, future patterns, Top companies, current development rate, & gross margin status is provided.

The Personalized Cell Therapies Industry landscape view, demand, revenue, market share & pricing structure analysis is offered. The changing Industry dynamics, plans, CAGR, COVID-19 impact on consumer demand, availability of raw materials is analyzed completely. The market development rate during 2020-2025 with past & present industry performance is assessed in this report.

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PCT Cell Therapy Services, LLC (U.S),S. Stem Cell, Inc. (U.S),Bellicum Pharmaceuticals, Inc. (U.S),Saneron CCEL Therapeutics, Inc. (U.S),StemGenex (U.S),Vericel Corporation.(U.S)

By Cell Type

Market Analysis By Regions

Asia-Pacific (China, Japan, Korea, India and Southeast Asia)

North America (United States, Canada and Mexico)

Europe (Germany, France, UK, Russia and Italy)

South America (Brazil, Argentina, Columbia)

Middle East and Africa (Saudi Arabia, UAE, Egypt, Nigeria and South Africa)

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Executive Summary

Assumptions and Acronyms Used

Research Methodology

Personalized Cell Therapies Market Overview

Personalized Cell Therapies Supply Chain Analysis

Personalized Cell Therapies Pricing Analysis

Global Personalized Cell Therapies Market Analysis and Forecast by Type

Global Personalized Cell Therapies Market Analysis and Forecast by Application

Global Personalized Cell Therapies Market Analysis and Forecast by Sales Channel

Global Personalized Cell Therapies Market Analysis and Forecast by Region

North America Personalized Cell Therapies Market Analysis and Forecast

Latin America Personalized Cell Therapies Market Analysis and Forecast

Europe Personalized Cell Therapies Market Analysis and Forecast

Asia Pacific Personalized Cell Therapies Market Analysis and Forecast

Middle East & Africa Personalized Cell Therapies Market Analysis and Forecast

Competition Landscape

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Personalized Cell Therapies Market Trends, Outlook, and Opportunity Analysis up to 2021 focuses on major key players PCT Cell Therapy Services, LLC...

Stem Cell And Platelet Rich Plasma Prp Alopecia Therapies Market Size, Share, Types, Products, Trends, Growth, Applications and Forecast 2020 to 2027…

New Jersey, United States,- The research report on Stem Cell And Platelet Rich Plasma Prp Alopecia Therapies market comprises of insights in terms of pivotal parameters such as production as well as the consumption patterns alongside revenue estimations for the projected timeframe. Speaking of production aspects, the study offers an in-depth analysis regarding the manufacturing processes along with the gross revenue amassed by the leading producers operating in this business arena. The unit cost deployed by these producers in various regions during the estimated timeframe is also mentioned in the report.

Significant information pertaining to the product volume and consumption value is enlisted in the document. Additionally, the report contains details regarding the consumption graphs, Individual sale prices, and import & export activities. Additional information concerning the production and consumption patterns are presented in the report.

In market segmentation by manufacturers, the report covers the following companies-

Exploring the growth rate over a period

Business owners looking to scale up their business can refer this report that contains data regarding the rise in sales within a given consumer base for the forecast period, 2020 to 2027. Product owners can use this information along with the driving factors such as demographics and revenue generated from other products discussed in the report to get a better analysis of their products and services. Besides, the research analysts have compared the market growth rate with product sales to enable business owners to determine the success or failure of a specific product or service.

By Type

By Application

Regions Covered in the Global Stem Cell And Platelet Rich Plasma Prp Alopecia Therapies Market:

The Middle East and Africa (GCC Countries and Egypt)

North America (the United States, Mexico, and Canada)

South America (Brazil etc.)

Europe (Turkey, Germany, Russia UK, Italy, France, etc.)

