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临床试验/NCT02873013
NCT02873013Enrolling By Invitation不适用

Research Concerning Background Factors at Time of Diagnosis and Initial Treatment and Treatment Progress Cancer Patients in Asia

Japan Study Group of Prostate Cancer1 个研究点 分布在 1 个国家目标入组 20,000 人开始时间: 2016年3月最近更新:
适应症

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
入组人数
20,000
试验地点
1
主要终点
Patients background at time of diagnosis of prostate cancer, treatment progress and prognosis with the reason for progression and subsequent treatment methods

研究概览

简要总结

This study will target patients who have received a histopathological diagnosis of prostate cancer and who are undergoing treatment in various forms, including active PSA surveillance, surgical treatment, radiotherapy, endocrine therapy, and chemotherapy. The study will survey information about the patient at time of diagnosis, clinical staging, details of initial treatment, status of disease progression, and prognosis at the end point of the study. The purpose of the study is to clarify distribution of staging, the actual status of treatment choices and treatment outcomes.

详细描述

The A-CaP will collect information in a linkable anonymized format from all medical institutions in Asian countries participating in the study and will engage in data analysis. J-CaP which has previous experience of engaging in a similar study in 2010 wll be a sponsor for A-CaP study, the aggregated results of which have been reported. The registration period for this study will be three years followed by 7 years of follow-up study, and research will be implemented across a wider range of Asian countries, with new institutions participating for the purposes of this study. As this study will be an observational study the acquisition of data will be relatively simple, and as the content of the study will be almost identical to the study conducted by J-CaP in 2010, a system for research implementation is already established at J-CaP.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
Male
接受健康志愿者

入选标准

  • Patients who have received a histopathological diagnosis of prostate cancer between January 1,2016,and December 31,
  • Patients who, having received a diagnosis within the abovementioned period, began initial treatment for prostate cancer(including active surveillance).
  • Patients who are either hospitalized as outpatients.

排除标准

  • Patients for whom information about the time of diagnosis, including histopathological diagnosis, cannot be acquired.

结局指标

主要结局

Patients background at time of diagnosis of prostate cancer, treatment progress and prognosis with the reason for progression and subsequent treatment methods

时间窗: three years

The following items are examined for primary outcome measure. 1. Patient background which is represented by month and year of birth; height and weight; ethnicity and family history; medical history; and name of condition/disease for which currently receiving treatment at hospital. 2. Information pertaining to prostate cancer which is represented by PSA value at time of prostate cancer diagnosis and Gleason score. 3. Prognosis information which is survival or death at end point of the Study.

次要结局

  • Patient QOL measured by SF-36 during treatment by comparison with A-Cap data and data in the United States and Australia(three years)

研究者

发起方
Japan Study Group of Prostate Cancer
申办方类型
Other
责任方
Principal Investigator
主要研究者

Hideyuki Akaza

Professor

Japan Study Group of Prostate Cancer

研究点 (1)

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