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首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >Sequential mitoxantrone/prednisone followed by docetaxel/estramustine in patients with hormone refractory metastatic prostate cancer: results of a phase II study.
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Sequential mitoxantrone/prednisone followed by docetaxel/estramustine in patients with hormone refractory metastatic prostate cancer: results of a phase II study.

机译:激素难治性转移性前列腺癌患者的序贯米托蒽醌/泼尼松,然后多西他赛/雌莫司汀:II期研究的结果。

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BACKGROUND: Mitoxantrone/prednisone ameliorates symptoms in hormone refractory prostate cancer (HRPC) but has no effect on survival. Docetaxel (Taxotere)/estramustine improves response but with significant toxicity. We reasoned that a sequential administration of the two regimens could be a viable alternative for delivering full doses of chemotherapy, avoiding overlapping toxicity and preserving dose intensity. PATIENTS AND METHODS: Thirty HRPC patients were treated with mitoxantrone 10 mg/m(2), day 1, every 3 weeks, plus prednisone 5 mg twice daily, for three cycles, followed by estramustine phosphate, 280 mg three times daily, days 1 to 5, plus docetaxel 75 mg/m(2), day 2, every 3 weeks for a maximum of 10 cycles. RESULTS: All patients were assessable for response and toxicity. After mitoxantrone/prednisone treatment, the prostate-specific antigen (PSA) response rate was 23%, which increased to 63% after completion of sequential mitoxantrone/prednisone and docetaxel/estramustine treatment (12 partialand 7 complete responses). With a median follow-up of 18 months, median survival for all patients was 18 months, and median progression-free survival was 10 months. The mitoxantrone/prednisone regimen was well tolerated, and the only grade 3-4 toxicity was grade 3 neutropenia in four (13%) patients. Twenty-nine patients received a total of 173 cycles of docetaxel/estramustine (median, 6 cycles/patient). Six (20%) patients had grade 3-4 neutropenia and two (6%) patients had febrile neutropenia episodes. The most frequent non-hematological toxic effects were asthenia, nausea and vomiting, edemas and onycholysis. Two (6%) patients had deep venous thrombosis. CONCLUSIONS: Mitoxantrone/prednisone followed by docetaxel/estramustine is a well-tolerated and active regimen in HRPC. Sequential therapy is feasible and can be used to integrate novel, more active regimens.
机译:背景:米托蒽醌/泼尼松可改善激素难治性前列腺癌(HRPC)的症状,但对生存没有影响。多西紫杉醇(紫杉醇)/雌莫司汀可改善反应,但有明显的毒性。我们认为,按顺序给药两种方案可能是可行的替代方案,可用于全剂量化疗,避免重叠毒性并保持剂量强度。患者和方法:30例HRPC患者每3周接受米托蒽醌10 mg / m(2)的治疗,每3周一次,再加泼尼松5 mg每天两次,共三个周期,然后是磷酸雌莫司汀,每天3次,每天1次,第1天到5,再加上多西他赛75 mg / m(2),第2天,每3周一次,最多10个周期。结果:所有患者的反应和毒性均可以评估。米托蒽醌/泼尼松治疗后,前列腺特异性抗原(PSA)响应率为23%,在连续的米托蒽醌/泼尼松和多西他赛/雌莫司汀治疗完成后(12个部分反应和7个完全反应),增加至63%。中位随访期为18个月,所有患者的中位生存期为18个月,中位无进展生存期为10个月。米托蒽醌/泼尼松方案的耐受性良好,四名(13%)患者的唯一3-4级毒性是3级中性粒细胞减少。 29名患者总共接受了173个周期的多西他赛/雌莫司汀治疗(中位,每个患者6个周期)。六名(20%)患者患有3-4级中性粒细胞减少症,两名(6%)患者具有发热性中性粒细胞减少症发作。最常见的非血液学毒性作用是乏力,恶心和呕吐,水肿和强直性溶血。 2名(6%)患者有深静脉血栓形成。结论:米托蒽醌/泼尼松,然后多西他赛/雌莫司汀是HRPC中耐受良好且有效的方案。序贯疗法是可行的,可用于整合新的,更积极的治疗方案。

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