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Pattern of relapse in childhood ALL: challenges and lessons from a uniform treatment protocol
Laxman Singh Arya1, S P Kotikanyadanam, Manorama Bhargava
1Division of Pediatric Oncology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India. lsarya@rediffmail.com
Insights
This study analyzed 254 children treated with the MCP-841 protocol, finding a 17.9% relapse rate. Relapse patterns and risk factors like lymphadenopathy necessitate protocol reappraisal for improved outcomes in pediatric cancer patients.
Area of Science:
- Pediatric Oncology
- Clinical Research
- Cancer Treatment Efficacy
Background:
- The MCP-841 protocol was used to treat 254 children under 15 with cancer between 1992 and 2002.
- Understanding relapse patterns is crucial for improving pediatric cancer treatment strategies.
Purpose of the Study:
- To identify relapse patterns in children treated with the MCP-841 protocol.
- To determine management gaps and inform future treatment protocol revisions.
Main Methods:
- Retrospective analysis of 254 pediatric patients treated with the MCP-841 protocol.
- Data collected on remission, relapse sites (bone marrow, CNS, testes), timing of relapse (on-therapy vs. post-therapy), and patient characteristics.
Main Results:
- Complete remission achieved in 87.8% of patients; 17.9% relapsed.
- Common relapse sites included bone marrow (57.5%) and central nervous system (17.5%).
- Lymphadenopathy was a significant predictor of relapse; high-risk features (age, WBC count) associated with early on-therapy relapse.
Conclusions:
- The MCP-841 protocol shows modest survival outcomes (67%), with significant rates of on-therapy relapse, particularly in the CNS and testes.
- Reappraisal of the current treatment protocol is needed, focusing on identifying high-risk groups for intensified, risk-stratified chemotherapy.
Abstract:
This retrospective analysis of 254 children less than 15 years of age treated with MCP-841 protocol from June 1992 to June 2002 was undertaken to identify the pattern of relapse and determine management lacunae. Two hundred twenty-three (87.8%) children achieved a complete remission of whom 40 (17.9%) relapsed. The mean age of relapsed patients was 6.5 years. The male/female ratio was 9:1. There were 23 (57.5%) isolated bone marrow (BM), 7 (17.5%) isolated central nervous system (CNS), 2 (5%) isolated testicular, 5 (12.5%) BM+testes and 1 each of BM+CNS, CNS+testes, and isolated bone relapses. Twenty-seven children (67.5%) relapsed on-therapy whereas 13 (32.5%) relapsed posttherapy. All 9 CNS relapses occurred on-therapy whereas 5/8 (62.5%) of testicular relapses occurred posttherapy. Lymphadenopathy was the only significant predictor for relapse. High-risk features such as age less than 1 year and greater than 10 years (P=0.047) and white cell count greater than 50.0 x 10(9)/L (P=0.044) were significantly more frequent in patients with early on-therapy relapse than in patients with off-therapy relapse. The overall survival in the entire study cohort was 67+/-3.5%. Modest survival outcome, relapse while on chemotherapy and the higher incidence of CNS and testicular relapse indicate the need for reappraisal of our treatment protocol. There is a need of identifying risk factors and high-risk groups in our set of patients and risk-stratified intensification of chemotherapy in them.
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