von Eiff Damian, Bozorgmehr Farastuk, Chung Inn, Bernhardt Denise, Rieken Stefan, Liersch Stephan, Muley Thomas, Kobinger Sonja, Thomas Michael, Christopoulos Petros, Steins Martin
Department of Thoracic Oncology, Thoraxklinik at Heidelberg University Hospital, Heidelberg, Germany.
Translational Lung Research Center Heidelberg (TLRC-H), Member of the German Center for Lung Research (DZL), Germany.
J Thorac Dis. 2020 Mar;12(3):782-793. doi: 10.21037/jtd.2019.12.74.
Etoposide-/platinum-based chemotherapy is the standard first-line treatment for extensive-disease small cell lung cancer (SCLC), but responses are short-lived and subsequent options limited. Here, we present our experience with paclitaxel in advanced treatment lines.
We retrospectively studied the clinical course of all paclitaxel-treated SCLC patients between 2005 and 2015 in our institution. Prognostic and predictive factors were analyzed by Kaplan-Meier and Cox regression analyses.
A total of 185 patients [119 men, median age 65 years, median ECOG performance status (PS) 1] were identified. One hundred and sixty-eight patients had extensive disease (ED) at the time of paclitaxel therapy. Paclitaxel was mainly given as third- or fourth-line therapy (93%). The response rate (RR) was 17% and disease control rate (DCR) 28%. Patients reached a median progression-free survival (PFS) of 1.6 (95% CI: 1.4-1.8) months and median overall survival (OS) of 3.3 (95% CI: 2.8-3.9) months. Main toxicities were fatigue (25%) and polyneuropathy (17%). Dose reduction of ≥25% was associated with shorter PFS [1.9 (95% CI: 1.5-2.3) . 1.4 (95% CI: 1.3-1.5) months; P=0.004]. Further independent predictive factors for PFS were gender, age, and hepatic/brain metastases (P<0.05). Tumor response to paclitaxel, PS, number and location of metastases, dose reduction, and smoking history were significant factors for OS in univariable analyses (P<0.05), while PS, dose reduction, status of cerebral/hepatic metastases, tumor response, and smoking history were retained as independent prognostic factors in multivariable testing. Notably, ECOG PS 2 patients had toxicity rates similar to ECOG PS 0-1 patients (63% . 62%), as well as a comparable DCR (29% . 28%), which was associated with prolonged survival (4.5 3.2 months for refractory cases, P=0.034).
Paclitaxel has clinically relevant activity in heavily pretreated SCLC. While patients with good PS and no cerebral/hepatic metastases derive the greatest benefit, ECOG PS 2 per se should not be used as a criterion to exclude patients.
依托泊苷/铂类化疗是广泛期小细胞肺癌(SCLC)的标准一线治疗方案,但缓解期短暂且后续治疗选择有限。在此,我们介绍我们在晚期治疗线中使用紫杉醇的经验。
我们回顾性研究了2005年至2015年在我们机构接受紫杉醇治疗的所有SCLC患者的临床病程。通过Kaplan-Meier和Cox回归分析来分析预后和预测因素。
共确定了185例患者[119例男性,中位年龄65岁,中位东部肿瘤协作组(ECOG)体能状态(PS)为1]。168例患者在接受紫杉醇治疗时已处于广泛期(ED)。紫杉醇主要作为三线或四线治疗(93%)。缓解率(RR)为17%,疾病控制率(DCR)为28%。患者的中位无进展生存期(PFS)为1.6(95%置信区间:1.4 - 1.8)个月,中位总生存期(OS)为3.3(95%置信区间:2.8 - 3.9)个月。主要毒性反应为疲劳(25%)和多发性神经病变(17%)。剂量减少≥25%与较短的PFS相关[1.9(95%置信区间:1.5 - 2.3)对1.4(95%置信区间:1.3 - 1.5)个月;P = 0.004]。PFS的其他独立预测因素为性别、年龄和肝/脑转移(P < 0.05)。在单变量分析中,肿瘤对紫杉醇的反应、PS、转移灶的数量和位置、剂量减少以及吸烟史是OS的显著因素(P < 0.