Lebenthal Justin M, Kontoyiannis Panayiotis D, Hahn Andrew W, Lim Zita D, Rao Priya, Cheng Jessica P, Chan Beei, Daw Najat C, Sheth Rahul A, Karam Jose A, Tang Chad, Tannir Nizar M, Msaouel Pavlos
Division of Cancer Medicine, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
The University of Texas Health Science Center at Houston, Houston, TX, USA.
Eur Urol Oncol. 2025 Apr;8(2):315-323. doi: 10.1016/j.euo.2024.07.002. Epub 2024 Jul 15.
SMARCB1-deficient renal medullary carcinoma (RMC) is a rare kidney cancer associated with sickle cell hemoglobinopathies with poor outcomes described only in case reports and small series. We report disease and management characteristics as well as contemporary survival outcomes in a large cohort of patients with RMC.
Data were extracted retrospectively from all patients with RMC treated at MD Anderson Cancer Center between January 2003 and December 2023. Multivariable Cox regression was used to estimate overall survival (OS) by diagnosis period.
Among 135 patients (median follow-up of 54.9 mo), only nine did not harbor a sickle hemoglobinopathy and were categorized as having renal cell carcinoma, unclassified with medullary phenotype (RCCU-MP). Most patients (78%) presented with metastatic disease, predominantly to the retroperitoneal lymph nodes (81.7%), and hematuria was the most frequent presenting symptom (60%) in RMC associated with sickle hemoglobinopathy. Survival outcomes improved by diagnosis year (adjusted hazard ratio 0.70, 95% confidence interval 0.53-0.92, p = 0.01). RCCU-MP occurred in slightly older patients with median OS of 19.5 mo from diagnosis, did not show a predilection to the right kidney or male predominance, and afflicted mainly Caucasians (89%). The study is limited by its retrospective nature conducted at one center.
RMC frequently presents with hematuria and is highly likely to spread to the retroperitoneal lymph nodes. Survival outcomes are improving with contemporary management. RCCU-MP is very rare and may be slightly less aggressive.
Renal medullary carcinoma (RMC) is a rare and aggressive subtype of kidney cancer afflicting primarily young men and women of African descent. There exist limited data regarding patient demographics and disease characteristics. We reported our institution's experience in treating patients with RMC. The first symptom most patients with RMC reported was blood in the urine, and the most common places where the cancer spread were the lymph nodes around the kidney. Patients with RMC are living longer with contemporary treatments.
SMARCB1缺陷型肾髓质癌(RMC)是一种罕见的肾癌,与镰状细胞血红蛋白病相关,预后较差,仅在病例报告和小系列研究中有描述。我们报告了一大群RMC患者的疾病和管理特征以及当代生存结果。
回顾性提取2003年1月至2023年12月在MD安德森癌症中心接受治疗的所有RMC患者的数据。采用多变量Cox回归按诊断时间估计总生存期(OS)。
在135例患者中(中位随访54.9个月),只有9例不伴有镰状血红蛋白病,被归类为肾细胞癌,髓质表型未分类(RCCU-MP)。大多数患者(78%)表现为转移性疾病,主要转移至腹膜后淋巴结(81.7%),血尿是与镰状血红蛋白病相关的RMC中最常见的首发症状(60%)。生存结果随诊断年份有所改善(调整后风险比0.70,95%置信区间0.53 - 0.92,p = 0.01)。RCCU-MP发生在年龄稍大的患者中,诊断后中位OS为19.5个月,未显示出对右肾的偏好或男性优势,主要累及白种人(89%)。该研究受限于在单一中心进行的回顾性研究性质。
RMC常表现为血尿,极易扩散至腹膜后淋巴结。当代治疗使生存结果有所改善。RCCU-MP非常罕见,侵袭性可能稍低。
肾髓质癌(RMC)是一种罕见且侵袭性强的肾癌亚型,主要影响非洲裔年轻男女。关于患者人口统计学和疾病特征的数据有限。我们报告了我们机构治疗RMC患者的经验。大多数RMC患者报告的首个症状是血尿,癌症最常见的扩散部位是肾周围的淋巴结。当代治疗使RMC患者的生存期延长。