Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, New York, USA.
Ipsen, Cambridge, Massachusetts, USA.
Cancer Med. 2023 Apr;12(8):9496-9505. doi: 10.1002/cam4.5714. Epub 2023 Mar 19.
Subgroup analyses of the NAPOLI-1 study identified that among patients who were irinotecan naïve prior to entering the clinical trial, a survival benefit was observed between the study arm and control arm. This treatment benefit was not observed among those previously exposed to irinotecan. This study sought to understand the impact of prior exposure to irinotecan on clinical outcomes among patients treated with liposomal irinotecan in the real-world setting.
This retrospective observational study utilized a nationwide electronic health record (EHR)-derived deidentified database. Data for adult patients with mPDAC treated with liposomal irinotecan-based regimens between January 2016 and October 2020 were analyzed. Patient characteristics, overall survival (OS), and progression-free survival (PFS) were assessed. Cox proportional hazard methods were used to calculate hazard ratios (HRs). HRs were adjusted for demographics and relevant clinical covariates.
Six hundred and seventy-five patients with mPDAC treated with a liposomal irinotecan-based regimen were included. The unadjusted OS HR was 1.3 (95% CI: 1.1-1.6, p < 0.001) and unadjusted PFS was HR 1.4 (95% CI: 1.2-1.7, p < 0.001). After adjustment for baseline characteristics, the adjusted OS HR was 1.0 (95% CI: 0.8-1.3, p = 0.8836) and the adjusted PFS HR was 1.1 (95% CI: 0.8-1.4, p = 0.5626).
Prior irinotecan was not found to be a significant predictor of patient outcomes in those later treated with liposomal irinotecan. Thus, the results may inform the rationale for utilizing liposomal irinotecan combination therapy following prior irinotecan exposure in mPDAC, in particular where the prior irinotecan exposure was more distant in time.
NAPOLI-1 研究的亚组分析表明,在进入临床试验之前未曾接受伊立替康治疗的患者中,研究组与对照组之间观察到生存获益。而在先前接受过伊立替康治疗的患者中未观察到这种治疗益处。本研究旨在了解在真实环境中接受脂质体伊立替康治疗的患者中,先前暴露于伊立替康对临床结局的影响。
这是一项回顾性观察性研究,利用了全国性的电子健康记录(EHR)衍生的去识别数据库。分析了 2016 年 1 月至 2020 年 10 月期间接受脂质体伊立替康为基础方案治疗的 mPDAC 成年患者的数据。评估了患者特征、总生存期(OS)和无进展生存期(PFS)。使用 Cox 比例风险方法计算风险比(HRs)。HRs 针对人口统计学和相关临床协变量进行了调整。
共纳入 675 例接受脂质体伊立替康为基础方案治疗的 mPDAC 患者。未经调整的 OS HR 为 1.3(95%CI:1.1-1.6,p<0.001),未经调整的 PFS HR 为 1.4(95%CI:1.2-1.7,p<0.001)。在调整基线特征后,调整后的 OS HR 为 1.0(95%CI:0.8-1.3,p=0.8836),调整后的 PFS HR 为 1.1(95%CI:0.8-1.4,p=0.5626)。
先前使用伊立替康并不是随后接受脂质体伊立替康治疗的患者结局的显著预测因素。因此,这些结果可能为在 mPDAC 中,在先前接受过伊立替康治疗的情况下,特别是在先前接受伊立替康治疗的时间较为久远的情况下,使用脂质体伊立替康联合治疗提供依据。