Systemic and surgical treatment in renal cell carcinoma: Does timing matter?

Authors

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Konstantin Egon Seitzer

Department of Urology and Pediatric Urology, West German Cancer Center, University Hospital Münster, Münster, Germany

Konstantin Egon Seitzer , Christopher Darr , Thomas Hilser , Andres Jan Schrader , Linda Huberth , Anne Mausbach , Martin Janssen , Laura-Maria Krabbe , Barbara Heitplatz , Boris A. Hadaschik , Martin Boegemann , Katrin Schlack , Viktor Grünwald

Organizations

Department of Urology and Pediatric Urology, West German Cancer Center, University Hospital Münster, Münster, Germany, Department of Urology, University of Duisburg-Essen and German Cancer Consortium (DKTK)-University Hospital Essen, Essen, Germany, Department of Medical Oncology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany, Department of Urology and Pediatric Urology, West German Cancer Center, University Hospital Münster, Muenster, Germany, Department of Urology, University Hospital Essen, Essen, Germany, Essen, Germany, Department of Urology, Vivantes Humboldt Hospital Berlin, Berlin, Germany, Gerhard-Domagk-Institute of Pathology, University Hospital Münster, Muenster, Germany, Department of Urology and pediatric Urology, University Hospital Münster, Münster, Germany, Clinic for Internal Medicine (Tumor Research) and Department of Urology, University of Duisburg-Essen and German Cancer Consortium (DKTK)-University Hospital Essen, Essen, Germany

Research Funding

No funding sources reported

Background: Today, targeted systemic therapy is standard 1st line treatment of advanced/metastatic renal cell carcinoma (aRCC). Upfront cytoreductive nephrectomy (CN) has been an important treatment option. Recently its role is under debate, especially in combination with the new 1st line treatments. Our study evaluated the current relevance of initial surgical intervention and the role of inductive systemic therapy in aRCC. Methods: We included 33 patients with aRCC from the University Hospitals in Essen and Münster initiating 1st line treatment from 03/18 to 01/23 pre or post surgery. We retrospectively formed two cohorts, either CN followed by systemic therapy (cohort 1; 13 patients) or vice versa (cohort 2; 20 patients). Patients received either Ipilimumab/Nivolumab (Ipi/Nivo) (42.4%) or a checkpoint inhibitor and tyrosine kinase inhibitor (CPI/TKI) combination (57.6%). Progression-free survival (PFS) was estimated with Kaplan-Meier-method from initiation of systemic therapy or CN to progression or death. In Cohort 2, we additionally analyzed the radiologic response of the primary measured by change of the longest diameter. The radiographic response was analysed according to RECIST1.1. Results: Patients’ age ranged from 44 to 80 years with a median of 63 years. Intermediate and poor prognosis occurred in 61.3% and 38.7% of cases. The two cohorts did not differ significantly regarding baseline characteristics. Median PFS was 8 vs. 23 months (p=0.03) in cohort 1 (95% CI 0.9-15.1) compared to cohort 2 (95% CI 18.8-27.2). In cohort 2 the time between start of systemic therapy and surgery was in median 8.5 months (95% CI 3.3-21.1), the primary had a median diameter of 10.7 cm (95% CI 4.5-13.3). Median reduction of the primary was in total 32.2%, 28.9% in the Ipi/Nivo and 34.7% in the CPI/TKI group (p=0.74). In seven patients (35%) response led to modification of the surgical approach, enabling partial instead of radical nephrectomy. Conclusions: The sequence of systemic therapy followed by surgery was associated with a significant PFS benefit. In addition, prior systemic therapy led to a primary reduction and better operability, in some cases even to kidney sparing surgery. Major limitation is the retrospective nature of our analysis and a potential selection bias. However, the sequence of prior systemic therapy followed by surgery in aRCC was associated with notably better outcomes.

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Abstract Details

Meeting

2024 ASCO Genitourinary Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session C: Renal Cell Cancer; Adrenal, Penile, and Testicular Cancers

Track

Renal Cell Cancer,Adrenal Cancer,Penile Cancer,Testicular Cancer

Sub Track

Therapeutics

Citation

J Clin Oncol 42, 2024 (suppl 4; abstr 417)

DOI

10.1200/JCO.2024.42.4_suppl.417

Abstract #

417

Poster Bd #

G20

Abstract Disclosures