Adjuvant pembrolizumab (pembro) for renal cell carcinoma (RCC) across UCLA Integrated Staging System (UISS) risk groups and disease stage: Subgroup analyses from the KEYNOTE-564 study.

Author:

Choueiri Toni K.1,Tomczak Piotr2,Park Se Hoon3,Venugopal Balaji4,Ferguson Tom5,Symeonides Stefan N.6,Hajek Jaroslav7,Chang Yen-Hwa8,Lee Jae-Lyun9,Sarwar Naveed10,Thiery-Vuillemin Antoine11,Gross-Goupil Marine12,Mahave Mauricio13,Haas Naomi B.14,Sawrycki Piotr15,Zhang Tian16,Xu Lei17,Imai Kentaro17,Poehlein Christian Heinrich17,Powles Thomas18

Affiliation:

1. Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA

2. Poznan University of Medical Sciences, Poznan, Poland

3. Sungkyunkwan University, Samsung Medical Center, Seoul, South Korea

4. Beatson West of Scotland Cancer Centre and University of Glasgow, Glasgow, United Kingdom

5. Fiona Stanley Hospital, Perth, Western Australia, Australia

6. Edinburgh Cancer Centre and University of Edinburgh, Edinburgh, United Kingdom

7. Fakultni Nemocnice Ostrava, Ostrava, Czech Republic

8. Taipei Veterans General Hospital, Taipei, Taiwan

9. Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea

10. Imperial College Healthcare NHS Trust, London, United Kingdom

11. University Hospital Jean Minjoz, Besançon, France

12. University Hospital of Bordeaux-St. Andrews Hospital, Bordeaux, France

13. Fundación Arturo López Pérez, Santiago, Chile

14. Abramson Cancer Center, Penn Medicine, Philadelphia, PA

15. Provincial Hospital in Torun, Torun, Poland

16. The University of Texas Southwestern Medical Center, Dallas, TX

17. Merck & Co., Inc., Rahway, NJ

18. Barts Health NHS Trust and the Royal Free NHS Foundation Trust, Barts Cancer Institute, and Queen Mary University of London, London, United Kingdom

Abstract

679 Background: Adjuvant pembro prolonged disease-free survival (DFS) for patients (pts) with RCC at increased risk of recurrence after nephrectomy in the phase 3 KEYNOTE-564 study (NCT03142334). This post hoc exploratory analysis evaluated efficacy of adjuvant pembro in pt subgroups based on UISS and disease stage. Methods: Pts with histologically confirmed clear cell RCC (pT2, Grade [G] 4 or sarcomatoid, N0, M0; pT3 or pT4, any G, N0, M0; any pT, any G, N+, M0; or M1 NED) were randomly assigned 1:1 to receive pembro 200 mg IV or placebo (pbo) every 3 weeks for ≤17 cycles (~1 y). DFS was assessed by investigator. UISS risk groups were derived retrospectively from TNM stage, Fuhrman nuclear grade, and ECOG PS. UISS groups were intermediate risk (pT2, G4, N0, M0; pT3, G1, N0, M0; or pT3, G2-4, N0, M0, ECOG 0), high risk (pT3, G2-4, N0, M0, ECOG PS 1; pT4, any G, N0, M0; or N1, M0), or M1 NED. Other subgroups were evaluated based on disease stage. Results: Baseline characteristics were balanced within subgroups. Median follow-up was 30.1 mo (range 20.8-47.5). Of 994 enrolled pts, most had UISS intermediate risk (n = 732, 73.6%; pembro n = 359; pbo n = 373); 195 pts (19.6%; pembro n = 100; pbo n = 95) had UISS high risk, and 58 pts (5.8%; pembro and pbo n = 29 each) had M1 NED. In the UISS intermediate risk group, the hazard ratio (HR) for DFS was 0.65 (95% CI, 0.48-0.88; 24-mo rates, pembro: 81.5%, pbo: 72.4%). In the UISS high-risk group, HR for DFS was 0.77 (95% CI, 0.49-1.20; 24-mo rates, pembro: 65.0%, pbo: 55.9%). In the M1 NED group, HR for DFS was 0.28 (95% CI, 0.12-0.66; 24-mo rates, pembro: 78.4%, pbo: 37.9%). DFS by disease stage is in the Table. Conclusions: Consistent with the results of the intention-to-treat (ITT) population, adjuvant pembro prolonged DFS compared with pbo for all subgroups. Results of this exploratory analysis further support the use of adjuvant pembro after nephrectomy as standard of care for pts with RCC at increased risk of recurrence. Clinical trial information: NCT03142334 . [Table: see text]

Funder

Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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