Li Qingsong, Hu Cheng, Su Shengfa, Ma Zhu, Geng Yichao, Hu Yinxiang, Li Huiqin, Lu Bing
Department of Thoracic Oncology, Affiliated Hospital of Guizhou Medical University, Guiyang, People's Republic of China.
Department of Thoracic Oncology, Affiliated Cancer Hospital of Guizhou Medical University, Guiyang, People's Republic of China.
Cancer Manag Res. 2022 Nov 28;14:3347-3358. doi: 10.2147/CMAR.S385818. eCollection 2022.
The impact of primary tumour radiotherapy on the prognosis for non-small-cell lung cancer (NSCLC) with controlled malignant pleural effusion (MPE-C) (MPE-C-NSCLC) is unclear. This study aimed to analyze the efficacy and safety of primary tumor radiotherapy in patients with MPE-C-NSCLC.
A total of 186 patients with MPE-C-NSCLC were enrolled and divided into two groups. The patients in the D group were treated with only drugs. Those in the RD group were treated with drugs plus primary tumour radiotherapy. The Kaplan-Meier method was used for survival analysis, and the Log rank test was used for between-group analysis and univariate prognostic analysis. The Cox proportional hazards model was used to perform multivariate analyses to assess the impacts of factors on survival. Propensity score matching (PSM) was matched based on clinical characteristics, systematic drug treatment and drug response to further adjust for confounding factors.
The overall survival (OS) rates at 1, 2, and 3 years for the RD group and D group were 54.4%, 26.8%, and 13.3% and 31.1%, 11.5%, and 4.4%, respectively; the corresponding MSTs were 14 months and 8 months, respectively ( =15.915, p<0.001). There was a significant difference in survival by PSM (p=0.027).Before PSM, multivariate analysis showed that metastasis status (organ≤3 and metastasis≤5), primary tumour radiotherapy, chemotherapy cycles≥4, and drug best response (CR+PR) were independent predictors of prolonged OS. After PSM, primary tumour radiotherapy and drug best response (CR+PR) were independent predictors of prolonged OS were still independent predictors of prolonged OS. There were no grade 4-5 radiation toxicities.
For MPE-C-NSCLC, the response of systemic drug treatment plays a crucial role in survival outcomes, and we also should pay attention to primary tumour radiotherapy in addition to systematic drug treatment.
原发性肿瘤放疗对恶性胸腔积液得到控制的非小细胞肺癌(MPE-C-NSCLC)预后的影响尚不清楚。本研究旨在分析原发性肿瘤放疗在MPE-C-NSCLC患者中的疗效和安全性。
共纳入186例MPE-C-NSCLC患者,分为两组。D组患者仅接受药物治疗。RD组患者接受药物治疗加原发性肿瘤放疗。采用Kaplan-Meier法进行生存分析,Log rank检验用于组间分析和单因素预后分析。采用Cox比例风险模型进行多因素分析,以评估各因素对生存的影响。基于临床特征、系统药物治疗和药物反应进行倾向评分匹配(PSM),以进一步调整混杂因素。
RD组和D组1年、2年和3年的总生存率(OS)分别为54.4%、26.8%和13.3%以及31.1%、11.5%和4.4%;相应的中位总生存期(MST)分别为14个月和8个月(χ²=15.915,p<0.001)。PSM分析显示生存存在显著差异(p=0.027)。在PSM之前,多因素分析表明转移状态(器官≤3且转移灶≤5)、原发性肿瘤放疗、化疗周期≥4以及药物最佳反应(完全缓解+部分缓解)是OS延长的独立预测因素。PSM之后,原发性肿瘤放疗和药物最佳反应(完全缓解+部分缓解)仍是OS延长的独立预测因素。未出现4-5级放射毒性反应。
对于MPE-C-NSCLC,全身药物治疗的反应对生存结局起着关键作用,除全身药物治疗外,还应重视原发性肿瘤放疗。