{"id":23213,"date":"2020-04-23T12:00:00","date_gmt":"2020-04-23T12:00:00","guid":{"rendered":"https:\/\/www.cancer.gov\/news-events\/cancer-currents-blog\/2020\/car-t-cell-nci-manufacturing-clinical-trials"},"modified":"2024-11-03T15:16:48","modified_gmt":"2024-11-03T15:16:48","slug":"nci-initiative-aims-to-boost-car-t-cell-therapy-clinical-trials","status":"publish","type":"post","link":"https:\/\/ogkologos.com\/en\/nci-initiative-aims-to-boost-car-t-cell-therapy-clinical-trials\/","title":{"rendered":"NCI Initiative Aims to Boost CAR T-Cell Therapy Clinical Trials"},"content":{"rendered":"

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Through a recently launched initiative, NCI will manufacture CAR T-cell therapies for clinical trials being conducted at multiple hospitals.<\/p>\n

Credit: National Cancer Institute<\/p>\n<\/div>\n<\/figcaption><\/figure>\n<\/div>\n

In 2010, an NCI research team published the first study of a new form of cancer treatment called CAR T-cell therapy, reporting on a single patient with advanced lymphoma whose disease, they recounted, \u201cunderwent a dramatic regression\u201d following the treatment<\/a>. The next year, researchers from the University of Pennsylvania reported a similar result using CAR T-cell therapy<\/a> to treat a patient with an advanced form of leukemia<\/a>.<\/p>\n

Within 7 years, the Food and Drug Administration (FDA) approved the first two CAR T-cell therapies<\/a>, and with a third approval expected sometime this year, research groups around the world are rapidly developing new CAR T-cell therapies<\/a>.<\/p>\n

These cancer treatments have captured public attention, and researchers\u2019 imaginations, like few others. In part, that\u2019s because of the remarkable way they can eliminate cancer in some people with advanced blood cancers. It\u2019s also because of where they come from: a patient\u2019s own blood. Components of that blood are then used to create the treatment.<\/p>\n

Transforming those components into the therapy that is eventually returned to the patient requires a highly complex manufacturing process. And that\u2019s part of what sets CAR T-cell therapy apart from most other cancer treatments, explained Anthony Welch, Ph.D., a project officer in NCI\u2019s Division of Cancer Treatment and Diagnosis (DCTD)<\/a>.<\/p>\n

\u201cWith CAR T cells, the process is the product,\u201d Dr. Welch said. That process is also expensive, complicated, and highly regulated.<\/p>\n

That\u2019s part of what makes conducting human clinical trials<\/a> testing these individualized CAR T-cell therapies more challenging than those involving \u201coff-the-shelf\u201d drugs that are manufactured in massive batches. Few laboratories and centers have the capability to make CAR T cells, which has limited the ability to test them more broadly.<\/p>\n

To help address these challenges, more than a year ago, DCTD and NCI leaders turned to their experts at the Frederick National Lab for Cancer Research (FNLCR)<\/a> and tasked them with developing the capability to produce cellular therapies like CAR T cells for cancer. Specifically, the goal was to accelerate the ability to test these therapies in clinical trials to be conducted at multiple hospital sites.\u00a0<\/p>\n

The initial clinical trial supported by this effort will be the first trial to test a CAR T-cell therapy designed to target a protein on cancer cells called CD33 in children and young adults with advanced forms of acute myeloid leukemia (AML)<\/a>. It will ultimately enroll patients at six different sites, starting at the NIH Clinical Center in Bethesda, MD, and the Children\u2019s Hospital of Philadelphia (CHOP).<\/p>\n

Having multiple sites for the first trial will be good for both the investigators and the patients, said the trial\u2019s co-lead investigator, Richard Aplenc, M.D., of CHOP, where the first patient on the trial was enrolled in January.\u00a0<\/p>\n

\u201cIt will really expand access to this investigational therapy,\u201d Dr. Aplenc continued. \u201cWe have sites on both coasts and in the middle of the country.\u201d<\/p>\n

And as researchers look to expand CAR T-cell therapy as an option for other cancers, including solid tumors<\/a>, Dr. Welch said, lowering the barriers to their success will be critical.<\/p>\n

\u201cThat\u2019s the idea we\u2019re trying to support,\u201d he said. \u201cWe\u2019re taking some of the risk out of [developing] innovative concepts and ideas by helping to bring more of these therapies into early clinical trials.\u201d<\/p>\n

