Extended pleurectomy decortication and chemotherapy versus chemotherapy alone for pleural mesothelioma (MARS 2): a phase 3 randomised controlled trial.

IF 38.7 1区 医学 Q1 CRITICAL CARE MEDICINE Lancet Respiratory Medicine Pub Date : 2024-06-01 Epub Date: 2024-05-10 DOI:10.1016/S2213-2600(24)00119-X
Eric Lim, David Waller, Kelvin Lau, Jeremy Steele, Anthony Pope, Clinton Ali, Rocco Bilancia, Manjusha Keni, Sanjay Popat, Mary O'Brien, Nadza Tokaca, Nick Maskell, Louise Stadon, Dean Fennell, Louise Nelson, John Edwards, Sara Tenconi, Laura Socci, Robert C Rintoul, Kelly Wood, Amanda Stone, Dakshinamoorthy Muthukumar, Charlotte Ingle, Paul Taylor, Laura Cove-Smith, Raffaele Califano, Yvonne Summers, Zacharias Tasigiannopoulos, Andrea Bille, Riyaz Shah, Elizabeth Fuller, Andrew Macnair, Jonathan Shamash, Talal Mansy, Richard Milton, Pek Koh, Andreea Alina Ionescu, Sarah Treece, Amy Roy, Gary Middleton, Alan Kirk, Rosie A Harris, Kate Ashton, Barbara Warnes, Emma Bridgeman, Katherine Joyce, Nicola Mills, Daisy Elliott, Nicola Farrar, Elizabeth Stokes, Vikki Hughes, Andrew G Nicholson, Chris A Rogers
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引用次数: 0

Abstract

Background: Extended pleurectomy decortication for complete macroscopic resection for pleural mesothelioma has never been evaluated in a randomised trial. The aim of this study was to compare outcomes after extended pleurectomy decortication plus chemotherapy versus chemotherapy alone.

Methods: MARS 2 was a phase 3, national, multicentre, open-label, parallel two-group, pragmatic, superiority randomised controlled trial conducted in the UK. The trial took place across 26 hospitals (21 recruiting only, one surgical only, and four recruiting and surgical). Following two cycles of chemotherapy, eligible participants with pleural mesothelioma were randomly assigned (1:1) to surgery and chemotherapy or chemotherapy alone using a secure web-based system. Individuals aged 16 years or older with resectable pleural mesothelioma and adequate organ and lung function were eligible for inclusion. Participants in the chemotherapy only group received two to four further cycles of chemotherapy, and participants in the surgery and chemotherapy group received pleurectomy decortication or extended pleurectomy decortication, followed by two to four further cycles of chemotherapy. It was not possible to mask allocation because the intervention was a major surgical procedure. The primary outcome was overall survival, defined as time from randomisation to death from any cause. Analyses were done on the intention-to-treat population for all outcomes, unless specified. This study is registered with ClinicalTrials.gov, NCT02040272, and is closed to new participants.

Findings: Between June 19, 2015, and Jan 21, 2021, of 1030 assessed for eligibility, 335 participants were randomly assigned (169 to surgery and chemotherapy, and 166 to chemotherapy alone). 291 (87%) participants were men and 44 (13%) women, and 288 (86%) were diagnosed with epithelioid mesothelioma. At a median follow-up of 22·4 months (IQR 11·3-30·8), median survival was shorter in the surgery and chemotherapy group (19·3 months [IQR 10·0-33·7]) than in the chemotherapy alone group (24·8 months [IQR 12·6-37·4]), and the difference in restricted mean survival time at 2 years was -1·9 months (95% CI -3·4 to -0·3, p=0·019). There were 318 serious adverse events (grade ≥3) in the surgery group and 169 in the chemotherapy group (incidence rate ratio 3·6 [95% CI 2·3 to 5·5], p<0·0001), with increased incidence of cardiac (30 vs 12; 3·01 [1·13 to 8·02]) and respiratory (84 vs 34; 2·62 [1·58 to 4·33]) disorders, infection (124 vs 53; 2·13 [1·36 to 3·33]), and additional surgical or medical procedures (15 vs eight; 2·41 [1·04 to 5·57]) in the surgery group.

