Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Meldola, Italy
Department of Oncology, Azienda Socio Sanitaria Territoriale (ASST) Monza, Presidio San Gerardo, Monza, Italy.
Oncologist. 2019 Nov;24(11):e1165-e1171. doi: 10.1634/theoncologist.2018-0737. Epub 2019 Apr 17.
Nivolumab has shown a survival benefit compared with docetaxel as second-line treatment for patients with previously treated advanced squamous non-small cell lung cancer (NSCLC) in a randomized phase III trial. The experiences of patients and physicians in routine clinical practice are often different from those in a controlled clinical trial setting. We present data from the entire Italian cohort of patients with squamous NSCLC enrolled in a worldwide nivolumab NSCLC expanded access program.
Patients with pretreated advanced squamous NSCLC received nivolumab 3 mg/kg every 2 weeks for up to 24 months. Safety was monitored throughout; efficacy data collected included objective tumor response, date of progression, and survival information.
The Italian cohort comprised 371 patients who received at least one dose of nivolumab. In the overall population, the objective response rate (ORR) was 18%, the disease control rate (DCR) was 47%, and median overall survival (OS) was 7.9 months (95% confidence interval 6.2-9.6). In subgroup analyses, ORR, DCR, and median OS were, respectively, 17%, 48%, and 9.1 months in patients previously treated with two or more lines of therapy ( = 209) and 8%, 40%, and 10.0 months in patients treated beyond disease progression ( = 65). In the overall population, the rate of any-grade and grade 3-4 adverse events was 29% and 6%, respectively. Treatment-related adverse events led to treatment discontinuation in 14 patients (5%). There were no treatment-related deaths.
To date, this report represents the most extensive clinical experience with nivolumab in advanced squamous NSCLC in current practice outside the controlled clinical trial setting. These data suggest that the efficacy and safety profiles of nivolumab in a broad, real-world setting are consistent with those obtained in clinical trials.
Nivolumab is approved in the U.S. and Europe for the treatment of advanced non-small cell lung cancer (NSCLC) after failure of prior platinum-based chemotherapy. In this cohort of Italian patients with previously treated, advanced squamous NSCLC treated in a real-world setting as part of the nivolumab expanded access program, the efficacy and safety of nivolumab was consistent with that previously reported in nivolumab clinical trials.
纳武利尤单抗在经治的晚期鳞状非小细胞肺癌(NSCLC)患者中与多西他赛相比显示出生存获益,这是一项随机 III 期试验的结果。患者和医生在常规临床实践中的经验通常与对照临床试验环境中的经验不同。我们报告了参与纳武利尤单抗 NSCLC 扩展使用计划的全球范围内意大利鳞状 NSCLC 患者队列的全部数据。
接受过治疗的晚期鳞状 NSCLC 患者接受纳武利尤单抗 3 mg/kg,每 2 周一次,最多 24 个月。整个过程中监测安全性;收集的疗效数据包括客观肿瘤反应、进展日期和生存信息。
意大利队列包括 371 名至少接受过一次纳武利尤单抗治疗的患者。在总体人群中,客观缓解率(ORR)为 18%,疾病控制率(DCR)为 47%,中位总生存期(OS)为 7.9 个月(95%置信区间 6.2-9.6)。在亚组分析中,先前接受过 2 线或以上治疗的患者(n=209)的 ORR、DCR 和中位 OS 分别为 17%、48%和 9.1 个月,而疾病进展后治疗的患者(n=65)的 ORR、DCR 和中位 OS 分别为 8%、40%和 10.0 个月。在总体人群中,任何级别和 3-4 级不良事件的发生率分别为 29%和 6%。治疗相关不良事件导致 14 名患者(5%)停止治疗。没有治疗相关死亡。
迄今为止,这是在对照临床试验环境之外的当前实践中,纳武利尤单抗在晚期鳞状 NSCLC 中的最广泛临床经验报告。这些数据表明,纳武利尤单抗在广泛的真实世界环境中的疗效和安全性特征与临床试验中获得的一致。
纳武利尤单抗在美国和欧洲被批准用于治疗先前铂类化疗失败后的晚期非小细胞肺癌(NSCLC)。在该队列中,意大利的晚期鳞状 NSCLC 患者在纳武利尤单抗扩展使用计划中作为真实世界环境中的一部分进行治疗,纳武利尤单抗的疗效和安全性与纳武利尤单抗临床试验中报告的一致。