Efficacy of total neoadjuvant chemotherapy in the FLOT regimen in patients with locally advanced gastric and gastroesophageal junction: results of a phase II study

A. Y. Anokhin, P. Kononets, D. Kanner, D. Stroyakovsky, A. O. Shveykin, A. E. Kalinin, V. Y. Kirsanov, A. S. Tyulandina
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Abstract

Background. The established approach notably improving the therapeutic outcomes for locally advanced gastric cancer and gastroesophageal junction cancer, presently entails the amalgamation of perioperative chemotherapy aligned with the FLOT protocol and surgical intervention. However, this approach harbors limitations, as only half of the patient cohort successfully completes the entire prescribed course of drug therapy. The potential solution to this problem lies in the complete transfer of the chemotherapy volume to the preoperative period and the execution of total neoadjuvant chemotherapy with FLOT regimen.Aim. Aim is to conduct a comparative assessment of the efficacy and safety between total neoadjuvant and perioperative chemotherapy with FLOT regimen for patients with locally advanced gastric cancer and gastroesophageal junction cancer.Materials and methods. In a retrospective study we enrolled patients with histologically confirmed locally advanced gastric cancer and gastroesophageal junction cancer meeting clinical stage criteria T2–4 and N0–3, without of distant metastases, treated between 2014 and 2020 at Federal State Budgetary Institution “N. N. Blokhin National Medical Research Center of Oncology” оf the Ministry of Health of the Russian Federation and Moscow City Oncologic Hospital No. 62 Department of Healthcare of Moscow. Participants in the control group underwent 8 courses of perioperative chemotherapy (4 preoperatively and 4 postoperatively), while those in the experimental group received 8 courses of total neoadjuvant chemotherapy. Both groups received drug therapy according to the FLOT protocol: 5-fluorouracil 2600 mg/m2 , intravenous drip, over 24 hours, leucovorin 200 mg/m2 , intravenous drip, oxaliplatin 85 mg/m2 , intravenous drip, docetaxel 50 mg/m2 , intravenous drip, on day 1, with a 14-day intercourse interval. The primary endpoint was one-year progression-free survival.Results. In the study included 187 patients. Participants were divided into two groups: 95 in the total neoadjuvant chemotherapy group and 92 in the perioperative chemotherapy group. The one-year progression-free survival was higher in the total neoadjuvant chemotherapy group at 79 %, compared to 68 % in the perioperative chemotherapy group (HR 0.54, 95 % confidence interval 0.32–0.9, p = 0.02). Median disease-free survival was 27.2 and 19.5 months in the neoadjuvant and perioperative chemotherapy groups, respectively. The tolerability of the entire planned drug treatment regimen was superior in the total neoadjuvant chemotherapy group, reaching 88.4 %, as opposed to 57.6 % in the perioperative chemotherapy group (p = 0.0001).Conclusion. Among patients with locally advanced gastric cancer and gastroesophageal junction cancer, the application of total neoadjuvant chemotherapy according to the FLOT protocol, administered over 8 courses, demonstrated enhanced one-year progression-free survival and improved tolerability of the entire planned treatment regimen.
局部晚期胃和胃食管交界处患者接受 FLOT 方案新辅助化疗的疗效:II 期研究结果
背景。目前,改善局部晚期胃癌和胃食管交界处癌治疗效果的既定方法是将符合 FLOT 方案的围手术期化疗与手术干预相结合。然而,这种方法存在局限性,因为只有一半的患者能成功完成整个规定的药物治疗疗程。解决这一问题的潜在方法是将化疗量完全转移到术前阶段,并采用 FLOT 方案进行全面的新辅助化疗。目的是对局部晚期胃癌和胃食管交界处癌患者采用FLOT方案进行新辅助全化疗和围手术期化疗的疗效和安全性进行比较评估。在一项回顾性研究中,我们选取了2014年至2020年期间在俄罗斯联邦卫生部 "N. N. Blokhin 国家肿瘤医学研究中心"(Federal State Budgetary Institution "N. N. Blokhin National Medical Research Center of Oncology" оf the Ministry of Health)和莫斯科市第62肿瘤医院(Moscow City Oncologic Hospital No. 62 Department of Healthcare of Moscow)接受治疗的组织学确诊局部晚期胃癌和胃食管交界处癌患者。对照组患者接受了 8 个疗程的围手术期化疗(术前 4 个疗程,术后 4 个疗程),而实验组患者则接受了 8 个疗程的新辅助化疗。两组患者均按照 FLOT 方案接受药物治疗:5-氟尿嘧啶 2600 毫克/平方米,24 小时内静脉滴注;亮菌素 200 毫克/平方米,静脉滴注;奥沙利铂 85 毫克/平方米,静脉滴注;多西他赛 50 毫克/平方米,静脉滴注,第 1 天开始,间隔 14 天。主要终点是一年无进展生存期。研究共纳入 187 名患者。参与者分为两组:新辅助化疗组 95 人,围手术期化疗组 92 人。新辅助化疗组的一年无进展生存率为79%,高于围手术期化疗组的68%(HR为0.54,95%置信区间为0.32-0.9,P = 0.02)。新辅助化疗组和围手术期化疗组的中位无病生存期分别为27.2个月和19.5个月。新辅助化疗组对整个计划药物治疗方案的耐受性更好,达到88.4%,而围手术期化疗组为57.6%(P = 0.0001)。在局部晚期胃癌和胃食管交界处癌患者中,按照FLOT方案进行8个疗程的全新药辅助化疗可提高一年无进展生存率,并改善整个计划治疗方案的耐受性。
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