Renal Collision Tumor Composed of Clear Cell Carcinoma and Collecting Duct Carcinoma Treated with Nivolumab and Ipilimumab: Case Report and Literature Review

IF 0.3 Q4 ONCOLOGY International Journal of Surgery-Oncology Pub Date : 2021-08-11 DOI:10.29337/ijsonco.128
C. Szeto, Muhammad Krenawi, G. Ben-Arie, Benzion Samueli, O. Lavon, Shadi Abu-Swis, M. Zemel, D. Levitas, W. Kian, E. Mazor
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Abstract

Introduction and importance: Collision tumors refer to the phenomenon where two or more different and unrelated tumors occur in the same location of an organ and form a single lesion. We present the first case of renal collision tumors composed of clear cell carcinoma (ccRCC) and collecting duct carcinoma (CDC) treated with combined therapy of nivolumab and ipilimumab. Case presentation: An 89-year-old male presented to the emergency room with back pain. Imaging studies demonstrated a large tumor in the left kidney with renal vein thrombosis. After radical nephrectomy, the histopathological report showed collision tumors with ccRCC and CDC components. The patient was included in a treatment protocol based on nivolumab (220 mg) and ipilimumab (73 mg) every 21 days, however, obtaining no clinical responses after 5 cycles of treatments. Clinical Discussion: Immune checkpoint inhibitors have become a new standard of care for patients with advanced ccRCC. However, current literatures showed inconclusive evidence on the efficacy of immune checkpoint inhibitor for metastatic CDC. As collision tumors with ccRCC and CDC components were infrequently reported in the literature, we also discuss the histological and immunohistochemical findings, clinical outcomes, and a literature review on this type of renal collision tumors. Conclusion: CDC is a rare and highly aggressive type of renal neoplasms, with limited treatment choices. More studies are needed to evaluate the efficacy of immune checkpoint inhibitors on CDC and its associated collision tumors. Highlights: Collecting duct carcinoma is a rare and highly aggressive type of renal neoplasms, with a poor clinical outcome. Radical nephrectomy alone is rarely curative. The use of immune checkpoint inhibitors for collecting duct carcinoma needs further evaluation. The use of HMWCK as a histologic marker for differential diagnosis of collecting duct carcinoma may need to be evaluated.
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纳武单抗和伊匹利单抗联合治疗肾透明细胞癌和集管癌合并的碰撞瘤:1例报告及文献复习
简介及重要性:碰撞瘤是指两个或两个以上不同且不相关的肿瘤发生在同一器官的同一部位,形成单一病变的现象。我们报告了第一例由透明细胞癌(ccRCC)和集管癌(CDC)组成的肾碰撞肿瘤,采用纳武单抗和伊匹单抗联合治疗。病例介绍:一名89岁男性因背部疼痛被送往急诊室。影像学检查显示左肾一大肿瘤伴肾静脉血栓形成。根治性肾切除术后,组织病理学报告显示碰撞肿瘤具有ccRCC和CDC成分。患者被纳入基于纳武单抗(220 mg)和伊匹单抗(73 mg)每21天的治疗方案,然而,在5个周期的治疗后没有获得临床反应。临床讨论:免疫检查点抑制剂已成为晚期ccRCC患者治疗的新标准。然而,目前的文献显示,免疫检查点抑制剂对转移性CDC的疗效尚无定论。由于含有ccRCC和CDC成分的碰撞瘤在文献中很少报道,我们也讨论了这类肾碰撞瘤的组织学和免疫组化表现、临床结果和文献综述。结论:CDC是一种罕见的高侵袭性肾肿瘤,治疗选择有限。需要更多的研究来评估免疫检查点抑制剂对CDC及其相关碰撞肿瘤的疗效。摘要集管癌是一种罕见且侵袭性强的肾肿瘤,临床预后较差。单纯根治性肾切除术很少能治愈。使用免疫检查点抑制剂收集导管癌需要进一步的评估。使用HMWCK作为鉴别诊断收集管癌的组织学标记可能需要评估。
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