Division of Drug and Diagnostic Development Promotion, Department for the Promotion of Drug and Diagnostic Development, Translational Research Support Office, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa-shi, Chiba, 277-8577, Japan.
Department of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa-shi, Chiba, 277-8577, Japan.
Sci Rep. 2024 Jul 23;14(1):16906. doi: 10.1038/s41598-024-65689-8.
This study aimed to compare second-line treatment outcomes for patients with unresectable pancreatic cancer previously treated with gemcitabine plus nab-paclitaxel (GnP) therapy. We conducted an integrated analysis of two retrospective studies included 318 patients receiving nanoliposomal irinotecan + 5-fluorouracil/folinic acid (NFF) (n = 102), S-1 (n = 57), or FOLFIRINOX (n = 14) as second-line treatment. Median overall survival (OS) in the NFF group was 9.08 months, significantly better than S-1 (4.90 months, P = 0.002). FOLFIRINOX had a median OS of 4.77 months, not statistically different from NFF. Subgroup analyses of OS indicated NFF was generally superior, however, a statistical interaction was observed between the treatment regimen in serum Alb < 3.5 g/dL (P = 0.042) and serum CRP ≥ 0.3 mg/dL (P = 0.006). Median progression-free survival (PFS) was 2.93 months for NFF, significantly better than S-1 (2.53 months, P = 0.024), while FOLFIRINOX had a comparable PFS (3.04 months, P = 0.948). Multivariate analysis identified the serum CRP, serum CA19-9, duration of first-line GnP therapy, and use (yes/no) of S-1 for second-line treatment as independent predictors for OS. This study concludes that second-line NFF therapy demonstrated a more favorable OS compared to S-1 therapy, however, it is still important to consider the patient background characteristics while selecting the most appropriate treatment.
本研究旨在比较先前接受吉西他滨加 nab-紫杉醇(GnP)治疗的不可切除胰腺癌患者的二线治疗结果。我们对两项回顾性研究进行了综合分析,共纳入 318 例接受纳米脂质体伊立替康+5-氟尿嘧啶/亚叶酸(NFF)(n=102)、替吉奥(S-1)(n=57)或 FOLFIRINOX(n=14)作为二线治疗的患者。NFF 组的中位总生存期(OS)为 9.08 个月,显著优于 S-1 组(4.90 个月,P=0.002)。FOLFIRINOX 的 OS 中位数为 4.77 个月,与 NFF 无统计学差异。OS 的亚组分析表明 NFF 通常更优,但在血清 Alb<3.5 g/dL(P=0.042)和血清 CRP≥0.3 mg/dL(P=0.006)的患者中观察到治疗方案之间存在统计学交互作用。NFF 的中位无进展生存期(PFS)为 2.93 个月,显著优于 S-1(2.53 个月,P=0.024),而 FOLFIRINOX 的 PFS 相当(3.04 个月,P=0.948)。多变量分析确定血清 CRP、血清 CA19-9、一线 GnP 治疗持续时间以及二线治疗中是否使用(是/否)S-1 为 OS 的独立预测因素。本研究得出结论,与 S-1 治疗相比,二线 NFF 治疗显示出更有利的 OS,但在选择最合适的治疗方法时,仍需考虑患者的背景特征。
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