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肿瘤负担减少对上皮样恶性胸膜间皮瘤生存的影响。

Effects of Reduction in Tumor Burden on Survival in Epithelioid Malignant Pleural Mesothelioma.

机构信息

Division of Medical Oncology, Mayo Clinic, Rochester, MN.

Division of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, MN.

出版信息

Mayo Clin Proc. 2018 Aug;93(8):1026-1033. doi: 10.1016/j.mayocp.2018.01.032. Epub 2018 May 24.

DOI:10.1016/j.mayocp.2018.01.032
PMID:29804728
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6077096/
Abstract

OBJECTIVE

To understand the relationship between response and survival in malignant pleural mesothelioma (MPM).

PATIENTS AND METHODS

The original clinical trial was conducted from April 1999 through March 2001. Patients with epithelioid MPM (n=305) were categorized using modified pleural Response Evaluation Criteria in Solid Tumors by whether they responded to treatment. Median progression-free survival (PFS) and overall survival (OS) were estimated and hazard ratios for responders and nonresponders were estimated and compared using the log-rank test. Multivariable Cox proportional hazards models were used to adjust for baseline prognostic factors.

RESULTS

Patients who responded to frontline therapy had a significantly longer OS (hazard ratio, 0.34; 95% CI, 0.24-0.49; median, 20.6 months; 95% CI, 15.3 months to not reached) than did those who did not respond (median, 9.4 months; 95% CI, 8.1-11.0 months) (P<.001). Similarly, responders had a significantly longer PFS (hazard ratio, 0.50; 95% CI, 0.39-0.64; median, 7.8 months; 95% CI, 6.5-8.5 months) than did nonresponders (median, 3.7 months; 95% CI, 2.9-4.3 months) (P<.001). These results were confirmed when adjusting for baseline prognostic factors. We also observed a survival benefit associated with disease stabilization in MPM.

CONCLUSION

Our findings indicate that reduction in tumor burden or disease stabilization determined using modified pleural Response Evaluation Criteria in Solid Tumors is strongly associated with OS and PFS in epithelioid MPM.

摘要

目的

了解恶性胸膜间皮瘤(MPM)的反应与生存之间的关系。

患者和方法

原始临床试验于 1999 年 4 月至 2001 年 3 月进行。根据改良胸膜实体瘤反应评估标准,将上皮样 MPM(n=305)患者分为有反应和无反应两组。使用对数秩检验估计中位无进展生存期(PFS)和总生存期(OS),并估计和比较反应者和无反应者的风险比。使用多变量 Cox 比例风险模型调整基线预后因素。

结果

一线治疗有反应的患者 OS 显著延长(风险比,0.34;95%CI,0.24-0.49;中位,20.6 个月;95%CI,15.3 个月至未达到),无反应者 OS 显著缩短(中位,9.4 个月;95%CI,8.1-11.0 个月)(P<.001)。同样,反应者 PFS 显著延长(风险比,0.50;95%CI,0.39-0.64;中位,7.8 个月;95%CI,6.5-8.5 个月),无反应者 PFS 显著缩短(中位,3.7 个月;95%CI,2.9-4.3 个月)(P<.001)。调整基线预后因素后,这些结果得到了证实。我们还观察到疾病稳定与 MPM 生存获益相关。

结论

我们的发现表明,使用改良胸膜实体瘤反应评估标准确定的肿瘤负荷减少或疾病稳定与上皮样 MPM 的 OS 和 PFS 密切相关。

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本文引用的文献

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Validation of Progression-Free Survival as a Surrogate Endpoint for Overall Survival in Malignant Mesothelioma: Analysis of Cancer and Leukemia Group B and North Central Cancer Treatment Group (Alliance) Trials.无进展生存期作为恶性间皮瘤总生存期替代终点的验证:癌症与白血病B组及北中部癌症治疗组(联盟)试验分析
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Metabolic response assessment with 18F-FDG-PET/CT is superior to modified RECIST for the evaluation of response to platinum-based doublet chemotherapy in malignant pleural mesothelioma.在评估恶性胸膜间皮瘤对铂类双联化疗的反应时,18F-FDG-PET/CT代谢反应评估优于改良RECIST标准。
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A Multicenter Study of Volumetric Computed Tomography for Staging Malignant Pleural Mesothelioma.一项关于容积计算机断层扫描用于恶性胸膜间皮瘤分期的多中心研究。
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Arginine Deprivation With Pegylated Arginine Deiminase in Patients With Argininosuccinate Synthetase 1-Deficient Malignant Pleural Mesothelioma: A Randomized Clinical Trial.精氨酸剥夺联合聚乙二醇化精氨酸脱亚氨酶治疗精氨酸合成酶 1 缺陷型恶性胸膜间皮瘤的随机临床试验。
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