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REGOSARC: Regorafenib versus placebo in doxorubicin‐refractory soft‐tissue sarcoma—A quality‐adjusted time without symptoms of progression or toxicity analysis

BACKGROUND: In a placebo‐controlled, randomized phase 2 trial (ClinicalTrials.gov identifier NCT01900743), regorafenib improved progression‐free survival (PFS) for patients with doxorubicin‐pretreated advanced nonadipocytic sarcoma. A quality‐adjusted time without symptoms of progression or toxicity...

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Autores principales: Berry, Vincent, Basson, Laurent, Bogart, Emilie, Mir, Olivier, Blay, Jean‐Yves, Italiano, Antoine, Bertucci, François, Chevreau, Christine, Clisant‐Delaine, Stéphanie, Liegl‐Antzager, Bernadette, Tresch‐Bruneel, Emmanuelle, Wallet, Jennifer, Taieb, Sophie, Decoupigny, Emilie, Le Cesne, Axel, Brodowicz, Thomas, Penel, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485075/
https://www.ncbi.nlm.nih.gov/pubmed/28295221
http://dx.doi.org/10.1002/cncr.30661
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author Berry, Vincent
Basson, Laurent
Bogart, Emilie
Mir, Olivier
Blay, Jean‐Yves
Italiano, Antoine
Bertucci, François
Chevreau, Christine
Clisant‐Delaine, Stéphanie
Liegl‐Antzager, Bernadette
Tresch‐Bruneel, Emmanuelle
Wallet, Jennifer
Taieb, Sophie
Decoupigny, Emilie
Le Cesne, Axel
Brodowicz, Thomas
Penel, Nicolas
author_facet Berry, Vincent
Basson, Laurent
Bogart, Emilie
Mir, Olivier
Blay, Jean‐Yves
Italiano, Antoine
Bertucci, François
Chevreau, Christine
Clisant‐Delaine, Stéphanie
Liegl‐Antzager, Bernadette
Tresch‐Bruneel, Emmanuelle
Wallet, Jennifer
Taieb, Sophie
Decoupigny, Emilie
Le Cesne, Axel
Brodowicz, Thomas
Penel, Nicolas
author_sort Berry, Vincent
collection PubMed
description BACKGROUND: In a placebo‐controlled, randomized phase 2 trial (ClinicalTrials.gov identifier NCT01900743), regorafenib improved progression‐free survival (PFS) for patients with doxorubicin‐pretreated advanced nonadipocytic sarcoma. A quality‐adjusted time without symptoms of progression or toxicity (Q‐TWiST) post hoc exploratory analysis was applied to provide an integrated measure of its clinical benefit. METHODS: In the base‐case analysis, each patient's overall survival (OS) was partitioned into 3 mutually exclusive health states: the time with a grade 3 or 4 adverse event (TOX), the time without symptoms of disease or grade 3 or 4 toxicity from treatment, and the time after tumor progression or relapse. The time spent in each state was weighted with a health‐state utility associated with that state and was summed to calculate the Q‐TWiST. The stability of the base‐case analysis was explored with several sensitivity analyses. RESULTS: In nonadipocytic sarcoma, the PFS was (4.0 months [2.6‐5.5 months] with regorafenib vs 1.0 month [0.9‐1.8 months] with a placebo; hazard ratio, 0.36 [0.25‐0.53]; P < .0001); the OS was 13.4 months (8.6‐17.3 months) with regorafenib and 9.0 months (6.8‐12.5 months) with a placebo (hazard ratio, 0.67 [0.44‐1.02]). With the classic definition of TOX (including all grade 3 and 4 clinical adverse events), the Q‐TWiSTs were 8.0 months (7.0‐9.0 months) with regorafenib and 5.7 months (4.9‐6.4 months) with a placebo (P < .001). CONCLUSIONS: For patients with doxorubicin‐pretreated soft‐tissue sarcoma, regorafenib significantly improved quality‐adjusted survival in comparison with a placebo. Cancer 2017;123:2294–2302. © 2017 The Authors. Cancer published by Wiley Periodicals, Inc. on behalf of American Cancer Society. This is an open access article under the terms of the Creative Commons Attribution NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
