Division of Radiation Oncology, Allegheny Health Network Cancer Institute, Pittsburgh, PA.
Department of Radiation Oncology, University of Texas M.D. Anderson Cancer Center, Houston, TX.
Clin Lung Cancer. 2019 Jul;20(4):263-269. doi: 10.1016/j.cllc.2019.03.003. Epub 2019 Mar 26.
Management options for unresected malignant pleural mesothelioma (MPM) are largely limited to palliative chemotherapy and best supportive care. This study sought to delineate subgroups most likely to benefit from chemotherapy.
The National Cancer Database was queried for newly-diagnosed unresected sarcomatoid, biphasic, and/or metastatic (M1) MPM. Statistics included Kaplan-Meier overall survival (OS) analysis with and without propensity matching, landmark Kaplan-Meier analysis to address immortal time bias, and multivariable Cox proportional hazards modeling in all patients as well as within histologic/M-classification-based subcohorts.
Of 4655 patients (48% chemotherapy, 52% best supportive care), 15%, 27%, and 40% had epithelioid, biphasic, and sarcomatoid disease, respectively; 41% had M1 disease. The median OS in the chemotherapy and BSC cohorts was 10.4 versus 4.8 months (P < .001). OS differences persisted following landmark analysis (P = .038) and propensity matching (P < .001). Chemotherapy was associated with higher OS in M1 cases with unknown histology and M1 epithelioid patients (P < .001 for both). For non-epithelioid cases, chemotherapy was associated with higher OS for M0 (P < .001 for sarcomatoid and biphasic) but not M1 (P > .05 for both) disease.
Chemotherapy may benefit metastatic epithelioid and non-metastatic non-epithelioid MPM to a greater degree than metastatic non-epithelioid disease. Causation, however, is not implied, and careful patient selection in this population cannot be understated.
未切除的恶性胸膜间皮瘤(MPM)的治疗选择主要限于姑息性化疗和最佳支持治疗。本研究旨在确定最有可能从化疗中获益的亚组。
从国家癌症数据库中检索新诊断的未切除的肉瘤样、双相和/或转移性(M1)MPM。统计分析包括Kaplan-Meier 总生存(OS)分析,包括有无倾向匹配、解决不朽时间偏倚的里程碑 Kaplan-Meier 分析,以及所有患者以及基于组织学/M 分类的亚组的多变量 Cox 比例风险建模。
在 4655 名患者中(48%接受化疗,52%接受最佳支持治疗),分别有 15%、27%和 40%患有上皮样、双相和肉瘤样疾病,41%患有 M1 疾病。化疗组和 BSC 组的中位 OS 分别为 10.4 个月和 4.8 个月(P<0.001)。里程碑分析(P=0.038)和倾向匹配后(P<0.001),OS 差异仍然存在。在组织学未知和 M1 上皮样患者中,化疗与更高的 OS 相关(两者均 P<0.001)。对于非上皮样病例,化疗与 M0(肉瘤样和双相 P<0.001)而非 M1(两者均 P>0.05)疾病的更高 OS 相关。
与转移性非上皮样疾病相比,化疗可能使转移性上皮样和非转移性非上皮样 MPM 获益更大。但是,这并不意味着因果关系,并且在这一人群中,仔细的患者选择至关重要。