Department of Clinical Oncology, Aichi Cancer Center Hospital, 1-1 Kanokoden, Chikusa-ku, Nagoya, Aichi, 464-8681, Japan.
Department of Endoscopy, Aichi Cancer Center Hospital, Nagoya, Japan.
Sci Rep. 2024 Jun 3;14(1):12658. doi: 10.1038/s41598-024-61975-7.
The combination of trifluridine/tipiracil hydrochloride (FTD/TPI) plus ramucirumab has demonstrated clinical activity in patients with advanced gastric cancer (AGC). We evaluated the efficacy and safety of this combination compared with those of FTD/TPI monotherapy in patients with AGC. We retrospectively reviewed data of patients with AGC who received FTD/TPI plus ramucirumab or FTD/TPI monotherapy as third- or later-line treatment. This study included 36 patients treated with FTD/TPI plus ramucirumab and 70 patients receiving FTD/TPI monotherapy. The objective response rate (ORR) and disease control rate (DCR) were 25.8% and 58.1%, respectively, in the FTD/TPI plus ramucirumab group and 5.0% and 38.3%, respectively, in the FTD/TPI group (ORR, P = 0.007; DCR, P = 0.081). The median progression-free survival (PFS) was significantly longer in the FTD/TPI plus ramucirumab group (median PFS, 2.9 vs. 1.8 months; hazard ratio [HR]: 0.52; P = 0.001). A numerical survival benefit was also observed (median overall survival, 7.9 months vs. 5.0 months; HR: 0.68, P = 0.089). In the multivariate analysis, PFS was significantly longer in the FTD/TPI plus ramucirumab group than in the FTD/TPI monotherapy group (HR: 0.61, P = 0.030). The incidence of febrile neutropenia was higher in the FTD/TPI plus ramucirumab group than in the FTD/TPI group (13.8% vs. 2.9%); however, no new safety signals were identified. Compared with FTD/TPI monotherapy, FTD/TPI plus ramucirumab offers clinical benefits with acceptable toxicity in heavily pretreated patients with AGC. Further investigation via randomized trials is warranted to confirm these findings.
替氟尿苷/盐酸曲氟尿苷(FTD/TPI)联合雷莫芦单抗在晚期胃癌(AGC)患者中显示出临床疗效。我们评估了与 FTD/TPI 单药治疗相比,该联合治疗在 AGC 患者中的疗效和安全性。我们回顾性分析了接受 FTD/TPI 联合雷莫芦单抗或 FTD/TPI 单药治疗作为三线或后线治疗的 AGC 患者的数据。本研究纳入了 36 例接受 FTD/TPI 联合雷莫芦单抗治疗和 70 例接受 FTD/TPI 单药治疗的患者。FTD/TPI 联合雷莫芦单抗组的客观缓解率(ORR)和疾病控制率(DCR)分别为 25.8%和 58.1%,FTD/TPI 组分别为 5.0%和 38.3%(ORR,P=0.007;DCR,P=0.081)。FTD/TPI 联合雷莫芦单抗组的中位无进展生存期(PFS)显著长于 FTD/TPI 组(中位 PFS,2.9 个月 vs. 1.8 个月;风险比[HR]:0.52;P=0.001)。也观察到生存获益的数值增加(中位总生存期,7.9 个月 vs. 5.0 个月;HR:0.68,P=0.089)。在多变量分析中,FTD/TPI 联合雷莫芦单抗组的 PFS 显著长于 FTD/TPI 单药组(HR:0.61,P=0.030)。FTD/TPI 联合雷莫芦单抗组发热性中性粒细胞减少症的发生率高于 FTD/TPI 组(13.8% vs. 2.9%);然而,未发现新的安全性信号。与 FTD/TPI 单药治疗相比,FTD/TPI 联合雷莫芦单抗为 AGC 患者提供了具有可接受毒性的临床获益。需要通过随机试验进一步研究来证实这些发现。