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Axitinib plus pembrolizumab in patients with advanced renal-cell carcinoma: Long-term efficacy and safety from a phase Ib trial

  • Michael B. Atkins
  • , Elizabeth R. Plimack
  • , Igor Puzanov
  • , Mayer N. Fishman
  • , David F. McDermott
  • , Daniel C. Cho
  • , Ulka N. Vaishampayan
  • , Saby George
  • , Jamal C. Tarazi
  • , William Duggan
  • , Rodolfo Perini
  • , Mahgull Thakur
  • , Kathrine C. Fernandez
  • , Toni K. Choueiri
  • Georgetown University
  • Beth Israel Deaconess Medical Center
  • Tufts University
  • MedStar Georgetown University Hospital
  • Roswell Park Cancer Institute
  • Vanderbilt University
  • Roswell Park Comprehensive Cancer Center
  • University of South Florida
  • Dana-Farber/Harvard Cancer Center
  • Harvard University
  • Dana-Farber Cancer Institute
  • New York University
  • University of Michigan, Ann Arbor
  • Wayne State University
  • Memorial Sloan-Kettering Cancer Center
  • SUNY Buffalo
  • Pfizer
  • Merck & Co.
  • Dana-Farber/Brigham and Women's Cancer Center
  • Cancer Center
  • Brigham and Women's Hospital

Research output: Contribution to journalArticlepeer-review

24 Scopus citations

Abstract

Background: Axitinib plus pembrolizumab showed superior overall survival (OS), progression-free survival (PFS) and objective response rate (ORR) versus sunitinib in a randomised phase III trial in patients with advanced renal-cell carcinoma (RCC). We report long-term efficacy and safety of the axitinib/pembrolizumab from the phase I trial (NCT02133742), after 46–55 months from study initiation (data cut-off date, 23rd July 2019). Methods: Fifty-two treatment-naïve patients with advanced RCC were treated with oral axitinib 5 mg twice daily and intravenous pembrolizumab 2 mg/kg every 3 weeks. PFS, duration of response (DoR) and OS were summarised using the Kaplan–Meier method. Results: At a median follow-up of 42.7 months (95% confidence interval [CI]: 41.1–44.1), median OS was not reached; 38 (73.1%) patients were alive. The probability of being alive at 4 years was 66.8% (95% CI: 49.1–79.5). Median PFS in the overall population was 23.5 months (95% CI: 15.4–30.4). ORR was 73.1%; five patients had complete response. Median DoR was 22.1 months (95% CI: 15.1–34.5). Grade III/IV adverse events (AEs) were reported in 38 (73.1%) patients and 20 (38.5%) discontinued treatment because of AEs: 17 (32.7%) discontinued axitinib, 13 (25.0%) discontinued pembrolizumab, and 10 (19.2%) discontinued both drugs. Common AEs included diarrhoea (84.6%), fatigue (80.8%), hypertension (53.8%), cough (48.1%) and dysphonia (48.1%). There were no new AE terms reported and no treatment-related deaths. Conclusions: In patients with advanced RCC with ~4 years of follow-up, combination axitinib/pembrolizumab continued to demonstrate clinical benefit, with no new safety signals.

Original languageEnglish
Pages (from-to)1-10
Number of pages10
JournalEuropean Journal of Cancer
Volume145
DOIs
StatePublished - Mar 2021

Keywords

  • Antibodies, Monoclonal, Humanized/adverse effects
  • Antineoplastic Combined Chemotherapy Protocols/adverse effects
  • Axitinib/adverse effects
  • Carcinoma, Renal Cell/drug therapy
  • Female
  • Humans
  • Kidney Neoplasms/drug therapy
  • Male
  • Middle Aged
  • Progression-Free Survival
  • Time Factors
  • United States

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