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Active symptom control with or without chemotherapy in the treatment of patients with malignant pleural mesothelioma (MS01): a multicentre randomised trial

BACKGROUND: Malignant pleural mesothelioma is almost always fatal, and few treatment options are available. Although active symptom control (ASC) has been recommended for the management of this disease, no consensus exists for the role of chemotherapy. We investigated whether the addition of chemoth...

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Autores principales: Muers, Martin F, Stephens, Richard J, Fisher, Patricia, Darlison, Liz, Higgs, Christopher MB, Lowry, Erica, Nicholson, Andrew G, O'Brien, Mary, Peake, Michael, Rudd, Robin, Snee, Michael, Steele, Jeremy, Girling, David J, Nankivell, Matthew, Pugh, Cheryl, Parmar, Mahesh KB
Formato: Texto
Lenguaje:English
Publicado: Lancet Publishing Group 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2431123/
https://www.ncbi.nlm.nih.gov/pubmed/18486741
http://dx.doi.org/10.1016/S0140-6736(08)60727-8
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author Muers, Martin F
Stephens, Richard J
Fisher, Patricia
Darlison, Liz
Higgs, Christopher MB
Lowry, Erica
Nicholson, Andrew G
O'Brien, Mary
Peake, Michael
Rudd, Robin
Snee, Michael
Steele, Jeremy
Girling, David J
Nankivell, Matthew
Pugh, Cheryl
Parmar, Mahesh KB
author_facet Muers, Martin F
Stephens, Richard J
Fisher, Patricia
Darlison, Liz
Higgs, Christopher MB
Lowry, Erica
Nicholson, Andrew G
O'Brien, Mary
Peake, Michael
Rudd, Robin
Snee, Michael
Steele, Jeremy
Girling, David J
Nankivell, Matthew
Pugh, Cheryl
Parmar, Mahesh KB
author_sort Muers, Martin F
collection PubMed
description BACKGROUND: Malignant pleural mesothelioma is almost always fatal, and few treatment options are available. Although active symptom control (ASC) has been recommended for the management of this disease, no consensus exists for the role of chemotherapy. We investigated whether the addition of chemotherapy to ASC improved survival and quality of life. METHODS: 409 patients with malignant pleural mesothelioma, from 76 centres in the UK and two in Australia, were randomly assigned to ASC alone (treatment could include steroids, analgesic drugs, bronchodilators, palliative radiotherapy [n=136]); to ASC plus MVP (four cycles of mitomycin 6 mg/m(2), vinblastine 6 mg/m(2), and cisplatin 50 mg/m(2) every 3 weeks [n=137]); or to ASC plus vinorelbine (one injection of vinorelbine 30 mg/m(2) every week for 12 weeks [n=136]). Randomisation was done by minimisation, with stratification for WHO performance status, histology, and centre. Follow-up was every 3 weeks to 21 weeks after randomisation, and every 8 weeks thereafter. Because of slow accrual, the two chemotherapy groups were combined and compared with ASC alone for the primary outcome of overall survival. Analysis was by intention to treat. This study is registered, number ISRCTN54469112. FINDINGS: At the time of analysis, 393 (96%) patients had died (ASC 132 [97%], ASC plus MVP 132 [96%], ASC plus vinorelbine 129 [95%]). Compared with ASC alone, we noted a small, non-significant survival benefit for ASC plus chemotherapy (hazard ratio [HR] 0·89 [95% CI 0·72–1·10]; p=0·29). Median survival was 7·6 months in the ASC alone group and 8·5 months in the ASC plus chemotherapy group. Exploratory analyses suggested a survival advantage for ASC plus vinorelbine compared with ASC alone (HR 0·80 [0·63–1·02]; p=0·08), with a median survival of 9·5 months. There was no evidence of a survival benefit with ASC plus MVP (HR 0·99 [0·78–1·27]; p=0·95). We observed no between-group differences in four predefined quality-of-life subscales (physical functioning, pain, dyspnoea, and global health status) at any of the assessments in the first 6 months. INTERPRETATION: The addition of chemotherapy to ASC offers no significant benefits in terms of overall survival or quality of life. However, exploratory analyses suggested that vinorelbine merits further investigation. FUNDING: Cancer Research UK and the Medical Research Council (UK).
