Department of Radiation Oncology, Duke Cancer Institute, Durham, NC, USA.
Department of Radiation Oncology, Institut Gustave Roussy, Villejuif, France.
Eur Urol. 2015 Oct;68(4):683-91. doi: 10.1016/j.eururo.2014.08.009. Epub 2014 Sep 22.
Technological advances in radiation therapy delivery have permitted the use of high-dose-per-fraction radiation therapy (RT) for early-stage prostate cancer (PCa). Level 1 evidence supporting the safety and efficacy of hypofractionated RT is evolving as this modality becomes more widely utilized and refined.
To perform a systematic review of the current evidence on the safety and efficacy of hypofractionated RT for early-stage PCa and to provide in-context recommendations for current application of this technology.
Embase, PubMed, and Scopus electronic databases were queried for English-language articles from January 1990 through June 2014. Prospective studies with a minimum of 50 patients were included. Separate consideration was made for studies involving moderate hypofractionation (doses of 2.5-4Gy per fraction) and extreme hypofractionation (5-10Gy in 4-7 fractions).
Six relatively small superiority designed randomized trials of standard fractionation versus moderate hypofractionation in predominantly low- and intermediate-risk PCa have been published with follow-up ranging from 4 to 8 yr, noting similar biochemical control (5-yr freedom from biochemical failure in modern studies is >80% for low-risk and intermediate-risk patients) and late grade ≥2 genitourinary and gastrointestinal toxicities (between 2% and 20%). Noninferiority studies are pending. In prospective phase 2 studies, extreme hypofractionation has promising 2- to 5-yr biochemical control rates of >90% for low-risk patients. Results from a randomized trial are expected in 2015.
Moderate hypofractionation has 5-yr data to date establishing safety compared with standard fractionation, but 10-yr outcomes and longer follow-up are needed to establish noninferiority for clinical effectiveness. Extreme hypofractionation is promising but as yet requires reporting of randomized data prior to application outside of a clinical protocol.
Hypofractionation for prostate cancer delivers relatively high doses of radiation per treatment. Prospective studies support the safety of moderate hypofractionation, while extreme fractionation may have greater toxicity. Both show promising cancer control but long-term results of noninferiority studies of both methods are required before use in routine treatment outside of clinical protocols.
放射治疗技术的进步使得早期前列腺癌(PCa)能够采用高剂量分割放射治疗(RT)。随着这种治疗方式的应用越来越广泛和完善,支持分割剂量 RT 安全性和有效性的 1 级证据也在不断发展。
对早期 PCa 采用分割剂量 RT 的安全性和有效性的现有证据进行系统评价,并针对该技术的当前应用提供具体建议。
通过 Embase、PubMed 和 Scopus 电子数据库,检索 1990 年 1 月至 2014 年 6 月期间发表的英文文献。纳入至少 50 例患者的前瞻性研究。分别考虑中等分割剂量(每次分割 2.5-4Gy)和大分割剂量(每次分割 5-10Gy,共 4-7 次)的研究。
目前已发表了 6 项相对较小的设计优势随机试验,比较了标准分割剂量与中分割剂量在主要为低危和中危 PCa 患者中的应用,随访时间为 4-8 年,提示生化控制效果相似(现代研究中,5 年生化无失败率对于低危和中危患者而言>80%),且晚期≥2 级泌尿生殖系统和胃肠道毒性相似(2%-20%之间)。非劣效性研究正在进行中。在前瞻性 2 期研究中,低危患者接受大分割剂量治疗的 2-5 年生化控制率>90%,结果令人鼓舞。预计 2015 年会公布一项随机试验的结果。
截至目前,中分割剂量治疗已有 5 年的数据证实其安全性优于标准分割剂量,但需要 10 年以上的结果和更长时间的随访来证实其在临床疗效方面不劣于后者。大分割剂量治疗有前途,但在临床方案之外应用前,还需要报告随机数据。
前列腺癌的分割放疗每次治疗给予相对较高的放射剂量。前瞻性研究支持中等分割剂量的安全性,而大分割剂量可能具有更大的毒性。两种方法的肿瘤控制均有较好的前景,但在常规临床治疗之外,还需要非劣效性研究的长期结果来支持这两种方法的应用。