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
1646P - A multicohort phase II trial of androgen deprivation therapy (ADT), docetaxel (DOCE) and nivolumab (NIVO) in patients (pts) with newly diagnosed metastatic hormone sensitive prostate cancer (mHSPC) enriched for inflamed tumours and DNA damage repair (DDR) alterations: Cohort 3 results
Presenter: Xiao Wei
Session: Poster session 11
1647P - Clinical validity of plasma DNA testing to identify BRCA-mutated (BRCA+) patients in the MAGNITUDE study
Presenter: Gerhardt Attard
Session: Poster session 11
1649P - Impact of concomitant medications on safety in patients with high-volume metastatic hormone-sensitive prostate cancer (mHSPC) receiving rezvilutamide (Rez) plus androgen-deprivation therapy (ADT): A post-hoc analysis of the randomized phase III CHART trial
Presenter: Dingwei Ye
Session: Poster session 11
1650P - Fuzuloparib plus abiraterone acetate and prednisone (AA-P) in patients (pts) with metastatic castration-resistant prostate cancer (mCRPC): A phase I study
Presenter: Tao Dai
Session: Poster session 11
1651P - Characteristics, tolerance and effectiveness of patients aged more or less than 75 years treated with [177Lu]Lu-PSMA-617 as part of France’s early access program
Presenter: David Tonnelet
Session: Poster session 11
1652P - SAABR: Single arm phase II study of androgen receptor pathway inhibitor (ARPI) + atezolizumab + GnRH analog (ADT) and stereotactic body radiotherapy (SBRT) to the prostate in men with de novo hormone-sensitive metastatic prostate cancer (mHSPC)
Presenter: Dana Rathkopf
Session: Poster session 11
1653P - Molecular and immunologic correlates of high PSMA/FOLH1 mRNA expression in prostate cancer (PC)
Presenter: Rana McKay
Session: Poster session 11
1654P - TAMARACK: Randomized Phase II trial of the B7-H3 targeting antibody drug conjugate (ADC) vobramitamab duocarmazine (vobra duo) in metastatic castration-resistant prostate cancer (mCRPC)
Presenter: Johann de Bono
Session: Poster session 11
1655P - Association of location of BRCA1/2 pathogenic variants with benefit from PARP-inhibitors in metastatic castration-resistant prostate cancers: Results from the PROGRESS study
Presenter: Lorena Incorvaia
Session: Poster session 11