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纳武利尤单抗联合化疗用于FGFR2和PD-L1共表达的转移性胃癌:一项前瞻性2期NIVOFGFR2研究

Nivolumab Combined with Chemotherapy in FGFR2 and PD-L1 Co-Expressing Metastatic Gastric Cancer: A Prospective Phase 2 NIVOFGFR2 Study.

作者信息

Tsimafeyeu Ilya, Musayeva Gunel, Mahmudova Samira, Otkhozoria Nana, Abbasov Bahadur, Kahharov Alisher, Guliyev Fuad

机构信息

Bureau for Cancer Research - BUCARE, 526 W 158Th Str, New York, NY, 10032, USA.

National Center of Oncology, Baku, Azerbaijan.

出版信息

J Gastrointest Cancer. 2025 Jan 11;56(1):40. doi: 10.1007/s12029-025-01172-5.

Abstract

BACKGROUND

Immunotherapy is increasingly significant in treating metastatic gastric cancer. This prospective phase 2 study investigates the efficacy and safety of combining nivolumab with chemotherapy in patients with metastatic gastric cancer co-expressing FGFR2 and PD-L1.

METHODS

Eligible patients were aged 18 years or older, with previously untreated HER-2 negative, PD-L1 positive, and FGFR2 positive metastatic gastric adenocarcinoma. Patients received nivolumab (360 mg every 3 weeks) in combination with chemotherapy (CAPOX: capecitabine 1000 mg/m twice daily on days 1-14 and oxaliplatin 130 mg/m on day 1, every 3 weeks). Tumor assessments were conducted using RECIST v1.1 every 8 weeks for 48 weeks, then every 12 weeks. The primary endpoint was the 1-year progression-free survival (PFS) rate. Secondary endpoints included median PFS, overall survival (OS), objective response rate (ORR), and grade ≥ 3 adverse events (AEs).

RESULTS

From June 2022 to October 2023, 194 patients were assessed for eligibility, with 23 patients enrolled and treated. At a median follow-up of 17.3 months, the 1-year PFS rate was 30.4%, with a median PFS of 6.0 months (95% CI, 4.3-7.7). The median OS was 15.1 months (95% CI, 13.2-16.8). The ORR was 21.7%, with one complete response and four partial responses. Grade 3 or higher TRAEs were reported in 34.8% of patients, primarily associated with chemotherapy. No treatment-related deaths occurred.

CONCLUSIONS

While the primary endpoint of improved 1-year PFS rate was not met, the study offers valuable insights into the potential benefits of combining nivolumab with chemotherapy in FGFR2 and PD-L1 co-expressing metastatic gastric cancer. Future research should optimize patient selection, assess combined immunotherapy and targeted anti-FGFR2 therapy, and further investigate the role of subsequent treatments to maximize therapeutic benefits.

摘要

背景

免疫疗法在转移性胃癌治疗中日益重要。这项前瞻性2期研究调查了纳武利尤单抗与化疗联合应用于共表达FGFR2和PD-L1的转移性胃癌患者的疗效和安全性。

方法

符合条件的患者年龄在18岁及以上,患有先前未接受过治疗的HER-2阴性、PD-L1阳性且FGFR2阳性的转移性胃腺癌。患者接受纳武利尤单抗(每3周360mg)联合化疗(CAPOX:卡培他滨1000mg/m²,第1 - 14天每日2次,奥沙利铂130mg/m²,第1天,每3周一次)。每8周进行一次肿瘤评估,持续48周,之后每12周进行一次,采用RECIST v1.1标准。主要终点是1年无进展生存期(PFS)率。次要终点包括中位PFS、总生存期(OS)、客观缓解率(ORR)和≥3级不良事件(AE)。

结果

2022年6月至2023年10月,对194例患者进行了资格评估,23例患者入组并接受治疗。中位随访17.3个月时,1年PFS率为30.4%,中位PFS为6.0个月(95%CI,4.3 - 7.7)。中位OS为15.1个月(95%CI,13.2 - 16.8)。ORR为21.7%,包括1例完全缓解和4例部分缓解。34.8%的患者报告了3级或更高等级的治疗相关不良事件(TRAE),主要与化疗相关。未发生与治疗相关的死亡。

结论

虽然未达到改善1年PFS率的主要终点,但该研究为纳武利尤单抗与化疗联合应用于FGFR2和PD-L1共表达的转移性胃癌的潜在益处提供了有价值的见解。未来的研究应优化患者选择,评估联合免疫疗法和靶向抗FGFR2疗法,并进一步研究后续治疗的作用以最大化治疗益处。

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