Long-term outcomes in patients (pts) with ipilimumab (ipi)-naive advanced melanoma in the phase 3 KEYNOTE-006 study who completed pembrolizumab (pembro) treatment.

Author:

Robert Caroline1,Long Georgina V.2,Schachter Jacob3,Arance Ana4,Grob Jean Jacques5,Mortier Laurent6,Daud Adil7,Carlino Matteo S.8,McNeil Catriona M.9,Lotem Michal10,Larkin James M. G.11,Lorigan Paul12,Neyns Bart13,Blank Christian U.14,Petrella Teresa M.15,Hamid Omid16,Zhou Honghong17,Homet Moreno Blanca17,Ibrahim Nageatte17,Ribas Antoni18

Affiliation:

1. Gustave Roussy, Villejuif, France;

2. Melanoma Institute Australia, The University of Sydney, Royal North Shore and Mater Hospitals, Sydney, Australia;

3. Sheba Medical Center, Tel Hashomer, Israel;

4. Hospital Clínic de Barcelona, Barcelona, Spain;

5. Aix Marseille University, Hôpital de la Timone, Marseille, France;

6. Universite Lille, Centre Hospitalier Regional Universitaire de Lille, Lille, France;

7. University of California, San Francisco, San Francisco, CA;

8. Westmead and Blacktown Hospitals and Melanoma Institute Australia, Sydney, Australia;

9. Chris O’Brien Lifehouse, Camperdown, Australia;

10. Sharett Institute of Oncology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel;

11. Royal Marsden Hospital, London, United Kingdom;

12. University of Manchester and The Christie NHS Foundation Trust, Manchester, United Kingdom;

13. Universitair Ziekenhuis Brussel, Brussels, Belgium;

14. Netherlands Cancer Institute, Amsterdam, Netherlands;

15. Sunnybrook Health Sciences Centre, Toronto, ON, Canada;

16. The Angeles Clinic and Research Institute, Los Angeles, CA;

17. Merck & Co., Inc., Kenilworth, NJ;

18. University of California, Los Angeles, Los Angeles, CA;

Abstract

9504 Background: Pembro demonstrated superior PFS and OS vs ipi in ipi-naive pts with advanced melanoma in the phase 3 KEYNOTE-006 study (NCT01866319). Here, we present long-term outcomes for all pts and in those pts who completed pembro therapy. Methods: Eligible pts (N = 834) were randomized 1:1:1 to pembro 10 mg/kg Q2W, pembro 10 mg/kg Q3W, or ipi 3 mg/kg Q3W for 4 doses. Treatment was continued for 2 yr (pembro only) or until disease progression, intolerable toxicity, or pt/investigator decision to discontinue. Per protocol, pts could interrupt pembro for ≤12 wk before discontinuation was required. Tumor imaging was performed at wk 12, then every 6 wk up to wk 48 and every 12 wk thereafter. After the prespecified final analysis, response assessments were per immune-related response criteria (irRC) by investigator review. Results: As of the data cutoff (Nov 3, 2016), median follow-up in the total population was 33.9 mo (range, 32.1-37.6). 33-mo OS rates were 50% in the pooled pembro arms (n = 556) and 39% in the ipi arm (n = 278); 33-mo PFS rates were 31% and 14%. ORR was 42% and 16%. Median duration of response was not reached for pembro (range 1.0+ to 33.8+ mo) or ipi (1.1+ to 34.8+ mo); 46 (68%) pembro-treated pts and 7 (58%) ipi-treated pts had a response lasting ≥30 mo. Among the 104/556 (19%) pts who completed pembro, median exposure to pembro was 24.0 mo (range 22.1-25.9). After a median follow-up of 9.0 mo after completion of pembro, 102 (98%) pts were alive. Responses were durable in pts who completed pembro; 9.7 mo after completion of pembro, estimated PFS (95% CI) was 91% (80-96) in all 104 pts, 95% (69-99) in pts with complete response (n = 24), 91% (74-97) in pts with partial response (n = 68), and 83% (48-96) in pts with stable disease (n = 12). Conclusions: Pembro provides durable efficacy after stopping the protocol-specified duration of treatment in pts with ipi-naive advanced melanoma in KEYNOTE-006. The estimated risk for progression or death nearly 10 mo after completing pembro is 9% and does not appear to differ by best response to pembro. Clinical trial information: NCT01866319.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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