Kobayashi H, Obata K
Department of Urology, Japanese Red Cross Nagoya Second Hospital.
Cancer Chemother Pharmacol. 1994;35 Suppl:S14-7. doi: 10.1007/BF00686912.
From 1980 to 1991, 59 patients with advanced urothelial cancer (pathological stage, > pT3) underwent radical operations. Of these 59 patients, 33 had nodal involvement. This study focused on those 33 patients with nodal involvement. The primary site was the urinary bladder in 20 patients and the upper urinary tract (renal pelvis and/or ureter) in 13. In all, 13 patients underwent adjuvant chemotherapy with an M-VAC or M-VEC [methotrexate (M), vinblastine, doxorubicin (ADM) or epirubicin, and cisplatin (CDDP)] regimen, and another 8 patients were treated with other insufficient chemotherapies [CDDP + ADM or CDDP + ADM + etoposide (VP-16)]. A group of 12 patients did not receive any additional treatment. Most of the patients in the M-VAC and M-VEC groups received more than 2 cycles of the regimen (median, 3.2 cycles; range, 1-9 cycles). The overall 5-year survival rate of the M-VAC and M-VEC group was 31%, whereas the rate was 0 for the other insufficient-chemotherapy groups and the no-chemotherapy group. Of the 13 patients in the M-VAC group, 4 (31%) patients were alive without disease progression and 9 (69%) were dead due to progressive disease. In the other groups, only 1 patient was alive without progression. Our results suggest that adjuvant M-VAC or M-VEC chemotherapy may extend the median survival of patients with advanced urothelial cancer, but it failed to reduce the rate of cancer death.
1980年至1991年期间,59例晚期尿路上皮癌患者(病理分期>pT3)接受了根治性手术。在这59例患者中,33例有淋巴结转移。本研究聚焦于这33例有淋巴结转移的患者。原发部位为膀胱的有20例患者,上尿路(肾盂和/或输尿管)的有13例。总共有13例患者接受了以M-VAC或M-VEC[甲氨蝶呤(M)、长春碱、阿霉素(ADM)或表阿霉素和顺铂(CDDP)]方案进行的辅助化疗,另外8例患者接受了其他不充分的化疗[CDDP + ADM或CDDP + ADM +依托泊苷(VP-16)]。12例患者未接受任何额外治疗。M-VAC和M-VEC组的大多数患者接受了超过2个周期的该方案化疗(中位数为3.2个周期;范围为1 - 9个周期)。M-VAC和M-VEC组的总体5年生存率为31%,而其他不充分化疗组和未化疗组的生存率为0。M-VAC组的13例患者中,4例(31%)患者存活且无疾病进展,9例(69%)因疾病进展死亡。在其他组中,只有1例患者存活且无进展。我们的结果表明,辅助性M-VAC或M-VEC化疗可能会延长晚期尿路上皮癌患者的中位生存期,但未能降低癌症死亡率。