4.4 Article

Ocular Late Effects in Childhood and Adolescent Cancer Survivors: A Report From the Childhood Cancer Survivor Study

期刊

PEDIATRIC BLOOD & CANCER
卷 54, 期 1, 页码 103-109

出版社

WILEY
DOI: 10.1002/pbc.22277

关键词

chemotherapy; late effects of cancer therapy; radiation therapy

资金

  1. National Cancer Institute, Bethesda, MD [U24 CA55727]
  2. Children's Cancer Research Fund (Minneapolis, MN)
  3. American Lebanese Syrian Associated Charities (ALSAC)
  4. NATIONAL CANCER INSTITUTE [U24CA055727] Funding Source: NIH RePORTER

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Introduction. Approximately 80% of children currently survive 5 years following diagnosis of their cancer. Studies based on limited data have implicated certain cancer therapies in the development of ocular sequelae in these survivors. Procedure. The Childhood Cancer Survivor Study (CCSS) is a retrospective cohort study investigating health outcomes of 5+ year survivors diagnosed and treated between 1970 and 1986 compared to a sibling cohort. The baseline questionnaire included questions about the first occurrence of six ocular conditions. Relative risks (RR) and 95% confidence intervals (CI) were calculated from responses of 14,362 survivors and 3,901 siblings. Results. Five or more years from the diagnosis, survivors were at increased risk of cataracts (RR: 10.8; 95% CI: 6.2-18.9), glaucoma (RR: 2.5; 95% CI: 1.1-5.7), legal blindness (RR: 2.6; 95% CI: 1.7-4.0), double vision (RR: 4.1; 95%, CI: 2.7-6.1), and dry eyes (RR: 1.9; 95% CI: 1.6-2.4), when compared to siblings. Dose of radiation to the eye was significantly associated with risk of cataracts, legal blindness, double vision, and dry eyes, in a dose-dependent manner. Risk of cataracts were also associated with radiation 3,000+cGy to the posterior fossa (RR: 8.4; 95% CI: 5.0-14.3), temporal lobe (RR: 9.4; 95% CI: 5.6-15.6), and exposure to prednisone (RR: 2.3; 95% CI: 1.6-3.4). Conclusions. Childhood cancer survivors are at risk of developing late occurring ocular complications, with exposure to glucocorticoids and cranial radiation being important determinants of increased risk. Longterm follow-up is needed to evaluate potential progression of ocular deficits and impact on quality of life. Pediatr Blood Cancer 2010;54:103-109. (C) 2009 Wiley-Liss, Inc.

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