A phase III randomized study comparing perioperative nivolumab vs. observation in patients with localized renal cell carcinoma undergoing nephrectomy (PROSPER RCC).

Author:

Harshman Lauren Christine1,Puligandla Maneka1,Haas Naomi B.2,Allaf Mohamad3,Drake Charles G.4,McDermott David F.5,Signoretti Sabina6,Cella David7,Gupta Rajan T8,Bhatt Rupal Satish5,Van Allen Eliezer Mendel1,Choueiri Toni K.9,Lara Primo10,Kapoor Anil11,Heng Daniel Yick Chin12,Shuch Brian M.13,Jewett Michael A.S.14,George Daniel J.15,Michaelson M Dror16,Carducci Michael Anthony17,

Affiliation:

1. Dana-Farber Cancer Institute, Boston, MA;

2. Abramson Cancer Center, Philadelphia, PA;

3. Johns Hopkins University School of Medicine, Baltimore, MD;

4. Columbia University Herbert Irving Comprehensive Cancer Center, New York, NY;

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

6. Brigham and Women's Hospital, Boston, MA;

7. Feinberg School of Medicine, Northwestern University, Chicago, IL;

8. Duke University Medical Center, Department of Radiology, Durham, NC;

9. Dana-Farber Cancer Institute and Brigham and Women's Hospital, Boston, MA;

10. University of California, Davis, Sacramento, CA;

11. Juravinski Cancer Centre, McMaster University, Hamilton, ON, Canada;

12. Tom Baker Cancer Centre, Calgary, AB, Canada;

13. Yale School of Medicine, New Haven, CT;

14. Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada;

15. Duke Cancer Institute, Duke University Medical Center, Durham, NC;

16. Massachusetts General Hospital Cancer Center, Boston, MA;

17. Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University, Baltimore, MD;

Abstract

TPS4596 Background: The anti-PD-1 antibody nivolumab (nivo) improves overall survival (OS) in metastatic treatment refractory RCC and is generally tolerable. In 2017, there is no standard adjuvant therapy proven to increase OS over surgery alone in non-metastatic (M0) disease. Mouse solid tumor models have revealed an OS benefit with a short course of neoadjuvant PD-1 blockade compared to adjuvant therapy. Two ongoing phase 2 studies of perioperative nivo in RCC patients (pts) have shown preliminary feasibility and safety with no surgical delays or complications. The PROSPER RCC trial will examine if the addition of perioperative nivo to radical or partial nephrectomy can improve clinical outcomes in pts with locally advanced RCC. With the goal of increasing cure and recurrence-free survival (RFS) rates in M0 RCC, we propose a three-pronged, multidisciplinary approach of presurgical priming with nivo followed by resection and adjuvant PD-1 blockade. Methods: Tumorbiopsy prior to randomization is mandatory to ensure the correct diagnosis and will permit unparalleled correlative science in this global, randomized, unblinded, phase 3 National Clinical Trials Network study. 766 pts with clinical stage ≥T2 or any node positive M0 RCC of any histology will be enrolled. The study arm will receive nivo 240mg IV for 2 doses prior to surgery followed by nivo adjuvantly for 9 months (q2 wks x 3 mo followed by q4 wks x 6 mo). The control arm will undergo the current standard of care: surgical resection followed by observation. Pts are stratified by clinical T stage, node positivity, and histology. There is 84.2% power to detect a 14.4% absolute increase in the primary endpoint of RFS from the ASSURE historical control of 55.8% to 70.2% at 5 yrs (HR 0.70). The study is also powered to detect a significant OS benefit (HR 0.67). Key safety, feasibility, and quality of life endpoints are incorporated. PROSPER RCC exemplifies team science with a host of planned correlative work to investigate the significance of the baseline immune milieu and changes after neoadjuvant priming and to identify predictive gene expression patterns. Additional collaborations are welcomed.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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