Clinical Outcomes and Targeted Genomic Analysis of Renal Cell Carcinoma Brain Metastases Treated with Stereotactic Radiosurgery.

Brain metastases Genomics Kidney cancer Phosphoinositide 3-kinase Pseudoprogression Radiation Renal cell carcinoma Stereotactic radiosurgery mTOR

Journal

European urology oncology
ISSN: 2588-9311
Titre abrégé: Eur Urol Oncol
Pays: Netherlands
ID NLM: 101724904

Informations de publication

Date de publication:
05 Aug 2024
Historique:
received: 02 05 2023
revised: 28 06 2024
accepted: 09 07 2024
medline: 7 8 2024
pubmed: 7 8 2024
entrez: 6 8 2024
Statut: aheadofprint

Résumé

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). To identify clinicogenomic features of RCC BMs treated with SRS in a large patient cohort. A single-institution retrospective analysis was conducted of all RCC BM patients treated with SRS from January 1, 2010 to March 31, 2021. SRS for RCC BMs. 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. 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). 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. 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.

Sections du résumé

BACKGROUND 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 OBJECTIVE
To identify clinicogenomic features of RCC BMs treated with SRS in a large patient cohort.
DESIGN, SETTING, AND PARTICIPANTS METHODS
A single-institution retrospective analysis was conducted of all RCC BM patients treated with SRS from January 1, 2010 to March 31, 2021.
INTERVENTION METHODS
SRS for RCC BMs.
OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS METHODS
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 CONCLUSIONS
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 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 RESULTS
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.

Identifiants

pubmed: 39107179
pii: S2588-9311(24)00178-0
doi: 10.1016/j.euo.2024.07.005
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 European Association of Urology. Published by Elsevier B.V. All rights reserved.

Auteurs

Jennifer Ma (J)

Department of Radiation Oncology and Brain Metastasis Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Luke Del Balzo (L)

Department of Radiation Oncology and Brain Metastasis Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA; Medical College of Georgia, Augusta, GA, USA.

Henry Walch (H)

Department of Epidemiology-Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Sari Khaleel (S)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Andrea Knezevic (A)

Department of Epidemiology-Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Jessica Flynn (J)

Department of Epidemiology-Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Zhigang Zhang (Z)

Department of Epidemiology-Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Jordan Eichholz (J)

Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Sahil D Doshi (SD)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Martin H Voss (MH)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Benjamin Freeman (B)

Department of Surgical Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

A Ari Hakimi (A)

Department of Surgical Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Chung-Han Lee (CH)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Tejus A Bale (TA)

Department of Molecular Diagnostics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Daniel Kelly (D)

Technology Division, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Boris A Mueller (BA)

Department of Radiation Oncology and Brain Metastasis Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Justin Mann (J)

Department of Radiation Oncology and Brain Metastasis Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Yao Yu (Y)

Department of Radiation Oncology and Brain Metastasis Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Melissa Zinovoy (M)

Department of Radiation Oncology and Brain Metastasis Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Linda Chen (L)

Department of Radiation Oncology and Brain Metastasis Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

John Cuaron (J)

Department of Radiation Oncology and Brain Metastasis Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Atif Khan (A)

Department of Radiation Oncology and Brain Metastasis Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Yoshiya Yamada (Y)

Department of Radiation Oncology and Brain Metastasis Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Jacob Y Shin (JY)

Department of Radiation Oncology and Brain Metastasis Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Kathryn Beal (K)

Department of Radiation Oncology and Brain Metastasis Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Nelson S Moss (NS)

Department of Neurosurgery and Brain Metastasis Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Maria I Carlo (MI)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Robert J Motzer (RJ)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Brandon S Imber (BS)

Department of Radiation Oncology and Brain Metastasis Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Ritesh R Kotecha (RR)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Luke R G Pike (LRG)

Department of Radiation Oncology and Brain Metastasis Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA. Electronic address: Pikel@mskcc.org.

Classifications MeSH