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spelling pubmed-24311232008-07-09 Active symptom control with or without chemotherapy in the treatment of patients with malignant pleural mesothelioma (MS01): a multicentre randomised trial Muers, Martin F Stephens, Richard J Fisher, Patricia Darlison, Liz Higgs, Christopher MB Lowry, Erica Nicholson, Andrew G O'Brien, Mary Peake, Michael Rudd, Robin Snee, Michael Steele, Jeremy Girling, David J Nankivell, Matthew Pugh, Cheryl Parmar, Mahesh KB Lancet Articles BACKGROUND: Malignant pleural mesothelioma is almost always fatal, and few treatment options are available. Although active symptom control (ASC) has been recommended for the management of this disease, no consensus exists for the role of chemotherapy. We investigated whether the addition of chemotherapy to ASC improved survival and quality of life. METHODS: 409 patients with malignant pleural mesothelioma, from 76 centres in the UK and two in Australia, were randomly assigned to ASC alone (treatment could include steroids, analgesic drugs, bronchodilators, palliative radiotherapy [n=136]); to ASC plus MVP (four cycles of mitomycin 6 mg/m(2), vinblastine 6 mg/m(2), and cisplatin 50 mg/m(2) every 3 weeks [n=137]); or to ASC plus vinorelbine (one injection of vinorelbine 30 mg/m(2) every week for 12 weeks [n=136]). Randomisation was done by minimisation, with stratification for WHO performance status, histology, and centre. Follow-up was every 3 weeks to 21 weeks after randomisation, and every 8 weeks thereafter. Because of slow accrual, the two chemotherapy groups were combined and compared with ASC alone for the primary outcome of overall survival. Analysis was by intention to treat. This study is registered, number ISRCTN54469112. FINDINGS: At the time of analysis, 393 (96%) patients had died (ASC 132 [97%], ASC plus MVP 132 [96%], ASC plus vinorelbine 129 [95%]). Compared with ASC alone, we noted a small, non-significant survival benefit for ASC plus chemotherapy (hazard ratio [HR] 0·89 [95% CI 0·72–1·10]; p=0·29). Median survival was 7·6 months in the ASC alone group and 8·5 months in the ASC plus chemotherapy group. Exploratory analyses suggested a survival advantage for ASC plus vinorelbine compared with ASC alone (HR 0·80 [0·63–1·02]; p=0·08), with a median survival of 9·5 months. There was no evidence of a survival benefit with ASC plus MVP (HR 0·99 [0·78–1·27]; p=0·95). We observed no between-group differences in four predefined quality-of-life subscales (physical functioning, pain, dyspnoea, and global health status) at any of the assessments in the first 6 months. INTERPRETATION: The addition of chemotherapy to ASC offers no significant benefits in terms of overall survival or quality of life. However, exploratory analyses suggested that vinorelbine merits further investigation. FUNDING: Cancer Research UK and the Medical Research Council (UK). Lancet Publishing Group 2008-05-01 /pmc/articles/PMC2431123/ /pubmed/18486741 http://dx.doi.org/10.1016/S0140-6736(08)60727-8 Text en 2008 Elsevier Ltd. All rights reserved. This document may be redistributed and reused, subject to certain conditions (http://www.elsevier.com/wps/find/authorsview.authors/supplementalterms1.0) .
spellingShingle Articles
Muers, Martin F
Stephens, Richard J
Fisher, Patricia
Darlison, Liz
Higgs, Christopher MB
Lowry, Erica
Nicholson, Andrew G
O'Brien, Mary
Peake, Michael
Rudd, Robin
Snee, Michael
Steele, Jeremy
Girling, David J
Nankivell, Matthew
Pugh, Cheryl
Parmar, Mahesh KB
Active symptom control with or without chemotherapy in the treatment of patients with malignant pleural mesothelioma (MS01): a multicentre randomised trial
title Active symptom control with or without chemotherapy in the treatment of patients with malignant pleural mesothelioma (MS01): a multicentre randomised trial
title_full Active symptom control with or without chemotherapy in the treatment of patients with malignant pleural mesothelioma (MS01): a multicentre randomised trial
title_fullStr Active symptom control with or without chemotherapy in the treatment of patients with malignant pleural mesothelioma (MS01): a multicentre randomised trial
title_full_unstemmed Active symptom control with or without chemotherapy in the treatment of patients with malignant pleural mesothelioma (MS01): a multicentre randomised trial
title_short Active symptom control with or without chemotherapy in the treatment of patients with malignant pleural mesothelioma (MS01): a multicentre randomised trial
title_sort active symptom control with or without chemotherapy in the treatment of patients with malignant pleural mesothelioma (ms01): a multicentre randomised trial
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2431123/
https://www.ncbi.nlm.nih.gov/pubmed/18486741
http://dx.doi.org/10.1016/S0140-6736(08)60727-8
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