Advances in targeted therapy for the treatment of patients with relapsed/refractory multiple myeloma

Emmanuelle Le Ray1, Sundar Jagannath2, Antonio Palumbo3

  • 1a Hematology Department , CHU Cochin, Paris V René Descartes University , Paris , France.

Expert Review of Hematology
|November 13, 2015
PubMed

Insights

New targeted therapies offer improved outcomes for relapsed/refractory multiple myeloma (RRMM) patients. This review covers new proteasome inhibitors and immunotherapies for RRMM treatment.

Area of Science:

  • Oncology
  • Hematology
  • Pharmacology

Background:

  • Relapsed/refractory multiple myeloma (RRMM) outcomes have improved with proteasome inhibitors (PIs) and immunomodulatory drugs.
  • However, treatment resistance and limited efficacy remain challenges in managing multiple myeloma.
  • The incurable nature of multiple myeloma necessitates continuous development of novel therapeutic agents.

Purpose of the Study:

  • To provide an overview of recent advances in targeted therapy for RRMM.
  • To discuss newly approved agents and emerging treatment strategies.
  • To focus on monotherapy and combination targeted therapies for RRMM.

Main Methods:

  • Literature review of recent clinical trials and studies.
  • Analysis of data on novel oral PIs, immunotherapies (e.g., CD38- or SLAMF7-targeted antibodies), and small molecules.
  • Synthesis of information on efficacy and safety of targeted agents in RRMM.

Main Results:

  • Recent approvals include new oral PIs (ixazomib) and novel immunotherapies.
  • Combination targeted therapies show promise in overcoming drug resistance.
  • Ongoing research focuses on expanding treatment options for RRMM patients.

Conclusions:

  • Targeted therapies, including novel PIs and immunotherapies, represent significant progress in RRMM management.
  • Personalized treatment approaches combining targeted agents are crucial for improving patient outcomes.
  • Continued research and development are essential to address unmet needs in multiple myeloma therapy.

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