Department of Clinical Oncology, The Christie NHS Foundation Trust, Manchester, United Kingdom; Rural Clinical School, University of New South Wales, Coffs Harbour, New South Wales, Australia.
Department of Clinical Oncology, The Christie NHS Foundation Trust, Manchester, United Kingdom.
Int J Radiat Oncol Biol Phys. 2020 Jun 1;107(2):288-296. doi: 10.1016/j.ijrobp.2020.01.008. Epub 2020 Jan 25.
Although high-level evidence supports moderately hypofractionated radiation therapy for definitive prostate treatment, there is less evidence for its use in the postprostatectomy setting. We externally validated a contemporary nomogram predicting biochemical failure (BF) after salvage radiation therapy (SRT) and report long-term disease control outcomes for hypofractionated SRT to the prostate bed.
A retrospective review was performed for 112 patients treated with hypofractionated SRT (52.5 Gy in 20 fractions using 3-dimensional conformal radiation therapy) for pT2-4R0-1N0/XM0 prostate adenocarcinoma, with postoperative prostate-specific antigen (PSA) greater than 0.1 ng/mL or rising. Freedom from BF (FFBF), distant metastasis, cancer-specific mortality, and overall survival were analyzed from commencement of radiation therapy. Cox regression was performed on FFBF to account for covariates. BF was defined as a PSA ≥0.4 ng/mL and rising after SRT. Early SRT was defined as SRT commencing at a pre-SRT PSA of ≤0.2 ng/mL.
Median follow-up was 10.0 years (interquartile range, 9.3-10.7 years), median pre-SRT PSA was 0.4 ng/mL, and androgen deprivation therapy was used in 14% of patients. The 5/10-year FFBF, distant metastasis, cancer-specific mortality, and overall survival were 68%/51%, 7%/16%, 5%/11%, and 90%/75%, respectively. FFBF for early SRT compared with late SRT was 81% versus 66% at 5 years and 68% versus 49% at 10 years. On multivariable analysis, pre-SRT PSA, International Society of Urologic Pathology grade group, seminal vesicle invasion, and androgen deprivation therapy use were associated with FFBF. The nomogram c-index was 0.67, and it overestimated FFBF by 10% and 15% at 5 and 10 years, respectively, with confidence intervals overlapping the line of unity.
Hypofractionated SRT provides long-term disease control outcomes comparable to conventionally fractionated radiation therapy. Early SRT provides improved disease control, with two-thirds of patients with pre-SRT PSA of ≤0.2 ng/mL free of BF at 10 years. We performed the first external validation of the Tendulkar salvage nomogram, which showed a robust model performance.
虽然高水平证据支持对明确的前列腺治疗进行中度适形分割放射治疗,但在前列腺切除术后使用这种方法的证据较少。我们对预测挽救性放射治疗(SRT)后生化失败(BF)的当代列线图进行了外部验证,并报告了前列腺床适形分割 SRT 的长期疾病控制结果。
对 112 例接受适形分割 SRT(52.5Gy/20 次,使用 3 维适形放射治疗)治疗术后前列腺特异性抗原(PSA)大于 0.1ng/ml 或升高的 pT2-4R0-1N0/XM0 前列腺腺癌患者进行回顾性分析。从开始放射治疗时分析 BF 无失败(FFBF)、远处转移、癌症特异性死亡率和总生存率。采用 Cox 回归对 FFBF 进行分析,以考虑协变量。BF 定义为 SRT 后 PSA≥0.4ng/ml 且持续升高。早期 SRT 定义为 SRT 开始时 PSA≤0.2ng/ml。
中位随访时间为 10.0 年(四分位间距,9.3-10.7 年),中位 PSA 为 0.4ng/ml,14%的患者接受了雄激素剥夺治疗。5/10 年 FFBF、远处转移、癌症特异性死亡率和总生存率分别为 68%/51%、7%/16%、5%/11%和 90%/75%。早期 SRT 与晚期 SRT 相比,5 年时 FFBF 为 81%比 66%,10 年时为 68%比 49%。多变量分析显示,SRT 前 PSA、国际泌尿病理学会分级组、精囊侵犯和雄激素剥夺治疗与 FFBF 相关。列线图 c 指数为 0.67,分别高估了 5 年和 10 年时的 FFBF 10%和 15%,置信区间与单位线重叠。
适形分割 SRT 可提供与常规分割放射治疗相当的长期疾病控制结果。早期 SRT 可改善疾病控制,2/3 例 SRT 前 PSA≤0.2ng/ml 的患者 10 年时无 BF。我们首次对 Tendulkar 挽救性列线图进行了外部验证,结果显示该模型具有良好的性能。