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本文引用的文献

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Long-Term Analysis of NRG Oncology RTOG 0415: A Randomized Phase III Noninferiority Study Comparing Two Fractionation Schedules in Patients With Low-Risk Prostate Cancer.NRG Oncology RTOG 0415 长期分析:一项比较低危前列腺癌患者两种分割方案的随机 III 期非劣效性研究。
J Clin Oncol. 2024 Jul 10;42(20):2377-2381. doi: 10.1200/JCO.23.02445. Epub 2024 May 17.
2
Hypofractionated Radiation Therapy for Localized Prostate Cancer: Executive Summary of an ASTRO, ASCO, and AUA Evidence-Based Guideline.局限性前列腺癌的分割放疗:ASTRO、ASCO 和 AUA 循证指南的执行摘要。
Pract Radiat Oncol. 2018 Nov-Dec;8(6):354-360. doi: 10.1016/j.prro.2018.08.002. Epub 2018 Oct 11.
3
Randomized Trial of Hypofractionated, Dose-Escalated, Intensity-Modulated Radiation Therapy (IMRT) Versus Conventionally Fractionated IMRT for Localized Prostate Cancer.随机分组试验:低分割、剂量递增、强度调制放射治疗(IMRT)对比常规分割 IMRT 治疗局限性前列腺癌。
J Clin Oncol. 2018 Oct 10;36(29):2943-2949. doi: 10.1200/JCO.2018.77.9868. Epub 2018 Aug 14.
4
Moderate Hypofractionation in High-Risk, Organ-Confined Prostate Cancer: Final Results of a Phase III Randomized Trial.中高危局限性前列腺癌的适度分割放疗:III 期随机试验的最终结果。
J Clin Oncol. 2017 Jun 10;35(17):1891-1897. doi: 10.1200/JCO.2016.70.4189. Epub 2017 Mar 29.
5
Hypofractionated versus conventionally fractionated radiotherapy for patients with prostate cancer (HYPRO): late toxicity results from a randomised, non-inferiority, phase 3 trial.对于前列腺癌患者,采用低分割与常规分割放射治疗(HYPRO):一项随机、非劣效性、3 期试验的晚期毒性结果。
Lancet Oncol. 2016 Apr;17(4):464-474. doi: 10.1016/S1470-2045(15)00567-7. Epub 2016 Mar 9.
6
Recurrent prostate cancer following external beam radiotherapy: follow-up strategies and management.外照射放疗后复发性前列腺癌:随访策略与管理
Urol Clin North Am. 2003 Nov;30(4):751-63. doi: 10.1016/s0094-0143(03)00051-x.

大分割、剂量递增放疗与常规分割放疗治疗局限性前列腺癌:一项III期前瞻性随机对照试验的长期更新

Hypofractionated, Dose-Escalated Radiation Versus Conventionally Fractionated Radiation for Localized Prostate Cancer: Long-Term Update of a Phase III, Prospective, Randomized Controlled Trial.

作者信息

Hassanzadeh Comron, Kuban Deborah, Pasyar Sarah, Bassett Roland, Troncoso Patricia, Ansari Maheen, Schlembach Pamela, McGuire Sean, Nguyen Quynh, Frank Steven, Mok Henry, Mohamad Osama, Park Ryan, Tang Chad, Du Weiliang, Kudchadker Rajat, Choi Seungtaek, Hoffman Karen

机构信息

Department of Genitourinary Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX.

出版信息

J Clin Oncol. 2025 Jun 20;43(18):2044-2048. doi: 10.1200/JCO-24-02057. Epub 2025 May 14.

DOI:10.1200/JCO-24-02057
PMID:40367400
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12170155/
Abstract

The MD Anderson dose-escalated, hypofractionated prostate radiation study was a phase III randomized trial comparing conventionally fractionated intensity-modulated radiation therapy (CIMRT, 75.6 Gy in 1.8-Gy fractions) with dose-escalated, hypofractionated intensity-modulated radiation (HIMRT, 72 Gy in 2.4-Gy fractions) in patients with localized prostate cancer, predominantly low-risk and intermediate-risk disease. The initial publication highlighted statistically fewer treatment failures in the HIMRT arm. We present long-term updated 13-year outcomes to determine whether cancer control benefit was maintained and to evaluate distant metastases post hoc. With a median follow-up of 13.2 years (IQR, 8.8-15.9 years), treatment failure occurred less frequently in men undergoing HIMRT (n = 13) compared with those undergoing CIMRT (n = 22), although the difference no longer meets statistical significance ( .08). Distant metastases were rare, and no statistically significant difference was noted ( = .2). There remained no statistically significant difference in late GI 2+ (10-year 10% HIMRT 4% CIMRT, = .09) or genitourinary grade 2+ toxicity (10-year 26% 23%, = .5).

摘要

MD安德森剂量递增、大分割前列腺放疗研究是一项III期随机试验,比较了常规分割调强放疗(CIMRT,1.8Gy分割,共75.6Gy)与剂量递增的大分割调强放疗(HIMRT,2.4Gy分割,共72Gy)在局限性前列腺癌患者中的疗效,这些患者主要为低风险和中风险疾病。最初的研究报告强调,HIMRT组的治疗失败在统计学上较少。我们展示了13年的长期更新结果,以确定癌症控制获益是否得以维持,并事后评估远处转移情况。中位随访时间为13.2年(四分位间距,8.8 - 15.9年),接受HIMRT治疗的男性(n = 13)与接受CIMRT治疗的男性(n = 22)相比,治疗失败发生频率更低,尽管差异不再具有统计学意义(P = 0.08)。远处转移很少见,未观察到统计学上的显著差异(P = 0.2)。晚期胃肠道2级及以上毒性(10年时,HIMRT组为10%,CIMRT组为4%,P = 0.09)或泌尿生殖系统2级及以上毒性(10年时,分别为26%和23%,P = 0.5)仍无统计学显著差异。