Interpretation: Extended pleurectomy decortication was associated with worse survival to 2 years, and more serious adverse events for individuals with resectable pleural mesothelioma, compared with chemotherapy alone.

Funding: National Institute for Health and Care Research (NIHR) Health Technology Assessment programme (15/188/31), Cancer Research UK Feasibility Studies Project Grant (A15895).

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胸膜间皮瘤扩大胸膜切除术和化疗与单纯化疗(MARS 2):三期随机对照试验。
背景:在随机试验中,从未对胸膜间皮瘤大体上完全切除的胸膜切除术进行过评估。本研究旨在比较胸膜切除术后加化疗与单纯化疗的疗效:MARS 2是一项在英国进行的全国性、多中心、开放标签、平行两组、务实、优势随机对照试验。该试验在 26 家医院进行(21 家医院只招收病人,1 家医院只做手术,4 家医院招收病人并做手术)。经过两个化疗周期后,符合条件的胸膜间皮瘤患者通过安全的网络系统被随机分配(1:1)接受手术和化疗或单纯化疗。年龄在16岁或16岁以上、患有可切除胸膜间皮瘤、器官和肺功能正常的患者均可参加。只接受化疗组的参与者将继续接受两到四个周期的化疗,而手术和化疗组的参与者将接受胸膜切除术或扩大胸膜切除术,然后再接受两到四个周期的化疗。由于干预是一项重大外科手术,因此无法掩盖分配情况。主要结果是总生存期,即从随机分配到任何原因死亡的时间。除特别说明外,所有结果的分析均在意向治疗人群中进行。该研究已在ClinicalTrials.gov注册,编号为NCT02040272,不再接受新参与者:2015年6月19日至2021年1月21日期间,在1030名通过资格评估的参与者中,335名参与者被随机分配(169名接受手术和化疗,166名接受单纯化疗)。291名(87%)参与者为男性,44名(13%)为女性,288名(86%)被诊断为上皮样间皮瘤。中位随访时间为22-4个月(IQR 11-3-30-8),手术和化疗组的中位生存期(19-3个月(IQR 10-0-33-7))短于单纯化疗组(24-8个月(IQR 12-6-37-4)),2年的限制性平均生存期差异为-1-9个月(95% CI -3-4至-0-3,P=0-019)。手术组有318例严重不良事件(≥3级),化疗组有169例(发生率比3-6[95% CI 2-3至5-5],P解释:与单纯化疗相比,扩展胸膜切除术与可切除胸膜间皮瘤患者更差的2年生存率和更多的严重不良事件有关:国家健康与护理研究所(NIHR)健康技术评估项目(15/188/31)、英国癌症研究中心可行性研究项目资助(A15895)。
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来源期刊
Lancet Respiratory Medicine
Lancet Respiratory Medicine RESPIRATORY SYSTEM-RESPIRATORY SYSTEM
CiteScore
87.10
自引率
0.70%
发文量
572
期刊介绍: The Lancet Respiratory Medicine is a renowned journal specializing in respiratory medicine and critical care. Our publication features original research that aims to advocate for change or shed light on clinical practices in the field. Additionally, we provide informative reviews on various topics related to respiratory medicine and critical care, ensuring a comprehensive coverage of the subject. The journal covers a wide range of topics including but not limited to asthma, acute respiratory distress syndrome (ARDS), chronic obstructive pulmonary disease (COPD), tobacco control, intensive care medicine, lung cancer, cystic fibrosis, pneumonia, sarcoidosis, sepsis, mesothelioma, sleep medicine, thoracic and reconstructive surgery, tuberculosis, palliative medicine, influenza, pulmonary hypertension, pulmonary vascular disease, and respiratory infections. By encompassing such a broad spectrum of subjects, we strive to address the diverse needs and interests of our readership.
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