Clinical Characteristics and Treatment Outcomes of Patients with Waldenstrom Macroglobulinemia

Gaurav Prakash1, Charanpreet Singh1, Pradeep Reddy1

  • 1Department of Clinical Hematology and Medical Oncology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

Insights

This study analyzed Waldenstrom macroglobulinemia (WM) patient data from India. Outcomes were comparable to Western literature, with a lower incidence of MYD88 mutations observed in Indian WM patients.

Area of Science:

  • Hematology
  • Oncology
  • Rare Diseases

Background:

  • Waldenstrom macroglobulinemia (WM) is a rare B-cell lymphoproliferative disorder.
  • Limited data exists on WM characteristics and outcomes specifically from India.
  • This study addresses the need for Indian-specific WM data.

Purpose of the Study:

  • To describe the clinical characteristics and treatment outcomes of WM patients in India.
  • To compare findings with existing Western literature.
  • To investigate the incidence of MYD88 mutations in Indian WM patients.

Main Methods:

  • Retrospective analysis of 55 WM patients treated at a single center from 2009-2023.
  • Data collection included patient demographics, clinical presentation, laboratory values, MYD88 mutation status, treatment regimens, and outcomes.
  • Statistical analysis of survival and response rates.

Main Results:

  • The median age of patients was 62 years, with a male predominance (3.2:1).
  • Common symptoms included those attributable to WM (76.4%) and Immunoglobulin M (IgM) related issues (9.1%).
  • Median hemoglobin was 7.4 g/dL, median serum IgM was 4.87 g/L. MYD88 mutation was positive in 53.3% of tested patients.
  • Chemo-immunotherapy, particularly Bendamustine-Rituximab, was the most common first-line treatment.
  • Overall and major response rates to front-line therapy were 78.2% and 69.1%, respectively.
  • Median event-free survival, time to next therapy, and overall survival were 45, 51, and 150 months, respectively.
  • Progressive disease was the most common cause of death (42.9%).

Conclusions:

  • Indian WM patients present with characteristics and outcomes comparable to those reported in Western literature.
  • A lower incidence of MYD88 mutations was observed in this Indian cohort compared to some Western studies.
  • This study provides valuable insights into WM management and epidemiology in the Indian subcontinent.