Division of Cancer Medicine, Department of Gastrointestinal Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Division of Hematology and Oncology, Department of Medicine, University of Arizona College of Medicine, Tucson, Arizona.
Clin Cancer Res. 2022 Jun 1;28(11):2229-2236. doi: 10.1158/1078-0432.CCR-21-3548.
VEGF receptor-2 (VEGFR-2)-mediated angiogenesis contributes to pathogenesis of biliary tract cancers (BTC). We investigated ramucirumab, a mAb targeting VEGFR-2 for treatment of advanced, chemorefractory BTC.
This is a phase II, single-arm trial for advanced, unresectable, pre-treated patients with BTC with ECOG 0/1, adequate liver, renal, and marrow functions. Ramucirumab was administered at 8 mg/kg, 2 weekly with restaging performed 8 weekly. Primary endpoint was progression-free survival (PFS). Secondary endpoints were overall response rate (ORR), disease control rate (DCR), overall survival (OS), and toxicity. Exploratory endpoints included correlation of tumor mutational status with PFS and OS.
61 patients were enrolled: the median age was 58.5 years; 59 with stage IV disease; 62%, intrahepatic cholangiocarcinoma; 22%, gallbladder cancer; and 16%, extrahepatic cholangiocarcinoma. All received prior chemotherapy: 52% had 1 prior, and rest ≥2 prior lines. Median treatment duration was 10.1 weeks (range, 2.1-86). Median PFS was 3.2 months [95% confidence interval (CI), 2.1-4.8]; median OS, 9.5 months (95% CI, 5.8-13.6). One (1.7%) patient achieved partial response; 26 (43.3%), stable disease; and 25 (41.7%), disease progression; DCR, 45%. Median 6-month PFS and OS rates were 32% (95% CI, 0.22-0.46) and 58% (95% CI, 0.47-0.72). The majority of toxicities were grade 1 or 2; grade 3 proteinuria (1, 2%), hypertension (13, 22%), and pulmonary embolism (1, 2%), and grade 4 gastrointestinal bleeding (1, 2%) occurred.
Ramucirumab was well tolerated and resulted in PFS similar to that achieved with other chemotherapy regimens used historically for chemorefractory BTC.
血管内皮生长因子受体-2(VEGFR-2)介导的血管生成有助于胆道癌(BTC)的发病机制。我们研究了雷莫芦单抗,一种针对 VEGFR-2 的单克隆抗体,用于治疗晚期、化疗耐药的 BTC。
这是一项针对晚期、不可切除、预处理的 BTC 患者的 II 期、单臂试验,ECOG 0/1,肝脏、肾脏和骨髓功能充足。雷莫芦单抗的剂量为 8mg/kg,每 2 周一次,每 8 周进行一次重新分期。主要终点是无进展生存期(PFS)。次要终点包括总缓解率(ORR)、疾病控制率(DCR)、总生存期(OS)和毒性。探索性终点包括肿瘤突变状态与 PFS 和 OS 的相关性。
共纳入 61 例患者:中位年龄为 58.5 岁;59 例为 IV 期疾病;62%为肝内胆管癌;22%为胆囊癌;16%为肝外胆管癌。所有患者均接受过化疗:52%接受过 1 线治疗,其余患者接受过 2 线以上治疗。中位治疗持续时间为 10.1 周(范围 2.1-86)。中位 PFS 为 3.2 个月[95%置信区间(CI),2.1-4.8];中位 OS 为 9.5 个月(95%CI,5.8-13.6)。1 例(1.7%)患者部分缓解;26 例(43.3%)患者疾病稳定;25 例(41.7%)患者疾病进展;DCR 为 45%。中位 6 个月 PFS 和 OS 率分别为 32%(95%CI,0.22-0.46)和 58%(95%CI,0.47-0.72)。大多数毒性反应为 1 级或 2 级;3 级蛋白尿(1,2%)、高血压(13,22%)和肺栓塞(1,2%),以及 4 级胃肠道出血(1,2%)。
雷莫芦单抗耐受性良好,PFS 与历史上用于化疗耐药 BTC 的其他化疗方案相似。