Phase I Trial of Weekly Docetaxel, Total Androgen Blockade, and Image-Guided Intensity-Modulated Radiotherapy for Localized High-Risk Prostate Adenocarcinoma

被引:6
作者
Marshall, David T. [1 ]
Ramey, Stephen [1 ]
Golshayan, Ali-Reza [1 ]
Keane, Thomas E. [1 ]
Kraft, Andrew S. [1 ]
Chaudhary, Uzair [2 ]
机构
[1] Med Univ S Carolina, Charleston, SC 29425 USA
[2] Univ Calif San Francisco, San Francisco, CA 94143 USA
关键词
Androgen deprivation therapy; Docetaxel; High-risk prostate cancer; Radiotherapy; MITOXANTRONE PLUS PREDNISONE; CONFORMAL RADIATION-THERAPY; DOSE-ESCALATION TRIAL; RADICAL PROSTATECTOMY; III TRIAL; CANCER; ESTRAMUSTINE; CONCURRENT; BRACHYTHERAPY; DEPRIVATION;
D O I
10.1016/j.clgc.2013.11.019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This phase I trial provided the maximum tolerated dose (MTD) of 25 mg/m(2) for docetaxel when combined with androgen deprivation therapy (ADT) and high-dose intensity-modulated radiotherapy (IMRT) to the prostate and seminal vesicles for high-risk localized prostate cancer. No patients had severe side effects at this dose, and it should be used in future trials to test the efficacy of this treatment paradigm. Background: This was a phase I study to find the maximum tolerable dose (MTD) of weekly docetaxel combined with high-dose intensity-modulated radiotherapy (IMRT) and androgen deprivation therapy (ADT). Patients and Methods: Men with localized high-risk prostate cancer (HRPC) were treated with weekly docetaxel at 10 to 30 mg/m2 concurrent with IMRT of 77.4 Gy to the prostate and 45 Gy to the seminal vesicles. ADT consisted of a gonadotropin-releasing hormone agonist (GnRHa) and bicalutamide beginning 2 months before and during chemoradiation. GnRHa was continued for 24 months. Results: Nineteen patients were enrolled. No dose-limiting toxicity (DLT) was seen with docetaxel doses up to 25 mg/m(2). At the 30 mg/m(2) level, 2 of 4 patients experienced DLTs of both grade 3 fatigue and dyspepsia. At 41 months' median follow-up, 2 patients had died-1 from metastatic prostate cancer and the other from heart failure. Two other patients experienced biochemical failure. One patient with bladder invasion at diagnosis experienced late grade 2 urinary hesitancy 9 months after completion of radiotherapy, requiring short-term intermittent catheterization. All patients had erectile dysfunction, but no late toxicities worse than grade 2 were identified. Conclusion: Weekly docetaxel may be combined with high-dose IMRT and long-term ADT up to a MTD of 25 mg/m2. Acute toxicities and long-term side effects of this regimen were acceptable. Future studies evaluating the efficacy of docetaxel, ADT, and IMRT for localized HRPC should use a weekly dose of 25 mg/m(2) when limiting the irradiated volume to the prostate and seminal vesicles. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:80 / 86
页数:7
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