Abstract 1712P
Background
This study investigated real-world efficacy of 1st-line nivolumab plus ipilimumab (NI) and its clinicopathologic predictive biomarkers in patients with advanced renal cell carcinoma (aRCC).
Methods
This study retrospectively analyzed 455 patients with aRCC who received 1st-line NI between 2018 and 2022 at 20 centers in Korea. Primary outcome was objective response rate (ORR). Secondary outcomes were progression-free survival (PFS), overall survival (OS) and identifying its practical clinicopathologic biomarkers.
Results
The median age of the patients was 65 years (range, 31 to 89 years), and 77.8% were male. Most of patients were intermediate (n=285, 62.6%) or poor (n=160, 35.2%) International Metastatic RCC Database Consortium (IMDC) risk groups. ORR was 41.5% including 4.8% of complete response, and median duration of response was 8.4 months (range 0.2-50.4). Achievement of objective response was significantly associated to male (odd ratio, OR 2.0, P=0.017), previous nephrectomy (OR 2.1, P=0.001), and lung metastasis (OR 2.4, P=0.001). With a median follow-up duration of 13.6 months (range 12.2-15.0), the median PFS and OS were 13.5 months (95% confidence interval [CI], 8.7-18.4) and 51.5 months (95% CI, 34.9-68.1), respectively. In multivariate analysis, Eastern Cooperative Oncology Group performance status (ECOG PS) 0-1 (vs. ≥2) (hazard ratio, HR 0.7, P=0.073 and HR 0.5, P=0.007), IMDC intermediate risk (vs. poor risk) (HR 0.7, P=0.043 and HR 0.5, P=0.002), and completion of 4 cycles of NI (vs. 1-3) (HR 0.3, P<0.001 and HR 0.3, P<0.001) were significantly associated with better PFS and OS. Although using antibiotics before the initiation of NI was significantly associated with shorter OS (HR 1.7, P=0.014), durable responders showed significantly longer OS (HR 0.02, P=0.001).
Conclusions
First-line NI showed comparable real-world efficacy in Korean patients with aRCC. ECOG PS, IMDC risk, and completion of 4 cycles of NI might affect both PFS and OS. Although previous use of antibiotics might adversely affect OS, male gender, lung metastasis or prior nephrectomy might be practical predictors of objective response, which itself could predict better OS.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All 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