IMmotion151: A Randomized Phase III Study of Atezolizumab Plus Bevacizumab vs Sunitinib in Untreated Metastatic Renal Cell Carcinoma (mRCC)

Author:

Motzer Robert J.1,Powles Thomas2,Atkins Michael B.3,Escudier Bernard4,McDermott David F.5,Suarez Cristina6,Bracarda Sergio7,Stadler Walter Michael8,Donskov Frede9,Lee Jae-Lyun10,Hawkins Robert E.11,Ravaud Alain12,Alekseev Boris Y.13,Staehler Michael D.14,Uemura Motohide15,Donaldson Francis16,Li Shi17,Huseni Mahrukh A.17,Schiff Christina17,Rini Brian I.18

Affiliation:

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

2. Barts Health NHS Trust – St Bartholomew’s Hospital, London, United Kingdom;

3. Georgetown University Lombardi Comprehensive Cancer Center, Washington, DC;

4. Gustave Roussy Institute, Villejuif, France;

5. Beth Israel Deaconess Medical Center, Boston, MA;

6. Vall d’Hebron Institute of Oncology, Vall d’Hebron University Hospital, Universitat Autònoma de Barcelona, Barcelona, Spain;

7. Ospedale San Donato, Arezzo, Italy;

8. University of Chicago, Chicago, IL;

9. Aarhus University Hospital, Aarhus, Denmark;

10. University of Ulsan College of Medicine/ Asan Medical Center, Seoul, Korea, Republic of (South);

11. Christie Hospital NHS Foundation Trust, Manchester, United Kingdom;

12. Bordeaux University Hospital, Bordeaux, France;

13. Federal State Institution, Moscow Research Oncological Institute, Moscow, Russia;

14. University Hospital Munich-Grosshadern, Ludwig Maximilian University, Munich, Germany;

15. Osaka University Graduate School of Medicine, Osaka, Japan;

16. F. Hoffmann-La Roche Ltd., Basel, Switzerland;

17. Genentech, Inc., South San Francisco, CA;

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

Abstract

578 Background: Atezolizumab (atezo; anti–PD-L1) + bevacizumab (bev; anti-VEGF) showed first-line (1L) anti-tumor activity with a manageable safety profile in PD-L1+ mRCC pts in a Phase II study (McDermott ASCO-GU 2017). Here we describe the first randomized Phase III trial of a PD-L1/PD-1 pathway inhibitor combined with an anti-VEGF agent in 1L mRCC. Methods: IMmotion151 (NCT02420821) enrolled treatment-naïve pts regardless of prognostic risk group randomized 1:1 to receive atezo 1200 mg IV q3w + bev 15 mg/kg IV q3w or sunitinib (sun) 50 mg PO QD 4 wk on/2 wk off. Pts were stratified by PD-L1 status (< 1% vs ≥ 1% PD-L1 expression on tumor-infiltrating immune cells [IC]; SP142 IHC assay). Coprimary endpoints: progression-free survival (PFS; by investigator per RECIST v1.1) in PD-L1+ pts (≥ 1% IC) and overall survival (OS) in intent-to-treat (ITT) pts. Secondary endpoints included PFS in ITT pts, ORR and DOR. Results: Baseline characteristics were comparable between arms within PD-L1+ (40% of ITT) and ITT pts. Median survival follow-up was 15 mo. PFS HR for atezo + bev vs sun was 0.74 (95% CI 0.57, 0.96) in PD-L1+ pts and 0.83 (95% CI 0.70, 0.97) in ITT pts. OS was immature at first interim analysis. PFS benefit was consistent across analyzed subgroups, including MSKCC risk, liver metastases and sarcomatoid histology. In PD-L1+ pts, ORR was 43% and DOR was not reached for atezo + bev vs 35% and 12.9 mo for sun. 40% of atezo + bev–treated pts and 54% of sun-treated pts had treatment-related Gr 3-4 AEs; 12% and 8% of treatment-related all-Gr AEs led to discontinuation, respectively. Conclusions: The study showed longer PFS for atezo + bev vs sun in PD-L1+ pts. Improved PFS was also observed in ITT pts. Safety was consistent with that of the individual agents. These results support the use of atezo + bev as a 1L treatment option in mRCC. Clinical trial information: NCT02420821. [Table: see text]

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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