Five-year overall survival from the anti-PD1 brain collaboration (ABC Study): Randomized phase 2 study of nivolumab (nivo) or nivo+ipilimumab (ipi) in patients (pts) with melanoma brain metastases (mets).

Author:

Long Georgina V.1,Atkinson Victoria2,Lo Serigne3,Guminski Alexander David4,Sandhu Shahneen Kaur5,Brown Michael Paul6,Gonzalez Maria7,Scolyer Richard A.8,Emmett Louise9,McArthur Grant A.10,Menzies Alexander M.11

Affiliation:

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

2. Princess Alexandra Hospital, University of Queensland, Greenslopes, Brisbane, QLD, Australia;

3. Melanoma Institute Australia, The University of Sydney, Sydney, NSW, Australia;

4. Royal North Shore Hospital, Sydney, Australia;

5. Peter MacCallum Cancer Center, Melbourne, VIC, Australia;

6. Royal Adelaide Hospital, Adelaide, Australia;

7. Melanoma Institute Australia, Sydney, Australia;

8. Melanoma Institute Australia, The University of Sydney, Sydney, Australia;

9. St Vincent’s Clinic Medical Imaging and Nuclear Medicine, Darlinghurst, Australia;

10. Melanoma and Skin Service and Cancer Therapeutics Program, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia;

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

Abstract

9508 Background: Preliminary data from the ABC (76 pts) and CheckMate 204 (94 pts) trials showed that nivo and nivo+ipi have activity in active melanoma brain metastases, with durable responses in a subset of pts. Here, we report updated 5-yr data from all pts enrolled on the ABC trial (NCT02374242). Methods: This open-label ph2 trial enrolled 3 cohorts of pts with active melanoma brain mets naïve to anti-PD1/PDL1/PDL2/CTLA4 from Nov 2014-Apr 2017. Pts with asymptomatic brain mets with no prior local brain therapy were randomised to cohort A (nivo 1mg/kg + ipi 3mg/kg, Q3Wx4, then nivo 3mg/kg Q2W) or cohort B (nivo 3mg/kg Q2W). Cohort C (nivo 3mg/kg Q2W) had brain mets i) that failed local therapy, ii) with neuro symptoms and/or iii) with leptomeningeal disease. Prior BRAF inhibitor (BRAFi) was allowed. The primary endpoint was best intracranial response (ICR) ≥wk12. Key secondary endpoints were IC PFS, overall PFS, OS, & safety. Results: A total of 76 pts (med f/u 54 mo) were enrolled; median age 59y, 78% male. For cohorts A, B and C: elevated LDH 51%, 58% and 19%; V600BRAF 54%, 56% and 81%; prior BRAFi 23%, 24%, 75%. Efficacy and toxicity are shown in the table. There were no treatment-related deaths. 1/17 deaths in cohort A & 4/16 in cohort B were due to IC progression only. Conclusions: Nivo monotherapy and ipi+nivo are active in melanoma brain mets, with durable responses in the majority of patients who received ipi+nivo upfront. A study of upfront ipi+nivo+/-SRS is underway (NCT03340129). Clinical trial information: NCT02374242. [Table: see text]

Funder

BMS

Other Foundation

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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