Department of Oncology, Faculty of Medicine and Dentistry, University Hospital Olomouc, Palacky University, 771 47 Olomouc, Czech Republic.
Department of Urology, Faculty of Medicine and Dentistry, University Hospital Olomouc, Palacky University, 771 47 Olomouc, Czech Republic.
Curr Oncol. 2022 Aug 3;29(8):5475-5488. doi: 10.3390/curroncol29080433.
Renal cell carcinoma with sarcomatoid dedifferentiation represents a rare histological entity characterized by aggressive behavior, limited efficacy of tyrosine kinase inhibitors or mTOR inhibitors, and poor outcome. The immune checkpoint inhibitor therapy regimen combining ipilimumab with nivolumab represents a new standard of care for this patient population due to a hitherto unprecedented response rate and overall survival. On the other hand, the role of cytoreductive nephrectomy in metastatic renal cell carcinoma, in particular, with sarcomatoid histology, remains controversial.
In the present case series, we report six patients with locally advanced or synchronous metastatic sarcomatoid renal cell carcinoma and intermediate or poor International Metastatic RCC Database Consortium (IMDC) risk score, five of whom were successfully subjected to cytoreductive nephrectomy.
All six patients received the combination regimen of ipilimumab with nivolumab. Five of these patients underwent upfront cytoreductive nephrectomy followed by systemic treatment without any significant delay, with a durable treatment outcome. Notably, two patients with poor prognostic features achieved a long-term major partial response to therapy. We also performed a review of the literature on optimal treatment strategies for patients with sarcomatoid renal cell carcinoma.
Herein, we highlight the feasibility of performing cytoreductive nephrectomy in patients with intermediate/poor prognosis metastatic renal cell carcinoma with sarcomatoid dedifferentiation followed by immunotherapy with ipilimumab and nivolumab. To enhance the chances of immunotherapy success, cytoreductive nephrectomy should also be considered for patients presenting with a disease with adverse prognostic parameters.
具有肉瘤样去分化的肾细胞癌是一种罕见的组织学实体,其特点是侵袭性行为、酪氨酸激酶抑制剂或 mTOR 抑制剂疗效有限以及预后不良。免疫检查点抑制剂联合伊匹单抗和纳武单抗的治疗方案代表了这一患者群体的新标准,因为其反应率和总生存率前所未有。另一方面,细胞减积性肾切除术在转移性肾细胞癌中的作用,特别是肉瘤样组织学,仍然存在争议。
在本病例系列中,我们报告了 6 例局部晚期或同步转移性肉瘤样肾细胞癌且具有中间或不良国际转移性肾细胞癌数据库联盟(IMDC)风险评分的患者,其中 5 例成功接受了细胞减积性肾切除术。
所有 6 例患者均接受了伊匹单抗联合纳武单抗的联合治疗方案。其中 5 例患者在接受系统治疗之前接受了细胞减积性肾切除术,没有明显的延迟,并且获得了持久的治疗效果。值得注意的是,2 例具有不良预后特征的患者对治疗产生了长期的主要部分缓解。我们还对肉瘤样肾细胞癌患者的最佳治疗策略进行了文献回顾。
在此,我们强调了在具有肉瘤样去分化的中间/不良预后转移性肾细胞癌患者中进行细胞减积性肾切除术的可行性,随后进行伊匹单抗和纳武单抗免疫治疗。为了提高免疫治疗成功的机会,对于具有不良预后参数的疾病患者,也应考虑进行细胞减积性肾切除术。