Incidence of second sarcomas: a cancer registry-based study.

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2014

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info:eu-repo/semantics/altIdentifier/doi/10.1007/s10552-014-0349-7

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info:eu-repo/semantics/altIdentifier/pmid/24463790

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info:eu-repo/semantics/altIdentifier/eissn/1573-7225

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info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_2209623178335

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F. Levi et al., « Incidence of second sarcomas: a cancer registry-based study. », Serveur académique Lausannois, ID : 10.1007/s10552-014-0349-7


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BACKGROUND: In high-quality cancer registration systems, about one in eight incident cancers are second primary cancers. This is due to a combination of careful diagnostic ascertainment, shared genetic determinants, shared exposure to environmental factors and consequences of treatment for first cancer. METHODS: We used data derived from the Swiss population-based cancer Registries of Vaud and Neuchâtel, including 885,000 inhabitants. RESULTS: Among 107,238 (52% males) first cancers occurring between 1976 and 2010, a total of 126 second sarcomas were observed through active and passive follow-up versus 68.2 expected, corresponding to a standardized incidence ratio (SIR) of 1.85 (95 % CI 1.5-2.2). Significant excess sarcoma risks were observed after skin melanoma (SIR = 3.0), breast cancer (2.2), corpus uteri (2.7), testicular (7.5), thyroid cancer (4.2), Hodgkin lymphoma (5.7) and leukemias (4.0). For breast cancer, the SIR was 3.4 ≥5 years after sarcoma diagnosis. CONCLUSIONS: The common denominator of these neoplasms is the utilization of radiotherapy in their management. Some sarcomas following breast cancer may be due to shared genetic components (i.e., in the Li-Fraumeni syndrome), as well as possibly to shared environmental factors, with sarcomas, including overweight, selected dietary and reproductive factors which are, however, too little defined for any quantitative risk assessment.

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