Treatment Recommendations for Relapsed Multiple Myeloma

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Article
ONCOLOGY® CompanionONCOLOGY® Companion, Volume 37, Supplement 11
Volume 37
Issue 11
Pages: 18

Experts in the multiple myeloma space met to discuss the treatment and monitoring after bispecific antibodies.

CancerNetwork hosted a Training Academy focused on various treatment options for patients with relapsed multiple myeloma.

Meet the Experts

Meet the Experts

Management of Relapsed Multiple Myeloma

  • With multiple treatments available, clinicians will determine the stage of relapse and provide the appropriate therapy.
    • Early relapse can be treated with combination therapies with the bases of these combinations including lenalidomide (Revlimid), pomalidomide (Pomalyst), or bortezomib (Velcade).
  • Although triplet combinations are preferred, the treatment must be individualized to the patient based on patient preference, condition, and disease progression.
  • For 1 to 3 lines of therapy, triplet combinations are available, including the following:
    • Carfilzomib (Krypolis), daratumumab (Darzalex), and dexamethasone
    • Daratumumab, pomalidomide, and dexamethasone
    • Bortezomib, selinexor (Xpovio), and dexamethasone
  • However, their trial data have not been compared head-to-head.
  • For late relapse, chimeric antigen receptor (CAR) T-cell therapy, B-cell maturation antigens, and bispecific therapies are available.
    • Immunotherapeutic options are also available.

Deciding Between CAR T-Cell and Bispecific Therapies

  • Typically decisions are made based on access and availability of the product.
    • Each center has different availability of treatments or waiting-list times.
    • Of note, because these therapies are new, clinics and institutions are still transitioning.
  • CAR T-cell therapy and bispecific treatments are optimally used as fourth-line therapy and beyond.


Step-Up Dosing of Teclistamab (Tecvayli)

  • This can vary between institutions and community practices.
  • Patients can be admitted as an inpatient, or treatment can be administered in an outpatient setting.
  • The FDA requires patients to be admitted for 48 hours after administration to monitor for cytokine release syndrome.
  • Step-up dosing is usually given on days 1, 4, and 7.
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