Sato Naohide, Akakura Koichiro, Isaka Shigeo, Nakatsu Hiroomi, Tanaka Masashi, Ito Haruo, Masai Motoyuki
Department of Urology, Ichihara Hospital, Teikyo University School of Medicine, Chiba, Japan.
Urology. 2004 Aug;64(2):341-5. doi: 10.1016/j.urology.2004.03.032.
To clarify the effect of intermittent androgen suppression on the time to androgen-independent progression and changes in quality of life (QOL).
Patients with locally advanced or metastatic prostate cancer were treated with a combination of leuprolide acetate and flutamide for 36 weeks. When the serum prostate-specific antigen (PSA) levels at 24 and 32 weeks were less than 4.0 ng/mL, treatment was withheld until the PSA level reached 15 ng/mL or the pretreatment level. This cycle of on-treatment and off-treatment was repeated until PSA failure (three consecutive increases in PSA level greater than 4.0 ng/mL during the on-treatment period) or symptomatic progression was observed. Changes in QOL were assessed by a self-assessment questionnaire.
Forty-nine patients (26 with T3N0M0, 8 with T2-T3N1M0, 2 with T4N0M0, and 13 with T2-T3N0M1) were enrolled. The mean follow-up period was 136.5 weeks. Thirty-one patients finished cycle 1, six finished cycle 2, and three finished cycle 3. The mean off-treatment duration in cycles 1, 2, and 3 was 46.1, 36.9, and 23.3 weeks, respectively. In the off-treatment period, statistically significant improvements in the QOL score were observed in the categories of potency (11.4 versus 2.4) and social/family well-being (20.3 versus 16.1) compared with those in the on-treatment period. PSA failure occurred in 6 patients (3 with T3N0M0 and 3 with T2-T3N1M0), and all patients were alive at last follow-up.
Our interim analysis indicated that QOL is remarkably improved during the off-treatment period. Intermittent androgen suppression would be a viable option for treatment of advanced prostate cancer, although a randomized controlled study is required to determine whether intermittent androgen suppression prolongs the time to androgen-independent cancer. We will continue follow-up in this study to a minimum of 3 years.
阐明间歇性雄激素抑制对雄激素非依赖性进展时间及生活质量(QOL)变化的影响。
局部晚期或转移性前列腺癌患者接受醋酸亮丙瑞林和氟他胺联合治疗36周。当24周和32周时血清前列腺特异性抗原(PSA)水平低于4.0 ng/mL时,停止治疗直至PSA水平达到15 ng/mL或治疗前水平。重复这种治疗期和非治疗期的循环,直到观察到PSA失败(治疗期内PSA水平连续三次升高超过4.0 ng/mL)或出现症状性进展。通过自我评估问卷评估生活质量的变化。
共纳入49例患者(26例T3N0M0,8例T2 - T3N1M0,2例T4N0M0,13例T2 - T3N0M1)。平均随访期为136.5周。31例患者完成第1周期,6例完成第2周期,3例完成第3周期。第1、2和3周期的平均非治疗期分别为46.1、36.9和23.3周。与治疗期相比,在非治疗期,性功能(11.4对2.4)和社会/家庭幸福感(20.3对16.1)类别的生活质量评分有统计学意义的改善。6例患者出现PSA失败(3例T3N0M0和3例T2 - T3N1M0),所有患者在最后一次随访时均存活。
我们的中期分析表明,在非治疗期生活质量显著改善。间歇性雄激素抑制可能是晚期前列腺癌治疗的一个可行选择,尽管需要进行随机对照研究来确定间歇性雄激素抑制是否能延长雄激素非依赖性癌症的发生时间。我们将继续对本研究进行至少3年的随访。