Idecabtagene vicleucel

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(Redirected from Abecma)

What is Idecabtagene vicleucel?[edit | edit source]

  • Idecabtagene vicleucel (Abecma) is a B-cell maturation antigen (BCMA)-directed genetically modified autologous T cell immunotherapy used to treat multiple myeloma.



What are the uses of this medicine?[edit | edit source]

  • Idecabtagene vicleucel (Abecma) is for the treatment of multiple myeloma in patients who have received at least four kinds of treatment regimens that have not worked or have stopped working. Abecma is a medicine made from your own white blood cells; the cells are genetically modified to recognize and attack your multiple myeloma cells.

Multiple myeloma:


How does this medicine work?[edit | edit source]

  • (uh-BEK-muh) A drug used to treat adults with multiple myeloma that relapsed (came back) or did not get better after treatment with at least four other anticancer therapies, including an anti-CD38 monoclonal antibody, a proteasome inhibitor, and an immunomodulating agent. It is also being studied in the treatment of other types of cancer.
  • Abecma is made using a patient’s T cells (a type of immune system cell).
  • A gene for a special receptor called chimeric antigen receptor (CAR) is added to the T cells in the laboratory.
  • These changed T cells called CAR T cells are grown in large numbers in the laboratory and given to the patient by infusion.
  • Upon administration, idecabtagene vicleucel specifically recognizes and kills BCMA-expressing tumor cells.
  • BCMA, a tumor-specific antigen and a receptor for both a proliferation-inducing ligand (APRIL) and B-cell activating factor (BAFF), is a member of the tumor necrosis factor receptor superfamily (TNFRSF) and plays a key role in plasma survival; it is found on the surfaces of plasma cells and overexpressed on malignant plasma cells.


Who Should Not Use this medicine ?[edit | edit source]

  • This medicine have no usage limitations.


What drug interactions can this medicine cause?[edit | edit source]

  • HIV and the lentivirus used to make Abecma have limited, short spans of identical genetic material (RNA).
  • Therefore, some commercial HIV nucleic acid tests may yield false-positive results in patients who have received Abecma.


Is this medicine FDA approved?[edit | edit source]

  • Idecabtagene vicleucel was approved for medical use in the United States in March 2021.


How should this medicine be used?[edit | edit source]


Recommended dosage:

  • Abecma is provided as a single dose for infusion containing a suspension of chimeric antigen receptor (CAR)-positive T cells in one or more infusion bags.
  • The recommended dose range is 300 to 460 × 106 CAR-positive T cells.


Administration:

  • Abecma is made from your own white blood cells, so your blood will be collected by a process called "leukapheresis" (LOO-kuh-feh-REE-sis).
  • Your blood cells will be sent to a manufacturing center to make your Abecma.
  • When your Abecma is ready, your healthcare provider will give Abecma to you through a catheter (tube) placed into your vein (intravenous infusion). Your dose of Abecma may be given in one or more infusion bags. The infusion usually takes up to 30 minutes for each infusion bag.
  • You will be monitored at the certified healthcare facility where you received your treatment daily for at least 7 days after the infusion.
  • You should plan to stay within 2 hours of this location for at least 4 weeks after getting Abecma.


What are the dosage forms and brand names of this medicine?[edit | edit source]

This medicine is available in fallowing doasage form:

  • As suspension for intravenous infusion
  • A single dose of Abecma contains a cell suspension of 300 to 460 × 106 CAR-positive T cells in one or more infusion bags.

This medicine is available in fallowing brand namesː

  • Abecma


What side effects can this medication cause?[edit | edit source]

The most common side effects of this medicine include:

  • fatigue
  • fever (100.4°F/38°C or higher)
  • chills/shivering
  • severe nausea or diarrhea
  • decreased appetite
  • headache
  • dizziness/lightheadedness
  • confusion
  • difficulty speaking or slurred speech
  • cough
  • difficulty breathing
  • fast or irregular heartbeat


What special precautions should I follow?[edit | edit source]

  • Abecma can cause a very common side effect called cytokine release syndrome. Counsel patients to seek immediate medical attention should signs or symptoms of CRS occur at any time.
  • Neurologic toxicities, which may be severe or life-threatening, occurred following treatment with Abecma, including concurrently with CRS, after CRS resolution, or in the absence of CRS. Counsel patients to seek immediate medical attention should signs or symptoms of neurologic toxicity occur at any time.
  • Allergic reactions may occur with the infusion of Abecma. Monitor for hypersensitivity reactions during infusion.
  • Abecma should not be administered to patients with active infections or inflammatory disorders. Severe, life-threatening, or fatal infections occurred in patients after Abecma infusion. Monitor patients for signs and symptoms of infection; treat appropriately.
  • Patients may exhibit prolonged cytopenias following lymphodepleting chemotherapy and Abecma infusion. Monitor blood counts prior to and after Abecma infusion.
  • Plasma cell aplasia and hypogammaglobulinemia can occur in patients receiving treatment with Abecma. Monitor and consider immunoglobulin replacement therapy.
  • Patients treated with Abecma may develop secondary malignancies. In the event that a secondary malignancy occurs after treatment with Abecma, contact Bristol-Myers Squibb at 1-888-805-4555.
  • Due to the potential for neurologic events, including altered mental status or seizures, patients receiving Abecma are at risk for altered or decreased consciousness or coordination in the 8 weeks following Abecma infusion. Advise patients to refrain from driving and engaging in hazardous occupations or activities, such as operating heavy or potentially dangerous machinery, during this initial period.


What to do in case of emergency/overdose?[edit | edit source]

  • In case of overdose, call the poison control helpline of your country. In the United States, call 1-800-222-1222.


Can this medicine be used in pregnancy?[edit | edit source]

  • There are no available data with Abecma use in pregnant women.
  • It is not known if Abecma has the potential to be transferred to the fetus.


Can this medicine be used in children?[edit | edit source]

  • The safety and efficacy of Abecma in patients under 18 years of age have not been established.


What are the active and inactive ingredients in this medicine?[edit | edit source]

Active ingredient:

  • IDECABTAGENE VICLEUCEL

Inactive ingredients:

  • DIMETHYL SULFOXIDE
  • WATER


Who manufactures and distributes this medicine?[edit | edit source]

Manufactured by:

Marketed by:

  • Celgene Corporation, a Bristol-Myers Squibb Company (Summit, NJ 07901), and bluebird bio, Inc.


What should I know about storage and disposal of this medication?[edit | edit source]

  • Store Abecma frozen in the vapor phase of liquid nitrogen (less than or equal to minus 130°C).
  • Thaw Abecma prior to infusion.


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