Asia-Pacific (Vietnam, China, Malaysia, Japan, Philippines, Korea, Thailand, India, Indonesia, and Australia)

Highlights of the Report:

Accurate market size and CAGR forecasts for the period 2020-2026

Identification and in-depth assessment of growth opportunities in key segments and regions

Detailed company profiling of top players of the global Stem Cell And Platelet Rich Plasma Prp Alopecia Therapies market

Exhaustive research on innovation and other trends of the global Stem Cell And Platelet Rich Plasma Prp Alopecia Therapies market

Reliable industry value chain and supply chain analysis

Comprehensive analysis of important growth drivers, restraints, challenges, and growth prospects

The scope of the Report:

The report offers a complete company profiling of leading players competing in the global Stem Cell And Platelet Rich Plasma Prp Alopecia Therapies marketwith a high focus on the share, gross margin, net profit, sales, product portfolio, new applications, recent developments, and several other factors. It also throws light on the vendor landscape to help players become aware of future competitive changes in the global Stem Cell And Platelet Rich Plasma Prp Alopecia Therapies market.

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Stem Cell And Platelet Rich Plasma Prp Alopecia Therapies Market Size, Share, Types, Products, Trends, Growth, Applications and Forecast 2020 to 2027...

COVID-19 Impact Analysis on Stem Cell Banking Industry. Insights on Strategies of Key Players Bulletin Line – Bulletin Line

One of the major factors fuelling the increasing popularity of stem cell banking is the increasing prevalence of chronic diseases such as cancer across the world. As per the World Health Organization (WHO), one of the major causes of mortality and morbidity throughout the world is cancer, with almost 14 million people getting affected by the disease in 2012. Furthermore, the number of new cancer cases is predicted to increase by 70% all around the world in the next two decades.

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Stem cell therapies are being increasingly adopted in many countries, because of their huge success in treating cancer and other types of chronic diseases. Moreover, the rising awareness amongst the people about the need for preserving stem cells will further boost the demand for stem cell banking in future. Due to these factors, the global stem cell banking market is expected to register unprecedented growth during the forecast period (20202030). Stem cells are basically, used for generating new cells and tissues for the treatment of various diseases such as Parkinsons disease, Alzheimers disease, arthritis, diabetes, and heart diseases.

Stem cell banking is widely used for the treatment of leukemia, autism, diabetes, thalassemia, and cerebral palsy. Out of these, the prevalence of leukemia is rising at a rapid pace across the world, which is in turn, fuelling the progress of the stem cell banking market all over the world. As per the Leukemia and Lymphoma Society (LLS), which is a voluntary healthcare organization focussing on providing access to blood cancer patients for treatments and funding research activities regarding the same, one person is diagnosed with blood cancer in the U.S. at almost every 3 minutes.

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COVID-19 Impact Analysis on Stem Cell Banking Industry. Insights on Strategies of Key Players Bulletin Line - Bulletin Line

Limited Reporting of Adverse Events Tied to Regenerative Treatments Leaves Consumers Vulnerable – The Pew Charitable Trusts

The Food and Drug Administration (FDA) has taken a series of actions in recent years to crack down on businesses marketing high-risk, unapproved regenerative medicine interventions, including unproven stem cell treatments, but more needs to be done to ensure consumers are protected.

The proliferation of clinics offering these interventionsmore than 700 in the United Statesposes a significant risk to public health and has led to multiple instances of patient harm, including blindness and life-threatening infections. Although FDAs efforts so far are encouraging, additional steps can be taken to fully address the risks posed by businesses marketing these products.

In particular, better reporting by patients and physicians of adverse events caused by unapproved stem cell interventions will help FDA and other regulatory authorities identify the riskiest practices and take targeted action to protect patients.

In June, FDA sent a warning letter to Las Vegas-based EUCYT Laboratories LLC for marketing a range of unapproved regenerative products derived from umbilical cord blood, amniotic fluid, and other human cells and tissues. The company said the products could treat or prevent various diseases and conditions, including COVID-19.

According to the letter, one of the companys exosome products caused multiple serious adverse events in patients in Nebraska late last year, including severe infections requiring hospitalization. Exosomes are small, membrane-enclosed vesicles, or packages, of materials released by individual cells. They are thought to play a role in cell communication or molecule transmission. Researchers are studying them for a variety of potential clinical applications, but FDA has not yet approved any exosome products.

Other companies also have marketed unapproved exosomes to patients. Last December, the agency issued a general safety alert, noting that multiple clinics that manufactured or marketed illegal stem cell products had begun offering exosome treatments and warning the public that these approaches had not been evaluated for safety or efficacy. FDA then wrote to another firm, Kimera Labs in Miramar, Florida, noting that the company had been marketing exosomes to treat diseases or conditions such as Parkinsons, multiple sclerosis, brain injuries, diabetes, stroke, and spinal cord injuries.

