Overall survival and independent review of response in CheckMate 214 with 42-month follow-up: First-line nivolumab + ipilimumab (N+I) versus sunitinib (S) in patients (pts) with advanced renal cell carcinoma (aRCC).

Author:

Tannir Nizar M.1,McDermott David F.2,Escudier Bernard3,Hammers Hans J.4,Aren Osvaldo Rudy5,Plimack Elizabeth R.6,Barthelemy Philippe7,Neiman Victoria8,George Saby9,Porta Camillo10,Powles Thomas11,Donskov Frede12,Grimm Marc-Oliver13,Amin Asim14,Tykodi Scott S.15,Tomita Yoshihiko16,Rini Brian I.17,McHenry M. Brent18,Saggi Shruti Shally18,Motzer Robert J.19

Affiliation:

1. University of Texas MD Anderson Cancer Center, Houston, TX;

2. Beth Israel Deaconess Medical Center, Dana-Farber/Harvard Cancer Center, Boston, MA;

3. Gustave Roussy, Villejuif, France;

4. The University of Texas Southwestern, Dallas, TX;

5. Centro Internacional de Estudios Clinicos, Santiago, Chile;

6. Fox Chase Cancer Center, Philadelphia, PA;

7. Hôpitaux Universitaires de Strasbourg, Strasbourg, France;

8. Davidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel;

9. Roswell Park Cancer Institute, Buffalo, NY;

10. University of Pavia, Pavia, Italy;

11. Barts Cancer Institute, Queen Mary University of London, Royal Free NHS Trust, London, United Kingdom;

12. Department of Oncology, Aarhus University Hospital, Aarhus, Denmark;

13. Jena University Hospital, Jena, Germany;

14. Levine Cancer Institute, Carolinas HealthCare System, Atrium Health, Charlotte, NC;

15. University of Washington and Fred Hutchinson Cancer Research Center, Seattle, WA;

16. Department of Urology, Department of Molecular Oncology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan;

17. Cleveland Clinic Taussig Cancer Institute, Cleveland, OH;

18. Bristol-Myers Squibb, Princeton, NJ;

19. Memorial Sloan Kettering Cancer Center, New York, NY;

Abstract

609 Background: N+I demonstrated superior OS and ORR v S in intention-to-treat (ITT) and intermediate/poor-risk (IP) pts with aRCC in CheckMate 214. Here, we report OS, response outcomes per independent radiology review committee (IRRC), and safety with extended min follow-up of 42 mo. Methods: Pts with clear cell aRCC were randomized 1:1 to N 3 mg/kg + I 1 mg/kg Q3W×4 and then N 3 mg/kg Q2W, or S 50 mg daily for 4 wk on, 2 wk off. Endpoints were OS, ORR, and PFS per IRRC using RECIST v1.1 in IP (primary), ITT (secondary), and favorable pts (FAV; exploratory). Results: OS remained superior in ITT (HR 0.72) and IP (HR 0.66) pts with N+I v S (Table). ORR per IRRC was higher and more responses were ongoing with N+I v S (68% v 53% [ITT] and 68% v 52% [IP]). More pts achieved complete response (CR) with N+I and these were ongoing in 86% [ITT] and 84% [IP] of pts. The PFS probability with N+I stabilized after 24 mo at ~35% in ITT and IP pts, whereas probabilities declined over time with S. Among FAV pts, while ORR was 29% with N+I v 54% with S, more pts achieved CR (13% v 6%), and more responses were ongoing (69% v 54%) with N+I v S; 94% of CRs in FAV pts were ongoing with N+I. OS benefits were similar in both arms and PFS probabilities are stabilizing with N+I and declining with S in FAV pts. The incidence of any and grade 3–4 treatment-related AEs was consistent with previous reports and no new drug-related deaths occurred in either arm. Response outcomes per investigator will also be reported. Conclusions: Superior OS and ORR with N+I v S was maintained in ITT and IP pts. More pts treated with N+I experienced CR compared with S, responses and CRs were durable, and PFS probabilities stabilized with N+I after extended follow-up. No new safety signals emerged. Clinical trial information: NCT02231749 .[Table: see text]

Funder

Bristol-Myers Squibb

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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