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Survival outcome in childhood ALL: experience from a tertiary care centre in North India
K P Kulkarni1, R K Marwaha, A Trehan
1Division of Pediatric Hematology-Oncology, Advanced Pediatric Center, PGIMER, Chandigarh, India.
Insights
Childhood acute lymphoblastic leukemia (ALL) survival lags in developing nations. Key risk factors include symptom-diagnosis interval, high white cell count (WCC), and low platelet count, impacting treatment outcomes.
Area of Science:
- Pediatric Oncology
- Hematology
- Epidemiology
Background:
- Childhood acute lymphoblastic leukemia (ALL) survival rates in developing countries lag significantly behind those in developed nations.
- This study aimed to evaluate survival data and identify critical risk factors in a cohort of children with ALL in a developing nation.
Purpose of the Study:
- To assess the survival outcomes of children diagnosed with acute lymphoblastic leukemia (ALL).
- To identify clinical and demographic risk factors influencing survival in pediatric ALL patients.
Main Methods:
- Analysis of clinical-demographic data from 762 pediatric ALL patients.
- Generation of Kaplan-Meier survival curves to evaluate overall survival (OS) and event-free survival (EFS).
- Multivariate Cox regression analysis to identify significant predictors of outcome.
Main Results:
- The 5-year OS and EFS were 46% and 43%, respectively.
- Significant predictors of outcome included symptom-diagnosis interval, high white cell count (WCC), low platelet count, bulk disease, mediastinal adenopathy, and receipt of two intensification blocks.
- Approximately 30% of patients opted out of therapy, with high rates of treatment default, loss to follow-up, and infection-related deaths.
Conclusions:
- Effective management of childhood ALL necessitates adequate financial resources and supportive care.
- Addressing high rates of therapy refusal, default, loss to follow-up, and infection-related mortality is crucial for improving cure rates.
- Implementing targeted remedial measures can enhance ALL treatment outcomes in developing nations.
Background:
Survival of children with ALL, in developing nations has not kept pace with cure rates in developed countries. Our study was designed to assess survival data and identify risk factors.
Procedure:
Data of 762 patients with ALL were analyzed. Information regarding the clinical-demographic profile, therapy and course of illness were recorded. Status and duration at last follow-up were utilized to generate Kaplan-Meier survival curves.
Results:
The mean age was 5.7 +/- 0.23 years (M/F, 3.2:1). Parents of 230 (30.2%) patients opted for no therapy. There were 68 and 60 deaths in induction and remission phases respectively. Besides these, 111 children either defaulted therapy or were lost to follow up. Relapsed disease was documented in 125 cases. The 5-year OS and EFS was 46% and 43% respectively. Survival analysis, using the Cox multivariate regression, for gender (P = 0.659, CI: 0.852-1.161), age (P = 0.943, CI: 0.725-1.225), symptom-diagnosis interval (P = 0.002, CI: 1.116-1.668), WCC (P < 0.001, CI: 1.353-1.814) and platelet count (P = 0.001, CI: 0.546-0.849) was performed. Bulk disease (P = 0.049, CI: 0.428-0.986), mediastinal adenopathy (P = 0.045, CI: 1.040-3.697), WCC (P = 0.016, CI: 1.395-2.691), platelet count (P = 0.031, CI: 0.431-0.967) and administration of 2 intensification blocks (P = 0.012, CI: 0.624-0.940) were found to be significant predictors of outcome by multivariate analysis.
Conclusions:
The management of ALL requires financial resources and access to quality supportive care. One third of our patients opted for no therapy. The other problem areas were a high proportion of therapy defaulters, lost to follow up and infection related deaths during induction and remission phases. The introduction of remedial measures for resolving the difficulties identified would hopefully improve cure rates in ALL in developing nations.
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