Sella A, Flex D, Gafni D, Rabinovitz O, Sulkes A, Baniel J
Dept. of Oncology, Rabin Medical Center, Petah Tikva.
Harefuah. 1999 Feb 15;136(4):268-71, 340, 339.
The treatment of metastatic urothelial cancer is based on the combination of cisplatin, methotrexate, vinblastine and adriamycin (M-VAC). From November 1994 to May 1997 we treated 25 patients (51 men, 3 women, aged 50-77) with M-VAC. The tumor originated from the urinary bladder in 14 (56%) and the upper urinary tract in 11 (44%). Disease sites included: primary--5 (25%), lymph nodes--17 (68%), lungs--10 (40%), bones--8 (32%), pelvic mass and liver each--4 (16%), with an overall median of 2 (1-5) sites per patient. 9 patients (38%) had complete responses and 8 (32%) had partial responses, for an overall response rate of 68% (95% CI 48.5%-85%). The median duration of response was 15.3 (1.6-29.6+) months. Median survival of responders was 19.1 (4.8-35.7+) months compared to 6.2 (0.7-11.2) for the non-responders (p < 0.05). 13 (52%) of patients are alive, of whom 8 (32%) are free of disease and 5 with a single metastatic site on presentation at follow-up. In the 118 treatment cycles we observed grade III-IV toxicity: myelosuppression 53 (45%), thrombocytopenia 4 (3%), stomatitis 8 (6.7%), diarrhea 3 (2.5%). There were 22 infectious episodes and 1 patient died of sepsis. We achieved a high response rate with the combination M-VAC. However, only a third had long-term disease-free states and treatment was associated with excessive toxicity. Therapeutic approaches with new agents are required to improve the response rate and toxicity.
转移性尿路上皮癌的治疗是以顺铂、甲氨蝶呤、长春碱和阿霉素(M-VAC)联合用药为基础。1994年11月至1997年5月,我们用M-VAC治疗了25例患者(51名男性,3名女性,年龄50 - 77岁)。肿瘤起源于膀胱的有14例(56%),起源于上尿路的有11例(44%)。疾病部位包括:原发灶——5例(25%),淋巴结——17例(68%),肺——10例(40%),骨——8例(32%),盆腔肿块和肝脏各4例(16%),每位患者受累部位的总体中位数为2(1 - 5)个。9例患者(38%)完全缓解,8例(32%)部分缓解,总缓解率为68%(95%可信区间48.5% - 85%)。缓解持续时间的中位数为15.3(1.6 - 29.6 +)个月。缓解者的中位生存期为19.1(4.8 - 35.7 +)个月,相比之下,未缓解者为6.2(0.7 - 11.2)个月(p < 0.05)。13例(52%)患者存活,其中8例(32%)无疾病,5例在随访时呈现单个转移部位。在118个治疗周期中,我们观察到Ⅲ - Ⅳ级毒性反应:骨髓抑制53例(45%),血小板减少4例(3%),口腔炎8例(6.7%),腹泻3例(2.5%)。有22次感染发作,1例患者死于败血症。我们用M-VAC联合用药取得了较高的缓解率。然而,只有三分之一的患者达到长期无病状态,且治疗伴有过度毒性。需要采用新药物的治疗方法来提高缓解率并降低毒性。