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Risk of subsequent gastrointestinal cancer among childhood cancer survivors: A systematic review.

Jop C Teepen ,
Suzanne L de Vroom ,
Flora E van Leeuwen ,
Wim J Tissing ,
Leontien C Kremer ,
Cécile M Ronckers

Abstract

METHODS

A systematic search of the literature databases Medline/PubMed (1945-2014) and Embase (1947-2014) was performed to identify studies that consisted of ⩾1000 CCS and assessed incidence of or mortality from subsequent GI cancer as an outcome.

CONCLUSION

Abdominal radiotherapy is a risk factor for developing a subsequent GI cancer. Few studies examined detailed treatment-related risk factors and most studies had small number of GI cancer cases. Therefore, no conclusions could be drawn on the effect of time since childhood cancer on GI cancer risk and on outcome after a subsequent GI cancer. Additional research is necessary to further explore risk factors for and outcome after a subsequent GI cancer, and to systematically evaluate the harms and benefits of GI screening among high-risk survivors in order to give sound screening recommendations.

RESULTS

A total of 45 studies were included. Studies that reported risk measures for subsequent GI cancer compared to the general population showed a 3.2 to 9.7-fold elevated risk in cohort studies including all childhood cancer types. Abdominal radiotherapy was associated with an increased risk of subsequent GI cancer in all four studies that assessed this risk. Survivors who had received procarbazine and platinum agents were also suggested to be at increased risk.

BACKGROUND

Childhood cancer survivors (CCS) are at increased risk of developing subsequent malignant neoplasms, including gastrointestinal (GI) cancer. We performed a systematic review to summarize all available literature on the risk of, risk factors for, and outcome after subsequent GI cancer among CCS.

More about this publication

Cancer treatment reviews

Volume 43
Pages 92-103
Publication date 01-02-2016

Full text links

Publisher website (DOI) 10.1016/j.ctrv.2015.12.002
Europe PubMed Central 26827697
Pubmed 26827697

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