Abstract
The development of treatment-induced cancer is one of the most devastating late complications of cancer therapy. Fortunately, these are quite uncommon in adult patients, that is, less than 1 in 200 at 20 years. In pediatric patients the risks are higher and may approach 1 in 5 at 20 years for patients with Ewing’s sarcoma and retinoblastoma.
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Spiro, I.J., Suit, H.D. (1997). Radiation-induced bone and soft tissue sarcomas: Clinical aspects and molecular biology. In: Verweij, J., Pinedo, H.M., Suit, H.D. (eds) Soft Tissue Sarcomas: Present Achievements and Future Prospects. Cancer Treatment and Research, vol 91. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-6121-7_10
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