Synapse - Clinical outcomes and targeted genomic analysis of renal cell carcinoma brain metastases treated with stereotactic radiosurgery

Clinical outcomes and targeted genomic analysis of renal cell carcinoma brain metastases treated with stereotactic radiosurgery Journal Article

Authors:	Ma, J.; del Balzo, L.; Walch, H.; Khaleel, S.; Knezevic, A.; Flynn, J.; Zhang, Z.; Eichholz, J.; Doshi, S. D.; Voss, M. H.; Freeman, B.; Hakimi, A. A.; Lee, C. H.; Bale, T. A.; Kelly, D.; Mueller, B. A.; Mann, J.; Yu, Y.; Zinovoy, M.; Chen, L.; Cuaron, J.; Khan, A.; Yamada, Y.; Shin, J. Y.; Beal, K.; Moss, N. S.; Carlo, M. I.; Motzer, R. J.; Imber, B. S.; Kotecha, R. R.; Pike, L. R. G.
Article Title:	Clinical outcomes and targeted genomic analysis of renal cell carcinoma brain metastases treated with stereotactic radiosurgery
Abstract:	Background: Molecular profiles of renal cell carcinoma (RCC) brain metastases (BMs) are not well characterized. Effective management with locoregional therapies, including stereotactic radiosurgery (SRS), is critical as systemic therapy advancements have improved overall survival (OS). Objective: To identify clinicogenomic features of RCC BMs treated with SRS in a large patient cohort. Design, setting, and participants: A single-institution retrospective analysis was conducted of all RCC BM patients treated with SRS from January 1, 2010 to March 31, 2021. Intervention: SRS for RCC BMs. Outcome measurements and statistical analysis: Next-generation sequencing was performed to identify gene alterations more prevalent in BM patients. Clinical factors and genes altered in >= 10% of samples were assessed per patient using Cox proportional hazards models and per individual BM using clustered competing risks regression with competing risk of death. Results and limitations: Ninety-one RCC BM patients underwent SRS to 212 BMs, with a median follow-up of 38.8 mo for patients who survived. The median intracranial progression-free survival and OS were 7.8 (interquartile range [IQR] 5.7-11) and 21 (IQR 16-32) mo, respectively. Durable local control of 83% was achieved at 12 mo after SRS, and 59% of lesions initially meeting the radiographic criteria for progression at 3-mo evaluation would be considered to represent pseudoprogression at 6-mo evaluation. A comparison of genomic alterations at both the gene and the pathway level for BM+ patients compared with BM- patients revealed phosphoinositide 3-kinase (PI3K) pathway alterations to be more prevalent in BM+ patients (43% vs 16%, p = 0.001, q = 0.01), with the majority being PTEN alterations (17% vs 2.7%, p = 0.003, q = 0.041). Conclusions: To our knowledge, this is the largest study investigating genomic profiles of RCC BMs and the only such study with annotated intracranial outcomes. SRS provides durable in-field local control of BMs. Recognizing post-SRS pseudoprogression is crucial to ensure appropriate management. The incidence of PI3K pathway alterations is more prevalent in BM+ patients than in BM- patients and warrants further investigation in a prospective setting. Patient summary: We examined the outcomes of radiotherapy for the treatment of brain metastases in kidney cancer patients at a single large referral center. We found that radiation provides good control of brain tumors, and certain genetic mutations may be found more commonly in patients with brain metastasis. (c) 2024 European Association of Urology. Published by Elsevier B.V. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
Keywords:	radiation; renal cell carcinoma; genomics; stereotactic radiosurgery; kidney cancer; checkpoint; brain metastases; pseudoprogression; inhibition; combination; cancer; phosphoinositide 3-kinase mtor
Journal Title:	European Urology Oncology
Volume:	8
Issue:	2
ISSN:	2588-9311
Publisher:	Elsevier BV
Date Published:	2025-04-01
Start Page:	338
End Page:	346
Language:	English
ACCESSION:	WOS:001452190000001
DOI:	10.1016/j.euo.2024.07.005
PROVIDER:	wos
PUBMED:	39107179
Notes:	Article -- MSK Cancer Center Support Grant (P30 CA008748) acknowledged in PDF -- MSK corresponding author is Luke Pike -- Source: Wos