Neoplasma. 2018;65(1):132-139. doi: 10.4149/neo_2018_170206N78.
Malignant pleural effusion (MPE) is a common complication occurring in cancer patients, and its management affects the prognosis of these patients. Preclinical and clinical studies have reported that treatment with nanoparticle albumin-bound paclitaxel (nab-paclitaxel) plus carboplatin (CBDCA) is effective against intraperitoneal malignant tumors. To investigate the effectiveness of nab-paclitaxel plus CBDCA therapy for MPEs arising in patients with non-small cell lung cancer (NSCLC), we retrospectively analyzed the clinicopathological characteristics of 40 patients with stage IIIb or IV NSCLC who were treated with nab-paclitaxel plus CBDCA from 2013 to 2016. Out of 26 patients with MPEs who were treated with nab-paclitaxel plus CBDCA in this study, 21 patients (80.8%) had effective responses in MPEs; 6 of 21 patients exhibited complete responses (23.1%) and 15 of 21 had partial responses (57.7%). Kaplan-Meier survival curves and log-rank tests to evaluate the effectiveness of nab-paclitaxel plus CBDCA therapy against MPEs showed longer median progression-free survival (323 days vs. 26 days; p=0.009) and overall survival (not reached vs. 199 days; p=0.047) in patients with complete responses compared with those who achieved no response. There were no statistical differences between therapeutic effects on MPEs and those on systemic lesions. Nab-paclitaxel plus CBDCA therapy may be a preferred therapeutic option for patients with NSCLC who experience MPEs, and its effectiveness in treatment of MPEs may need to be evaluated separately from its therapeutic responses in systemic lesions.
恶性胸腔积液(MPE)是癌症患者常见的并发症,其治疗会影响这些患者的预后。临床前和临床研究报告称,纳米白蛋白结合紫杉醇(nab-紫杉醇)加卡铂(CBDCA)治疗对腹腔恶性肿瘤有效。为了研究 nab-紫杉醇加 CBDCA 治疗非小细胞肺癌(NSCLC)患者 MPE 的疗效,我们回顾性分析了 2013 年至 2016 年期间接受 nab-紫杉醇加 CBDCA 治疗的 40 例 IIIb 或 IV 期 NSCLC 患者的临床病理特征。在本研究中,26 例 MPE 患者接受了 nab-紫杉醇加 CBDCA 治疗,其中 21 例(80.8%)对 MPE 有有效反应;21 例患者中有 6 例(23.1%)完全缓解,15 例(57.7%)部分缓解。Kaplan-Meier 生存曲线和对数秩检验评估 nab-紫杉醇加 CBDCA 治疗对 MPE 的疗效显示,完全缓解患者的中位无进展生存期(323 天 vs. 26 天;p=0.009)和总生存期(未达到 vs. 199 天;p=0.047)均长于无反应患者。MPE 治疗效果与全身病变治疗效果之间无统计学差异。nab-紫杉醇加 CBDCA 治疗可能是 NSCLC 合并 MPE 患者的首选治疗方案,其对 MPE 的疗效可能需要与全身病变的疗效分别评估。