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spelling pubmed-54850752017-07-11 REGOSARC: Regorafenib versus placebo in doxorubicin‐refractory soft‐tissue sarcoma—A quality‐adjusted time without symptoms of progression or toxicity analysis Berry, Vincent Basson, Laurent Bogart, Emilie Mir, Olivier Blay, Jean‐Yves Italiano, Antoine Bertucci, François Chevreau, Christine Clisant‐Delaine, Stéphanie Liegl‐Antzager, Bernadette Tresch‐Bruneel, Emmanuelle Wallet, Jennifer Taieb, Sophie Decoupigny, Emilie Le Cesne, Axel Brodowicz, Thomas Penel, Nicolas Cancer Original Articles BACKGROUND: In a placebo‐controlled, randomized phase 2 trial (ClinicalTrials.gov identifier NCT01900743), regorafenib improved progression‐free survival (PFS) for patients with doxorubicin‐pretreated advanced nonadipocytic sarcoma. A quality‐adjusted time without symptoms of progression or toxicity (Q‐TWiST) post hoc exploratory analysis was applied to provide an integrated measure of its clinical benefit. METHODS: In the base‐case analysis, each patient's overall survival (OS) was partitioned into 3 mutually exclusive health states: the time with a grade 3 or 4 adverse event (TOX), the time without symptoms of disease or grade 3 or 4 toxicity from treatment, and the time after tumor progression or relapse. The time spent in each state was weighted with a health‐state utility associated with that state and was summed to calculate the Q‐TWiST. The stability of the base‐case analysis was explored with several sensitivity analyses. RESULTS: In nonadipocytic sarcoma, the PFS was (4.0 months [2.6‐5.5 months] with regorafenib vs 1.0 month [0.9‐1.8 months] with a placebo; hazard ratio, 0.36 [0.25‐0.53]; P < .0001); the OS was 13.4 months (8.6‐17.3 months) with regorafenib and 9.0 months (6.8‐12.5 months) with a placebo (hazard ratio, 0.67 [0.44‐1.02]). With the classic definition of TOX (including all grade 3 and 4 clinical adverse events), the Q‐TWiSTs were 8.0 months (7.0‐9.0 months) with regorafenib and 5.7 months (4.9‐6.4 months) with a placebo (P < .001). CONCLUSIONS: For patients with doxorubicin‐pretreated soft‐tissue sarcoma, regorafenib significantly improved quality‐adjusted survival in comparison with a placebo. Cancer 2017;123:2294–2302. © 2017 The Authors. Cancer published by Wiley Periodicals, Inc. on behalf of American Cancer Society. This is an open access article under the terms of the Creative Commons Attribution NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. John Wiley and Sons Inc. 2017-03-10 2017-06-15 /pmc/articles/PMC5485075/ /pubmed/28295221 http://dx.doi.org/10.1002/cncr.30661 Text en © 2017 American Cancer Society This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Berry, Vincent
Basson, Laurent
Bogart, Emilie
Mir, Olivier
Blay, Jean‐Yves
Italiano, Antoine
Bertucci, François
Chevreau, Christine
Clisant‐Delaine, Stéphanie
Liegl‐Antzager, Bernadette
Tresch‐Bruneel, Emmanuelle
Wallet, Jennifer
Taieb, Sophie
Decoupigny, Emilie
Le Cesne, Axel
Brodowicz, Thomas
Penel, Nicolas
REGOSARC: Regorafenib versus placebo in doxorubicin‐refractory soft‐tissue sarcoma—A quality‐adjusted time without symptoms of progression or toxicity analysis
title REGOSARC: Regorafenib versus placebo in doxorubicin‐refractory soft‐tissue sarcoma—A quality‐adjusted time without symptoms of progression or toxicity analysis
title_full REGOSARC: Regorafenib versus placebo in doxorubicin‐refractory soft‐tissue sarcoma—A quality‐adjusted time without symptoms of progression or toxicity analysis
title_fullStr REGOSARC: Regorafenib versus placebo in doxorubicin‐refractory soft‐tissue sarcoma—A quality‐adjusted time without symptoms of progression or toxicity analysis
title_full_unstemmed REGOSARC: Regorafenib versus placebo in doxorubicin‐refractory soft‐tissue sarcoma—A quality‐adjusted time without symptoms of progression or toxicity analysis
title_short REGOSARC: Regorafenib versus placebo in doxorubicin‐refractory soft‐tissue sarcoma—A quality‐adjusted time without symptoms of progression or toxicity analysis
title_sort regosarc: regorafenib versus placebo in doxorubicin‐refractory soft‐tissue sarcoma—a quality‐adjusted time without symptoms of progression or toxicity analysis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485075/
https://www.ncbi.nlm.nih.gov/pubmed/28295221
http://dx.doi.org/10.1002/cncr.30661
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