Long-Term Morbidity and Mortality Among Survivors of Neuroblastoma Diagnosed During Infancy: A Report From the Childhood Cancer Survivor Study. Academic Article uri icon

Overview

abstract

  • PURPOSE: To describe the risk of late mortality, subsequent malignant neoplasms (SMNs), and chronic health conditions (CHCs) in survivors of neuroblastoma diagnosed in infancy by treatment era and exposures. METHODS: Among 5-year survivors of neuroblastoma in the Childhood Cancer Survivor Study diagnosed age < 1 year between 1970 and 1999, we examined the cumulative incidence of late (> 5 years from diagnosis) mortality, SMN, and CHCs (grades 2-5 and 3-5). Multivariable Cox regression models estimated hazard ratios (HRs) and 95% CIs by decade and treatment (surgery-alone v chemotherapy with or without surgery [C ± S] v radiation with or without chemotherapy ± surgery [R ± C ± S]) among survivors and between survivors and 5,051 siblings. RESULTS: Among 1,397 eligible survivors, the 25-year cumulative incidence of late mortality was 2.1% (95% CI, 1.3 to 3.9) with no difference by treatment era. Among 990 participants who completed a baseline survey, fewer survivors received radiation in more recent eras (51.2% 1970s, 20.4% 1980s, and 10.1% 1990s; P < .001). Risk of SMN was elevated only among individuals treated with radiation-containing regimens compared with surgery alone (HR[C ± S], 3.2 [95% CI, 0.9 to 11.6]; HR[R ± C ± S], 5.7 [95% CI, 1.2 to 28.1]). In adjusted models, there was a 50% reduction in risk of grade 3-5 CHCs in the 1990s versus 1970s (HR, 0.5 [95% CI, 0.3 to 0.9]; P = .01); individuals treated with radiation had a 3.6-fold risk for grade 3-5 CHCs (95% CI, 2.1 to 6.2) versus those treated with surgery alone. When compared with siblings, risk of grade 3-5 CHCs for survivors was lowest in the most recent era (HR[1970s], 4.7 [95% CI, 3.4 to 6.5]; HR[1980s], 4.6 [95% CI, 3.3 to 6.4]; HR[1990s], 2.5 [95% CI, 1.7 to 3.9]). CONCLUSION: Neuroblastoma survivors treated during infancy have a relatively low absolute burden of late mortality and SMN. Encouragingly, risk of CHCs has declined in more recent eras with reduced exposure to radiation therapy.

authors

  • Friedman, Danielle Novetsky
  • Goodman, Pamela J
  • Leisenring, Wendy M
  • Diller, Lisa R
  • Cohn, Susan L
  • Howell, Rebecca M
  • Smith, Susan A
  • Tonorezos, Emily
  • Wolden, Suzanne L
  • Neglia, Joseph P
  • Ness, Kirsten K
  • Gibson, Todd M
  • Nathan, Paul C
  • Weil, Brent R
  • Robison, Leslie L
  • Oeffinger, Kevin C
  • Armstrong, Gregory T
  • Sklar, Charles A
  • Henderson, Tara O

publication date

  • December 16, 2022

Research

keywords

  • Cancer Survivors
  • Neoplasms, Second Primary
  • Neuroblastoma

Identity

PubMed Central ID

  • PMC10043581

Scopus Document Identifier

  • 85150000883

Digital Object Identifier (DOI)

  • 10.1200/JCO.22.01732

PubMed ID

  • 36525618

Additional Document Info

volume

  • 41

issue

  • 8