Real-World Evaluation of Talquetamab for the Treatment of Relapsed/Refractory Multiple Myeloma (RRMM): An International Myeloma Working Group Immunotherapy Registry Real-World Analysis - Summary - MDSpire
Coming Soon: Introducing MDSpire News. Learn more
Conexiant’s news site is now MDSpire News. Learn more

Assessment of Talquetamab in Treating Relapsed/Refractory Multiple Myeloma: Insights from an International Immunotherapy Registry Analysis

  • By

  • Murali Janakiram

  • Carlyn R. Tan

  • Hira Mian

  • Chiung-Yu Huang

  • Rakesh Popat

  • Joaquín Martínez-Lopez

  • Efsthathios Kastritis

  • Wee-Joo Chng

  • Prashant Kapoor

  • Mrugakshi Dave

  • Susan Bal

  • Laurent Garderet

  • Andre De Menezes Silva Corraes

  • Christine Riedhammer

  • Torsten Steinbrunn

  • Magdalene Corona

  • Chandramouli Nagarajan

  • Hermann Einsele

  • Tom Martin

  • Amrita Krishnan

  • Yi Lin

  • May 19, 2026

Share

Objective:

To characterize real-world patterns of talquetamab use, evaluate safety and tolerability, and assess real-world outcomes including response rates, progression-free survival (PFS), and overall survival (OS) in patients with relapsed refractory multiple myeloma (RRMM).

Approach:
  • Study Design: International multicenter retrospective study involving nine academic centers across five countries, focusing on patients treated with talquetamab.
  • Patient Inclusion: Patients who received at least one cycle of talquetamab were included; those receiving it as bridging for CART therapy were excluded from survival analyses.
  • Data Collection: Data on patient characteristics, treatment details, and adverse events (AEs) were collected and analyzed using IMWG response criteria.
Key Findings:
  • A total of 151 patients were included, with a median age of 64 years; 91% were triple-refractory and 53% were penta-refractory.
  • Cytokine release syndrome (CRS) occurred in 26% of patients after the first step-up dose, primarily low grade.
  • Skin and nail toxicities were reported in 40% of patients, with skin dryness being the most common manifestation.
Interpretation:

Real-world data indicate that talquetamab is associated with manageable safety profiles and response rates in a heavily pretreated RRMM population.

Limitations:
  • The study's retrospective nature may introduce biases.
  • Strict eligibility criteria in clinical trials may limit generalizability of findings.
Conclusion:

Talquetamab demonstrates a favorable safety profile and efficacy in real-world settings for patients with RRMM.

Original Source(s)

Related Content