Wang Emily, Rupe Eric S, Mukhida Sagar S, Johns Andrew C, Campbell Matthew T, Shah Amishi Y, Zurita Amado J, Gao Jianjun, Goswami Sangeeta, Jonasch Eric, Msaouel Pavlos, Tannir Nizar M, Hahn Andrew W
Pharmacy Clinical Programs, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Department of Abdominal Imaging, Division of Diagnostic Imaging, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Eur Urol Focus. 2025 Jan;11(1):150-158. doi: 10.1016/j.euf.2024.09.007. Epub 2024 Sep 21.
Belzutifan, a hypoxia-inducible factor 2 alpha inhibitor, was approved initially for patients with von Hippel-Lindau disease and more recently for sporadic, metastatic clear cell renal cell carcinoma (ccRCC) based on the results of LITESPARK-005. There is a paucity of data regarding real-world experience with belzutifan in patients with sporadic, metastatic ccRCC. This study aims to describe clinical outcomes with belzutifan in patients with sporadic, metastatic ccRCC.
A retrospective study of 22 patients who received belzutifan at MD Anderson Cancer Center prior to the Food and Drug Administration approval was conducted. Progression-free survival (PFS) and objective response rate (ORR) were assessed by a blinded radiologist using Response Evaluation Criteria In Solid Tumors (RECIST) version 1.1. PFS and overall survival (OS) were measured from belzutifan initiation.
The median follow-up time was 14.9 mo. Most patients had International Metastatic RCC Database Consortium intermediate-risk disease, more than three metastatic sites, and a median of five prior lines of treatment at initiation of belzutifan; all patients received prior immune checkpoint therapy (ICT) and vascular endothelial growth factor receptor tyrosine kinase inhibitors (VEGFR-TKIs). The median PFS was 8.51 mo (95% confidence interval [CI] 0-18.4) and ORR was 36.4%. The median OS was 14.72 mo (95% CI 7.34-22.10). Of 22 patients, four (18.2%) patients required dose reductions and three (13.6%) patients discontinued belzutifan because of adverse drug events (ADEs). The most common ADEs were anemia (77.3%; 17/22) and hypoxia (36.4%; 8/22). There were no treatment-related deaths.
In a heavily pretreated cohort of patients with sporadic, metastatic ccRCC, belzutifan had meaningful clinical activity and was well tolerated. These real-world results add to the results of LITESPARK-005 and support the use of belzutifan after progression on ICT and VEGFR-TKIs.
Belzutifan is a new medicine used to treat a type of clear cell kidney cancer that has spread to other parts of the body (metastasized). A study at MD Anderson Cancer Center followed 22 patients who were treated with belzutifan, and found that it worked to control the cancer for almost 9 mo and caused the cancer to shrink in 36% of patients. This study confirms that belzutifan can be effective and safe, even after other treatments have not worked.
贝佐替凡(belzutifan)是一种缺氧诱导因子2α抑制剂,最初被批准用于治疗希佩尔-林道病患者,最近基于LITESPARK-005试验结果被批准用于治疗散发性、转移性透明细胞肾细胞癌(ccRCC)。关于贝佐替凡在散发性、转移性ccRCC患者中的真实世界经验的数据较少。本研究旨在描述贝佐替凡在散发性、转移性ccRCC患者中的临床疗效。
对22例在食品药品监督管理局批准之前于MD安德森癌症中心接受贝佐替凡治疗的患者进行了一项回顾性研究。由一名盲法放射科医生使用实体瘤疗效评价标准(RECIST)1.1版评估无进展生存期(PFS)和客观缓解率(ORR)。PFS和总生存期(OS)从开始使用贝佐替凡时开始测量。
中位随访时间为14.9个月。大多数患者患有国际转移性肾细胞癌数据库联盟中危疾病,有超过三个转移部位,在开始使用贝佐替凡时既往接受过治疗的中位数为五线;所有患者均接受过既往免疫检查点治疗(ICT)和血管内皮生长因子受体酪氨酸激酶抑制剂(VEGFR-TKIs)。中位PFS为8.51个月(95%置信区间[CI]0-18.4),ORR为36.4%。中位OS为14.72个月(95%CI 7.34-22.10)。在22例患者中,4例(18.2%)患者需要减量,3例(13.6%)患者因药物不良事件(ADEs)停用贝佐替凡。最常见的ADEs是贫血(77.3%;17/22)和缺氧(36.4%;8/22)。没有与治疗相关的死亡。
在一组接受过大量治疗的散发性、转移性ccRCC患者中,贝佐替凡具有显著的临床活性且耐受性良好。这些真实世界的结果补充了LITESPARK-005试验的结果,并支持在ICT和VEGFR-TKIs治疗进展后使用贝佐替凡。
贝佐替凡是一种用于治疗已扩散至身体其他部位(转移)的透明细胞肾癌的新药。MD安德森癌症中心的一项研究对22例接受贝佐替凡治疗的患者进行了随访,发现它能有效控制癌症近9个月,使36%的患者癌症缩小。这项研究证实,即使在其他治疗无效后,贝佐替凡也可能有效且安全。