From a Blood Collection to an Engineered Cell Therapy<\/h2>\n

In a nutshell, the manufacturing of a CAR T-cell therapy works like this.<\/p>\n

First, a patient\u2019s own blood is collected and the white blood cells from that collection are separated out, with the remaining red blood cells and plasma returned to the patient, a process known as leukapheresis<\/a>.<\/p>\n

Once the collected white blood cells are in hand, research groups use various methods to isolate specific T cells from the other white blood cells. Then, a disarmed virus is used to deliver genetic instructions to the T cells telling them to produce the chimeric antigen receptor<\/a> (CAR), which ends up on their surfaces, and co-stimulatory molecules, which reside inside the cell. (By delivering signals that keep the T cells active, the co-stimulatory molecules help the CAR T cells to survive and grow once introduced back into the patient.)<\/p>\n

Next, this small batch of CAR T cells is\u00a0induced to multiply until they number in the millions, a process that is carefully monitored to ensure that they grow enough in number to achieve the appropriate \u201cdose\u201d of T cells.<\/p>\n

The final step in the manufacturing journey requires some important housekeeping to ensure the purity and quality of the CAR T cells, at which point they are ready to be infused back into the patient.<\/p>\n

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In CAR T-cell therapy, after patients undergo leukapheresis, their T cells are subject to a complex process that produces hundreds of millions of genetically modified T cells that they then receive via intravenous infusion.<\/p>\n

Credit: Adapted from Blood Cancer Journal. January 2019. doi: https:\/\/doi.org\/10.1038\/s41408-018-0164-6. CC BY 4.0.<\/p>\n<\/div>\n<\/figcaption><\/figure>\n<\/div>\n

At the moment, only a small group of research labs have the ability to make CAR T cells, said Nirali Shah, M.D., of NCI\u2019s Center for Cancer Research<\/a>, the co-lead investigator on the CD33 CAR T-cell trial.<\/p>\n

\u201cYou can\u2019t just manufacture cells in any lab and give them to patients,\u201d said Dr. Shah, who has led several trials of CAR T-cell therapies in children with blood cancers at the NIH Clinical Center in Bethesda, MD. \u201cYou need to have the infrastructure and the support and the knowledge to be able to do this well.\u201d<\/p>\n

With an existing facility, the Biopharmaceutical Development Program (BDP) at the FNLCR in Frederick, MD, for manufacturing biological products, Dr. Welch said, there was an opportunity for NCI to help meet a critical need to help accelerate CAR T-cell research.\u00a0<\/p>\n

\u201cThe BDP has\u00a0experience manufacturing viruses, antibodies<\/a>, proteins<\/a>, and vaccines<\/a> to support early trials,\u201d he added. \u201cIt has experience with quality manufacturing processes.\u201d<\/p>\n

What the program didn\u2019t have, however, was experience manufacturing CAR T cells.<\/p>\n

Collaborations Critical to Quick Action<\/h2>\n

With a commitment from NCI leadership to back the manufacturing effort, the next steps were to identify the first trial to be supported and establish the manufacturing process.\u00a0<\/p>\n

Having some of the country\u2019s leading experts in developing and testing CAR T-cell therapies at NCI helped with the first step. Dr. Shah and her colleagues in NCI\u2019s Pediatric Oncology Branch (POB)<\/a> were already working on a CD33 CAR T cell that they were moving toward a trial for children with AML. This specific CAR was initially developed by Terry Fry, M.D., formerly of the POB and now at the University of Colorado School of Medicine.<\/p>\n

\u201cWhen the CD33 concept was first developed, we were all thinking it would be a single-center phase 1 trial, because we previously did not have the infrastructure to plan for a multicenter trial,\u201d Dr. Shah said.<\/p>\n

But the community of researchers like Drs. Shah and Aplenc, whose work focuses on developing and testing treatments, including stem cell transplants, for children with blood cancers is highly collaborative, she said. And with the NCI manufacturing initiative coming online, she added, \u201cthere was now a mechanism to think about a multicenter trial.\u201d<\/p>\n

That research community includes the Center for International Blood and Marrow Transplant Research, which came on board as the trial\u2019s primary sponsor, and the National Marrow Donor Program, which will manage its overall conduct (e.g., overseeing and coordinating the shipping of cells, monitoring patient safety).<\/p>\n

