Yamada Yoshiya, Kollmeier Marisa A, Pei Xin, Kan Chu Cheng, Cohen Gil'ad N, Donat Sherri M, Cox Brett W, Zelefsky Michael J
Department of Radiation Oncology, Memorial Sloan-Kettering Cancer Center, New York, NY.
Department of Radiation Oncology, Memorial Sloan-Kettering Cancer Center, New York, NY.
Brachytherapy. 2014 Mar-Apr;13(2):111-6. doi: 10.1016/j.brachy.2013.11.005. Epub 2013 Dec 25.
We report the toxicity and biochemical tumor control outcome of a prospective Phase II study using high-dose-rate brachytherapy (HDR) alone as a salvage therapy for recurrent disease after external beam radiotherapy (EBRT).
Forty-two patients with biopsy-proven recurrence were enrolled on a Phase II study of salvage HDR monotherapy using iridium-192. Median pretreatment EBRT dose was 8100 cGy (6840-8640 cGy) and the median time from completion of EBRT to salvage HDR was 73 months. The protocol prescription dose of 3200 cGy was delivered in four fractions over 30 hours in a single insertion. Median followup after salvage HDR was 36 months (6-67 months).
The actuarial prostate-specific antigen biochemical relapse-free survival and distant metastases-free survival rates at 5 years were 68.5% and 81.5%, respectively. Cause-specific survival was 90.3%. Late genitourinary Grade 1and 2 toxicities were found in 38% and 48%, respectively, and one patient developed Grade 3 urinary incontinence. Late Grade 1 and 2 gastrointestinal toxicity was noted in 17% and 8% of patients, respectively. Three patients (7%) developed Grade 2 late urinary toxicity (urethral stricture), which were corrected with urethral dilatation, and one patient developed Grade 3 urinary incontinence. No Grade 4 toxicities were observed.
Genitourinary toxicity was the most commonly encountered toxicity observed after salvage HDR but severe toxicities were uncommon. Salvage HDR is an effective and well-tolerated modality for locally recurrent prostate cancer and should be considered even for patients who have previously been treated with ultra-high dose levels of EBRT.
我们报告一项前瞻性II期研究的毒性和生化肿瘤控制结果,该研究使用高剂量率近距离放射疗法(HDR)单独作为外照射放疗(EBRT)后复发性疾病的挽救治疗。
42例经活检证实复发的患者参加了一项使用铱-192的挽救性HDR单一疗法的II期研究。预处理EBRT的中位剂量为8100 cGy(6840 - 8640 cGy),从EBRT完成到挽救性HDR的中位时间为73个月。方案规定剂量3200 cGy在单次插入中于30小时内分4次给予。挽救性HDR后的中位随访时间为36个月(6 - 67个月)。
5年时精算前列腺特异性抗原生化无复发生存率和无远处转移生存率分别为68.5%和81.5%。病因特异性生存率为90.3%。分别在38%和48%的患者中发现了1级和2级晚期泌尿生殖系统毒性,1例患者出现3级尿失禁。分别在17%和8%的患者中观察到1级和2级晚期胃肠道毒性。3例患者(7%)出现2级晚期泌尿系统毒性(尿道狭窄),经尿道扩张矫正,1例患者出现3级尿失禁。未观察到4级毒性。
泌尿生殖系统毒性是挽救性HDR后最常见的毒性,但严重毒性并不常见。挽救性HDR是局部复发性前列腺癌的一种有效且耐受性良好的治疗方式,即使对于先前接受过超高剂量EBRT治疗的患者也应考虑使用。