Such efforts to enforce regulations for businesses marketing potentially dangerous interventions will likely expand significantly later this year, when the agencys regulatory framework for regenerative medicine products takes full effect. In 2017, FDA released four guidance documents to clarify how it would regulate this burgeoning field and more clearly delineate which products must be reviewed before they go on the market.

At the same time, the agency granted businesses three years of enforcement discretion to give manufacturers time to comply with the new regulatory policy and begin moving their products through the review process. During this periodwhich was slated to end in November but has been extended for six months because of the COVID-19 pandemicFDA has taken a risk-based approach to enforcement, acting only against those products that pose a significant safety concern. Since 2017, the agency has filed injunctions against two companies and issued at least 35 regulatory letters to businesses marketing unapproved regenerative products.

Reports of patients being harmed prompted the agencys early actions. For example, in 2019, FDA and the Department of Justice sought and won a permanent injunction against a clinic that injected unproven stem cell products into three women suffering from age-related macular degeneration. The products blinded one and severely damaged the vision of the others.

Reports of such adverse events reach the agency through a variety of channels, including FDAs MedWatch database, which includes mandatory reports from manufacturers, suppliers, and distributors, as well as voluntary reports from physicians and consumers. Because many regenerative medicine products on the market are not FDA-approved, adverse events related to their use are likely to be reported only by patients and their physicians, and even then, only when those individuals know about the database.

This means that adverse events linked to unapproved regenerative products are underreported, perhaps significantly, making it difficult to know how widespread the harm is, or which businesses may be driving the problems. In general, adverse events for all medical products are underreported.

FDA acknowledged this challenge with regenerative therapies in a recent article in the Journal of the American Medical Association and encouraged more thorough reporting by patients and their clinicians. Improved reporting would allow the agency to target enforcement activities more effectively and reinforce the case for tighter regulation of this market. As awareness of the harms grows, fewer patients may be willing to undergo these treatments in the first place.

The agency should consider additional steps to encourage reporting. For example, although the number of consumer reports to the MedWatch database has increased in recent years, patient knowledge of the database appears to be limited. Targeted public awareness campaigns could help boost that knowledge and encourage broader use. The agency also could consider updating the instructions for patients in the MedWatch online reporting system to facilitate easier and more complete reporting of adverse events related to unapproved stem cell productsincluding essential information on where patients receive these treatments.

Most important, however, will be how effectively FDAand potentially otherregulatory authoritiesuse adverse event information to target enforcement activities. Once the period of enforcement discretion ends, the agency will need to take aggressive action against possibly hundreds of businesses across the countryincluding issuing warning letters and, where necessary, seizing products, filing injunctions or pursuing criminal prosecutions to stop the spread of these interventions and protect patients from harm.

Liz Richardson directs The Pew Charitable Trusts health care products project.

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Limited Reporting of Adverse Events Tied to Regenerative Treatments Leaves Consumers Vulnerable - The Pew Charitable Trusts

How airway cells work together in regeneration and aging – Newswise

Newswise The study, published in Cell Stem Cell, also sheds light on how aging can cause lung regeneration to go awry, which can lead to lung cancer and other diseases.

There currently are few therapies that target the biology of lung diseases, said Dr. Brigitte Gomperts, a professor and vice chair of research in pediatric hematology-oncology at the UCLA Childrens Discovery and Innovation Institute and the papers senior author. These findings will inform our efforts to develop a targeted therapy to improve airway health.

The airways, which carry the air that is breathed in from the nose and mouth to the lungs, are the bodys first line of defense against airborne particles like germs and pollution that can cause illness.

Two types of airway cells play a vital role in this process: mucus cells, which secrete mucus to trap harmful particles, and ciliated cells, which use their finger-like projections to sweep the mucus-engulfed particles up to the back of the throat, where they can be cleared out of the lungs.

The infectious or toxic particles that people breathe in every day can injure the airways and when that happens, airway basal stem cells which are capable of self-renewing and producing the mucus and ciliated cells that line the airways activate to repair the damage.

To keep the right balance of each cell type, airway basal stem cells must transition from the proliferative phase, during which they produce more of themselves, to the differentiation phase, during which they give rise to mature airway cells.

