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
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