Stereotactic Ablative Radiotherapy for the Comprehensive Treatment of Oligometastatic Cancers: Long-Term Results of the SABR-COMET Phase II Randomized Trial

David A. Palma(London Health Sciences Centre), Robert Olson(Positive Living North), Stephen Harrow(Beatson West of Scotland Cancer Centre), Stewart Gaede(London Health Sciences Centre), Alexander V. Louie(Sunnybrook Health Science Centre), Cornelis J.A. Haasbeek(Amsterdam University Medical Centers), Liam Mulroy(Nova Scotia Cancer Centre), Michael Lock(London Health Sciences Centre), George Rodrigues(London Health Sciences Centre), Brian Yaremko(London Health Sciences Centre), Devin Schellenberg(Surrey Place Centre), Belal Ahmad(London Health Sciences Centre), Sashendra Senthi(Alfred Health), Anand Swaminath(Juravinski Cancer Centre), Neil Kopek(McGill University Health Centre), Mitchell Liu, Karen Moore(Beatson West of Scotland Cancer Centre), Suzanne Currie(Beatson West of Scotland Cancer Centre), Roel Schlijper(Positive Living North), Glenn Bauman(London Health Sciences Centre), Joanna Laba(London Health Sciences Centre), Xiaotao Qu(London Health Sciences Centre), Andrew Warner(London Health Sciences Centre), Suresh Senan(Amsterdam University Medical Centers)
Journal of Clinical Oncology
June 2, 2020
Cited by 1,227Open Access
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Abstract

PURPOSE The oligometastatic paradigm hypothesizes that patients with a limited number of metastases may achieve long-term disease control, or even cure, if all sites of disease can be ablated. However, long-term randomized data that test this paradigm are lacking. METHODS We enrolled patients with a controlled primary malignancy and 1-5 metastatic lesions, with all metastases amenable to stereotactic ablative radiotherapy (SABR). We stratified by the number of metastases (1-3 v 4-5) and randomized in a 1:2 ratio between palliative standard-of-care (SOC) treatments (arm 1) and SOC plus SABR (arm 2). We used a randomized phase II screening design with a primary end point of overall survival (OS), using an α of .20 (wherein P < .20 indicates a positive trial). Secondary end points included progression-free survival (PFS), toxicity, and quality of life (QOL). Herein, we present long-term outcomes from the trial. RESULTS Between 2012 and 2016, 99 patients were randomly assigned at 10 centers internationally. The most common primary tumor types were breast (n = 18), lung (n = 18), colorectal (n = 18), and prostate (n = 16). Median follow-up was 51 months. The 5-year OS rate was 17.7% in arm 1 (95% CI, 6% to 34%) versus 42.3% in arm 2 (95% CI, 28% to 56%; stratified log-rank P = .006). The 5-year PFS rate was not reached in arm 1 (3.2%; 95% CI, 0% to 14% at 4 years with last patient censored) and 17.3% in arm 2 (95% CI, 8% to 30%; P = .001). There were no new grade 2-5 adverse events and no differences in QOL between arms. CONCLUSION With extended follow-up, the impact of SABR on OS was larger in magnitude than in the initial analysis and durable over time. There were no new safety signals, and SABR had no detrimental impact on QOL.


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