Survival improvement by decade of patients aged 0-14 years with acute lymphoblastic leukemia: a SEER analysis

Haiqing Ma1, Huanhuan Sun2, Xiaoping Sun1

  • 1Department of Laboratory Medicine and the Center for Stem Cell and Developmental Biology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, United States.

Scientific Reports
|February 28, 2014
PubMed

Insights

Survival rates for childhood acute lymphoblastic leukemia (ALL) have significantly improved over three decades. Continued advances in targeted and personalized therapies promise further gains for pediatric ALL patients.

Area of Science:

  • Pediatric Oncology
  • Epidemiology
  • Cancer Survival Rates

Background:

  • Assessing long-term treatment outcomes for childhood acute lymphoblastic leukemia (ALL) is crucial for understanding therapeutic progress.
  • The Surveillance, Epidemiology, and End Results (SEER) database provides a valuable resource for analyzing population-based cancer survival data.

Observation:

  • This study analyzed 12,096 pediatric ALL patients diagnosed between 1981 and 2010 across 18 SEER sites.
  • Five-year survival improved from 74.8% to 88.6%, and 10-year survival increased from 69.3% to 85.5% over the three decades.
  • While survival improved across most age groups, infants with ALL showed persistently low 10-year survival rates (54.7%).
  • Girls consistently demonstrated higher survival rates than boys, particularly in the 0-14 age group during 2001-2010 (10-year relative survival: 87.8% vs. 83.6%).

Findings:

  • Pediatric ALL survival rates have shown a statistically significant, decade-over-decade improvement.
  • Significant progress was noted in older children (10-14 years), with a >20 percentage point increase in 10-year survival.
  • Disparities in survival rates were observed based on age (infants) and sex (girls vs. boys).

Implications:

  • The findings highlight the substantial impact of evolving treatment strategies on pediatric ALL outcomes.
  • Further advancements in targeted and personalized therapies are expected to continue improving survival rates for childhood ALL.
  • Addressing specific challenges in infant ALL and understanding sex-based differences may further enhance treatment efficacy and outcomes.