恶性胸膜间皮瘤患者胸膜内光动力治疗联合胸膜切除/去皮后化疗的可行性研究

S. Mordon, C. Munck, E. Surmei-Pintilie, R. Akkad, E. Wasielewski, G. Baert, P. Deleporte, H. Porte, A. Scherpereel
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引用次数: 0

摘要

背景:多模式联合手术(胸膜切除/去皮,P/D)和静脉辅助化疗(铂/培美曲塞)是一些恶性胸膜间皮瘤(MPM)患者的有效治疗选择。术中胸膜光动力治疗(iPDT)已成为改善这种多模式治疗结果的有希望的选择(Friedberg J, Ann Thorac Surg. 2017)。MesoPDT试验(NCT02662504)旨在评估这种方法的可行性,目前只有两个美国专家中心执行包括iPDT在内的多模式治疗。方法:设计单中心临床试验,评估iPDT方案在里尔大学医院的可行性。为了应用iPDT方案,并评估其在美国中心以外的适用性和安全性,预计最多有6名患者。结果:2016-2017年,连续纳入4例可评估患者,并按方案治疗,达到研究成果截止值。iPDT的具体程序已与美国专家合作实施和管理。安全概况是有利的。主要和最具体的不良事件是iPDT后72小时内发生的急性肺损伤,这可能导致可逆性呼吸窘迫,通过适当的重症监护可以控制。4例患者完成了全部计划方案。结论:iPDT多模式治疗MPM在欧洲专家中心是适用的和可管理的,涉及当地技能和专门的团队。iPDT在里尔中心的安全性是有利的,正如外部板验证的那样。中位总生存期很有希望(≈28个月),与之前美国的结果相似。我们的中心有望很快加入一项大型II期随机多中心美国试验,评估MPM多模式治疗(P/D,化疗)±iPDT (NCT02153229;美国宾夕法尼亚大学)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Feasibility trial assessing intrapleural photodynamic therapy combined with pleurectomy/decortication then chemotherapy in malignant pleural mesothelioma patients
Background: Multimodal treatment associating surgery (pleurectomy/decortication, P/D) then IV adjuvant chemotherapy (platinum/pemetrexed) is an effective therapeutic option for some selected malignant pleural mesothelioma (MPM) patients. Intra-operative pleural photodynamic therapy (iPDT) has emerged as a promising option to improve this multimodal treatment outcome (Friedberg J, Ann Thorac Surg. 2017). The MesoPDT trial (NCT02662504) aimed at assessing the feasibility of such procedure outside the only two US expert centers performing multimodal treatment including iPDT to date. Methods: A single-center pilot clinical trial was designed to assess the feasibility of iPDT protocol in Lille University Hospital. A pool of maximum six patients was expected in order to apply the iPDT protocol, and to assess its applicability and safety outside US center expert. Results: In 2016-2017, four consecutive assessable patients were included and treated per protocol, reaching the study achievement cut-off. iPDT specific procedures have been applied and managed in partnership with US experts. The safety profile was favorable. The main and most specific adverse event was acute lung injury occurring within 72 hours after iPDT, which may lead to reversible respiratory distress, manageable with adequate intensive care. The 4 patients achieved the full scheduled protocol. Conclusion: The iPDT multimodal treatment for MPM is applicable and manageable in a European expert center, involving local skills and dedicated teams. The safety profile of the iPDT in Lille center was favorable, as validated by an external board. Median overall survival was promising (≈28 months), similar to previous US results. Our center is expected to join soon a large phase II randomized, multicentric US trial assessing MPM multimodal treatment (P/D, chemotherapy) ±iPDT (NCT02153229; UPENN, USA).
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