Kantoff P W, Halabi S, Conaway M, Picus J, Kirshner J, Hars V, Trump D, Winer E P, Vogelzang N J
Lank Center for Genitourinary Oncology and Breast Oncology Center, Department of Adult Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115-6084, USA.
J Clin Oncol. 1999 Aug;17(8):2506-13. doi: 10.1200/JCO.1999.17.8.2506.
Approximately 40,000 men die each year of hormone-refractory prostate cancer (HRPC). The results of treatment with chemotherapy have been disappointing to date, with no trials demonstrating a benefit with respect to survival duration. Corticosteroids and mitoxantrone each have been shown to be active agents in this disease. The purpose of this study was to demonstrate an advantage of mitoxantrone and hydrocortisone (M+H) over hydrocortisone alone with respect to survival duration.
Two hundred forty-two patients with HRPC were randomized to receive either M+H or hydrocortisone alone. Patients were monitored for survival, time to disease progression, time to treatment failure, response, and quality-of-life (QOL) parameters.
Treatment in both arms was well tolerated. Although there was a delay in time to treatment failure and disease progression in favor of M+H over hydrocortisone alone, there was no difference in overall survival (12.3 months for M+H v 12.6 months for hydrocortisone alone). There was an indication that QOL was better with M+H, in particular with respect to pain control.
M+H generated more frequent responses and a delay in both time to treatment failure and disease progression compared with hydrocortisone alone. In addition, there was a possible benefit of M+H with respect to pain control over hydrocortisone alone. No improvement in survival was observed. Although M+H could be viewed as a palliative option for patients with HRPC, new drugs and novel strategies are needed to improve survival for this disease.
每年约有40000名男性死于激素难治性前列腺癌(HRPC)。迄今为止,化疗的治疗结果令人失望,尚无试验表明其在生存时间方面有获益。皮质类固醇和米托蒽醌均已被证明是该疾病的有效药物。本研究的目的是证明米托蒽醌与氢化可的松联合用药(M+H)在生存时间方面优于单独使用氢化可的松。
242例HRPC患者被随机分为接受M+H或单独使用氢化可的松治疗。对患者的生存情况、疾病进展时间、治疗失败时间、反应及生活质量(QOL)参数进行监测。
两组治疗的耐受性均良好。虽然M+H组在治疗失败时间和疾病进展时间上较单独使用氢化可的松组有所延迟,但总生存期无差异(M+H组为12.3个月,单独使用氢化可的松组为12.6个月)。有迹象表明M+H组的生活质量更好,尤其是在疼痛控制方面。
与单独使用氢化可的松相比,M+H组的反应更频繁,治疗失败时间和疾病进展时间均延迟。此外,M+H组在疼痛控制方面可能比单独使用氢化可的松更具优势。未观察到生存期的改善。虽然M+H可被视为HRPC患者的一种姑息治疗选择,但仍需要新的药物和新的策略来改善该疾病患者的生存期。