Shah Amishi Y, Karam Jose A, Malouf Gabriel G, Rao Priya, Lim Zita D, Jonasch Eric, Xiao Lianchun, Gao Jianjun, Vaishampayan Ulka N, Heng Daniel Y, Plimack Elizabeth R, Guancial Elizabeth A, Fung Chunkit, Lowas Stefanie R, Tamboli Pheroze, Sircar Kanishka, Matin Surena F, Kimryn Rathmell W, Wood Christopher G, Tannir Nizar M
MD Anderson Cancer Center, Houston, TX, USA.
Groupe Hospitalier Pitié-Salpêtrière, University Pierre and Marie Curie, Paris, France.
BJU Int. 2017 Dec;120(6):782-792. doi: 10.1111/bju.13705. Epub 2016 Dec 9.
To describe the management strategies and outcomes of patients with renal medullary carcinoma (RMC) and characterise predictors of overall survival (OS).
RMC is a rare and aggressive malignancy that afflicts young patients with sickle cell trait; there are limited data on management to date. This is a study of patients with RMC who were treated in 2000-2015 at eight academic institutions in North America and France. The Kaplan-Meier method was used to estimate OS, measured from initial RMC diagnosis to date of death. Cox regression analysis was used to determine predictors of OS.
In all, 52 patients (37 males) were identified. The median (range) age at diagnosis was 28 (9-48) years and 49 patients (94%) had stage III/IV. The median OS for all patients was 13.0 months and 38 patients (75%) had nephrectomy. Patients who underwent nephrectomy had superior OS compared to patients who were treated with systemic therapy only (median OS 16.4 vs 7.0 months, P < 0.001). In all, 45 patients received chemotherapy and 13 (29%) had an objective response; 28 patients received targeted therapies, with 8-week median therapy duration and no objective responses. Only seven patients (13%) survived for >24 months.
RMC carries a poor prognosis. Chemotherapy provides palliation and remains the mainstay of therapy, but <20% of patients survive for >24 months, underscoring the need to develop more effective therapy for this rare tumour. In this study, nephrectomy was associated with improved OS.
描述肾髓质癌(RMC)患者的管理策略及预后,并确定总生存期(OS)的预测因素。
RMC是一种罕见的侵袭性恶性肿瘤,主要影响具有镰状细胞特征的年轻患者;目前关于其治疗的数据有限。本研究纳入了2000年至2015年期间在北美和法国的八家学术机构接受治疗的RMC患者。采用Kaplan-Meier法估计OS,从RMC初始诊断至死亡日期进行测量。使用Cox回归分析确定OS的预测因素。
共纳入52例患者(37例男性)。诊断时的中位(范围)年龄为28(9 - 48)岁,49例患者(94%)为III/IV期。所有患者的中位OS为13.0个月,38例患者(75%)接受了肾切除术。接受肾切除术的患者的OS优于仅接受全身治疗的患者(中位OS 16.4个月对7.0个月,P < 0.001)。共有45例患者接受了化疗,13例(29%)有客观缓解;28例患者接受了靶向治疗,中位治疗持续时间为8周,无客观缓解。只有7例患者(13%)存活超过24个月。
RMC预后较差。化疗可提供姑息治疗,仍是主要治疗手段,但<20%的患者存活超过24个月,这凸显了为这种罕见肿瘤开发更有效治疗方法的必要性。在本研究中,肾切除术与OS改善相关。