根据FOLFIRINOX方案治疗局部晚期胃和心食管交界处腺癌的总新辅助化疗:中期结果

M. V. Sedova, M. A. Batov, A. A. Kolomeytseva, V. M. Khomyakov, N. N. Volchenko, A. A. Fedenko
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The tumor regression grade was assessed in accordance with Becker, Mandard and G. A. Lavnikova scales. Results. The study included 136 patients, 119 of whom started treatment according to the protocol (ITT population). Fiſty-nine patients were enrolled into the FLOT group and 60 into the FOLFIRINOX group. One-year progression-free survival (PFS) was 67,5 % in the FLOT group and 90,4 % in the FOLFIRINOX group (p = 0,29). The estimated 2-year PFS in the FLOT group was 61,4 % [95 % CI, 48,4–77,9 %]. Median PFS and overall survival (OS) were not reached. The incidence of events (progression or death) was lower in the FOLFIRINOX group (odds ratio [OR] 0,40 [95 % CI 0,16–0,97, p = 0,047]). Adverse prognostic factors regardless of treatment were lymphatic (L1), vascular (V1) and perineural invasion (Pn1), and regional lymph node involvement aſter chemotherapy (ypN+) [p = 0,046; p = 0,014; p = 0,0021; p = 0,04, respectively]. 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引用次数: 0

摘要

目的。研究全新辅助化疗(NACT)联合FOLFIRINOX方案治疗局部晚期胃(GC)和心食管结(CEJ)癌的疗效和安全性。患者和方法。组织学证实的局部晚期胃腺癌和CEJ,临床分期cT3或更高,和/或区域淋巴结累及(cN+),无远处转移证据的患者纳入了我们的开放标签、单中心、非随机研究。FLOT对照组术前4个疗程,术后4个疗程并随访。FOLFIRINOX组采用新辅助方式化疗8个疗程,术后进行手术观察。根据Becker、manard和G. A. Lavnikova量表评估肿瘤消退等级。结果。该研究包括136例患者,其中119例根据方案开始治疗(ITT人群)。59例患者入组FLOT, 60例入组FOLFIRINOX。FLOT组的一年无进展生存率(PFS)为67.5%,FOLFIRINOX组为94.4% (p = 0.29)。估计FLOT组的2年PFS为61.4% [95% CI, 48,4 - 77,9%]。中位PFS和总生存期(OS)均未达到。FOLFIRINOX组的事件发生率(进展或死亡)较低(优势比[or] 0,40 [95% CI 0,16 - 0,97, p = 0,047])。不良预后因素包括淋巴(L1)、血管(V1)和神经周围浸润(Pn1)以及化疗后局部淋巴结受累(ypN+) [p = 0.046;P = 0.014;P = 0,0021;P = 0,04]。病理完全缓解与生存率无相关性。结论。对于局部晚期GC/ CEJ, FOLFIRINOX方案的总新辅助化疗与围手术期FLOT的一年PFS率相当。未发现肿瘤消退等级与生存结果之间存在关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Total neoadjuvant chemotherapy according to the FOLFIRINOX regimen for locally advanced adenocarcinoma of the stomach and cardioesophageal junction: interim results
Purpose. To study the efficacy and safety of total neoadjuvant chemotherapy (NACT) with the FOLFIRINOX regimen for locally advanced gastric (GC) and cardioesophageal junction (CEJ) cancer. Patients and methods . Patients with histologically confirmed locally advanced gastric adenocarcinoma and CEJ, clinical stage cT3 or higher and/or regional lymph node involvement (cN+), without evidence of distant metastasis were included in our open-label, single-centre, non-randomised study. In the FLOT control group, patients received 4 courses preoperatively and 4 postoperatively with follow-up. I In the FOLFIRINOX group 8 courses of chemotherapy were administered in neoadjuvant mode, followed by surgery and observation. The tumor regression grade was assessed in accordance with Becker, Mandard and G. A. Lavnikova scales. Results. The study included 136 patients, 119 of whom started treatment according to the protocol (ITT population). Fiſty-nine patients were enrolled into the FLOT group and 60 into the FOLFIRINOX group. One-year progression-free survival (PFS) was 67,5 % in the FLOT group and 90,4 % in the FOLFIRINOX group (p = 0,29). The estimated 2-year PFS in the FLOT group was 61,4 % [95 % CI, 48,4–77,9 %]. Median PFS and overall survival (OS) were not reached. The incidence of events (progression or death) was lower in the FOLFIRINOX group (odds ratio [OR] 0,40 [95 % CI 0,16–0,97, p = 0,047]). Adverse prognostic factors regardless of treatment were lymphatic (L1), vascular (V1) and perineural invasion (Pn1), and regional lymph node involvement aſter chemotherapy (ypN+) [p = 0,046; p = 0,014; p = 0,0021; p = 0,04, respectively]. There was no correlation between pathological complete response and survival rates. Conclusion . Total neoadjuvant chemotherapy with the FOLFIRINOX regimen for locally advanced GC/ CEJ demonstrated comparable to the perioperative FLOT one-year PFS rate. No association was found between tumor regression grade and survival outcomes.
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