These stem cells have to maintain a really delicate equilibrium, said Gomperts, who is also co-director of the cancer and stem cell biology program at the UCLA Jonsson Comprehensive Cancer Center. They have to produce just the right amount of mucus and ciliated cells to keep harmful particles out of the lungs, but they also have to self-replicate to ensure there will be enough stem cells to respond to the next injury.

In the new study, the researchers examined mice with lung injuries, analyzing how the different types of cells found in the niche the supportive environment that surrounds airway basal stem cells work together to orchestrate the repair response.

They found that a group of molecules known as the Wnt/beta-catenin signaling pathway activates to stimulate the airway basal stem cells to respond to injury. The researchers were surprised to discover that this group of molecules originates in one cell type to initiate proliferation and another cell type to initiate differentiation.

In the proliferation phase of repair, a connective tissue cell called a fibroblast secretes the Wnt molecule, which signals to the stem cells that its time to self-renew. In the differentiation phase of repair, the Wnt molecule is secreted by an epithelial cell, which make up the lining of tissues and organs, to signal to the stem cells that its time to produce mature airway cells.

Understanding how regeneration occurs in healthy lungs is a critical first step to understanding how disease can arise when the process goes wrong. Seeking insights into what role this process and the cells that activate it might play in disease, the scientists studied its activity in older mice.

We were surprised to find that in the aging airways, the Wnt/beta-catenin signaling pathway is active in the stem cells even when there is no injury, in contrast to the young airways where it is only activated when necessary, said Cody Aros, the papers first author, a UCLA medical student who recently completed his doctoral research. When this pathway is active, it stimulates the stem cells to produce more of themselves and more airway cells even if theyre not needed.

Previous research by Gomperts lab has established a link between a more active Wnt/beta-catenin pathway and lung cancer.

The more a cell divides, the more likely it is that a proofreading error or mutation can occur and lead to cancer, Gomperts said.

The new paper builds on that work by establishing not just what goes wrong but precisely when it goes wrong in otherwise healthy people as part of the aging process.

These findings give us insight into which cell types are important, which pathway is important and when we might want to think about intervening with therapies to prevent the formation of cancer, Aros said.

This work was supported by the UCLA Medical Scientist Training Program, the National Institutes of Health, a UCLA Broad Stem Cell Research Center Rose Hills Foundation Graduate Scholarship, the Tobacco Related Disease Research Program, a STOP Cancer Award and the UCLA Jonsson Comprehensive Cancer Center and UCLA Broad Stem Cell Research Center Ablon Scholars Program.

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Global Animal Stem Cell Therapy Market 2020 Trends Analysis and Coronavirus (COVID-19) Effect Analysis | Key Players Market With COVID-19 Impact…

The globalAnimal Stem Cell Therapy marketreport has been updated by theMarket Data Analyticsowing to the changed market conditions because of COVID-19. Although, the world is still in hope that everything will come back to normal but the WHO finds no positive signs. The WHO has clearly mentioned that people will have to start living with this disease as there are very less chances that the coronavirus infection will go. The conditions in the global market have changed drastically and every single country is facing economic crunch owing to the slowing down of the business. Thus, it was necessary to update the Animal Stem Cell Therapy market report.

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The latest report consists of the following parts:

Part 1 In the first part of the Animal Stem Cell Therapy market report the market introduction or the market overview is included. In this part the target audience for the Animal Stem Cell Therapy market is also defined for better understanding the market and clients.

Part 2 In the second part the research methodologies and the market tools that were incorporated for studying the market is explained in detail. There are also details about the primary and secondary researches that were conducted by the research analysts.

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Part 3 In the third part the qualitative information about the Animal Stem Cell Therapy market is included. This information is mainly about the Animal Stem Cell Therapy market drivers, restraints, opportunities, and challenges.

Part 4 The fourth part of the report deals with the market segmentation. The Animal Stem Cell Therapy market includes the following segmentations:{Dogs, Horses, Others};{Veterinary Hospitals, Research Organizations}. A detailed analysis of every single category in the market segments has been included. The data includes both statistics and qualitative information which are depicted in the form of tables and figures in the report.

