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苯丁酸氮芥与洛莫司汀(CL56)用于治疗激素绝对抵抗性前列腺癌:内分泌敏感性的重新诱导——一项意外发现。

Chlorambucil and lomustine (CL56) in absolute hormone refractory prostate cancer: re-induction of endocrine sensitivity an unexpected finding.

作者信息

Shamash J, Dancey G, Barlow C, Wilson P, Ansell W, Oliver R T D

机构信息

Department of Medical Oncology, St Bartholomew's Hospital, London EC1A 7BE, UK.

出版信息

Br J Cancer. 2005 Jan 17;92(1):36-40. doi: 10.1038/sj.bjc.6602263.

Abstract

The management of androgen independent prostate cancer is increasingly disputed. Diethylstilbestrol and steroids have useful second-line activity in its management. The value of chemotherapy still remains contentious. This paper reports a phase 2 study of two orally active chemotherapy drugs in patients who are absolutely hormone refractory having failed primary androgen blockade and combined oestrogens and corticosteroids. In total, 37 patients who were biochemically castrate with absolute hormone refractory prostate cancer and performance status of 0-3 were enrolled. Therapy consisted of chlorambucil 1 mg kg(-1) given as 6 mg a day until the total dose was reached and lomustine 2 mg kg(-1) given every 56 days (CL56). During this time all hormone therapy was stopped. One patient normalised his PSA with a further two having a greater than 50% decline leading to an objective response rate of 10%. The median time to progression was 3.6 months with an overall survival of 7.1 months. The median survival of this group of patients from first becoming androgen independent was 23.5 months. Eight of 17 (47%) patients who were subsequently re-challenged with hormonal therapy following failure of chemotherapy had a further PSA reduction, three (17%) of which were >50%. The median progression-free interval for the eight patients was 4 months. In conclusion, CL56 has a low objective response rate in the management of absolute hormone refractory prostate cancer. Toxicity was mild. Re-induction of hormone sensitivity following failure of chemotherapy was an unexpected finding that requires further study.

摘要

雄激素非依赖性前列腺癌的治疗争议越来越大。己烯雌酚和类固醇在其治疗中具有有效的二线活性。化疗的价值仍存在争议。本文报告了一项针对两种口服活性化疗药物的2期研究,研究对象为原发性雄激素阻断、联合雌激素和皮质类固醇治疗失败后绝对激素抵抗的患者。总共招募了37例生化去势、患有绝对激素抵抗性前列腺癌且体能状态为0 - 3的患者。治疗方案包括苯丁酸氮芥1 mg·kg⁻¹,每日给药6 mg,直至达到总剂量,以及洛莫司汀2 mg·kg⁻¹,每56天给药一次(CL56方案)。在此期间,所有激素治疗均停止。1例患者的前列腺特异性抗原(PSA)恢复正常,另有2例患者的PSA下降超过50%,客观缓解率为10%。中位疾病进展时间为3.6个月,总生存期为7.1个月。这组患者从首次出现雄激素非依赖性开始的中位生存期为23.5个月。17例化疗失败后随后接受激素治疗重新挑战的患者中,有8例(47%)的PSA进一步降低,其中3例(17%)下降超过50%。这8例患者的中位无进展生存期为4个月。总之,CL56方案在绝对激素抵抗性前列腺癌的治疗中客观缓解率较低。毒性较轻。化疗失败后激素敏感性的重新诱导是一个意外发现,需要进一步研究。

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