Tisagenlecleucel

Tisagenlecleucel, also known by its brand name Kymriah, is a groundbreaking CAR T-cell therapy being studied in clinical trials for various B-cell malignancies. These trials aim to explore its effectiveness, safety, and potential combinations with other treatments to improve outcomes for patients with challenging blood cancers, including leukemia and lymphoma.

Table of Contents

What is Tisagenlecleucel?

Tisagenlecleucel, also known by its brand name Kymriah, is a groundbreaking type of cancer treatment called CAR T-cell therapy[3]. CAR stands for Chimeric Antigen Receptor, which is a special protein added to T-cells (a type of immune cell) to help them fight cancer. This therapy is considered a form of immunotherapy because it uses the patient’s own immune system to combat cancer cells.

Tisagenlecleucel is what’s known as a “second-generation CAR-T” therapy. It consists of three main parts[3]:

  • A CD19 antigen-binding domain: This part helps the modified T-cells recognize and attach to cancer cells that have the CD19 protein on their surface.
  • A 4-1BB costimulatory domain: This component helps the T-cells multiply and survive longer in the body.
  • A CD3-ζ signaling domain: This part activates the T-cells to attack the cancer cells once they’ve been recognized.

How Does It Work?

The process of tisagenlecleucel treatment involves several steps[1][2]:

  1. T-cell collection: First, some of the patient’s own T-cells are collected from their blood.
  2. Genetic modification: These T-cells are then sent to a laboratory where they are genetically modified to produce the special CAR protein that can recognize and attack cancer cells.
  3. Cell multiplication: The modified T-cells are grown in large numbers in the lab.
  4. Lymphodepletion: Before receiving the modified T-cells, the patient undergoes a process called lymphodepletion. This involves chemotherapy to reduce the number of existing immune cells in the body, making room for the new CAR T-cells.
  5. Infusion: The modified CAR T-cells are then infused back into the patient’s bloodstream.
  6. Cancer-fighting action: Once in the body, these CAR T-cells multiply and begin to recognize and attack cancer cells that have the CD19 protein on their surface.

What Conditions Does Tisagenlecleucel Treat?

Tisagenlecleucel is primarily used to treat certain types of blood cancers. Based on the clinical trials information provided, it is being studied for or used in the treatment of[1][2][3]:

  • Acute Lymphoblastic Leukemia (ALL): This is a type of cancer that affects the blood and bone marrow. It progresses quickly and creates immature blood cells rather than mature ones.
  • Large B-cell Lymphoma: This is a type of non-Hodgkin lymphoma that develops in B-cells, a type of white blood cell. It includes several subtypes:
    • Diffuse Large B-cell Lymphoma (DLBCL)
    • High-Grade B-Cell Lymphoma
    • Transformed Follicular Lymphoma to Diffuse Large B-Cell Lymphoma
Importantly, tisagenlecleucel is typically used for patients whose cancer has either come back after initial treatment (relapsed) or has not responded well to other treatments (refractory).

How is Tisagenlecleucel Administered?

Tisagenlecleucel is administered as a single infusion[1]. However, the entire treatment process involves several steps:

  1. Preparatory treatments: Patients may receive what’s called “bridging” chemotherapy to help control their cancer while the CAR T-cells are being prepared[3].
  2. Lymphodepleting chemotherapy: Just before receiving tisagenlecleucel, patients undergo lymphodepleting chemotherapy. This usually involves drugs like fludarabine and cyclophosphamide, or sometimes bendamustine[3].
  3. Tisagenlecleucel infusion: The CAR T-cells are then infused into the patient’s bloodstream. This is typically done in a hospital setting where the patient can be closely monitored.
  4. Monitoring: After the infusion, patients are closely watched for potential side effects and to assess the treatment’s effectiveness.

Current Clinical Trials

Several clinical trials are currently underway to further study tisagenlecleucel and explore new ways to enhance its effectiveness:

  • Combination with CD22 CAR T-cells: A study is looking at using tisagenlecleucel followed by another type of CAR T-cell therapy targeting CD22 in children and young adults with B-cell cancers[1]. This approach aims to improve outcomes for patients who might not respond fully to CD19-targeted therapy alone.
  • Combination with NT-I7 (efineptakin alfa): Another trial is investigating the use of NT-I7, a long-acting form of interleukin-7, after tisagenlecleucel treatment in patients with large B-cell lymphoma[2]. The goal is to see if NT-I7 can help the CAR T-cells expand and persist longer in the body.
  • Comparison with standard care: A large phase III trial called BELINDA compared tisagenlecleucel to standard care in adults with aggressive B-cell non-Hodgkin lymphoma[3]. This study aimed to determine if tisagenlecleucel could be more effective than current standard treatments.

Potential Side Effects

While tisagenlecleucel can be very effective, it can also cause some serious side effects. Two of the most significant are[2]:

  • Cytokine Release Syndrome (CRS): This is a condition where the immune system becomes highly activated, causing symptoms like fever, low blood pressure, and difficulty breathing. It usually occurs within the first week after infusion but can be managed with appropriate care.
  • Immune Effector Cell-Associated Neurotoxicity Syndrome (ICANS): This can cause neurological symptoms like confusion, difficulty speaking, or seizures. Like CRS, it’s usually temporary and can be managed with proper medical care.
Other potential side effects include infections, low blood cell counts, and B-cell aplasia (a lack of normal B-cells, which can increase the risk of infections).

