Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
The University of Texas, MD Anderson Cancer Center, Houston, Texas, USA.
Hepatology. 2023 Sep 1;78(3):758-770. doi: 10.1097/HEP.0000000000000365. Epub 2023 Apr 1.
Biliary tract cancers are rare, heterogeneous cancers with poor prognoses. Bintrafusp alfa, a first-in-class bifunctional fusion protein composed of the extracellular domain of TGF-βRII (a TGF-β "trap") fused to a human IgG1 monoclonal antibody blocking programmed death ligand 1, was evaluated in patients with locally advanced/metastatic chemorefractory biliary tract cancers.
This multicenter, single-arm, open-label, phase 2 study (NCT03833661) enrolled adults with locally advanced or metastatic biliary tract cancer that was intolerant to or had failed first-line systemic platinum-based chemotherapy. Patients received 1200 mg bintrafusp alfa intravenously Q2W. The primary endpoint was confirmed objective response according to Response Evaluation Criteria in Solid Tumors 1.1 assessed by IRC. Secondary endpoints included duration of response, durable response rate, safety, progression-free survival, and overall survival.Between March 2019 and January 2020, 159 patients were enrolled. Median follow-up was 16.1 (range, 0.0-19.3) months; 17 patients (10.7%; 95% CI: 6.4%-16.6%) achieved an objective response. Median duration of response was 10.0 (range, 1.9-15.7) months; 10 patients (6.3%; 95% CI: 3.1%-11.3%) had a durable response (≥6 mo). Median progression-free survival was 1.8 months (95% CI: 1.7-1.8 mo); median overall survival was 7.6 months (95% CI: 5.8-9.7 mo). Overall survival rates were 57.9% (6 mo) and 38.8% (12 mo). Grade ≥3 adverse events occurred in 26.4% of patients, including one treatment-related death (hepatic failure). Frequent grade ≥3 adverse events included anemia (3.8%), pruritus (1.9%), and increased alanine aminotransferase (1.9%).
Although this study did not meet its prespecified primary endpoint, bintrafusp alfa demonstrated clinical activity as second-line treatment in this hard-to-treat cancer, with durable responses and a manageable safety profile.
胆道癌是一种罕见的、异质性的癌症,预后较差。Bintrafusp alfa 是一种首创的双功能融合蛋白,由 TGF-βRII 的细胞外结构域(TGF-β“陷阱”)与一种阻断程序性死亡配体 1 的人 IgG1 单克隆抗体融合而成,在局部晚期/转移性化疗耐药的胆道癌患者中进行了评估。
这是一项多中心、单臂、开放标签、2 期研究(NCT03833661),纳入了局部晚期或转移性胆道癌患者,这些患者对一线系统铂类化疗不耐受或已失败。患者接受 1200mg Bintrafusp alfa 静脉注射,每 2 周 1 次。主要终点是根据独立审查委员会评估的实体瘤反应评估标准 1.1 确认的客观缓解。次要终点包括缓解持续时间、持久缓解率、安全性、无进展生存期和总生存期。2019 年 3 月至 2020 年 1 月期间,共纳入 159 例患者。中位随访时间为 16.1 个月(范围,0.0-19.3);17 例患者(10.7%;95%CI:6.4%-16.6%)达到客观缓解。中位缓解持续时间为 10.0 个月(范围,1.9-15.7);10 例患者(6.3%;95%CI:3.1%-11.3%)有持久缓解(≥6 个月)。中位无进展生存期为 1.8 个月(95%CI:1.7-1.8 个月);中位总生存期为 7.6 个月(95%CI:5.8-9.7 个月)。总生存率为 57.9%(6 个月)和 38.8%(12 个月)。≥3 级不良事件发生率为 26.4%,包括 1 例治疗相关死亡(肝衰竭)。常见的≥3 级不良事件包括贫血(3.8%)、瘙痒(1.9%)和丙氨酸氨基转移酶升高(1.9%)。
尽管本研究未达到预设的主要终点,但 Bintrafusp alfa 作为二线治疗在这种难以治疗的癌症中显示出了临床活性,具有持久的缓解和可管理的安全性。