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首页> 外文期刊>International Journal of Radiation Oncology, Biology, Physics >Results of a phase II trial of transrectal ultrasound-guided permanent radioactive implantation of the prostate for definitive management of localized adenocarcinoma of the prostate (radiation therapy oncology group 98-05).
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Results of a phase II trial of transrectal ultrasound-guided permanent radioactive implantation of the prostate for definitive management of localized adenocarcinoma of the prostate (radiation therapy oncology group 98-05).

机译:经直肠超声引导的前列腺永久性放射性植入物以明确治疗前列腺局部腺癌的II期试验结果(放射治疗肿瘤学组98-05)。

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PURPOSE: To evaluate the effectiveness of transrectal ultrasound-guided permanent radioactive (125)I implantation of the prostate for organ-confined adenocarcinoma of the prostate compared with historical data of prostatectomy and external beam radiotherapy within a cooperative group setting. METHODS AND MATERIALS: Patients accrued to this study had histologically confirmed, locally confined, adenocarcinoma of the prostate with clinical Stage T1b, T1c, or T2a, no nodal or metastatic disease, prostate-specific antigen level of < or =10 ng/mL, and Gleason score of < or =6. All patients underwent transrectal ultrasound-guided radioactive (125)I permanent seed implantation into the prostate. The prescribed dose was 145 Gy to the prostate planning target volume. RESULTS: A total of 27 institutions accrued a total of 101 patients to this protocol, with no institution accruing >8 patients. Six patients were ineligible, leaving 95 properly entered as eligible in the study. The median follow-up was 5.3 years (range, 0.4-6.5 years). At 5 years, 5 patients had local failure, 1 had evidence of distant failure, and 6 (6%) had biochemical failure. The overall survival rate at 5 years was 96.7%. At last follow-up, no patient had died of prostate cancer or related toxicities. Eight patients had a maximal acute toxicity level of 3, and no patient had Grade 4 or 5 acute toxicity. During follow-up, 2 patients had maximal Grade 3 toxicity, both related to bladder issues, and no patient experienced Grade 4 or 5 toxicity. CONCLUSION: The results of this clinical protocol (a multi-institutional trial of brachytherapy for localized adenocarcinoma of the prostate) have demonstrated that this type of trial can be successfully completed through the Radiation Therapy Oncology Group. Biochemical disease-free survival was comparable with other brachytherapy published series and with the results after surgery and external beam radiotherapy.
机译:目的:与合作组内的前列腺切除术和外部束放射疗法的历史数据进行比较,以评价经直肠超声引导的永久性放射性(125)I前列腺植入术治疗前列腺癌的局限性腺癌的有效性。方法和材料:该研究的患者经组织学证实为局部狭窄的前列腺腺癌,临床分期为T1b,T1c或T2a,无淋巴结或转移性疾病,前列腺特异性抗原水平≤10 ng / mL,格里森得分<或= 6。所有患者均接受经直肠超声引导的放射性(125)I永久种子植入前列腺。规定剂量为前列腺计划目标体积的145 Gy。结果:共有27家机构共计101名患者接受了该方案,而没有机构多于8名患者。有6名患者不符合条件,剩下95名符合研究条件。中位随访时间为5.3年(范围0.4-6.5年)。在5年时,有5例发生局部衰竭,有1例显示远距离衰竭,有6例(6%)发生生化衰竭。 5年总生存率为96.7%。在最后一次随访中,没有患者死于前列腺癌或相关毒性。八名患者的最大急性毒性水平为3,无患者有4级或5级急性毒性。在随访过程中,有2名患者具有最大的3级毒性,均与膀胱问题有关,并且没有患者经历4级或5级毒性。结论:该临床方案的结果(一项针对前列腺局部腺癌的近距离放射治疗的多机构试验)表明,这种类型的试验可以通过放射治疗肿瘤学小组成功完成。生化无病生存率与其他近距离放射治疗系列以及手术和外照射放疗后的结果相当。

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