Weitzman A L, Shelton G, Zuech N, Owen C E, Judge T, Benson M, Sawczuk I, Katz A, Olsson C A, Bagiella E, Pfaff C, Newhouse J H, Petrylak D P
Department of Medicine, Columbia Presbyterian Medical Center, New York, New York 10032, USA.
J Urol. 2000 Mar;163(3):834-7.
We evaluated the independent response rate of dexamethasone before docetaxel and estramustine administration as measured by changes in serum prostate specific antigen (PSA) in patients with androgen independent prostate cancer.
A total of 12 patients received 20 mg. dexamethasone orally every 6 hours for 3 doses repeated every 3 weeks before starting cytotoxic therapy with estramustine and docetaxel. After progression on dexamethasone 280 mg. estramustine orally 3 times daily on days 1 to 5 and 70 mg./m.2 docetaxel intravenously for 1 hour on day 2 were given.
None of the patients initially treated with dexamethasone monotherapy (median 1 cycle, range 1 to 5) had a PSA decline of 50% or greater. Median PSA increase on monotherapy was 47% (range 0% to 22%). On estramustine and docetaxel therapy PSA decreased 50% or greater in 11 patients (92%, 95% confidence intervals [CI] 60 to 99) and 80% or greater in 7 (58%, 95% CI 29 to 84), and normalized in 5 (42%, 95% CI 16 to 71), with a median duration of response of 153 (range 42 to 371), 132 (range 84 to 287) and 84 (range 21 to 174) days, respectively. Median times to reach 50% and 80% decreases in baseline PSA were 21 (range 21 to 209) and 63 (range 21 to 138) days, respectively. In 9 patients (75%, 95% CI 43 to 93) PSA decreased at least 50% by week 9. Of 4 patients with bidimensionally measurable disease 3 had a partial response. Median time to progression was 263 days (range 91 to 378).
Administration of 20. mg. dexamethasone orally every 6 hours for 3 doses every 3 weeks does not significantly contribute to the PSA response rate of estramustine and docetaxel.
我们评估了在多西他赛和雌莫司汀给药前使用地塞米松的独立缓解率,通过雄激素非依赖性前列腺癌患者血清前列腺特异性抗原(PSA)的变化来衡量。
共有12例患者在开始使用雌莫司汀和多西他赛进行细胞毒性治疗前,每6小时口服20毫克地塞米松,共3剂,每3周重复一次。在地塞米松治疗进展后,于第1至5天每天口服280毫克雌莫司汀3次,并于第2天静脉注射70毫克/平方米多西他赛1小时。
最初接受地塞米松单药治疗的患者(中位1个周期,范围1至5个周期)中,无一例PSA下降50%或更多。单药治疗时PSA的中位增幅为47%(范围0%至22%)。在接受雌莫司汀和多西他赛治疗时,11例患者(92%,95%置信区间[CI]60至99)的PSA下降50%或更多,7例患者(58%,95%CI29至84)的PSA下降80%或更多,5例患者(42%,95%CI16至71)的PSA恢复正常,缓解的中位持续时间分别为153天(范围42至371天)、132天(范围84至287天)和84天(范围21至174天)。达到基线PSA下降50%和80%的中位时间分别为21天(范围21至209天)和63天(范围21至138天)。9例患者(75%,95%CI43至93)在第9周时PSA至少下降了50%。在4例具有双维度可测量疾病的患者中,3例有部分缓解。中位进展时间为263天(范围91至378天)。
每6小时口服20毫克地塞米松,每3周3剂,对雌莫司汀和多西他赛的PSA缓解率没有显著贡献。