Abstract 1700P
Background
The BIONIKK trial showed promising efficacy of N+/-I and TKI in L1 mRCC according to tumor molecular group. S/R comp. are associated with poor prognosis but conversely may predict the efficacy of immune checkpoint inhibitors. We report on the impact of S/R on the efficacy of L1 in the BIONIKK trial.
Methods
Patients (pts) with mRCC were randomized according to ccrcc1-4 molecular group to receive N (58), NI (101) or TKI (40) in L1. Centralized pathological review was performed to identify ISUP grade, to quantify S/R comp. and the immune infiltrate (scale 0 to 3). Endpoints were objective response rate (ORR), progression-free survival (PFS) and overall survival (OS) according to S/R. Median follow-up was 46.6 months (IQR: 41.2-54.4).
Results
Of the 199 pts included, S, R and S+R was found in 23 (27.6%), 23 and 32 (co-presence: 58%) tumors respectively. Compared to pts with non-S/R tumors, those with S/R are more often IMDC int+poor (82%/78% vs 63%), have their tumors enriched in ccrcc1+4 (78%/69% vs 50%) and more immune infiltrates (2+3 in 87% vs 57%). Compared with pts without S, S-mRCC pts treated with N tended to have a higher rate of progressive disease (50% vs 34%), a shorter PFS (HR 1.23 [95%CI 0.68-2.22]), and a shorter OS (HR 2.56 [95%CI 1.28-5]), as did pts treated with TKI. Conversely, S-mRCC pts treated with NI had a higher ORR (68% vs. 42%), a longer PFS (HR 0.73 [95%CI 0.43-1.23]), and a similar OS (HR 1.03 [95%CI 0.52-2.04]). Compared with ISUP 4 tumors without S/R, S/R were associated with shorter PFS and OS with N or with TKI, and a higher ORR, PFS and OS with NI (table). Table: 1700P
Nivo | Nivo-ipi | TKI | ||
N= | S/R | 24 | 40 | 14 |
ISUP 4, no S/R | 3 | 13 | 5 | |
ORR (CR+PR) | S/R | 29% | 62% | 50% |
ISUP 4, no S/R | 33% | 8% | 80% | |
mPFS (95%CI), months | S/R | 2.4 (2.3-9.3) | 15.0 (10.3-32.8) | 9.1 (3.4-NA) |
ISUP 4, no S/R | 7.7 (2.16-NA) | 4.8 (2.5-NA) | 35.2 (14.4-NR) | |
HR (95%CI) | 0.78 (0.23-2.7) | 0.31 (0.16-0.62) | 3.44 (0.98-12.5) | |
mOS (95%CI), months | S/R | 21.2 (6.7-34.9) | 47.1 (33.8-NR) | 40.5 (12.9-NR) |
ISUP 4, no S/R | NR (29.4-NR) | 36.8 (29.4-NR) | NR (NR-NR) | |
HR (95%CI) | 4.76 (0.62-33.3) | 0.77 (0.32-1.85) | 4.0 (0.50-33.3) |
Conclusions
Within the BIONIKK study, we confirm the high co-occurrence of S and R comp. in mRCC, as well as a poor prognosis associated with the S comp. We also confirmed the particular efficacy of NI, but not N alone in S-mRCC. Results by ccrcc group, R comp. and %S/R will be presented.
Clinical trial identification
NCT02960906.
Editorial acknowledgement
Legal entity responsible for the study
ARTIC (Association pour la Recherche en Thérapeutiques Innovantes en Cancérologie).
Funding
ARTIC, Bristol Myers Squibb.
