Clinical Characteristics, Management, and Outcomes of Patients with Renal Medullary Carcinoma: A Single-center Retrospective Analysis of 135 Patients.

IF 8.3 1区 医学 Q1 ONCOLOGY
Justin M Lebenthal, Panayiotis D Kontoyiannis, Andrew W Hahn, Zita D Lim, Priya Rao, Jessica P Cheng, Beei Chan, Najat C Daw, Rahul A Sheth, Jose A Karam, Chad Tang, Nizar M Tannir, Pavlos Msaouel
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引用次数: 0

Abstract

Background and objective: 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.

Methods: 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.

Key findings and limitations: 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.

Conclusions and clinical implications: 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.

Patient summary: 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.

肾髓样癌患者的临床特征、管理和疗效:对 135 例患者的单中心回顾性分析。
背景和目的: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有关,其不良预后仅在病例报告和小型系列病例中有所描述。我们报告了一大批 RMC 患者的疾病和管理特征以及当代生存结果:我们从 2003 年 1 月至 2023 年 12 月期间在 MD 安德森癌症中心接受治疗的所有 RMC 患者中回顾性地提取了数据。采用多变量 Cox 回归估算诊断期间的总生存率(OS):在135名患者(中位随访54.9个月)中,只有9名患者不伴有镰状血红蛋白病,被归类为肾细胞癌,未分类为髓样表型(RCCU-MP)。大多数患者(78%)出现转移性疾病,主要是腹膜后淋巴结转移(81.7%),血尿是镰状血红蛋白病相关肾细胞癌患者最常见的症状(60%)。诊断年生存率有所提高(调整后危险比为 0.70,95% 置信区间为 0.53-0.92,P = 0.01)。RCCU-MP发生在年龄稍大的患者中,中位生存期为诊断后19.5个月,未显示出右肾偏向性或男性占优势,且主要为白种人(89%)。这项研究是在一个中心进行的回顾性研究,因此存在局限性:RMC常伴有血尿,并极有可能扩散至腹膜后淋巴结。随着现代治疗方法的应用,患者的生存率正在不断提高。RCCU-MP非常罕见,侵袭性可能稍弱:肾髓质癌(RMC)是一种罕见的侵袭性肾癌亚型,主要困扰非洲裔的年轻男性和女性。有关患者人口统计学和疾病特征的数据十分有限。我们报告了本机构治疗 RMC 患者的经验。大多数 RMC 患者报告的第一个症状是血尿,癌症最常见的扩散部位是肾脏周围的淋巴结。采用现代治疗方法后,RMC 患者的寿命更长。
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来源期刊
CiteScore
15.50
自引率
2.40%
发文量
128
审稿时长
20 days
期刊介绍: Journal Name: European Urology Oncology Affiliation: Official Journal of the European Association of Urology Focus: First official publication of the EAU fully devoted to the study of genitourinary malignancies Aims to deliver high-quality research Content: Includes original articles, opinion piece editorials, and invited reviews Covers clinical, basic, and translational research Publication Frequency: Six times a year in electronic format
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