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Ten-year outcomes of high-dose, intensity-modulated radiotherapy for localized prostate cancer.高强度聚焦超声治疗局限性前列腺癌十年疗效分析
Cancer. 2011 Apr 1;117(7):1429-37. doi: 10.1002/cncr.25467. Epub 2010 Nov 8.
2
Multi-institutional Phase II study of proton beam therapy for organ-confined prostate cancer focusing on the incidence of late rectal toxicities.多机构质子束治疗局限性前列腺癌的 II 期研究,重点关注晚期直肠毒性的发生率。
Int J Radiat Oncol Biol Phys. 2011 Oct 1;81(2):390-6. doi: 10.1016/j.ijrobp.2010.05.027. Epub 2010 Sep 9.
3
Long-term urinary, sexual, and rectal morbidity in patients treated with iodine-125 prostate brachytherapy followed up for a minimum of 5 years.接受碘-125前列腺近距离放射治疗且随访至少5年的患者的长期泌尿、性和直肠发病率。
Urology. 2007 Feb;69(2):338-42. doi: 10.1016/j.urology.2006.10.001.
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Tutorial in biostatistics: competing risks and multi-state models.生物统计学教程:竞争风险与多状态模型
Stat Med. 2007 May 20;26(11):2389-430. doi: 10.1002/sim.2712.
5
Proton therapy for prostate cancer: the initial Loma Linda University experience.前列腺癌的质子治疗:洛马林达大学的初步经验。
Int J Radiat Oncol Biol Phys. 2004 Jun 1;59(2):348-52. doi: 10.1016/j.ijrobp.2003.10.011.
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Studying radiation therapy using SEER-Medicare-linked data.利用与监测、流行病学和最终结果(SEER)计划及医疗保险相关联的数据研究放射治疗。
Med Care. 2002 Aug;40(8 Suppl):IV-49-54. doi: 10.1097/00005650-200208001-00007.
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Use of SEER-Medicare data for measuring cancer surgery.利用监测、流行病学与最终结果(SEER)-医疗保险数据来衡量癌症手术情况。
Med Care. 2002 Aug;40(8 Suppl):IV-43-8. doi: 10.1097/00005650-200208001-00006.
8
Overview of the SEER-Medicare data: content, research applications, and generalizability to the United States elderly population.SEER-医疗保险数据概述:内容、研究应用及对美国老年人群的普遍性
Med Care. 2002 Aug;40(8 Suppl):IV-3-18. doi: 10.1097/01.MLR.0000020942.47004.03.
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Prostate cancer radiation dose response: results of the M. D. Anderson phase III randomized trial.前列腺癌放疗剂量反应:MD安德森癌症中心III期随机试验结果
Int J Radiat Oncol Biol Phys. 2002 Aug 1;53(5):1097-105. doi: 10.1016/s0360-3016(02)02829-8.
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Construct validity of medicare chemotherapy claims: the case of 5FU.医疗保险化疗报销申请的结构效度:以5-氟尿嘧啶为例。
Med Care. 2002 Mar;40(3):201-11. doi: 10.1097/00005650-200203000-00004.

前列腺癌放射治疗后的迟发性胃肠道毒性。

Late gastrointestinal toxicities following radiation therapy for prostate cancer.

机构信息

The Cancer Institute of New Jersey, New Brunswick, NJ 08903, USA.

出版信息

Eur Urol. 2011 Nov;60(5):908-16. doi: 10.1016/j.eururo.2011.05.052. Epub 2011 Jun 12.

DOI:10.1016/j.eururo.2011.05.052
PMID:21684064
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3185133/
Abstract

BACKGROUND

Radiation therapy is commonly used to treat localized prostate cancer; however, representative data regarding treatment-related toxicities compared with conservative management are sparse.

OBJECTIVE

To evaluate gastrointestinal (GI) toxicities in men treated with either primary radiation or conservative management for T1-T2 prostate cancer.

DESIGN, SETTING, AND PARTICIPANTS: We performed a population-based cohort study, using Medicare claims data linked to the Surveillance Epidemiology and End Results data. Competing risk models were used to evaluate the risks.

MEASUREMENTS

GI toxicities requiring interventional procedures occurring at least 6 mo after cancer diagnosis.

RESULTS AND LIMITATIONS

Among 41,737 patients in this study, 28,088 patients received radiation therapy. The most common GI toxicity was GI bleeding or ulceration. GI toxicity rates were 9.3 per 1000 person-years after three-dimensional conformal radiotherapy, 8.9 per 1000 person-years after intensity-modulated radiotherapy, 5.3 per 1000 person-years after brachytherapy alone, 20.1 per 1000 person-years after proton therapy, and 2.1 per 1000 person-years for conservative management patients. Radiation therapy is the most significant factor associated with an increased risk of GI toxicities (hazard ratio [HR]: 4.74; 95% confidence interval [CI], 3.97-5.66). Even after 5 yr, the radiation group continued to experience significantly higher rates of new GI toxicities than the conservative management group (HR: 3.01; 95% CI, 2.06-4.39). Because our cohort of patients were between 66 and 85 yr of age, these results may not be applicable to younger patients.

CONCLUSIONS

Patients treated with radiation therapy are more likely to have procedural interventions for GI toxicities than patients with conservative management, and the elevated risk persists beyond 5 yr.

摘要

背景

放射治疗常用于治疗局限性前列腺癌,但关于与保守治疗相比的治疗相关毒性的代表性数据很少。

目的

评估接受原发放疗或保守治疗的 T1-T2 前列腺癌患者的胃肠道(GI)毒性。

设计、地点和参与者:我们进行了一项基于人群的队列研究,使用医疗保险索赔数据与监测、流行病学和最终结果数据相关联。使用竞争风险模型评估风险。

测量

癌症诊断至少 6 个月后需要介入治疗的胃肠道毒性。

结果和局限性

在这项研究的 41737 名患者中,有 28088 名患者接受了放射治疗。最常见的胃肠道毒性是胃肠道出血或溃疡。三维适形放疗后胃肠道毒性发生率为每 1000 人年 9.3 例,调强放疗后为每 1000 人年 8.9 例,单纯近距离放疗后为每 1000 人年 5.3 例,质子治疗后为每 1000 人年 20.1 例,保守治疗后为每 1000 人年 2.1 例。放射治疗是与胃肠道毒性风险增加最相关的因素(风险比[HR]:4.74;95%置信区间[CI]:3.97-5.66)。即使在 5 年后,放射组仍继续经历显著更高的新胃肠道毒性发生率,高于保守治疗组(HR:3.01;95%CI:2.06-4.39)。由于我们的患者队列年龄在 66 至 85 岁之间,这些结果可能不适用于年轻患者。

结论

与保守治疗相比,接受放射治疗的患者更有可能因胃肠道毒性而接受介入治疗,且这种风险升高持续超过 5 年。