Disclosure
Y. Vano: Financial Interests, Personal, Invited Speaker: Ipsen, BMS, MSD, Pfizer, Eisai; Financial Interests, Personal, Other, Congress and travel funding: Ipsen, MSD, Pfizer; Financial Interests, Institutional, Funding, Funding support for the CABIR study: Ipsen; Financial Interests, Institutional, Funding, Funding support for the BIONIKK study: Bristol Myers Squibb; Financial Interests, Personal, Steering Committee Member, Member of the scientific committee of the WITNESS study: Bristol Myers Squibb; Financial Interests, Institutional, Local PI: Tesaro. C. Tournigand: Non-Financial Interests, Leadership Role: GERCOR; Non-Financial Interests, Advisory Role: Fondation APHP. D. Borchiellini: Financial Interests, Personal, Advisory Board: Astellas, AstraZeneca, Bristol Myer Squibb, Ipsen, Janssen, Merck, Pfizer; Financial Interests, Institutional, Advisory Board: Bayer, MSD; Financial Interests, Personal, Invited Speaker: Accord HealthCare; Financial Interests, Institutional, Local PI, Clinical Research: Astellas, AstraZeneca, Bayer, Bristol Myer Squibb, Exelixis, Infinity, Janssen, MSD, Roche, Taiho Oncology; Financial Interests, Institutional, Local PI: Aveo, Gilead, Seagen. B. Laguerre: Financial Interests, Personal, Other, ASCO GU symposium 2023 (travel and registration): Pfizer; Financial Interests, Personal, Other, honoraria: Astellas, Janssen, Pfizer, Eisai, Bayer; Financial Interests, Personal, Other, registration ASCO virtual meeting 2022: BMS; Financial Interests, Personal, Other, registration ASCO GU symposium 2022 (virtual): MSD; Financial Interests, Personal, Other, registration and travel for ASCO meeting 2023: AstraZeneca; Financial Interests, Personal, Other, registration and travel meeting ASCO GU 2024: Ipsen; Financial Interests, Personal, Other, registration virtual meeting EMOS 2023: MSD. P. Barthelemy: Financial Interests, Personal, Advisory Board: BMS, MSD, Merck, Pfizer, Ipsen, Bayer, Janssen Cilag, Astellas, Novartis, Amgen, Gilead; Financial Interests, Personal, Invited Speaker: AstraZeneca. G. Gravis: Financial Interests, Institutional, Invited Speaker: AAA, AMGEN, Astellas, BMS, Janssen, MSD, Pfizer, Ipsen, AstraZeneca, alliance Merck Pfizer, Bayer, Eisai; Financial Interests, Institutional, Advisory Board: Alliance Merck-Pfizer, BMS, Janssen, Pfizer, Ipsen, Bayer, Eisai, Gilead, AstraZeneca, AAA Novartis, MSD; Financial Interests, Personal, Other, Support for attending meetings and/or travel: BMS, AstraZeneca, Bayer, Ipsen, MSD, Pfizer, Janssen, AAA Novartis; Financial Interests, Institutional, Funding: Janssen; Financial Interests, Institutional, Coordinating PI: BMS; Non-Financial Interests, Principal Investigator: IPSEN, BMS, Merck. S. Oudard: Financial Interests, Personal, Advisory Board, consultancy, advisory role: Sanofi; Financial Interests, Personal, Invited Speaker, public speaking and advisory role: Janssen; Financial Interests, Personal, Advisory Board, advisory role and public speaking: AstraZeneca, MSD, Merck, Astellas, Ipsen, Pfizer, Roche, Genentech; Financial Interests, Personal, Advisory Board, Advisory board and public speaking: BMS, Bayer, Novartis. All other authors have declared no conflicts of interest.
Resources from the same session
1617P - Multi-gene copy number variation risk-score for prediction of survival and therapy response outcome in treatment-naïve metastatic castrate resistant prostate cancer
Presenter: Manish Kohli
Session: Poster session 11
1618P - Clinical prognostic factors within the high volume subgroup of metastatic hormone sensitive prostate cancer (mHSPC) in ENZAMET (ANZUP 1304)
Presenter: Anis Hamid
Session: Poster session 11
1619P - Efficacy of carboplatin in patients with metastatic castration-resistant prostate cancer: Results from the biomarker-driven, randomised, outcome-adaptive ProBio trial
Presenter: Anna Kristiansen
Session: Poster session 11
1620P - Inherited variants in SRD5A genes and response to hormonal therapy in prostate cancer (SWOG S1216)
Presenter: Sue Ingles
Session: Poster session 11
Resources:
Abstract
1621P - Validation of a digital pathology-based multimodal artificial intelligence (MMAI) prostate biopsy biomarker in a prospective, real-world Swedish prostate cancer (PCa) cohort treated with radical prostatectomy
Presenter: Anders Bjartell
Session: Poster session 11
1622P - A phase II study of the first-in-class oral innate immune activator BXCL701 with pembrolizumab in patients with metastatic castration-resistant prostate cancer (mCRPC): Long-term follow-up
Presenter: Rahul Aggarwal
Session: Poster session 11
1623P - Prognostic value of circulating tumour DNA fraction in metastatic castration-resistant prostate cancer: Insights from the ProBio trial
Presenter: Alessio Crippa
Session: Poster session 11
1624P - Total and regional changes in body composition in metastatic hormone-sensitive prostate cancer (mHSPC) patients randomized to receive androgen deprivation + enzalutamide +/- zoledronic acid: The BonEnza study
Presenter: Martina Buffoni
Session: Poster session 11
1625P - Fuzuloparib combined with abiraterone in the neoadjuvant treatment of localised high-risk prostate cancer (FAST-PC): A single-arm phase II study
Presenter: Yao Zhu
Session: Poster session 11