Prognostic impact of lymphocyte kinetics and immune composition during bispecific antibody therapy in relapsed/refractory multiple myeloma - Report - MDSpire
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Influence of Lymphocyte Dynamics and Immune Profile on Outcomes of Bispecific Antibody Treatment in Relapsed/Refractory Multiple Myeloma

  • By

  • Mansi R. Shah

  • Aishee Bag

  • Asis Shrestha

  • Yetunde Ogunsesan

  • Anup Trikannad

  • Sruthi Vellanki

  • Sanjay Muttineni

  • Hira Cheema

  • Syed Naqvi

  • Sasya Dronavalli

  • Samer Al Hadidi

  • Sharmilan Thanendrarjan

  • Maurizio Zangari

  • Frits van Rhee

  • Aniko Szabo

  • Rajshekar Chakraborty

  • Meera Mohan

  • Carolina Schinke

  • August 22, 2026

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Clinical Report: Influence of Lymphocyte Dynamics on Bispecific Antibody Outcomes

Overview

This study investigates the impact of lymphocyte dynamics and immune profiles on the efficacy of bispecific antibodies in relapsed/refractory multiple myeloma. Key findings indicate that while baseline lymphopenia did not correlate with treatment response, significant changes in lymphocyte counts occurred during treatment, particularly among responders.

Background

Bispecific antibodies targeting BCMA and GPRC5D represent significant advancements in the treatment of relapsed/refractory multiple myeloma, achieving overall response rates of up to 70%. Understanding the factors influencing treatment outcomes, such as immune competence reflected by lymphocyte dynamics, is crucial for optimizing therapeutic strategies. This study aims to clarify the prognostic significance of lymphocyte kinetics during bispecific antibody treatment.

Data Highlights

ParameterValue
Median Age70 years
Male Patients52%
Median Baseline ALC0.91 × 10³/µL
Patients with Lymphopenia52%
2-Year PFS Rate (No Lymphopenia)28%
2-Year OS Rate (No Lymphopenia)55%

Key Findings

  • Overall response rates to bispecific antibodies in RRMM reached 70%.
  • Baseline lymphopenia was present in 52% of patients but did not correlate with treatment response.
  • Responders exhibited significantly higher ALC values on Day 14 compared to non-responders.
  • CD4 T-cell counts decreased significantly by Day 30, particularly in non-responders.
  • CD19 B-cell counts declined persistently throughout treatment without differences between responders and non-responders.

Clinical Implications

Clinicians should consider the dynamics of lymphocyte subsets when evaluating treatment responses to bispecific antibodies in RRMM. Monitoring ALC and lymphocyte subset changes may provide insights into patient immune competence and treatment efficacy.

Conclusion

The study highlights the importance of lymphocyte dynamics in understanding treatment outcomes with bispecific antibodies in relapsed/refractory multiple myeloma, suggesting that immune profile assessments may aid in patient management.

Related Resources & Content

  1. Bumma et al., Journal of Clinical Oncology, 2024 -- Relapsed or Refractory Multiple Myeloma: Activity of BCMA x CD3 Bispecific Antibody
  2. Abutalib et al., The ASCO Post, 2026 -- Navigating Early Relapse in Multiple Myeloma: New Evidence from the 2026 ASCO and EHA Congresses
  3. The ASCO Post, 2023 -- Bispecific Antibody REGN5459 Shows Activity in Patients With Relapsed or Refractory Multiple Myeloma
  4. Blood Cancer Journal, 2025 -- Analysis of Peripheral Blood Immune Cell Characteristics and Their Response to BCMA CAR-T Therapy in Relapsed Refractory Multiple Myeloma
  5. NCCN Clinical Practice Guidelines In Oncology, 2026 -- Multiple Myeloma, Version 5.2026
  6. Teclistamab in Relapsed or Refractory Multiple Myeloma, New England Journal of Medicine, 2022
  7. Blood Cancer Journal, 2026 -- Prognostic impact of lymphocyte kinetics and immune composition during bispecific antibody therapy in relapsed/refractory multiple myeloma
  8. Multiple Myeloma, Version 5.2026, NCCN Clinical Practice Guidelines In Oncology - PubMed
  9. Teclistamab in Relapsed or Refractory Multiple Myeloma | New England Journal of Medicine
  10. Prognostic impact of lymphocyte kinetics and immune composition during bispecific antibody therapy in relapsed/refractory multiple myeloma | Blood Cancer Journal

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