Next, it was time to nail down the manufacturing process. The location had already been identified: the BDP, which manufactures drugs and therapies from biological sources, such as bacteria and proteins, for research studies.<\/p>\n

The NCI team then turned to NIH for manufacturing expertise. The experts they consulted included David Stroncek, M.D., and Steve Highfill, Ph.D., of NIH\u2019s Center for Cellular Engineering<\/a>, which has extensive experience developing and manufacturing cell therapies, including CAR T cells, for investigators within NIH.\u00a0<\/p>\n

\u201cTheir expertise and experience was invaluable,\u201d Dr. Welch said.<\/p>\n

Armed with this guidance and feedback, the NCI team decided to use a relatively new, commercially available system for manufacturing CAR T cells.\u00a0<\/p>\n

The system, called Prodigy, is \u201cclosed,\u201d meaning that once the collected cells from the patient are put into the system, it takes care of the rest, producing a completed CAR T-cell product within 2 weeks, explained Jason Yovandich, Ph.D., also of DCTD.<\/p>\n

Up to this point, most laboratories and the companies that manufacture the two FDA-approved CAR T-cell therapies have used \u201copen\u201d systems, which require more manual manipulation to produce a final product. With a closed system, Dr. Yovandich said, \u201cthe only variable to account for is\u00a0the patient cells going in.\u201d<\/p>\n

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One of the CliniMACS Prodigy systems being used at NCI’s Frederick National Laboratory for Cancer Research to manufacture CAR T-cell therapies.<\/p>\n

Credit: National Cancer Institute<\/p>\n<\/div>\n<\/figcaption><\/figure>\n<\/div>\n

Currently, NCI has two Prodigy systems, with plans to add a third. Depending on how this initiative progresses, more could be added, he said.\u00a0<\/p>\n

A Different Model<\/h2>\n

Numerous clinical trials of CAR T-cell therapies have been conducted at CHOP. Dr. Aplenc said that, not unexpectedly, there are differences conducting a trial when the treatment is not being manufactured in house. But for a multicenter trial, a single manufacturer seems to be the ideal choice.<\/p>\n

\u201cIf NCI was not doing the cell manufacturing, it would be extremely challenging to do this [multicenter trial],\u201d he said.<\/p>\n

Dr. Aplenc said he doesn\u2019t expect any issues with having the CD33 CAR T cells made at a single location. Even when a CAR T-cell therapy is produced in house at a single institution, there are always logistics to deal with. For example, the manufacturing time \u201cis driven by the current queue at that center, which can be driven by patient volume and manufacturing throughput,\u201d he said.<\/p>\n

And even as the manufacturing of CAR T-cell therapies becomes more automated, which is expected to increase the number of labs involved in research involving these therapies, a centralized approach can play an important role in human clinical studies<\/a> of new treatments, Dr. Shah noted. \u201cI think a model like this has so much promise,\u201d she said.<\/p>\n

Dr. Welch emphasized that it\u2019s still early days for the manufacturing initiative and that it will take time to see how it plays out. \u201cWe\u2019re still taking baby steps,\u201d he said.<\/p>\n

Even so, it\u2019s taken a lot of work and collaboration to get this far. \u201cThat\u2019s what it takes to put something like this together,\u201d he said. The collaboration \u201chas been tremendous and critical to the progress we have made.\u201d<\/p>\n

Source<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"

April 23, 2020, by NCI Staff Through a recently launched initiative, NCI will manufacture CAR T-cell therapies for clinical trials being conducted at multiple hospitals. Credit: National Cancer Institute In 2010, an NCI research team published the first study of a new form of cancer treatment called CAR T-cell therapy, reporting on a single patient […]<\/p>\n","protected":false},"author":2,"featured_media":23214,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_monsterinsights_skip_tracking":false,"footnotes":""},"categories":[5137],"tags":[],"class_list":["post-23213","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-world-news"],"_links":{"self":[{"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/posts\/23213","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/comments?post=23213"}],"version-history":[{"count":1,"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/posts\/23213\/revisions"}],"predecessor-version":[{"id":45660,"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/posts\/23213\/revisions\/45660"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/media\/23214"}],"wp:attachment":[{"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/media?parent=23213"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/categories?post=23213"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/tags?post=23213"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}