Part 5 Geographical presence of the Animal Stem Cell Therapy market in the major regions such as North America, Europe, Latin America, Asia Pacific, and the Middle East and Africa is described in detail.

Part 6 The major market players in the Animal Stem Cell Therapy market includeMedivet Biologics LLC, VETSTEM BIOPHARMA, J-ARM, U.S. Stem Cell, Inc, VetCell Therapeutics, Celavet Inc., Magellan Stem Cells, Kintaro Cells Power, Animal Stem Care, Animal Cell Therapies, Cell Therapy Sciences, Animacel. Along with these many other industry players are profiled in this section.

Part 7 The last part deals with the market conclusions. The conclusions mainly include the observations and the comments from the research analysts and the market experts.

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AlloVir raises $276M IPO to run broad cell therapy program – FierceBiotech

AlloVir has raised $276 million in an upsized IPO to fund development of allogeneic T-cell treatments for viral diseases. The money will equip AlloVir to embark on a broad clinical development program for a phase 3-ready cell therapy that targets five viruses.

Massachusetts-based AlloVir generates off-the-shelf virus-specific T cells in donors before stimulating their peripheral blood mononuclear cells to selectively activate and expand the therapeutic cells. By giving patients T cells that partially match their HLA subtype, AlloVir thinks it can kill virus infected cells without harming healthy cells or causing graft-versus-host disease.

Viralym-M is the most advanced manifestation of the approach. Baylor College of Medicine has taken the treatment for five common viruses through phase 2, setting AlloVir up to push the drug toward approval while generating clinical proof-of-concept data in other indications.

AlloVir plans to spend $98 million to take Viralym-M through phase 3 trials in immunocompromised patients post allogeneic hematopoietic stem cell transplant (HSCT) who have complications linked to hemorrhagic cystitis, cytomegalovirus or adenovirus. The phase 2 linked adenovirus Viralym-M to a 93% clinical response rate in HSCT patients with one or more treatment-refractory infections.

The size of the IPO means AlloVir has enough money to pursue other opportunities. In addition to the three phase 3 trials, AlloVir plans to start three phase 2 trials to test Viralym-M in the prevention of multi-virus infections in HSCT patients, and the treatment of BK and cytomegalovirus in kidney and solid organ transplant recipients, respectively.

AlloVir has set aside $83 million for the phase 2 program, leaving it with cash to spend on two other assets. A second cell therapy, ALVR106, is due to enter the clinic in autologous and allogeneic HSCT patients with respiratory viral diseases in the fourth quarter. AlloVir has earmarked $56 million for work on ALVR106.

A further $33 million will go toward a phase 1/2 trial of AlloVirs COVID-19 prospect. AlloVir joined the race to develop a COVID-19 treatment in March, teaming up with Baylor College of Medicine to create an off-the-shelf cell therapy against SARS-CoV-2 and other coronaviruses. The resulting drug, ALVR109, is made of CD4+ and CD8+ virus-specific T cells generated from healthy donors.

Baylor filed an IND for ALVR109 in June, only for FDA to hit it with a clinical hold earlier this month amid safety concerns related to the quality of ancillary reagents unique to ALVR109. Despite the setback, AlloVir still expects the trial to get underway this year and deliver top-line data in 2021.

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What Is the Impact of COVID-19 on Cancer Stem Cells Market During Projected Period of 2020-2026? – Market Research Posts

The abrupt rise of the COVID-19 pandemic has enforced an optimistic impact on the global cancer stem cells market growth in 2020. Rising demand for treatment of metastatic stage cancer in the course of the COVID-19 pandemic is shoving the growth of the market. Analysts have predicted that the market will perceive continuous growth after the end of the COVID-19 disaster.

The latest report published by Research Dive on the global cancer stem cells reveals the impact of COVID-19 pandemic on the market growth. Before the rise of the pandemic, the market was expected to grow at a CAGR of 10.3% from 2019 to 2026. However, the sudden outburst of the COVID-19 pandemic has fueled the market growth. Our analysts have estimated that the market is expected to grow at 11.8% CAGR, post-COVID-19 upheaval. The market is anticipated to perceive growth owing to the mounting demand for increased mortality and morbidity rate of cancer during the course of the pandemic.

