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