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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.
Abstract:
Waldenstrom macroglobulinemia (WM) is a rare B-cell lympho-proliferative disorder. There is limited data from India regarding the characteristics and outcomes of patients with WM. We describe here the patients with WM treated at our center over the course of the past 15 years. This was a single center, retrospective analysis. Patients fulfilling the diagnosis of WM who were treated at our center between 2009 and 2023 were included in the study. Fifty-five patients were included in the study for analysis. The median age was 62 years with a Male: Female ratio of 3.2:1. Most patients (n = 42; 76.4%) had symptoms attributable to WM, while 5 patients (9.1%) had Immunoglobulin M (IgM) related symptoms and 8 patients (14.5%) had both. The median hemoglobin of the cohort was 7.4 g/dl and the median serum IgM level was 4.87 g/L. MYD88 mutation testing was done in 30 patients and was positive in 16 (53.3%). The most common first line therapy was chemo-immunotherapy (n = 36; 65.5%). Most common chemo-immunotherapy was Bendamustine-Rituximab followed by Rituximab-Cyclophosphamide-Dexamethasone. The overall response rate and major response rate to front-line therapy was 78.2% and 69.1% respectively. The median follow-up for the entire cohort was 30 months. Fourteen patients died during follow-up with the most common cause being progressive disease (n = 6; 42.9%). The median Event-free Survival, Time to Next therapy and Overall Survival were 45 months, 51 months and 150 months respectively. In our WM case series from India, we found a low incidence of MYD88 mutations with comparable treatment outcomes to western literature.
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.
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