Journal of Clinical Oncology, Vol 16, 3592-3600, Copyright © 1998 by American Society of Clinical Oncology
Increased mortality after successful treatment for Hodgkin's disease
MM Hudson, CA Poquette, J Lee, CA Greenwald, A Shah, X Luo, EI Thompson, JA Wilimas, LE Kun and WM Crist
Department of Hematology-Oncology, St Jude Children's Research Hospital, Memphis, TN 38105, USA. melissa.hudson@stjude.org
PURPOSE: To determine the impact of treatment toxicity on long-term
survival in pediatric Hodgkin's disease. PATIENTS AND METHODS: We studied
late events in 387 patients treated for pediatric Hodgkin's disease on four
consecutive clinical trials at St Jude Children's Research Hospital from
1968 to 1990. Relative risks, actuarial risks, and absolute excess risks
for cause-specific deaths were calculated. RESULTS: As of April 1997, 316
(82%) of patients were alive, with a median follow-up of 15.1 (range, 2.9
to 28.6) years. In this cohort, which represented 5,623 person-years of
follow-up, 71 fatal events resulted from Hodgkin's disease (n=36), second
malignancies (n=14), infections (n=7), accidents (n=7), cardiac disease
(n=6), and asphyxiation (n=1). The 5-year estimated event-free survival
(EFS) for the entire cohort was 79.6%+/-2.1 %, which declined to
63.1%+/-4.4% by 20 years. Cumulative incidences of cause-specific deaths at
25 years were 9.8%+/-1.6% for Hodgkin's disease, 8.1%+/-2.6% for second
malignancy, 4.0%+/-1.8% for cardiac disease, 3.9%+/-1.5% for infection, and
2.1%+/-0.8% for accidents. Standardized incidence ratios showed excess risk
for all second malignancies (12; 95% confidence interval [CI], 8 to 17),
acute myeloid leukemia (81; 95% CI, 16 to 237), solid tumors (11; 95% CI, 7
to 16), and breast cancer (33; 95% CI, 12 to 72). Standardized mortality
ratios also showed excess mortality from cardiac disease (22; 95% CI, 8 to
48) and infection (18; 95% CI, 7 to 38). CONCLUSION: Compared with age- and
sex-matched control populations, survivors of pediatric Hodgkin's disease
who were treated before 1990 face an increased risk of early mortality
related to second cancers, cardiac disease, and infection.
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