4.7 Article

Secondary Malignant Neoplasms Among Children, Adolescents, and Young Adults With Osteosarcoma

Journal

CANCER
Volume 120, Issue 24, Pages 3987-3993

Publisher

WILEY-BLACKWELL
DOI: 10.1002/cncr.28936

Keywords

osteosarcoma; secondary malignant neoplasm (SMN); late effects; children; adolescents; young adults

Categories

Funding

  1. Swim Across America
  2. National Center for Advancing Translational Sciences, National Institutes of Health, through University of California at San Francisco-Clinical and Translational Science Institute [UL1 TR000004]

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BACKGROUNDAs patients with osteosarcoma become long-term survivors, increasing attention has turned to the burden of late effects. The goal of the current study was to describe the incidence, characteristics, and outcomes of secondary malignant neoplasms (SMNs) in this population. METHODSPatients aged birth to 40 years at time of primary diagnosis with osteosarcoma and reported to the Surveillance, Epidemiology, and End Results (SEER) program between 1973 and 2010 were eligible for inclusion in the cohort. Competing risks methods were used to estimate the cumulative incidence of SMNs and potential risk factors for developing an SMN. Standardized incidence ratios (SIR) and overall survival after an SMN were estimated. RESULTSThe SEER database included 3379 patients who were diagnosed with osteosarcoma as their first malignancy. Of these, 89 patients were diagnosed with an SMN. The cumulative incidence of any SMN was 2.1% (95% confidence interval [95% CI], 1.6%-2.7%) at 10 years, 4.0% (95% CI, 3.1%-5.1%) at 20 years, and 7.4% (95% CI, 5.6%-9.5%) at 30 years. The median time from the primary diagnosis to an SMN diagnosis was 6.0 years. The SIR for SMNs for survivors of osteosarcoma compared with the general population was 1.6 (95% CI, 1.0-2.5) for patients diagnosed with osteosarcoma from 1973 through 1985 and 4.7 (95% CI, 3.3-6.4) for patients diagnosed with osteosarcoma from 1986 through 2010, with a 34-fold increased risk of leukemia in this most recent era. The overall survival rate at 5 years for patients with SMNs after a diagnosis of osteosarcoma was 44.5%. CONCLUSIONSSurvivors of osteosarcoma are at an increased risk of developing SMNs compared with the baseline population, with an increased risk noted in patients treated in the more recent era. Cancer 2014;120:3987-3993 (c) 2014 American Cancer Society. As patients with osteosarcoma become long-term survivors, increasing attention has turned to the burden of late effects. Survivors of osteosarcoma are at an increased risk of secondary malignant neoplasms compared with the baseline population, with an increased risk noted among patients treated in the more recent era.

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