Berry William, Dakhil Shaker, Modiano Manuel, Gregurich Maryann, Asmar Lina
U.S. Oncology, Houston, Texas, USA.
J Urol. 2002 Dec;168(6):2439-43. doi: 10.1016/S0022-5347(05)64163-8.
We compared median time to treatment failure of men with asymptomatic, hormone refractory, progressive prostate cancer treated with mitoxantrone plus prednisone versus prednisone alone.
In a multicenter phase III trial 120 men with asymptomatic, progressive, hormone refractory prostate cancer were randomly assigned to treatment with mitoxantrone and prednisone or prednisone alone. Patients received 12 mg./m. mitoxantrone intravenously once every 3 weeks for 6 cycles and 5 mg. prednisone twice daily with or without mitoxantrone. Time to treatment failure was assessed as an aggregate end point comprised of time to disease progression, time to toxicity or death, or time to initiation of alternate therapy.
Median followup was 21.8 months. Median time to treatment failure and median time to progression were the same: time to treatment failure and time to progression in the mitoxantrone and prednisone group was 8.1 months compared to 4.1 months in the prednisone alone group (p = 0.017 versus p = 0.018). More patients (27 or 48%) treated with mitoxantrone and prednisone achieved a 50% or greater reduction in prostate specific antigen levels than those who received only prednisone (15 or 24%, p = 0.007). There was no significant difference in median survival between the 2 groups, which was 23 and 19 months, respectively. Death was mainly attributable to disease progression.
Patients with hormone refractory prostate cancer who are asymptomatic but had progressive disease had a significantly higher response rate when treated with mitoxantrone and prednisone as demonstrated by the 50% or greater decrease in prostate specific antigen compared to treatment with prednisone alone. Time to treatment failure was significantly prolonged in the chemotherapy treated group but survival rates were not different.
我们比较了米托蒽醌联合泼尼松与单用泼尼松治疗无症状、激素难治性、进展性前列腺癌男性患者至治疗失败的中位时间。
在一项多中心III期试验中,120例无症状、进展性、激素难治性前列腺癌男性患者被随机分配接受米托蒽醌和泼尼松或单用泼尼松治疗。患者每3周静脉注射12mg/m²米托蒽醌,共6个周期,同时每日两次服用5mg泼尼松,服用米托蒽醌与否均可。至治疗失败时间被评估为一个综合终点,包括疾病进展时间、毒性或死亡时间或开始替代治疗的时间。
中位随访时间为21.8个月。至治疗失败的中位时间和至进展的中位时间相同:米托蒽醌和泼尼松组至治疗失败时间和至进展时间为8.1个月,而单用泼尼松组为4.1个月(分别为p = 0.017和p = 0.018)。与仅接受泼尼松治疗的患者(15例或24%,p = 0.007)相比,更多接受米托蒽醌和泼尼松治疗的患者(27例或48%)前列腺特异性抗原水平降低了50%或更多。两组的中位生存期无显著差异,分别为23个月和19个月。死亡主要归因于疾病进展。
无症状但患有进展性疾病的激素难治性前列腺癌患者,与单用泼尼松治疗相比,米托蒽醌联合泼尼松治疗时前列腺特异性抗原降低50%或更多,显示出显著更高的缓解率。化疗治疗组至治疗失败时间显著延长,但生存率无差异。