首页> 外文期刊>Urology >Combination of low-dose flutamide and finasteride for PSA-only recurrent prostate cancer after primary therapy.
【24h】

Combination of low-dose flutamide and finasteride for PSA-only recurrent prostate cancer after primary therapy.

机译:低剂量氟他胺和非那雄胺联合用于仅PSA的复发性前列腺癌。

获取原文
获取原文并翻译 | 示例
           

摘要

OBJECTIVES:To evaluate the efficacy and tolerability of combined finasteride and low-dose flutamide for prostate-specific antigen (PSA)-only recurrence after definitive therapy and to determine the predictors of recurrence-free survival. METHODS: Seventy-one men with biochemical recurrence after primary therapy for prostate cancer were prospectively enrolled from 1996 to 1998. Forty-two patients had undergone radical retropubic prostatectomy and 29 had undergone external beam radiotherapy. Radionuclide bone scans and computed tomography of the abdomen and pelvis showed no metastasis. The initial treatment with finasteride (5 mg twice daily) and flutamide (125 mg twice daily) was continued unless participants were unable to tolerate the agents or experienced PSA progression. RESULTS: At a mean of 44.4 months (range 12 to 92) of follow-up, 54 (76%) of 71 patients were available for measurement of disease status and response to therapy. Three patients had died of unrelated causes; 5 men withdrew from the study because of side effects and 1 patient for protocol violation. Eight patients were lost to follow-up. Twenty-seven patients (38%) continued receiving therapy with no evidence of PSA progression (PSA level less than 0.4 ng/mL), 6 patients maintained a more than 50% reduction in their baseline PSA level at the time of analysis, and 21 (29%) had PSA progression (ie, elevated PSA level on three consecutive tests more than 4 weeks apart). Major side effects were breast tenderness (90%), gynecomastia (72%), gastrointestinal disturbances (22%), fatigue (10%), and decreased libido (4%). The side effects were mild and well tolerated by most patients. CONCLUSIONS: The combination of finasteride and flutamide showed a moderate efficacy in patients with PSA-only recurrence after definitive therapy. The efficacy appears to be greater in patients who can achieve a PSA nadir of 0.1 ng/mL or less after the start of treatment.
机译:目的:评估非那雄胺和小剂量氟他胺联合用于最终治疗后仅前列腺特异性抗原(PSA)复发的疗效和耐受性,并确定无复发生存的预测指标。方法:从1996年至1998年,前瞻性纳入了71例前列腺癌主要治疗后生化复发的男性。其中42例接受了根治性耻骨后前列腺切除术,其中29例接受了体外放射治疗。放射性核素骨扫描和腹部和骨盆的计算机断层扫描未显示转移。除非参与者不能耐受药物或PSA进展,否则继续使用非那雄胺(每日两次,每次5 mg)和氟他胺(每天两次,一次125 mg)进行初始治疗。结果:平均随访44.4个月(范围12至92),有71位患者中的54位(76%)可以测量疾病状况和对治疗的反应。三例患者死于不相关原因。 5名男性因副作用退出研究,另有1名患者因违反协议而退出研究。 8名患者失去随访。二十七名患者(38%)继续接受治疗,没有PSA进展的证据(PSA水平低于0.4 ng / mL),六名患者在分析时基线PSA水平保持了超过50%的降低,而21名患者(29%)的PSA病情恶化(即,相隔4周以上的三个连续测试中PSA水平升高)。主要副作用是乳房压痛(90%),男性乳房发育症(72%),胃肠道不适(22%),疲劳(10%)和性欲下降(4%)。多数患者副作用较轻且耐受性良好。结论:非那雄胺和氟他胺的组合在明确治疗后仅PSA复发的患者中显示中等疗效。在开始治疗后PSA最低值可达到0.1 ng / mL或更低的患者中,疗效似乎更高。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号