Li Xujia, Huang Jinsheng, Wang Fenghua, Jiang Qi, Huang Lingli, Li Shengping, Guo Guifang
VIP Department, Sun Yat-sen University Cancer Center, Guangzhou, P.R. China.
State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, P.R. China.
Ther Adv Med Oncol. 2023 Jul 8;15:17588359231186029. doi: 10.1177/17588359231186029. eCollection 2023.
Modified fluorouracil/leucovorin/irinotecan/oxaliplatin (FOLFIRINOX) regimen (mFOLFIRINOX), comprised of fluorouracil, leucovorin, irinotecan and oxaliplatin, is the first-line standard chemotherapy in patients with advanced pancreatic cancer. The S-1/oxaliplatin/irinotecan (SOXIRI) regimen has also been studied recently under similar conditions. This study compared its efficacy and safety.
All cases of locally advanced or metastatic pancreatic cancer treated with the SOXIRI or mFOLFIRINOX regimen in Sun Yat-sen University Cancer Centre from July 2012 to June 2021 were reviewed retrospectively. The data of patients who satisfied the inclusion criteria were compared between two cohorts, including overall survival (OS), progression-free survival (PFS), objective response rate, disease control rate and safety.
A total of 198 patients were enrolled in the study, including 102 patients treated with SOXIRI and 96 patients treated with mFOLFIRINOX. There was no significant difference in OS [12.1 months 11.2 months, hazard ratio (HR) = 1.04, = 0.81] or PFS (6.5 months 6.8 months, HR = 0.99, = 0.96) between patients treated with SOXIRI and mFOLFIRINOX. In the subgroup analysis, patients with slightly elevated baseline total bilirubin (TBIL) or underweight patients before chemotherapy were more likely to have a longer OS or PFS from SOXIRI than from mFOLFIRINOX. In addition, the carbohydrate antigen (CA)19-9 decline was a good predictor for the efficacy and prognosis of both chemotherapy regimens. All grade adverse events were parallel in all kinds of toxicities except that anaemia was more common in the SOXIRI group than in the mFOLFIRINOX group (41.4% 24%, = 0.03). The occurrence of any grade 3 to 4 toxicity was similar in the two groups.
For locally advanced or metastatic pancreatic cancer patients, the SOXIRI regimen had similar efficacy and controllable safety compared with the mFOLFIRINOX regimen.
改良氟尿嘧啶/亚叶酸钙/伊立替康/奥沙利铂(FOLFIRINOX)方案(mFOLFIRINOX)由氟尿嘧啶、亚叶酸钙、伊立替康和奥沙利铂组成,是晚期胰腺癌患者的一线标准化疗方案。S-1/奥沙利铂/伊立替康(SOXIRI)方案最近也在类似情况下进行了研究。本研究比较了其疗效和安全性。
回顾性分析2012年7月至2021年6月在中山大学肿瘤防治中心接受SOXIRI或mFOLFIRINOX方案治疗的所有局部晚期或转移性胰腺癌病例。比较两个队列中符合纳入标准患者的数据,包括总生存期(OS)、无进展生存期(PFS)、客观缓解率、疾病控制率和安全性。
共198例患者纳入研究,其中102例接受SOXIRI治疗,96例接受mFOLFIRINOX治疗。接受SOXIRI和mFOLFIRINOX治疗的患者在OS[12.1个月对11.2个月,风险比(HR)=1.04,P=0.81]或PFS(6.5个月对6.8个月,HR=0.99,P=0.96)方面无显著差异。在亚组分析中,基线总胆红素(TBIL)轻度升高的患者或化疗前体重不足的患者接受SOXIRI治疗比接受mFOLFIRINOX治疗更有可能获得更长的OS或PFS。此外,糖类抗原(CA)19-9下降是两种化疗方案疗效和预后的良好预测指标。除贫血在SOXIRI组比mFOLFIRIN组更常见(41.4%对24%,P=0.03)外,所有级别的不良事件在各种毒性方面相似。两组3至4级毒性的发生率相似。
对于局部晚期或转移性胰腺癌患者,SOXIRI方案与mFOLFIRINOX方案疗效相似,安全性可控。