Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Clinical Trial
. 2023 May;24(5):553-562.
doi: 10.1016/S1470-2045(23)00097-9. Epub 2023 Mar 31.

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

Affiliations
Clinical Trial

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

Toni K Choueiri et al. Lancet Oncol. 2023 May.

Abstract

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-2α 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 63·0 years (IQR 57·5-68·5), 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 24·6 months (IQR 22·1-32·2). 16 (30·8% [95% CI 18·7-45·1]) 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.

Funding: Merck Sharp & Dohme (a subsidiary of Merck & Co) and the National Cancer Institute.

PubMed Disclaimer

Conflict of interest statement

Declaration of interests TKC reports institutional and personal, paid or unpaid support, or both, for research, advisory boards, consultancy, and honoraria from AstraZeneca, Aravive, Aveo, Bayer, Bristol Myers Squibb (BMS), Calithera, Circle Pharma, Eisai, EMD Serono, Exelixis, GlaxoSmithKline, IQVA, Infinity, Ipsen, Jansen, Kanaph, Lilly, Merck, Nikang, NuScan, Novartis, Pfizer, Roche, Sanofi/Aventis, Surface Oncology, Takeda, Tempest, Up-To-Date, and Continuing Medical Education events (Peerview, OncLive, and MJH). TKC has institutional patents filed on molecular alterations and immunotherapy response or toxicity, and ctDNA. TKC has stock or stock options in Tempest, Pionyr, Osel, Precede Bio, and CureResponse, and serves on committees for the National Comprehensive Cancer Network, Genitourinary Cancer Steering Committee, American Society of Clinical Oncology, European Society for Medical Oncology, Academic and Community Cancer Research United, and KidneyCan. TKC mentored several non-US citizens on research projects with potential funding (in part) from non-US sources or foreign components. TKC's institution (Dana-Farber Cancer Institute) might have received additional independent funding of drug companies or royalties potentially involved in research around the subject matter. DFM has received honoraria from BMS, Pfizer, Merck, Alkermes, EMD Serono, Eli Lilly, Werewolf Therapeutics, Calithera Biosciences, Synthekine, Johnson & Johnson, and Aveo and research support from BMS, Merck, Genentech, Pfizer, Exelixis, X4 Pharma, Alkermes, Checkmate Pharmaceuticals, and CRISPR Therapeutics. JM has received research grants from Merck, Eisai, Exelixis, Rubius Therapeutics, Corvus, Trishula, Genentech, Peloton, Vyriad, SillaJen, Seattle Genetics, Tocagen, and Replimune; royalties from UpToDate; and participated on an advisory board for Merck. TMB has received study support from Merck; and speaking or consulting fees from Pfizer, Bayer, Eli Lilly, and Bristol Myers Squibb. RF has received research grants from Merck. MDM has participated in advisory boards for Merck, Eisai, Janssen, and Exelixis. SZ has participated on an advisory board for Exelixis. AR, RP, and DV are employees of Merck & Co. SST has received research funding from Genentech, BMS, Merck Sharp & Dohme, Pfizer, Nektar, Exelixis, Clinigen Group, and Aveo Oncology; honoraria for FirstWord Pharma, Targeted Oncology, and Natera; and participated on an advisory board for Merck, BMS, and Exelixis. All other authors declare no competing interests.

Comment in

Publication types

MeSH terms

Supplementary concepts

Associated data

LinkOut - more resources