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低危前列腺癌的立体定向体部放射治疗:十年分析

Stereotactic Body Radiotherapy for Low-Risk Prostate Cancer: A Ten-Year Analysis.

作者信息

Katz Alan

机构信息

Flushing radiation.

出版信息

Cureus. 2017 Sep 9;9(9):e1668. doi: 10.7759/cureus.1668.

DOI:10.7759/cureus.1668
PMID:29152425
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5679773/
Abstract

Objective This study represents the first 10 year analysis of the efficacy and toxicity of stereotactic body radiotherapy (SBRT) in the treatment of early low-risk prostate cancer. Materials and methods Two hundred and thirty males were treated with Cyberknife SBRT to a dose of 35 Gray (Gy) or 36.25 Gy in five consecutive days. All patients had a Gleason score of six and a PSA < 10ng/ml. Median follow-up is nine years. The median age was 69.5 years and median prostate specific antigen (PSA) was 5.6ng/ml. The treatment was delivered with homogeneous planning with a dose prescription of 82-87% of the maximum dose to cover the planning target volume (PTV). Results Ten-year biochemical disease free survival was 93% with either dose. Local control was 98.4%. Median prostate specific antigen (PSA) dropped to 0.1 by five years and has remained there. Toxicity was mild with 10% of patients having Grade two-three late urinary toxicity and 4% having the late grade two rectal toxicity. Mean Expanded Prostate Cancer Index Composite (EPIC) Quality of Life (QOL) scores declined initially for bowel and urinary domains, but recovered to baseline, where they remain. EPIC sexual scores have declined by 40%. Discussion/Conclusions Stereotactic body radiotherapy to a dose of 35 Gy-36.25 Gy is an effective treatment for early low-risk prostate cancer, with acceptably low toxicity. There appears to be no benefit to increasing the dose beyond 35 Gy. Ten-year biochemical disease free survival appears to be higher than with standard intensity modulated radiotherapy (IMRT).

摘要

目的 本研究是对立体定向体部放疗(SBRT)治疗早期低危前列腺癌的疗效和毒性进行的首次10年分析。材料与方法 230名男性接受了射波刀SBRT治疗,连续5天给予35格雷(Gy)或36.25 Gy的剂量。所有患者的 Gleason评分为6分,前列腺特异性抗原(PSA)<10ng/ml。中位随访时间为9年。中位年龄为69.5岁,中位前列腺特异性抗原(PSA)为5.6ng/ml。采用均匀计划进行治疗,剂量处方为最大剂量的82-87%,以覆盖计划靶体积(PTV)。结果 两种剂量的10年无生化疾病生存率均为93%。局部控制率为98.4%。中位前列腺特异性抗原(PSA)在5年后降至0.1,并一直保持在该水平。毒性较轻,10%的患者有2-3级晚期泌尿毒性,4%的患者有2级晚期直肠毒性。平均扩展前列腺癌指数综合(EPIC)生活质量(QOL)评分在肠道和泌尿领域最初有所下降,但恢复到基线水平并保持在该水平。EPIC性功能评分下降了40%。讨论/结论 立体定向体部放疗剂量为35 Gy-36.25 Gy是治疗早期低危前列腺癌的有效方法,毒性低至可接受。超过35 Gy增加剂量似乎没有益处。10年无生化疾病生存率似乎高于标准调强放疗(IMRT)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f40/5679773/29f9b138d2dd/cureus-0009-00000001668-i05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f40/5679773/e7dd7784030e/cureus-0009-00000001668-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f40/5679773/1a5ce175dbc6/cureus-0009-00000001668-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f40/5679773/1266c72e15f4/cureus-0009-00000001668-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f40/5679773/627a4221e2bc/cureus-0009-00000001668-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f40/5679773/29f9b138d2dd/cureus-0009-00000001668-i05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f40/5679773/e7dd7784030e/cureus-0009-00000001668-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f40/5679773/1a5ce175dbc6/cureus-0009-00000001668-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f40/5679773/1266c72e15f4/cureus-0009-00000001668-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f40/5679773/627a4221e2bc/cureus-0009-00000001668-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f40/5679773/29f9b138d2dd/cureus-0009-00000001668-i05.jpg

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