CAR T-Cell Therapy, cancer treatment, Medrego biotech

Chimeric antigen receptor T-cell therapy, popularly referred to as CAR-T therapy, is reshaping the terrain of cancer treatment, presenting a beacon of hope for patients grappling with specific cancer types.

An Introduction to CAR T-Cell Therapy

CAR-T therapy is not just another treatment in the vast landscape of oncological interventions. It fundamentally transforms T-cells, vital components of the immune system responsible for recognizing and obliterating foreign entities, empowering them with the capability to latch onto and eradicate cancer cells.

Traditionally, CAR-T therapy has been a recourse for blood cancers. However, the scientific community is buzzing with activity to explore its potential for other cancer types. Dive deeper into the intricate workings, advantages, challenges, and future prospects of this revolutionary treatment.

Decoding the Mechanism of This New Cancer Therapy

T-cells are indispensable warriors in the immune system’s arsenal. Their primary function? To bind to alien proteins on unfamiliar cell surfaces. Some T-cells annihilate these invaders directly, while others rally the broader immune system.

However, for the immune system to counteract cancer cells, T-cells equipped with specific receptors are imperative. These specialized receptors allow T-cells to attach to distinct cancer cell proteins. The creation of these bespoke cells is the essence of CAR-T therapy.

Journey of a T-cell in CAR-T Therapy

  1. Extraction of T-cells from the patient’s bloodstream.
  2. Genetic modification in a controlled lab environment enables T-cells to produce chimeric antigen receptors tailored to the patient’s cancer type.
  3. Cultivation of these newly engineered T-cells in the lab, amplifying their numbers.
  4. Reintroduction of these T-cells into the patient’s bloodstream.

Furthermore, a regimen of low-dose chemotherapy might precede the T-cell infusion. This is not to combat cancer directly but to make room for the modified T-cells to function optimally.

Post-infusion, these empowered CAR T-cells set forth on their mission to identify, bind, and eliminate cancer cells. Although the primary action is swift, there’s evidence suggesting the persistence of these cells, continuously fighting cancer cells for months post-treatment.

It’s crucial to note, however, that CAR-T therapy isn’t a first-line treatment. Its administration requires prior ineffective treatments, varying based on cancer type. Its approval is primarily for blood cancers like:

  • Relapsed or refractory large B-cell lymphoma.
  • Relapsed or refractory follicular lymphoma.
  • Relapsed or refractory mantle cell lymphoma.
  • Pediatric relapsed or refractory acute lymphoblastic leukemia.
  • Relapsed or refractory multiple myeloma.

Advantages of CAR T-Cell Therapy

CAR-T therapy is a game-changer, especially for patients whose blood cancers remain unyielding to other treatments. It’s not merely a fallback but often a life-saver.

Efficacy Rates of CAR T-Cell Therapy

According to data from the National Cancer Institute, CAR-T therapy exhibits promising response rates:

  • Relapsed/refractory diffuse large B-cell lymphoma: Between 52 to 82 percent.
  • B-cell acute lymphoblastic leukemia: A staggering 80 percent.
  • Chronic lymphocytic leukemia/small lymphocytic lymphoma: 82 percent.

Many patients from these clinical trials experienced complete remission, signifying the groundbreaking potential of this treatment. Link to the study.

Understanding the Challenges and Risks of CAR T-Cell Therapy

No treatment is without challenges. With CAR-T therapy:

  • Efficacy concerns: Like most treatments, CAR-T therapy isn’t infallible. There’s a possibility it might not eliminate all cancer cells.
  • Relapse: The looming shadow of cancer recurrence persists even if initial results are positive. For instance, specific cancers like large B-cell lymphoma have shown tendencies to reappear post-treatment. Related study here.
  • Adverse effects: While side effects are a possibility with any treatment, CAR-T therapy has some significant ones.

Potential Side Effects of CAR T-Cell Therapy

The range of side effects can span from mild to severe, necessitating immediate medical attention if they intensify. These include:

  • Common reactions like fever, fatigue, nausea, diarrhea, rashes, muscle aches, joint stiffness, and appetite loss.
  • Severe reactions stemming from cytokine release syndrome, like rapid heart rate, kidney failure, multiple organ failure, hallucinations, and more.

Mitigative measures, like a combination of steroids and other specific drugs, are employed to manage these side effects.

Equine tendond and ligament treatment with stem cell therapy

Financial Aspects of CAR T-Cell Therapy

CAR-T therapy is undoubtedly groundbreaking but comes with a hefty price tag. Treatments like Axicabtagene ciloleucel (Yescarta) and tisagenlecleucel (Kymriah) cost $373,000 and $475,000 respectively, excluding ancillary medical expenses. See the related publication here.

Insurance might cover these costs, contingent on clinical appropriateness and FDA approvals. Both private insurance and Medicare provide varying degrees of coverage.

The Horizon of CAR T-Cell Therapy

CAR-T therapy is the epitome of hope for countless patients, especially those with stubborn blood cancers. While the treatment process can be arduous, necessitating hospital stays, the potential life extension it offers is invaluable.

Research continues to broaden the horizons of CAR-T therapy beyond blood cancers. The quest to enhance its safety and efficacy is relentless, signaling a future brimming with possibilities in the realm of cancer treatment.

The Medrego Biotech team is also heavily involved in the future of CAR T-cell Therapy. See more about cooperation options on this topic here – Medrego R&D services.


The Medrego Life Science team does not give any personal advice on a certain health condition, or provide instructions on how to cure or treat a health condition. We always suggest consulting a qualified medical professional for personalized advice.

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Experience in Gene and Cell therapy (ATMP) regulatory affairs and authorization in the EU. Senior consultant for private and public sector organisations. Previously member of the Committee for Advanced Therapies (ATMPs) at European Medicines Agency (EMA).