Segawa Takehiko, Kamoto Toshiyuki, Kinoshita Hidefumi, Kunishima Yasuharu, Yoshimura Koji, Ito Akihiro, Takahashi Takeshi, Higashi Shin, Nakamura Eijiro, Nishiyama Hirofumi, Ito Noriyuki, Yamamoto Shingo, Habuchi Tomonori, Ogawa Osamu
Department of Urology, Graduate School of Medicine, Kyoto University, 54 Shogoin-Kawaharacho, Kyoto 606-8507, Japan.
Int J Clin Oncol. 2005 Oct;10(5):333-7. doi: 10.1007/s10147-005-0513-x.
We aimed to determine the safety and efficacy of monthly paclitaxel and carboplatin with oral estramustine phosphate in patients with hormone-refractory prostate cancer (HRPC).
Patients with prostate cancer that was progressing despite androgen ablation therapy were treated with i.v. paclitaxel, 175 mg/m2, over 3 h, followed by carboplatin (area under the curve, 5) on day 1, with oral estramustine phosphate, 280 mg twice daily, for a 28-day treatment cycle. Estramustine phosphate was precluded in those patients who had experienced adverse effects during prior chemotherapies. Patients were evaluated for response every cycle, and the treatment was continued until the cancer progressed.
Twenty-one patients with progressive hormone-refractory disease were treated for a median of 4 cycles (range, 1 to 11 cycles). Estramustine phosphate was precluded in seven patients. Post-therapy decreases in serum prostate-specific antigen levels of 50% and 75%, respectively, were seen in 43% and 19% of the patients (95% confidence intervals, 22% to 64% and 2% to 36%). Of the nine patients with measurable disease, 1 (11%) had a complete response and 2 (22%) had a partial response. The overall median time to progression was 4 months, and the median survival time for all patients was 11 months. Major grade 3 or 4 adverse effects were anemia (29%), neutropenia (48%), and thrombocytopenia (24%). Mild peripheral neuropathy and myalgia/arthralgia were observed in 11 (52%) and 9 (43%) patients, respectively.
Monthly paclitaxel and carboplatin with oral estramustine phosphate has significant antitumor activity and is well tolerated in patients with progressive HRPC.
我们旨在确定每月使用紫杉醇、卡铂联合口服磷酸雌莫司汀治疗激素难治性前列腺癌(HRPC)患者的安全性和疗效。
尽管接受了雄激素剥夺治疗但病情仍进展的前列腺癌患者,静脉输注紫杉醇175mg/m²,持续3小时,于第1天接着给予卡铂(曲线下面积为5),同时口服磷酸雌莫司汀,每日2次,每次280mg,治疗周期为28天。曾在既往化疗期间出现不良反应的患者不使用磷酸雌莫司汀。每个周期对患者进行疗效评估,治疗持续至癌症进展。
21例病情进展的激素难治性疾病患者接受了中位4个周期(范围1至11个周期)的治疗。7例患者未使用磷酸雌莫司汀。治疗后分别有43%和19%的患者血清前列腺特异性抗原水平下降50%和75%(95%置信区间分别为22%至64%和2%至36%)。9例可测量疾病的患者中,1例(11%)完全缓解,2例(22%)部分缓解。总体中位进展时间为4个月,所有患者的中位生存时间为11个月。主要的3级或4级不良反应为贫血(29%)、中性粒细胞减少(48%)和血小板减少(24%)。分别有11例(52%)和9例(43%)患者观察到轻度周围神经病变和肌痛/关节痛。
每月使用紫杉醇、卡铂联合口服磷酸雌莫司汀对进展期HRPC患者具有显著的抗肿瘤活性且耐受性良好。