Staehler Michael, Haseke N, Schöppler G, Stadler T, Karl A, Siebels M, Ihrler S, Stief C G
Department of Urology, University of Munich, Klinikum Grosshadern, Marchioninistr. 15, 81377 München, Germany.
Eur J Med Res. 2008 Nov 24;13(11):531-5.
Carcinoma of the collecting ducts of Bellini of the kidney (CDC) is very rare but among the most aggressive urological entities. Standard therapy is not well defined with questionable efficacy.
We present two cases of male patients (49 and 66 years old) with pT3a pN2 CDC treated with a combination of cisplatin plus gemcitabine in an adjuvant setting. Following recurrence the multi-kinase inhibitor sunitinib was administered.
Radical nephrectomy with lymphadenectomy revealed CDC in stage pT3a pN2 M0 G3 R0 in both patients. 4 courses of adjuvant chemotherapy with cisplatin 70 mg/m superset2 and gemcitabine 1,500 mg/m superset2 were given. Side effects according to the NCI 3.0 common toxicity criteria were limited to grade 2 asthenia and grade 2 thrombozytopenia/leucopenia. Restaging revealed local recurrence and lymph node metastases. Both patients were re-operated and metastatic CDC was found. Second line therapy with sunitinb malatat (Sutent superset, Pfizer Inc. U.S.) at 50mg p.o. was given. Grade 3 leucopenia and thrombocytopenia and grade 2 asthenia and mucositis were not dose-limiting. After two cycles multiple liver, lung and bone metastases and mediastinal lymphopathy occured. 8 weeks later the patients died with a survival of 8 months from initial diagnosis.
Adjuvant gemcitabine plus cisplatin did not delay recurrence of CDC after surgery. Metastasectomy either had no influence on the course of disease. Anti-angiogenetic therapy with sunitinib treatment was not effective, possibly related to a low vascular density (CD31 expression) in CDC.
肾集合管癌(CDC)非常罕见,但却是最具侵袭性的泌尿系统疾病之一。标准治疗方法尚不明确,疗效也存在疑问。
我们报告两例男性患者(年龄分别为49岁和66岁),患有pT3a pN2期的CDC,在辅助治疗中接受了顺铂加吉西他滨的联合治疗。复发后给予多激酶抑制剂舒尼替尼。
两例患者行根治性肾切除术加淋巴结清扫术,病理分期均为pT3a pN2 M0 G3 R0期的CDC。给予4个周期的辅助化疗,顺铂剂量为70mg/m²,吉西他滨剂量为1500mg/m²。根据美国国立癌症研究所(NCI)3.0版常见毒性标准,副作用仅限于2级乏力和2级血小板减少/白细胞减少。再次分期显示局部复发和淋巴结转移。两名患者均再次手术,发现有转移性CDC。给予二线治疗,口服舒尼替尼(索坦,辉瑞公司,美国),剂量为50mg。3级白细胞减少和血小板减少以及2级乏力和粘膜炎均未达到剂量限制毒性。两个周期后出现多发肝、肺和骨转移以及纵隔淋巴结肿大。8周后,患者死亡,从初始诊断起存活8个月。
辅助性吉西他滨加顺铂治疗未能延迟CDC术后复发。转移灶切除术对疾病进程没有影响。舒尼替尼抗血管生成治疗无效,可能与CDC中血管密度低(CD31表达)有关。