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A review of ongoing trials of stereotactic ablative radiotherapy for oligometastatic disease in the context of new consensus definitions

期刊

ANNALS OF PALLIATIVE MEDICINE
卷 10, 期 5, 页码 6045-6051

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AME PUBL CO
DOI: 10.21037/apm-20-847

关键词

Oligometastatic; radiotherapy; stereotactic ablative radiotherapy (SABR); stereotactic body radiation therapy (SBRT); stereotactic

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Characterization and treatment of oligometastatic disease (OMD) are rapidly growing areas of research. Ongoing clinical trials evaluating stereotactic ablative radiotherapy (SABR) in OMD include patient populations with various OMD subsets, requiring consideration of the applicability of trial results within relevant OMD scenarios.
The characterization and treatment of oligometastatic disease (OMD) are rapidly growing areas of research. Consensus statements have recently been developed by European Society for Radiotherapy and Oncology (ESTRO)/American Society for Radiation Oncology (ASTRO) and ESTRO/European Organization for Research and Treatment of Cancer (EORTC) in an effort to harmonize terminology describing OMD. The purpose of this study was to assess patient populations eligible for ongoing clinical trials evaluating stereotactic ablative radiotherapy (SABR) in OMD in the context of key definitions from both statements. Using the clinicaltrials.gov database, a search of ongoing OMD clinical trials evaluating the use of SABR was performed from inception to January 2020, using the keywords oligometastasis, stereotactic radiotherapy, and related terms. Results were independently reviewed by two investigators, with discrepancies settled by a third. Information from these trials including study design, population criteria, and primary endpoints were extracted. OMD was defined in general as a limited number of metastases that could be safely treated with metastasis-directed therapy. States of OMD were broadly categorized into de novo, repeat, and induced, with synchronous and metachronous being subsets of de novo. The initial search strategy identified 293 trials, of which 85 met our eligibility criteria. Phase II trials were by far the most common (n=46, 52%). Most trials had a single treatment arm (n=43, 51%), and 31 (36%) were randomized. The majority of trials (n=65, 76%) had populations that included all three subsets of OMD. Notably, 70 trials (82%) also included oligoprogressive disease, which is debatably a distinct entity from OMD. Progression-free survival was the most common primary endpoint (n=31, 36%), followed by local control (n=17, 20%), toxicity (n=14, 16%) and overall survival (n=7, 8%). Although the use of SABR for OMD is an active area of prospective clinical trial research, ongoing studies include mixed populations as defined by new consensus statements. Therefore, the applicability of results from these trials should be considered within relevant OMD scenarios.

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