Division of Medical Oncology, Department of Onco-Hematology, IRCCS-CROB, Referral Cancer Center of Basilicata, via Padre Pio 1, 85028, Rionero, Vulture (PZ), Italy.
Medical Oncology Unit, Department of Medicine, Surgery and Neurosciences, University of Siena, Viale Bracci - Policlinico ″Le Scotte″, 53100, Siena, Italy.
Invest New Drugs. 2019 Jun;37(3):524-530. doi: 10.1007/s10637-019-00725-3. Epub 2019 Jan 28.
Purpose Few data described the activity of chemotherapy after ramucirumab plus paclitaxel progression in metastatic gastric cancer patients. The aim of this phase II study is to assess the efficacy and safety of the FOLFIRI regimen as a third-line of treatment. Methods The study enrolled patients with histologically proven metastatic gastric cancer or gastroesophageal junction carcinoma whose disease had progressed after ramucirumab-based second line of treatment. Treatment consisted of biweekly irinotecan 150 mg/m2 as a 1-h infusion on day 1, folinic acid 100 mg/m2 intravenously on days 1-2, and 5-fluorouracil as a 400 mg/m2 bolus and then 600 mg/m2 continuous infusion over 22 h on days 1-2. Primary end-point was tumor response rate (confirmed complete and partial response). Results Twenty-six patients were enrolled. Overall response rate and disease control rate were 11.5% and 38.5%. The median progression free survival (PFS) was 52 days (95% CI:42-74), and the median overall survival was 117 days (95% CI: 94-154). no unexpected adverse events have been observed. A longer PFS and OS were observed in patients who had achieved PFS ≥ 3 months during prior ramucirumab treatment. Conclusions Our findings suggest a poor efficacy of the FOLFIRI regimen in metastatic gastric or gastroesophageal junction cancer patients whose disease progressed during a ramucirumab-based second line of treatment. However, FOLFIRI could be an option for patients who responded to prior ramucirumab.
目的
在转移性胃癌患者接受雷莫芦单抗联合紫杉醇治疗进展后,很少有数据描述化疗的活性。本 II 期研究的目的是评估 FOLFIRI 方案作为三线治疗的疗效和安全性。
方法
该研究纳入了经组织学证实的转移性胃癌或胃食管交界处癌患者,这些患者的疾病在二线雷莫芦单抗治疗后进展。治疗包括每周两次伊立替康 150mg/m2,静脉输注 1 小时,第 1 天;亚叶酸 100mg/m2 静脉输注,第 1-2 天;5-氟尿嘧啶 400mg/m2 推注,然后 600mg/m2 持续输注 22 小时,第 1-2 天。主要终点是肿瘤反应率(确认完全和部分缓解)。
结果
共纳入 26 例患者。总缓解率和疾病控制率分别为 11.5%和 38.5%。中位无进展生存期(PFS)为 52 天(95%CI:42-74),中位总生存期为 117 天(95%CI:94-154)。未观察到意外的不良事件。在先前雷莫芦单抗治疗中 PFS≥3 个月的患者中,PFS 和 OS 更长。
结论
我们的研究结果表明,对于在二线雷莫芦单抗治疗期间疾病进展的转移性胃或胃食管交界处癌患者,FOLFIRI 方案疗效不佳。然而,对于对先前雷莫芦单抗有反应的患者,FOLFIRI 可能是一种选择。