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临床试验/NCT03162523
NCT03162523已完成不适用

Norwegian Experiences With Interstitial Radiation Treatment (Brachytherapy) for Men With High-risk Localised Prostate Cancer

Oslo University Hospital1 个研究点 分布在 1 个国家目标入组 325 人开始时间: 2004年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
325
试验地点
1
主要终点
Patient-reported side-effects after HDR-BT compared to conventional EBRT

研究概览

简要总结

There are 3 articles that will be written about the experience with HDR-brachytherapy (HDR-BT) in patients with high-risk prostate cancer in Norway as part of a doctorial thesis-project. The project will focus on survival, side-effects and dosimetry variables as the main points of interest.

详细描述

First article will compare overall and prostate cancer specific-mortality in patients who has received HDR-BT compared to patients who has received external beam radiation therapy only (EBRT). Patients who have been treated with HDR-BT have been enrolled in an approved registry at Oslo University Hospital since 2004. The control group (EBRT only) data are from the Lancet published hallmark study SPCG-7 (Scandinavian Prostate Cancer Group). This is a case-control study.

Second article will focus on side-effects of HDR-BT compared to EBRT patients. Patients included in the registry described above have been sent (and completed with a 72% answer rate) a questionnaire of the standard Expanded Prostate Cancer Index (EPIC-26) form. This will be compared to patients who already have answered the same questionnaire in a previously published study (approved by the Norwegian Ethical Committee).

The Third article will investigate if there are any association between patients reporting severe adverse effects after HDR-BT and the patients dosimetry reports (i.e are there a larger dose to the urethra or rectum in these patients?)

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Other

入排标准

年龄范围
— 至 75 Years(Child, Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • age, high-risk prostate cancer, general good Health, anatomical favourable condition for brachytherapy

排除标准

  • poor Health, metastasis, T3b stage tumour, Prostate Specific Antigen (PSA) Levels > 75, biological age > 75 years

结局指标

主要结局

Patient-reported side-effects after HDR-BT compared to conventional EBRT

时间窗: 1 year

Patient self-reported side-effects focusing on rectal, bladder, quality of life, sexual function and psycological bother will be recorded in both Groups and compared.

Overall- and Prostate-Cancer specific mortality in patients treated with HDR-BT compared to EBRT alone

时间窗: 24 weeks

The final measured outcome is death by prostate cancer, death due to other cause (overall mortality) or alive at 10 years.

Are there an Association between rectal dosage after HDR-BT and self-reported rectal bother in patients undergone HDR-BT treatment ?

时间窗: 2 years

Investigations into needle placement, dosage and anatomical variations will be examined in patients who report rectal problems 5 years after HDR-BT treatment.

次要结局

未报告次要终点

研究者

发起方
Oslo University Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Trude Baastad Wedde

Consultant oncologist

Oslo University Hospital

研究点 (1)

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