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

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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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          Most cited references25

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          Tumor metastasis: molecular insights and evolving paradigms.

          Metastases represent the end products of a multistep cell-biological process termed the invasion-metastasis cascade, which involves dissemination of cancer cells to anatomically distant organ sites and their subsequent adaptation to foreign tissue microenvironments. Each of these events is driven by the acquisition of genetic and/or epigenetic alterations within tumor cells and the co-option of nonneoplastic stromal cells, which together endow incipient metastatic cells with traits needed to generate macroscopic metastases. Recent advances provide provocative insights into these cell-biological and molecular changes, which have implications regarding the steps of the invasion-metastasis cascade that appear amenable to therapeutic targeting. Copyright © 2011 Elsevier Inc. All rights reserved.
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            Stereotactic ablative radiotherapy versus standard of care palliative treatment in patients with oligometastatic cancers (SABR-COMET): a randomised, phase 2, open-label trial

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              Local Consolidative Therapy Vs. Maintenance Therapy or Observation for Patients With Oligometastatic Non–Small-Cell Lung Cancer: Long-Term Results of a Multi-Institutional, Phase II, Randomized Study

              Our previously published findings reported that local consolidative therapy (LCT) with radiotherapy or surgery improved progression-free survival (PFS) and delayed new disease in patients with oligometastatic non-small-cell lung cancer (NSCLC) that did not progress after front-line systemic therapy. Herein, we present the longer-term overall survival (OS) results accompanied by additional secondary end points.
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                Author and article information

                Journal
                J Clin Oncol
                J. Clin. Oncol
                jco
                jco
                JCO
                Journal of Clinical Oncology
                American Society of Clinical Oncology
                0732-183X
                1527-7755
                1 September 2020
                2 June 2020
                1 September 2021
                : 38
                : 25
                : 2830-2838
                Affiliations
                [ 1 ]London Health Sciences Centre, London, Ontario, Canada
                [ 2 ]BC Cancer, Centre for the North, Prince George, British Columbia, Canada
                [ 3 ]Beatson West of Scotland Cancer Centre, Glasgow, Scotland
                [ 4 ]Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada
                [ 5 ]Amsterdam University Medical Center, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands
                [ 6 ]Nova Scotia Cancer Centre, Halifax, Nova Scotia, Canada
                [ 7 ]BC Cancer, Surrey Centre, Surrey, British Columbia, Canada
                [ 8 ]Alfred Health Radiation Oncology, Melbourne, Victoria, Australia
                [ 9 ]Juravinski Cancer Centre, Hamilton, Ontario, Canada
                [ 10 ]McGill University Health Centre, Montreal, Quebec, Canada
                [ 11 ]BC Cancer, Vancouver Centre, Vancouver, British Columbia, Canada
                Author notes
                David A. Palma, MD, PhD, London Health Sciences Centre, 800 Commissioners Rd E, PO Box 5010, STN B, London, Ontario N6A 5W9, Canada; Twitter: @drdavidpalma, @WesternU; e-mail: david.palma@ 123456lhsc.on.ca .
                Article
                2000818
                10.1200/JCO.20.00818
                7460150
                32484754
                cf0841ed-36f6-4773-ae80-086cd55fdcea
                © 2020 by American Society of Clinical Oncology

                Creative Commons Attribution Non-Commercial No Derivatives 4.0 License: https://creativecommons.org/licenses/by-nc-nd/4.0/

                History
                : 5 May 2020
                Page count
                Figures: 4, Tables: 1, Equations: 0, References: 27, Pages: 10
                Categories
                [BC], BREAST
                [GIC], GASTRO: COLORECTAL & ANAL
                [GUC], GENITOURINARY: PROSTATE, ADVANCED STAGE
                [RADN], RADIATION ONCOLOGY
                [THOR], THORACIC ONCOLOGY: LUNG
                RAPID COMMUNICATIONS
                Radiation Oncology
                Custom metadata
                v1

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