Shimoyama Rai, Imamura Yoshinori, Uryu Kiyoaki, Mase Takahiro, Fujimura Yoshiaki, Hayashi Maki, Ohtaki Megu, Ohtani Keiko, Shinozaki Nobuaki, Minami Hironobu
Department of General Surgery, Shonan Kamakura General Hospital, Kamakura, Kanagawa 247-8533, Japan.
Department of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Hyogo 650-0017, Japan.
Mol Clin Oncol. 2023 Oct 25;19(6):98. doi: 10.3892/mco.2023.2694. eCollection 2023 Dec.
The present study aimed to investigate temporal trends in treatment patterns and prognostic factors for overall survival (OS) among patients with metastatic pancreatic cancer. From the Tokushukai REAl-world Data project, 1,093 patients with metastatic pancreatic cancer treated with gemcitabine, tegafur/gimeracil/oteracil (S-1), gemcitabine plus S-1, gemcitabine plus nab-paclitaxel, or fluorouracil, folic acid, oxaliplatin and irinotecan (FOLFIRINOX) between April 2010 and March 2020 were identified. Stratified/conventional Cox regression analyses were conducted to examine associations between patient- and tumor-related factors, study period, hospital volume, hospital type and first-line chemotherapy regimens. Overall, 846 patients were selected (503 male patients; median age, 70 years) after excluding ineligible patients. Over a median follow-up of 5.4 months, the median OS was 6.8 months (95% confidence interval, 6.3-7.4). The median OS for gemcitabine, S-1, gemcitabine plus S-1, gemcitabine plus nab-paclitaxel and FOLFIRINOX regimens was 5.9, 5.3, 7.7, 9.0 and 9.5 months, respectively. The median OS for 2010-2013, 2014-2017 and 2017-2020 was 6.2, 7.1 and 7.8 months, respectively. Performance status, body mass index and first-line chemotherapy regimens were identified to be significant prognostic factors. In summary, the real-world data indicated that standard care, including chemotherapy, for metastatic pancreatic cancer was widely used in hospitals throughout Japan and verified the survival benefits of gemcitabine plus nab-paclitaxel and FOLFIRINOX observed in prior clinical trials. This trial has been registered in the University Hospital Medical Information Network Clinical Trials Registry as UMIN000050590 on April 1, 2023.
本研究旨在调查转移性胰腺癌患者治疗模式的时间趋势以及总生存期(OS)的预后因素。从德洲会真实世界数据项目中,确定了2010年4月至2020年3月期间接受吉西他滨、替吉奥(S-1)、吉西他滨加S-1、吉西他滨加白蛋白结合型紫杉醇或氟尿嘧啶、叶酸、奥沙利铂和伊立替康(FOLFIRINOX)治疗的1093例转移性胰腺癌患者。进行分层/传统Cox回归分析,以检查患者和肿瘤相关因素、研究时期、医院规模、医院类型和一线化疗方案之间的关联。总体而言,排除不符合条件的患者后,选择了846例患者(503例男性患者;中位年龄70岁)。在中位随访5.4个月时,中位OS为6.8个月(95%置信区间,6.3 - 7.4)。吉西他滨、S-1、吉西他滨加S-1、吉西他滨加白蛋白结合型紫杉醇和FOLFIRINOX方案的中位OS分别为5.9、5.3、7.7、9.0和9.5个月。2010 - 2013年、2014 - 2017年和2017 - 2020年的中位OS分别为6.2、7.1和7.8个月。体能状态、体重指数和一线化疗方案被确定为显著的预后因素。总之,真实世界数据表明,包括化疗在内的转移性胰腺癌标准治疗在日本各地的医院中广泛使用,并证实了先前临床试验中观察到的吉西他滨加白蛋白结合型紫杉醇和FOLFIRINOX的生存获益。该试验于2023年4月1日在大学医院医学信息网络临床试验注册中心注册为UMIN000050590。