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Characteristics and therapeutic strategies of brain and cranial radiation-induced sarcoma: analysis of 165 cases from our case experience and comprehensive review. | LitMetric

AI Article Synopsis

  • Radiation-induced sarcoma (RIS) develops as a potential side effect of radiation therapy for brain tumors, with unclear clinical characteristics and treatment options.
  • The study analyzed 165 RIS cases and found an average age of 39.6 years at diagnosis, with a mean latency period of about 11.8 years and a median overall survival of 11 months, varying by type (fibrosarcoma vs. osteosarcoma) and location (intracranial vs. extracranial).
  • Surgical intervention and postoperative chemotherapy were associated with improved survival outcomes, whereas radiation treatment for RIS did not show any survival benefit.

Article Abstract

Background: Radiation-induced sarcoma (RIS) is among the neoplasms potentially caused by radiation therapy (RT) for brain tumors. However, the clinical characteristics of and ideal treatment for RIS are unclear. We analysed our case experience and conducted a comprehensive literature review to reveal the characteristics of brain and cranial RIS.

Methods: We analysed 165 cases of RIS from the literature together with the RIS case treated at our institution. In each case, the latency period from irradiation to the development of each RIS and the median overall survival (OS) of the patients was analysed by Kaplan-Meier analysis. Spearman's correlation test was used to determine the relationship between the latency period and radiation dose or age at irradiation.

Results: The mean age at the development of RIS was 39.63 ± 17.84 years. The mean latency period was 11.79 ± 8.09 years. No factors associated with early development of RIS were detected. The median OS was 11 months, with fibrosarcoma showing significantly shorter OS compared with osteosarcoma and other sarcomas (p = 0.0021), and intracranial RIS showing a worse prognosis than extracranial RIS (p < 0.0001). Patients treated with surgery (p < 0.0001) and postoperative chemotherapy (p = 0.0157) for RIS presented significantly longer OS, whereas RT for RIS was not associated with a survival benefit.

Conclusions: Although prognosis for RIS is universally poor, pathological characteristics and locations are associated with worse prognosis. Surgery and chemotherapy may be the ideal treatment strategies for RIS.

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Source
http://dx.doi.org/10.1093/jjco/hyad078DOI Listing

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