Metastatic SMARCB1-Deficient Renal Medullary Carcinoma without Hemoglobinopathy with Durable and Dramatic Response to Pembrolizumab plus Lenvatinib: Case Report.

IF 0.7 Q4 ONCOLOGY
Case Reports in Oncology Pub Date : 2024-09-17 eCollection Date: 2024-01-01 DOI:10.1159/000540937
William McCamy, Maryam Yousefiasl, Maria Tretiakova, Minal Jagtiani, Evan Hall
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引用次数: 0

Abstract

Introduction: Renal medullary carcinoma (RMC) is a rare form of renal cell carcinoma (RCC) that is typically associated with a loss of function in SMARCB1 and diagnosis of sickle cell or other hemoglobinopathy. In rare cases, this disease can be seen in patients without hemoglobinopathy and is classified as "SMARCB1-deficient RMC without hemoglobinopathy" or referred to as "RCC unclassified with medullary phenotype" in some of the literature. Platinum-based cytotoxic chemotherapy is currently the recommended first-line treatment for this rare disease.

Case presentation: Here we report a 53-year-old male who was diagnosed with metastatic SMARCB1-deficient RMC without hemoglobinopathy after presenting with left flank and abdominal pain. After initiating first-line pembrolizumab and lenvatinib systemic therapy, imaging showed regression at 6 weeks. To date, this patient continues to show a near complete response to this treatment regimen.

Conclusion: To our knowledge, this is the first documented case of SMARCB1-deficient RMC without hemoglobinopathy to receive this treatment regimen and show such a response.

无血红蛋白病的转移性 SMARCB1 缺乏性肾髓样癌对 Pembrolizumab 加仑伐替尼有持久而显著的反应:病例报告。
导言:肾髓质癌(RMC)是一种罕见的肾细胞癌(RCC),通常与SMARCB1功能缺失和镰状细胞或其他血红蛋白病的诊断有关。在极少数情况下,这种疾病也会出现在没有血红蛋白病的患者身上,在一些文献中被归类为 "无血红蛋白病的SMARCB1缺失型RMC "或被称为 "未分类的髓样表型RCC"。以铂为基础的细胞毒化疗是目前治疗这种罕见疾病的一线推荐疗法:我们在此报告了一名 53 岁男性患者的病例,该患者因出现左翼和腹部疼痛而被诊断为无血红蛋白病的转移性 SMARCB1 缺失 RMC。在开始接受一线pembrolizumab和来伐替尼系统治疗后,6周时影像学显示病情有所缓解。迄今为止,该患者仍对这一治疗方案表现出近乎完全的反应:据我们所知,这是第一例接受这种治疗方案并显示出这种反应的无血红蛋白病的 SMARCB1 缺失 RMC 病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.40
自引率
12.50%
发文量
151
审稿时长
7 weeks
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