Saxman S B, Propert K J, Einhorn L H, Crawford E D, Tannock I, Raghavan D, Loehrer P J, Trump D
Indiana University School of Medicine, Indianapolis 46202, USA.
J Clin Oncol. 1997 Jul;15(7):2564-9. doi: 10.1200/JCO.1997.15.7.2564.
A previously reported randomized intergroup trial demonstrated that combination chemotherapy with methotrexate, vinblastine, doxorubicin, and cisplatin (M-VAC) was superior to single-agent cisplatin in patients with advanced urothelial carcinoma. We conducted a long-term analysis of patients included in the intergroup trial to examine factors associated with long-term survival.
Two-hundred fifty-five assessable patients with urothelial carcinoma were randomized to receive either single-agent cisplatin (70 mg/m2 on day 1) or combination chemotherapy with methotrexate (30 mg/m2 on days 1, 15, and 22), vinblastine (3 mg/m2 on days 2, 15, and 22), doxorubicin (30 mg/m2 on day 2), and cisplatin (70 mg/m2 on day 2). Courses were repeated every 28 days. The association between patient characteristics and survival was assessed using Cox proportional hazards models.
With long-term follow-up evaluation, survival in the M-VAC arm continues to be superior to cisplatin (P = .00015, log-rank test). Predictors of survival include performance status, histology, and the presence of liver or bone metastasis. Only 3.7% of the patients randomized to M-VAC are alive and continuously disease-free at 6 years.
Long-term follow-up evaluation of the intergroup trial confirms that M-VAC is superior to single-agent cisplatin in patients with advanced urothelial carcinoma; however, durable progression-free survival is rare. Patients with non-transitional-cell histology, poor performance status, and/or bone or visceral involvement fare poorly and are unlikely to benefit significantly from M-VAC chemotherapy.
一项先前报道的随机组间试验表明,对于晚期尿路上皮癌患者,甲氨蝶呤、长春碱、阿霉素和顺铂联合化疗(M-VAC)优于单药顺铂化疗。我们对参与该组间试验的患者进行了长期分析,以研究与长期生存相关的因素。
255例可评估的尿路上皮癌患者被随机分为两组,一组接受单药顺铂治疗(第1天70mg/m²),另一组接受甲氨蝶呤(第1、15和22天30mg/m²)、长春碱(第2、15和22天3mg/m²)、阿霉素(第2天30mg/m²)和顺铂(第2天70mg/m²)联合化疗。每28天重复一个疗程。使用Cox比例风险模型评估患者特征与生存之间的关联。
经过长期随访评估,M-VAC组的生存率仍优于顺铂组(P = 0.00015,对数秩检验)。生存的预测因素包括体能状态、组织学类型以及肝或骨转移的存在。随机分配至M-VAC组的患者中,只有3.7%在6年后仍存活且无疾病复发。
该组间试验的长期随访评估证实,对于晚期尿路上皮癌患者,M-VAC优于单药顺铂;然而,持久的无进展生存很少见。非移行细胞组织学类型、体能状态差和/或有骨或内脏受累的患者预后较差,不太可能从M-VAC化疗中显著获益。