Multimodal Treatments for Brain Metastases from Renal Cell Carcinoma: Results of a Multicentric Retrospective Study

Author:

Navarria Pierina1ORCID,Pessina Federico23,Minniti Giuseppe4,Franzese Ciro13ORCID,Marini Beatrice1,D’agostino Giuseppe1,Badalamenti Marco1,Raspagliesi Luca2,Reggiori Giacomo1,Lobefalo Francesca1,Fariselli Laura5ORCID,Franceschini Davide1ORCID,Bellu Luisa1ORCID,Clerici Elena1ORCID,Pinzi Valentina5ORCID,Scorsetti Marta13

Affiliation:

1. Radiotherapy and Radiosurgery Department, IRCCS Humanitas Research Hospital, Rozzano, 20089 Milan, Italy

2. Neurosurgery Department, IRCCS Humanitas Research Hospital, Rozzano, 20089 Milan, Italy

3. Department of Biomedical Sciences, Humanitas University, 20089 Milan, Italy

4. Department of Radiological Sciences, Oncology & Pathology, Sapienza University of Rome, 20089 Rome, Italy

5. Radiotherapy Unit, Istituto Neurologico Fondazione “Carlo Besta”, 20089 Milan, Italy

Abstract

The aim of this study was to evaluate the clinical outcomes of a large series of brain metastatic renal cell carcinoma (BMRCC) patients treated in three Italian centers. Methods: A total of 120 BMRCC patients with a total of 176 lesions treated were evaluated. Patients received surgery plus postoperative HSRS, single-fraction SRS, or hypofractionated SRS (HSRS). Local control (LC), brain distant failure (BDF), overall survival (OS), toxicities, and prognostic factors were assessed. Results: The median follow-up time was 77 months (range 16–235 months). Surgery plus HSRS was performed in 23 (19.2%) cases, along with SRS in 82 (68.3%) and HSRS in 15 (12.5%). Seventy-seven (64.2%) patients received systemic therapy. The main total dose and fractionation used were 20–24 Gy in single fraction or 32–30 Gy in 4–5 daily fractions. Median LC time and 6 month and 1, 2 and 3 year LC rates were nr, 100%, 95.7% ± 1.8%, 93.4% ± 2.4%, and 93.4% ± 2.4%. Median BDF time and 6 month and 1, 2 and 3 year BDF rates were n.r., 11.9% ± 3.1%, 25.1% ± 4.5%, 38.7% ± 5.5%, and 44.4% ± 6.3%, respectively. Median OS time and 6 month and 1, 2 and 3 year OS rates were 16 months (95% CI: 12–22), 80% ± 3.6%, 58.3% ± 4.5%, 30.9% ± 4.3%, and 16.9% ± 3.6, respectively. No severe neurological toxicities occurred. Patients with a favorable/intermediate IMDC score, a higher RCC-GPA score, an early occurrence of BMs from primary diagnosis, absence of EC metastases, and a combined local treatment (surgery plus adjuvant HSRS) had a better outcome. Conclusions: SRS/HSRS is proven to be an effective local treatment for BMRCC. A careful evaluation of prognostic factors is a valid step to manage the optimal therapeutic strategy for BMRCC patients.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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