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Lancet. 2021 Jan 30;397(10272):375-386. doi: 10.1016/S0140-6736(20)32714-8. Epub 2021 Jan 21.
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A multicentre randomised phase III trial comparing pembrolizumab versus single-agent chemotherapy for advanced pre-treated malignant pleural mesothelioma: the European Thoracic Oncology Platform (ETOP 9-15) PROMISE-meso trial.一项比较派姆单抗与单药化疗治疗晚期预处理恶性胸膜间皮瘤的多中心随机 III 期试验:欧洲胸部肿瘤平台(ETOP 9-15)PROMISE-meso 试验。
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根据真实世界队列中的组织学,化疗治疗恶性胸膜间皮瘤的疗效。

Efficacy of chemotherapy for malignant pleural mesothelioma according to histology in a real-world cohort.

机构信息

Oncology Department, Hospital Universitari Vall d'Hebron & Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.

Thoracic Cancers Translational Genomics Unit, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.

出版信息

Sci Rep. 2021 Nov 1;11(1):21357. doi: 10.1038/s41598-021-00831-4.

DOI:10.1038/s41598-021-00831-4
PMID:34725384
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8560806/
Abstract

CheckMate 743 trial demonstrated survival benefit of immunotherapy in first line in MPM with some differences in the efficacy of chemotherapy according to histology. The objective of this study is to characterize the impact of chemotherapy according to histology in patients diagnosed with MPM at our institution. Clinical records of all MPM patients diagnosed at Vall d'Hebron University Hospital between November 2002 and April 2020 were reviewed. Associations between clinical variables and outcomes were assessed with Cox regression models. Survival data were calculated by the Kaplan-Meier method. 189 patients were included with 76% of tumors classified as epithelioid subtype. First line chemotherapy was offered to 85% of patients. Median survival in overall population was 21.3 months (95% CI 17.2-24.3). We found that patients with epithelioid tumors had better overall survival (OS) and progression free survival (PFS). Median OS of epithelioid patients treated with first line chemotherapy was 26.7 months versus 15.0 months in non-epithelioid patients (HR 2.25 CI 95% 1.4-3.4; p < 0.001). Median PFS for patients with epithelioid tumors treated with chemotherapy was 4.8 months versus 3.6 months in non-epithelioid (HR 1.5 CI 95% 1.0-2.3; p = 0.03). The improvement of outcomes in patients with epithelioid histology was detected in patients treated with cisplatin or carboplatin. Histology was not a predictive factor for the platinum agent sensitivity (p of interaction PFS = 0.09, p of interaction OS = 0.65). In our series, patients with non-epithelioid tumors presented worse prognosis. Although epithelioid tumors exposed to cisplatin had higher PFS, histology was not a clear predictor of chemotherapy efficacy.

摘要

CheckMate 743 试验表明,免疫疗法在 MPM 的一线治疗中具有生存获益,并且根据组织学的不同,化疗的疗效也存在差异。本研究的目的是在我们的机构中,根据组织学特征来描述化疗对 MPM 患者的影响。回顾了 2002 年 11 月至 2020 年 4 月期间在 Vall d'Hebron 大学医院诊断为 MPM 的所有患者的临床记录。使用 Cox 回归模型评估临床变量与结局之间的相关性。通过 Kaplan-Meier 法计算生存数据。共纳入 189 例患者,其中 76%的肿瘤分类为上皮样亚型。一线化疗用于 85%的患者。总体人群的中位总生存期为 21.3 个月(95%CI 17.2-24.3)。我们发现,上皮样肿瘤患者的总生存(OS)和无进展生存(PFS)更好。接受一线化疗的上皮样患者的中位 OS 为 26.7 个月,而非上皮样患者为 15.0 个月(HR 2.25,95%CI 1.4-3.4;p<0.001)。接受化疗的上皮样肿瘤患者的中位 PFS 为 4.8 个月,而非上皮样肿瘤为 3.6 个月(HR 1.5,95%CI 1.0-2.3;p=0.03)。在接受顺铂或卡铂治疗的患者中,检测到上皮样组织学患者的结局改善。组织学不是铂类药物敏感性的预测因素(PFS 交互作用 p=0.09,OS 交互作用 p=0.65)。在我们的系列中,非上皮样肿瘤患者的预后较差。尽管接受顺铂治疗的上皮样肿瘤患者的 PFS 更高,但组织学并不是化疗疗效的明确预测因素。