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A phase 1b/2 study of cabozantinib in combination with pembrolizumab in advanced cutaneous melanoma. Cancer 2026 Feb 15;132(4):e70326

Date

02/17/2026

Pubmed ID

41701511

Pubmed Central ID

PMC12912253

DOI

10.1002/cncr.70326

Scopus ID

2-s2.0-105030268320 (requires institutional sign-in at Scopus site)

Abstract

BACKGROUND: Pembrolizumab is approved for advanced cutaneous melanoma (aCM). Cabozantinib, an oral multi-tyrosine kinase inhibitor, has demonstrated antitumor activity as monotherapy or in combination with anti-PD-1 therapy in malignancies. The objective of this study was to determine the safety and efficacy of cabozantinib and pembrolizumab for patients with aCM.

METHODS: This phase 1b/2 study enrolled 28 patients with unresectable aCM. In phase 1b, escalating dose levels of cabozantinib (20 mg, 40 mg, and 60 mg) were administered concurrently with pembrolizumab 200 mg intravenously every 3 weeks using a 3 + 3 design to determine recommended phase 2 dose (RP2D). In phase 2, patients received cabozantinib at RP2D in combination with pembrolizumab using a Simon 2 stage design. Primary end point of phase 2 was overall response rate (ORR). Secondary end points included disease control rate, progression-free survival (PFS), and overall survival (OS).

RESULTS: Phase 1b enrolled eight patients, cabozantinib 40 mg daily dose level was selected as RP2D. Response rate in stage 1 exceeded predefined criteria for proceeding to expansion phase; however, phase 2 was terminated after 20 patients due to low accrual in the setting of evolving standard of care. Among all treated patients, the most common grade ≥3 toxicities were hypertension (n = 10, 36%), hypokalemia (n = 5, 18%), hypophosphatemia (n = 4, 14%), and ALT elevation (n = 4, 14%). Among 20 patients treated in phase 2, ORR was 45%, median PFS was 6.6 months, and median OS was 29.5 months.

CONCLUSIONS: Cabozantinib and pembrolizumab combination was explored in treatment-naive aCM. Toxicity was consistent with known profiles, but discontinuation rates were notable.

Author List

Zakharia Y, Kim D, Freesmeier M, Frees M, Mott S, Monga V, Laux D, Javed A, Rieth J, Smestad J, Milhem M

Author

John Smestad PhD, BS, MD Assistant Professor in the Medicine department at Medical College of Wisconsin




MESH terms used to index this publication - Major topics in bold

Adult
Aged
Aged, 80 and over
Anilides
Antibodies, Monoclonal, Humanized
Antineoplastic Combined Chemotherapy Protocols
Female
Humans
Male
Melanoma
Middle Aged
Pyridines
Skin Neoplasms