Bempegaldesleukin Plus Nivolumab in Untreated Advanced Melanoma: The Open-Label, Phase III PIVOT IO 001 Trial Results

Author:

Diab Adi1ORCID,Gogas Helen2ORCID,Sandhu Shahneen3ORCID,Long Georgina V.4ORCID,Ascierto Paolo A.5ORCID,Larkin James6ORCID,Sznol Mario7ORCID,Franke Fabio8,Ciuleanu Tudor E.9,Pereira Caio10,Muñoz Couselo Eva11ORCID,Bronzon Damian Fernanda12ORCID,Schenker Michael13ORCID,Perfetti Aldo14,Lebbe Celeste15ORCID,Quéreux Gaëlle16,Meier Friedegund1718ORCID,Curti Brendan D.19ORCID,Rojas Carlos20,Arriaga Yull21,Yang Haisu21,Zhou Ming21ORCID,Ravimohan Shruthi22,Statkevich Paul23,Tagliaferri Mary A.24ORCID,Khushalani Nikhil I.25ORCID

Affiliation:

1. Melanoma Medical Oncology Department, The University of Texas MD Anderson Cancer Center, Houston, TX

2. First Department of Medicine, National and Kapodistrian University of Athens, Athens, Greece

3. Department of Medical Oncology, Peter MacCallum Cancer Centre, The University of Melbourne, Melbourne, VIC, Australia

4. Melanoma Institute Australia, Royal North Shore and Mater Hospitals, The University of Sydney, Sydney, NSW, Australia

5. Melanoma, Cancer Immunotherapy and Development Therapeutics Department, Istituto Nazionale Tumori IRCCS Fondazione G. Pascale, Naples, Italy

6. Medical Oncology, The Royal Marsden Hospital, London, United Kingdom

7. Medical Oncology, Yale Cancer Center, Yale University School of Medicine, Smilow Cancer Hospital Yale New Haven Health, New Haven, CT

8. Medical Oncology, Oncosite Centro de Pesquisa Clínica, Ijui, Brazil

9. Medical Oncology, Institutul Prof Dr Ion Chiricuţă, Cluj-Napoca, Romania

10. Fundação Pio XII, Hospital de Câncer de Barretos, Barretos, Brazil

11. Medical Oncology, Vall d’Hebron University Hospital, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain

12. Hospital São Lucas da PUCRS, Porto Alegre, Brazil

13. Sf Nectarie Oncology Center, University of Medicine and Pharmacy, Craiova, Romania

14. Clínica Adventista Belgrano, Buenos Aires, Argentina

15. AP-HP Department of Dermato-oncology and CIC, INSERM U976, Cancer Institute APHP, Nord-Université Paris Cite, Université Paris Cité, Paris, France

16. Department of Dermatology, CIC 1413, de Cancéro-Dermatologie-CIC Biothérapie Nantes, Nantes University Hospital, Nantes, France

17. Skin Cancer Center, National Center for Tumor Diseases, University Cancer Centre Dresden, Dresden, Germany

18. Department of Dermatology, University Hospital Carl Gustav Carus, Dresden, Germany

19. Earle A. Chiles Research Institute, Providence Cancer Institute, Portland, OR

20. Medical Oncology, Bradford Hill Clinical Research Center, Santiago, Chile

21. Medical Oncology, Bristol Myers Squibb, Princeton, NJ

22. Translational Medicine, Bristol Myers Squibb, Princeton, NJ

23. Clinical Pharmacology & Pharmacometrics, Bristol Myers Squibb, Princeton, NJ

24. Clinical Development Department, Nektar Therapeutics, San Francisco, CA

25. Department of Cutaneous Oncology, Moffitt Cancer Center, Tampa, FL

Abstract

PURPOSE Despite marked advances in the treatment of unresectable or metastatic melanoma, the need for novel therapies remains. Bempegaldesleukin (BEMPEG), a pegylated interleukin-2 (IL-2) cytokine prodrug, demonstrated efficacy in the phase II PIVOT-02 trial. PIVOT IO 001 (ClinicalTrials.gov identifier: NCT03635983 ) is a phase III, randomized, open-label study that builds on the PIVOT-02 results in first-line melanoma. METHODS Patients with previously untreated, unresectable, or metastatic melanoma were randomly assigned 1:1 to receive BEMPEG plus nivolumab (NIVO) or NIVO monotherapy. Primary end points were objective response rate (ORR) and progression-free survival (PFS) by blinded independent central review and overall survival (OS). Secondary and exploratory end points included additional efficacy measures, safety, and pharmacokinetics (PKs) and pharmacodynamics analyses. RESULTS In 783 patients (n = 391, BEMPEG plus NIVO; n = 392, NIVO monotherapy), the median follow-up was 11.6 months in the intent-to-treat population. The ORR with BEMPEG plus NIVO was 27.7% versus 36.0% with NIVO (two-sided P = .0311). The median PFS with BEMPEG plus NIVO was 4.17 months (95% CI, 3.52 to 5.55) versus 4.99 months (95% CI, 4.14 to 7.82) with NIVO (hazard ratio [HR], 1.09; 97% CI, 0.88 to 1.35; P = .3988). The median OS was 29.67 months (95% CI, 22.14 to not reached [NR]) with BEMPEG plus NIVO versus 28.88 months (95% CI, 21.32 to NR) with NIVO (HR, 0.94; 99.929% CI, 0.59 to 1.48; P = .6361). Grade 3-4 treatment-related adverse events (AEs) and serious AE rates were higher with the combination (21.7% and 10.1%, respectively) versus NIVO (11.5% and 5.5%, respectively). BEMPEG PK exposure and absolute lymphocyte count changes after BEMPEG plus NIVO were comparable between PIVOT IO 001 and PIVOT-02. CONCLUSION The PIVOT IO 001 study did not meet its primary end points of ORR, PFS, and OS. Increased toxicity was observed with BEMPEG plus NIVO versus NIVO.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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