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A MyMyelomaTeam Member asked a question 💭
Mill Creek, WA

I am wondering if anyone has undergone CarT therapy for RRMM, with new drug Carvykti ? If so, what was your response, side effects after infusion, and whether you would do it again ?
Thanks...have a good day !

February 7, 2023
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Reactions
A MyMyelomaTeam Member

Me too. Just got okayed for it yesterday by my insurance company.

February 21, 2023
A MyMyelomaTeam Member

My husband is planning on going thru the Carvykti transplant in the upcoming months, Would love to know if anyone else has had this too?

February 13, 2023
A MyMyelomaTeam Member

I had carvykti cart- t April 1st this year. I haven't had many of the bad side effects but at this point am still.not allowed to drive, but was recently told that I am in full remission. I can't say it hasn't been a battle getting here though.

July 31, 2024
A MyMyelomaTeam Member

My husband had a Carvytkti CAR-T in January of last year for MM and the manf messed up his cells and he did not get the approved dose and it failed.

July 31, 2024
MyMyelomaTeam

Carvykti, also known by its drug name Ciltacabtagene autoleucel, is a type of immunotherapy called chimeric antigen receptor (CAR) T-cell therapy. Here are some key points about Carvykti:

Overview
- Approval: Carvykti is approved by the U.S. Food and Drug Administration (FDA) to treat relapsed or refractory multiple Show Full Answer

Carvykti, also known by its drug name Ciltacabtagene autoleucel, is a type of immunotherapy called chimeric antigen receptor (CAR) T-cell therapy. Here are some key points about Carvykti:

Overview
- Approval: Carvykti is approved by the U.S. Food and Drug Administration (FDA) to treat relapsed or refractory multiple myeloma in adults who have already tried at least four lines of therapy. These therapies must include:
- A proteasome inhibitor
- An immunomodulatory agent
- An anti-CD38 monoclonal antibody

How It Works
- Mechanism: Carvykti is made from a person’s own T cells, which are harvested and genetically engineered to target a protein called B-cell maturation antigen (BCMA) found on myeloma cells.
- Process:
1. T Cell Harvesting: T cells are collected from the patient in a process similar to a blood transfusion.
2. Genetic Engineering: The harvested T cells are sent to a laboratory where they are genetically modified to express CARs that target BCMA.
3. Manufacturing: This process takes about four to five weeks.
4. Infusion: The modified T cells are then infused back into the patient after a round of chemotherapy called lymphodepletion to make room for the new T cells.

Administration
- Chemotherapy: Patients receive chemotherapy for a few days before the Carvykti infusion.
- Infusion: Carvykti is administered once as an intravenous infusion.

Side Effects
- Common Side Effects:
- Cytokine release syndrome (CRS), which can be severe and life-threatening, causing neurological effects like seizures, hallucinations, and tremors.
- Fever, low blood pressure, fatigue, infections, cough, chills, diarrhea, nausea, encephalopathy, low appetite, headache, fast heart rate, trouble breathing, edema, bleeding or blood clotting issues, constipation, vomiting, and pain in muscles, bones, or joints.
- Serious Side Effects:
- Immune effector cell-associated neurotoxicity syndrome
- Macrophage activation syndrome
- Hemophagocytic lymphohistiocytosis
- Increased risk of developing other types of cancer

For more detailed information, you can visit the official Carvykti website: [Carvykti — Janssen Biotech Inc.](https://www.carvykti.com)

This information is based on the knowledge base provided.

July 31, 2024

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