Royal Brompton and Harefield Hospitals, Guy's and St Thomas' NHS Foundation Trust, London, UK; Imperial College London, London, UK.
St Bartholomew's Hospital, London, UK.
Lancet Respir Med. 2024 Jun;12(6):457-466. doi: 10.1016/S2213-2600(24)00119-X. Epub 2024 May 10.
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).
背景:广泛胸膜切除术和剥除术(extended pleurectomy decortication,EPD)用于胸膜间皮瘤的完全宏观切除术,尚未在随机试验中进行评估。本研究旨在比较 EPD 加化疗与单纯化疗后的结果。
方法:MARS 2 是一项在英国进行的 3 期、全国性、多中心、开放性、平行两组、实用、优效性随机对照试验。该试验在 26 家医院进行(21 家仅招募、1 家仅手术、4 家招募和手术)。在完成两个周期的化疗后,符合条件的胸膜间皮瘤患者被随机分配(1:1)至手术和化疗组或单纯化疗组,使用安全的基于网络的系统。年龄在 16 岁及以上、可切除的胸膜间皮瘤且有足够的器官和肺功能的患者有资格入组。单纯化疗组的患者接受 2 至 4 个周期的化疗,手术和化疗组的患者接受胸膜切除术和剥除术或广泛胸膜切除术和剥除术,随后再接受 2 至 4 个周期的化疗。由于干预措施是一项主要的手术程序,因此无法进行分组盲法。主要结局是总生存时间,定义为从随机分组到任何原因死亡的时间。除非另有说明,否则所有结局的分析均基于意向治疗人群。该研究在 ClinicalTrials.gov 注册,NCT02040272,现已不再招募新的参与者。
结果:在 2015 年 6 月 19 日至 2021 年 1 月 21 日期间,对 1030 名符合条件的患者进行了评估,其中 335 名患者被随机分配(169 名患者分配至手术和化疗组,166 名患者分配至单纯化疗组)。291 名(87%)患者为男性,44 名(13%)为女性,288 名(86%)患者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时间(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 年时限制性平均生存时间的差异为-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<0.0001),心脏不良事件(30 例比 12 例;3.01 [1.13 至 8.02])和呼吸不良事件(84 例比 34 例;2.62 [1.58 至 4.33])、感染(124 例比 53 例;2.13 [1.36 至 3.33])、以及其他手术或医疗程序(15 例比 8 例;2.41 [1.04 至 5.57])的发生率更高。
解释:与单纯化疗相比,广泛胸膜切除术和剥除术与可切除性胸膜间皮瘤患者的 2 年生存率降低和更严重的不良事件相关。
资金来源:英国国家卫生与保健优化研究所(NIHR)卫生技术评估计划(15/188/31)、英国癌症研究基金会可行性研究项目资助(A15895)。
Interact Cardiovasc Thorac Surg. 2017-11-1
Nat Rev Dis Primers. 2025-8-7
Life Sci Alliance. 2025-7-31
Cancers (Basel). 2025-7-16
J Thorac Cardiovasc Surg. 2022-11
Eur J Cardiothorac Surg. 2020-7-1
J Thorac Oncol. 2018-8-16