The University of Queensland School of Medicine, Ochsner Clinical School, New Orleans, LA.
Ochsner Cancer Institute, New Orleans, LA.
Clin Genitourin Cancer. 2021 Dec;19(6):e395-e400. doi: 10.1016/j.clgc.2021.08.004. Epub 2021 Aug 27.
Renal medullary carcinoma (RMC) is a very rare, aggressive neoplasm occurring almost exclusively in adolescents and young adults with sickle cell trait. Given the rare nature of this tumor, accounting for less than 0.5% of all renal carcinomas, most of the published data on therapies is from case reports and small case series, and current treatments are insufficient, with most patients succumbing to their disease in months. We report our experience with a cytotoxic chemotherapy regimen consisting of platinum-based therapy, doxorubicin, and bortezomib.
Three patients with metastatic RMC at a single institution were treated off-label with a perioperative chemotherapy regimen for 4 cycles of 2 alternating regimens: regimen A consisting of cisplatin, doxorubicin, and bortezomib; regimen B consisting of carboplatin, paclitaxel, and gemcitabine. A radical nephrectomy was performed on all patients. Surveillance imaging was performed on all patients to assess response and disease burden. Patients received up to 12 months of maintenance therapy with everolimus.
Three African American patients - 2 males and 1 female aged 14, 28, and 31 - with sickle cell trait and metastatic disease were treated with this regimen. The median follow-up was 18 months. All had resection of the primary tumor - 2 patients after receiving neoadjuvant therapy, and one patient underwent resection prior to referral. All 3 patients achieved complete responses based on imaging, 2 of which lasted for 12 months, and another is still in remission over 7 years after diagnosis.
This regimen of alternating cycles of platinum-based chemotherapy with bortezomib appeared to be active against RMC and was generally well-tolerated. Given the extremely rare nature of this disease and dismal prognosis, new treatment modalities should be pursued, and whenever possible, patients should be enrolled in a clinical trial. We propose that a multiinstitution clinical trial of this regiment may be warranted.
肾髓质癌(RMC)是一种非常罕见的侵袭性肿瘤,几乎仅发生于镰状细胞特征的青少年和年轻成人。鉴于这种肿瘤的罕见性质,占所有肾癌的比例不到 0.5%,大多数关于治疗的已发表数据来自病例报告和小病例系列,目前的治疗方法不足,大多数患者在数月内死于该病。我们报告了我们在一个机构中使用包含铂类药物治疗、多柔比星和硼替佐米的细胞毒性化疗方案的经验。
3 名患有转移性 RMC 的患者在该机构接受了标签外治疗,使用了 4 个周期的 2 种交替方案的围手术期化疗方案:方案 A 由顺铂、多柔比星和硼替佐米组成;方案 B 由卡铂、紫杉醇和吉西他滨组成。所有患者均进行了根治性肾切除术。对所有患者进行监测影像学检查,以评估反应和疾病负担。所有患者接受长达 12 个月的依维莫司维持治疗。
3 名患有镰状细胞特征和转移性疾病的非裔美国患者(2 名男性和 1 名女性,年龄分别为 14、28 和 31 岁)接受了该方案治疗。中位随访时间为 18 个月。所有患者均切除了原发肿瘤——2 名患者在接受新辅助治疗后切除,1 名患者在转诊前切除。所有 3 名患者的影像学检查均达到完全缓解,其中 2 名患者的缓解持续时间为 12 个月,另 1 名患者在诊断后 7 年仍处于缓解状态。
这种铂类药物联合硼替佐米交替周期化疗方案似乎对 RMC 有效,且总体耐受性良好。鉴于这种疾病的罕见性质和预后极差,应寻求新的治疗方法,只要有可能,患者应参加临床试验。我们建议,可能有必要进行该方案的多机构临床试验。