Belzutifan plus cabozantinib for patients with advanced clear cell renal cell carcinoma previously treated with immunotherapy: an open-label, single-arm, phase 2 study

被引:65
作者
Choueiri, Toni K. [1 ]
McDermott, David F. [2 ]
Merchan, Jaime [3 ]
Bauer, Todd M. [4 ,5 ]
Figlin, Robert [6 ]
Heath, Elisabeth, I [7 ]
Michaelson, M. Dror [8 ]
Arrowsmith, Edward [9 ]
D'Souza, Anishka [10 ]
Zhao, Song [11 ]
Roy, Ananya
Perini, Rodolfo
Vickery, Donna
Tykodi, Scott S. [12 ]
机构
[1] Dana Farber Canc Inst, Lank Ctr Genitourinary Oncol, Boston, MA 02115 USA
[2] Beth Israel Deaconess Med Ctr, Boston, MA USA
[3] Univ Miami Hlth Syst, Miami, FL USA
[4] Sarah Cannon Res Inst, Nashville, TN USA
[5] Tennessee Oncol, Nashville, TN USA
[6] Cedars Sinai Med Ctr, Los Angeles, CA USA
[7] Karmanos Canc Inst, Detroit, MI USA
[8] Massachusetts Gen Hosp, Canc Ctr, Boston, MA USA
[9] Tennessee Oncol, Chattanooga, TN USA
[10] Univ Southern Calif, GU Med Oncol, Los Angeles, CA USA
[11] Swedish Canc Inst, Seattle, WA USA
[12] Fred Hutchinson Canc Ctr, Seattle, WA USA
关键词
EVEROLIMUS; NIVOLUMAB; SUNITINIB; AXITINIB; LENVATINIB; CANCER;
D O I
10.1016/S1470-2045(23)00097-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Few treatment options are available for patients with advanced renal cell carcinoma who have received previous anti-PD-1-based or anti-PD-L1-based immunotherapy. Combining belzutifan, an HIF-2 alpha inhibitor, with cabozantinib, a multitargeted tyrosine-kinase inhibitor of VEGFR, c-MET, and AXL, might provide more antitumoural effects than either agent alone. We aimed to investigate the antitumour activity and safety of belzutifan plus cabozantinib in patients with advanced clear cell renal cell carcinoma that was previously treated with immunotherapy.Methods This open-label, single-arm, phase 2 study was conducted at ten hospitals and cancer centres in the USA. Patients were enrolled into two cohorts. Patients in cohort 1 had treatment-naive disease (results will be reported separately). In cohort 2, eligible patients were aged 18 years or older with locally advanced or metastatic clear cell renal cell carcinoma, measurable disease according to Response Evaluation Criteria in Solid Tumours version 1.1, an Eastern Cooperative Oncology Group performance status score of 0 or 1, and had previously received immunotherapy and up to two systemic treatment regimens. Patients were given belzutifan 120 mg orally once daily and cabozantinib 60 mg orally once daily until disease progression, unacceptable toxicity, or patient withdrawal. The primary endpoint was confirmed objective response assessed by the investigator. Antitumour activity and safety were assessed in all patients who received at least one dose of study treatment. This trial is registered with ClinicalTrials.gov, NCT03634540, and is ongoing.Findings Between Sept 27, 2018, and July 14, 2020, 117 patients were screened for eligibility, 52 (44%) of whom were enrolled in cohort 2 and received at least one dose of study treatment. Median age was 63 center dot 0 years (IQR 57 center dot 5-68 center dot 5), 38 (73%) of 52 patients were male, 14 (27%) were female, 48 (92%) were White, two (4%) were Black or African American, and two were Asian (4%). As of data cutoff (Feb 1, 2022), median follow-up was 24 center dot 6 months (IQR 22 center dot 1-32 center dot 2). 16 (30 center dot 8% [95% CI 18 center dot 7-45 center dot 1]) of 52 patients had a confirmed objective response, including one (2%) who had a complete response and 15 (29%) who had partial responses. The most common grade 3-4 treatment-related adverse event was hypertension (14 [27%] of 52 patients). Serious treatment-related adverse events occurred in 15 (29%) patients. One death was considered treatment related by the investigator (respiratory failure).Interpretation Belzutifan plus cabozantinib has promising antitumour activity in patients with pretreated clear cell renal cell carcinoma and our findings provide rationale for further randomised trials with belzutifan in combination with a VEGFR tyrosine-kinase inhibitor.Copyright (c) 2023 Elsevier Ltd. All rights reserved.
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收藏
页码:553 / 562
页数:10
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