Ikezawa Kenji, Kiyota Ryosuke, Takada Ryoji, Daiku Kazuma, Maeda Shingo, Imai Toshihiro, Abe Yutaro, Kai Yugo, Yamai Takuo, Fukutake Nobuyasu, Nakabori Tasuku, Ashida Reiko, Uehara Hiroyuki, Tabuchi Takahiro, Katayama Kazuhiro, Ohkawa Kazuyoshi
Department of Hepatobiliary and Pancreatic Oncology Osaka International Cancer Institute Osaka Japan.
Department of Cancer Survey and Gastrointestinal Oncology Osaka International Cancer Institute Osaka Japan.
JGH Open. 2021 May 10;5(6):679-685. doi: 10.1002/jgh3.12555. eCollection 2021 Jun.
The optimal standard second-line chemotherapy for metastatic pancreatic cancer (MPC) remains unclear. Here, we evaluated the efficacy and safety of modified fluorouracil/leucovorin plus irinotecan and oxaliplatin (mFOLFIRINOX) compared with oral fluoropyrimidine S-1 as a second-line chemotherapy in patients with MPC.
We retrospectively reviewed 76 consecutive patients with metastatic pancreatic adenocarcinoma who underwent mFOLFIRINOX or S-1 treatment as a second-line chemotherapy after gemcitabine plus nab-paclitaxel (GnP) failure at our department between December 2014 and February 2019.
Patients who underwent mFOLFIRINOX treatment exhibited significantly better objective response rates (ORRs) and progression-free survival (PFS) than S-1 (ORR, 20.0% 0%, = 0.003; PFS, 3.7 2.1 months, = 0.010). Although baseline patient characteristics of age, performance status, and serum albumin levels differed significantly between the two groups, mFOLFIRINOX was identified as an independent factor of favorable PFS on multivariate analyses. Grade 3-4 neutropenia and peripheral sensory neuropathy occurred more frequently in the mFOLFIRINOX group. The median overall survival from the initiation of second-line chemotherapy was not significantly longer in the mFOLFIRINOX group than in the S1 group (8.5 5.8 months, respectively; = 0.213); however, the 8-month survival rate was significantly higher in the mFOLFIRINOX group (56.0% 27.5%, respectively; = 0.030).
mFOLFIRINOX as a second-line regimen contributed to favorable treatment outcomes, but induced more frequent adverse events than S-1. On multivariate analyses, mFOLFIRINOX was identified as an independent factor with favorable PFS, suggesting that mFOLFIRINOX could be a promising treatment option for patients with GnP failure.
转移性胰腺癌(MPC)的最佳标准二线化疗方案仍不明确。在此,我们评估了改良氟尿嘧啶/亚叶酸钙联合伊立替康和奥沙利铂(mFOLFIRINOX)与口服氟嘧啶S-1作为MPC患者二线化疗的疗效和安全性。
我们回顾性分析了2014年12月至2019年2月期间在我院接受吉西他滨联合纳米白蛋白紫杉醇(GnP)治疗失败后接受mFOLFIRINOX或S-1二线化疗的76例连续性转移性胰腺腺癌患者。
接受mFOLFIRINOX治疗的患者客观缓解率(ORR)和无进展生存期(PFS)显著优于S-1(ORR,20.0%对0%,P = 0.003;PFS,3.7个月对2.1个月,P = 0.010)。尽管两组患者的年龄、体能状态和血清白蛋白水平等基线特征存在显著差异,但在多因素分析中,mFOLFIRINOX被确定为PFS良好的独立因素。mFOLFIRINOX组3-4级中性粒细胞减少和周围感觉神经病变的发生率更高。二线化疗开始后的中位总生存期在mFOLFIRINOX组并不比S-1组显著延长(分别为8.5个月和5.8个月;P = 0.213);然而,mFOLFIRINOX组的8个月生存率显著更高(分别为56.0%和27.5%;P = 0.030)。
mFOLFIRINOX作为二线方案有助于取得良好的治疗效果,但比S-1诱导的不良事件更频繁。在多因素分析中,mFOLFIRINOX被确定为PFS良好的独立因素,表明mFOLFIRINOX可能是GnP治疗失败患者的一种有前景的治疗选择。