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Previously, the global cancer stem cells market was anticipated to garner a revenue of $956.6 million in 2020. However, in the present situation, i.e., in 2020, the market size is predicted to reach up to $982.5 million. Early therapy cannot remove or treat the tumor cells that are found in the body, and instead involves treatments that kill the tumor cells and improve better therapeutic longevity. The implementation of CSC therapy globally has a positive effect on the global cancer stem cells market.

According to our analysts, the global cancer stem cells market is projected to observe substantial growth in 2020 and will continue to grow at a significant growth rate after the end of the COVID-19 pandemic. In 2001, Gleevec was used to administer a genetic drug called chronic myelogenous leukemia (CML) for the treatment of rare cancer.

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Enhanced emphasis on customized diagnosis and strengthened cell-based research & development programs is predicted to broaden the application of CSC for the treatment of various kinds of cancer. Furthermore, CSCs are used to treat tumors of the nervous system, such as gliomas, medulloblastoma, and ependymomas. These factors are expected to fuel the demand expansion of cancer stem cells during the forecast period.

Besides, cumulative investments and rising advancements in the cancer stem cells are projected to unlock massive opportunities and thrust the growth of the global cancer stem cells market, post-COVID-19 pandemic.

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What Is the Impact of COVID-19 on Cancer Stem Cells Market During Projected Period of 2020-2026? - Market Research Posts

Global Outlook for Cell Reprogramming and Direct Reprogramming Services and Products Market to 2030, with Company Profiles of Leading Players…

DUBLIN, July 31, 2020 /PRNewswire/ -- The "Cell Reprogramming (iPSC Generation) / Direct Reprogramming Services and Products Market, 2020-2030" report has been added to ResearchAndMarkets.com's offering.

The 'Cell Reprogramming (iPSC Generation)/Direct Reprogramming Services and Products Market, 2020-2030' report features an extensive study of the current market landscape and the future potential of cell reprogramming services and products in treating different chronic conditions. It features an in-depth analysis, highlighting the capabilities of various stakeholders engaged in this domain.

In addition to other elements, the study includes:

One of the key objectives of the report was to understand the primary growth drivers and the future opportunity in cell reprogramming (iPSC generation)/ direct reprogramming services and products market. Based on multiple parameters, such as growth of the overall iPSC market, reprogramming cost and annual number of projects for stem cell therapies, we have provided an informed estimate of the likely evolution of the market in the short to mid-term and mid to long term, for the period, 2020-2030.

The report also features the likely distribution of the current and forecasted opportunity within cell reprogramming services and products market across [A] type of technology offered (sendai virus-based reprogramming, mRNA reprogramming, episomal reprogramming and other technologies), [B] Source cells for iPSC generation (fibroblasts, blood mononuclear cells, unspecified somatic cells and other cells), [C] type of application (research and therapeutic), and [D] key geographical regions (North America, Europe and Asia- Pacific and rest of the world). To account for the uncertainties associated with the development of reprogrammed cells and to add robustness to our model, we have provided three forecast scenarios, portraying the conservative, base and optimistic tracks of the market's evolution.

Key Topics Covered:

1. PREFACE

2. EXECUTIVE SUMMARY

3. INTRODUCTION

4. CURRENT MARKET LANDSCAPE

5. COMPANY COMPETITIVENESS ANALYSIS

6. COMPANY PROFILES 6.1. Chapter Overview 6.2. Allele Biotechnology 6.3. ALSTEM 6.4. Applied Biological Materials 6.5. Axol Bioscience 6.6. Creative Bioarray 6.7. DefiniGEN 6.8. FUJIFILM Cellular Dynamics International 6.9. Lonza 6.10. Mogrify 6.11. REPROCELL 6.12. Stemnovate 6.13. Thermo fisher Scientific

7. CASE STUDY: CLINICAL TRIAL ACTIVITY IN STEM CELL THERAPY DEVELOPMENT

8. PARTNERSHIPS AND COLLABORATIONS

9. LIKELY PARTNERSHIP OPPORTUNITIES

10. MARKET FORECAST

11. EXECUTIVE INSIGHTS

12. CONCLUDING REMARKS

For more information about this report visit https://www.researchandmarkets.com/r/dywciv

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Global Outlook for Cell Reprogramming and Direct Reprogramming Services and Products Market to 2030, with Company Profiles of Leading Players...