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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
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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Clinical Oncology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7460150/ https://www.ncbi.nlm.nih.gov/pubmed/32484754 http://dx.doi.org/10.1200/JCO.20.00818 |
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author | Palma, David A. Olson, Robert Harrow, Stephen Gaede, Stewart Louie, Alexander V. Haasbeek, Cornelis Mulroy, Liam Lock, Michael Rodrigues, George B. Yaremko, Brian P. Schellenberg, Devin Ahmad, Belal Senthi, Sashendra Swaminath, Anand Kopek, Neil Liu, Mitchell Moore, Karen Currie, Suzanne Schlijper, Roel Bauman, Glenn S. Laba, Joanna Qu, X. Melody Warner, Andrew Senan, Suresh |
author_facet | Palma, David A. Olson, Robert Harrow, Stephen Gaede, Stewart Louie, Alexander V. Haasbeek, Cornelis Mulroy, Liam Lock, Michael Rodrigues, George B. Yaremko, Brian P. Schellenberg, Devin Ahmad, Belal Senthi, Sashendra Swaminath, Anand Kopek, Neil Liu, Mitchell Moore, Karen Currie, Suzanne Schlijper, Roel Bauman, Glenn S. Laba, Joanna Qu, X. Melody Warner, Andrew Senan, Suresh |
author_sort | Palma, David A. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7460150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Society of Clinical Oncology |
record_format | MEDLINE/PubMed |
spelling | pubmed-74601502021-09-01 Stereotactic Ablative Radiotherapy for the Comprehensive Treatment of Oligometastatic Cancers: Long-Term Results of the SABR-COMET Phase II Randomized Trial Palma, David A. Olson, Robert Harrow, Stephen Gaede, Stewart Louie, Alexander V. Haasbeek, Cornelis Mulroy, Liam Lock, Michael Rodrigues, George B. Yaremko, Brian P. Schellenberg, Devin Ahmad, Belal Senthi, Sashendra Swaminath, Anand Kopek, Neil Liu, Mitchell Moore, Karen Currie, Suzanne Schlijper, Roel Bauman, Glenn S. Laba, Joanna Qu, X. Melody Warner, Andrew Senan, Suresh J Clin Oncol RAPID COMMUNICATIONS 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. American Society of Clinical Oncology 2020-09-01 2020-06-02 /pmc/articles/PMC7460150/ /pubmed/32484754 http://dx.doi.org/10.1200/JCO.20.00818 Text en © 2020 by American Society of Clinical Oncology https://creativecommons.org/licenses/by-nc-nd/4.0/ Creative Commons Attribution Non-Commercial No Derivatives 4.0 License: https://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | RAPID COMMUNICATIONS Palma, David A. Olson, Robert Harrow, Stephen Gaede, Stewart Louie, Alexander V. Haasbeek, Cornelis Mulroy, Liam Lock, Michael Rodrigues, George B. Yaremko, Brian P. Schellenberg, Devin Ahmad, Belal Senthi, Sashendra Swaminath, Anand Kopek, Neil Liu, Mitchell Moore, Karen Currie, Suzanne Schlijper, Roel Bauman, Glenn S. Laba, Joanna Qu, X. Melody Warner, Andrew Senan, Suresh Stereotactic Ablative Radiotherapy for the Comprehensive Treatment of Oligometastatic Cancers: Long-Term Results of the SABR-COMET Phase II Randomized Trial |
title | Stereotactic Ablative Radiotherapy for the Comprehensive Treatment of Oligometastatic Cancers: Long-Term Results of the SABR-COMET Phase II Randomized Trial |
title_full | Stereotactic Ablative Radiotherapy for the Comprehensive Treatment of Oligometastatic Cancers: Long-Term Results of the SABR-COMET Phase II Randomized Trial |
title_fullStr | Stereotactic Ablative Radiotherapy for the Comprehensive Treatment of Oligometastatic Cancers: Long-Term Results of the SABR-COMET Phase II Randomized Trial |
title_full_unstemmed | Stereotactic Ablative Radiotherapy for the Comprehensive Treatment of Oligometastatic Cancers: Long-Term Results of the SABR-COMET Phase II Randomized Trial |
title_short | Stereotactic Ablative Radiotherapy for the Comprehensive Treatment of Oligometastatic Cancers: Long-Term Results of the SABR-COMET Phase II Randomized Trial |
title_sort | stereotactic ablative radiotherapy for the comprehensive treatment of oligometastatic cancers: long-term results of the sabr-comet phase ii randomized trial |
topic | RAPID COMMUNICATIONS |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7460150/ https://www.ncbi.nlm.nih.gov/pubmed/32484754 http://dx.doi.org/10.1200/JCO.20.00818 |
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