Long‐term risk of second malignant neoplasms after neuroblastoma in childhood: Role of treatment

International Journal of Cancer - Tập 107 Số 5 - Trang 791-796 - 2003
Carolé Rubino1, Élisabeth Adjadj1, Sylvie Guérin1, Catherine Guibout1, Akhtar Shamsaldin2,1, Marie‐Gabrielle Dondon1, Dominique Valteau‐Couanet3, Olivier Hartmann3, Mike Hawkins4, Florent de Vathaire1
1Research Unit of Cancer Epidemiology (XU521 INSERM), Institut Gustave Roussy, Villejuif, France
2Department of Medical Physics and Radiotherapy, Institut Gustave Roussy, Villejuif, France
3Department of Pediatrics, Institut Gustave Roussy, Villejuif, France
4Centre for Childhood Cancer Survivor Studies, Department of Public Health and Epidemiology, University of Birmingham, Birmingham, United Kingdom

Tóm tắt

Abstract

The aim of our study was to quantify the risk of second malignant neoplasms (SMNs) among long‐term survivors of neuroblastoma and to study the influence of treatment on this risk. We studied data from 544 5‐year survival patients diagnosed with neuroblastoma before age 16 years at 8 French and British treatment centres from 1948 to 1986. After an average follow‐up of 15 years (range, 5–38 years), 12 children developed a total of 13 SMNs, whereas 1.19 were expected from general population rates. Among these SMNs, there were 5 thyroid and 3 breast cancers. Increases of the risks of SMN were observed with time since neuroblastoma diagnosis and attained age. In a multivariate analysis, the relative risk of SMN associated with radiotherapy was 4.3 (95% CI 0.8–78), whereas no increased risk of SMN was associated with the administration of chemotherapy as a whole (RR = 0.4, 95% CI 0.1–1.9). Young children treated for a neuroblastoma have significantly increased risks of SMN over 3 decades of follow‐up. Radiotherapy treatment was found to be an important risk factor for developing SMNs, whereas no effect of chemotherapy was evidenced. Although our findings reflect the late effects of past therapeutic modalities, they underscore the importance of long‐term surveillance of young children treated for a neuroblastoma. For these patients, many more years of follow‐up are required to appreciate their overall risks of treatment‐related SMNs. © 2003 Wiley‐Liss, Inc.

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