Future Research and Developments

Ongoing research is focused on several areas to improve tisagenlecleucel therapy:

  • Combination therapies: Studies are looking at combining tisagenlecleucel with other treatments to enhance its effectiveness or duration of response[1][2].
  • Expanding indications: Researchers are investigating the use of tisagenlecleucel in other types of cancers and in different stages of disease.
  • Improving safety: Work is ongoing to better understand and manage the side effects of CAR T-cell therapy.
  • Long-term follow-up: Studies are tracking patients long-term to understand the durability of responses and any late effects of treatment.
These ongoing efforts aim to make tisagenlecleucel an even more effective and safer treatment option for patients with certain blood cancers.

Aspect Details
Drug Name Tisagenlecleucel (Kymriah)
Type of Therapy CAR T-cell therapy
Target CD19 protein on B-cells
Conditions Studied B-cell malignancies including Acute Lymphoblastic Leukemia (ALL) and aggressive B-cell Non-Hodgkin Lymphoma
Administration Single infusion after lymphodepleting chemotherapy
Key Outcomes Measured Safety, efficacy, event-free survival, overall survival, response rates
Potential Side Effects Cytokine Release Syndrome (CRS), Immune Effector Cell-Associated Neurotoxicity Syndrome (ICANS)
Ongoing Research Combination therapies, timing of administration, use in various patient populations

Ongoing Clinical Trials on Tisagenlecleucel

  • Study on Extracellular Vesicles in Hematology Patients Treated with Brexucabtagene Autoleucel and Drug Combination

    Recruiting

    1 1 1 1
    France
  • Long-Term Follow-Up Study for Patients Treated with CAR T-Cell Therapy Using PHE885, YTB323, and Tisagenlecleucel

    Recruiting

    1 1 1 1
    Austria Belgium Denmark Finland France Germany +6
  • Study on Golcadomide for Patients with Relapsed or Refractory Aggressive Large B-Cell Lymphoma at High Risk of Relapse After CAR T-Cell Therapy

    Recruiting

    1 1 1
    Investigated diseases:
    France
  • Study of fludarabine phosphate in patients with blood cancer undergoing lymphodepletion before CAR-T cell therapy

    Not yet recruiting

    1 1 1 1
    Investigated diseases:
    Belgium
  • Study of Tisagenlecleucel for Treating Adult Patients with Resistant or Relapsed B-cell Acute Lymphoblastic Leukemia

    Not yet recruiting

    1 1
    Investigated drugs:
    Poland
  • Study on Nivolumab and Tisagenlecleucel for Children, Adolescents, and Young Adults with Acute Lymphoblastic Leukemia After Treatment Loss

    Not recruiting

    1 1 1
    Investigated diseases:
    France
  • Study on the Effectiveness and Safety of Tisagenlecleucel for Adults with Hard-to-Treat or Returning Follicular Lymphoma

    Not recruiting

    1 1 1
    Investigated drugs:
    Belgium France Germany Italy The Netherlands Norway +1
  • Study on Tisagenlecleucel for High-Risk B-Cell Acute Lymphoblastic Leukemia in Pediatric and Young Adult Patients with Minimal Residual Disease

    Not recruiting

    1 1 1
    Investigated drugs:
    Belgium Denmark France Italy The Netherlands Norway +2
  • Study of Tisagenlecleucel for Adults with Relapsed or Refractory Aggressive B-cell Non-Hodgkin Lymphoma

    Not recruiting

    1 1 1 1
    Austria France Germany Italy The Netherlands Norway +1
  • Study Comparing Tisagenlecleucel with Standard Treatment for Adults with Relapsed or Refractory Follicular Lymphoma

    Not recruiting

    1 1 1 1
    Austria Czechia Hungary Poland Romania Slovakia +1

Glossary

  • CAR T-cell therapy: A type of treatment that uses a patient's own T cells (a type of immune cell) that have been genetically modified to better recognize and attack cancer cells.
  • Tisagenlecleucel: A specific type of CAR T-cell therapy that targets CD19, a protein found on B-cells. It's also known by the brand name Kymriah.
  • B-cell malignancies: Cancers that affect B lymphocytes, a type of white blood cell. These include certain types of leukemia and lymphoma.
  • Acute Lymphoblastic Leukemia (ALL): A type of blood cancer that affects the lymphoid line of blood cells, particularly B-cells or T-cells.
  • Non-Hodgkin Lymphoma: A group of blood cancers that develop from lymphocytes (a type of white blood cell).
  • Cytokine Release Syndrome (CRS): A side effect of some immunotherapies where the immune system releases a large amount of inflammatory molecules called cytokines, potentially causing fever, low blood pressure, and other symptoms.
  • Immune Effector Cell-Associated Neurotoxicity Syndrome (ICANS): A neurological side effect that can occur with certain immunotherapies, potentially causing confusion, difficulty speaking, or other neurological symptoms.
  • Lymphodepleting chemotherapy: A type of chemotherapy given before CAR T-cell therapy to reduce the number of existing immune cells and help the engineered CAR T-cells work more effectively.
  • CD19: A protein found on the surface of B-cells that is targeted by Tisagenlecleucel.
  • CD22: Another protein found on B-cells that is being explored as a target for CAR T-cell therapy, sometimes in combination with CD19-targeted therapies.
  • Autologous: Referring to cells or tissues obtained from the same individual. In CAR T-cell therapy, the patient's own T-cells are used to create the treatment.
  • Refractory: Referring to a disease that does not respond to treatment.
  • Relapsed: Referring to the return of a disease after a period of improvement.

References