Ma Jennifer, Del Balzo Luke, Walch Henry, Khaleel Sari, Knezevic Andrea, Flynn Jessica, Zhang Zhigang, Eichholz Jordan, Doshi Sahil D, Voss Martin H, Freeman Benjamin, Ari Hakimi A, Lee Chung-Han, Bale Tejus A, Kelly Daniel, Mueller Boris A, Mann Justin, Yu Yao, Zinovoy Melissa, Chen Linda, Cuaron John, Khan Atif, Yamada Yoshiya, Shin Jacob Y, Beal Kathryn, Moss Nelson S, Carlo Maria I, Motzer Robert J, Imber Brandon S, Kotecha Ritesh R, Pike Luke R G
Department of Radiation Oncology and Brain Metastasis Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Radiation Oncology and Brain Metastasis Center, Memorial Sloan Kettering Cancer Center, New York, NY, USA; Medical College of Georgia, Augusta, GA, USA.
Eur Urol Oncol. 2025 Apr;8(2):338-346. doi: 10.1016/j.euo.2024.07.005. Epub 2024 Aug 5.
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.
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.
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.
肾细胞癌(RCC)脑转移瘤(BMs)的分子特征尚未得到充分表征。随着全身治疗的进展改善了总生存期(OS),包括立体定向放射外科(SRS)在内的局部区域治疗的有效管理至关重要。
在一个大型患者队列中确定接受SRS治疗的RCC BMs的临床基因组特征。
设计、设置和参与者:对2010年1月1日至2021年3月31日期间接受SRS治疗的所有RCC BM患者进行了单机构回顾性分析。
对RCC BMs进行SRS。
进行二代测序以确定在BM患者中更普遍的基因改变。使用Cox比例风险模型对每位患者评估临床因素和在≥10%的样本中发生改变的基因,对于每个个体BM,使用具有死亡竞争风险的聚类竞争风险回归进行评估。
91例RCC BM患者接受了SRS治疗212个BMs,存活患者的中位随访时间为38.8个月。颅内无进展生存期和OS的中位数分别为7.8(四分位间距[IQR]5.7 - 11)和21(IQR 16 - 32)个月。SRS后12个月实现了83%的持久局部控制,在3个月评估时最初符合影像学进展标准的病变中,59%在6个月评估时将被认为是假性进展。将BM +患者与BM -患者在基因和通路水平的基因组改变进行比较,发现磷酸肌醇3激酶(PI3K)通路改变在BM +患者中更普遍(43%对16%,p = 0.001,q = 0.01),其中大多数是PTEN改变(17%对2.7%,p = 0.003,q = 0.041)。
据我们所知,这是研究RCC BMs基因组特征的最大规模研究,也是唯一一项有颅内结局注释的此类研究。SRS可对BMs提供持久的瘤床局部控制。认识到SRS后的假性进展对于确保适当管理至关重要。PI3K通路改变的发生率在BM +患者中比在BM -患者中更普遍,值得在前瞻性研究中进一步探究。
我们在一个大型转诊中心检查了肾癌患者脑转移瘤放射治疗的结果。我们发现放疗能很好地控制脑肿瘤,并且某些基因突变可能在脑转移患者中更常见。