Abstract 107P
Background
Metastatic non-clear cell renal cell carcinoma (mnccRCC) currently lacks standard first-line treatment options. This study evaluated the effectiveness and safety of ICI plus tyrosine kinase inhibitor (TKI) in mnccRCC patients through multi-center real-world evidence, encompassing the largest sample size to date.
Methods
We conducted a retrospective analysis of treatment-naive metastatic non-clear cell renal cell carcinoma (mnccRCC) patients who received either TKI monotherapy or TKI + ICI combination therapy at four hospitals in China. Baseline characteristics were recorded, and comparisons were made between the two groups in terms of objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), overall survival (OS), and the incidence of adverse events (AEs).
Results
A total of 214 mnccRCC patients were enrolled from the four hospitals: 122 in the TKI monotherapy group and 92 in the TKI + ICI combination group. The median follow-up time was 36.5 months (interquartile range [IQR], 24.2–57.0), with a median age of 49 years and a majority of male patients (70.6%). Compared to the TKI group, the TKI + ICI group showed a significantly higher objective response rate (29.4% vs. 16.4%, P < 0.01) and disease control rate (78.3% vs. 48.4%, P < 0.01). Additionally, the combination therapy group had a longer progression-free survival [median PFS (95% CI): 15.2 (6.6–23.7) months vs. 5.9 (4.3–7.5) months, P < 0.001] and a longer overall survival [median OS (95% CI): not reached vs. 38.5 (26.6–50.4) months, P = 0.019]. The incidence of grade 3 or higher treatment-related adverse events was slightly higher in the combination therapy group, but the difference was not statistically significant (35.8% vs. 23.7%, P = 0.079).
Conclusions
Our retrospective real-world study demonstrates that, compared to TKI monotherapy, the combination of ICI and TKI significantly improves progression-free survival (PFS), objective response rate (ORR), and overall survival (OS) in patients with metastatic non-clear cell renal cell carcinoma (mnccRCC), with manageable safety. This study provides stronger evidence for the pharmacological treatment of metastatic non-clear cell renal cell carcinoma.
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
195P - Anti-CTLA4 therapy leads to early expansion of peripheral Th17 population and induction of Th1 cytokines
Presenter: Mari Nakazawa
Session: Poster Display session
Resources:
Abstract
196P - Single-cell analysis of stage-I high-grade serous ovarian carcinoma reveals the essential role of regulatory T cells in early tumor establishment
Presenter: Joanna Mikulak
Session: Poster Display session
Resources:
Abstract
197P - Comprehensive immunoprofiling of the intratumoral and peripheral T cell receptor gene repertoire in triple-negative breast cancer patients
Presenter: Antonios Mingos
Session: Poster Display session
Resources:
Abstract
198P - Association of types of treatment modalities with expression of T Lymphocytes (CD4, CD8, Treg) in breast cancer patients and their clinical outcome
Presenter: Arshi Rizwan
Session: Poster Display session
Resources:
Abstract
199P - Cancer neutrophil encyclopedia: A deep dive into antigen-presenting warriors
Presenter: Yingcheng Wu
Session: Poster Display session
Resources:
Abstract
200P - CXCR1+ neutrophil infiltration orchestrates response to third-generation EGFR-TKI in EGFR mutant NSCLC
Presenter: Haowei Wang
Session: Poster Display session
Resources:
Abstract
201P - Underlying mechanisms of neutrophil-mediated immunosuppression and resistance to treatment in breast cancer: Further evidence that these cells matter
Presenter: Bruna Filipa Correia
Session: Poster Display session
Resources:
Abstract
202P - Mining tumor infiltrating B cells to discover antibody-target pairs and develop novel therapies
Presenter: Matthieu Delince
Session: Poster Display session
Resources:
Abstract
203P - Targeting IL-33 reprograms tumor microenvironment and potentiates antitumor response to anti-PD-L1 immunotherapy
Presenter: Xuyao Zhang
Session: Poster Display session
Resources:
Abstract
204P - Deciphering the crosstalk between tumor and circulating immune microenvironment in advanced NSCLC patients undergoing immunotherapy
Presenter: Prisca Tamarozzi
Session: Poster Display session
Resources:
Abstract