Factors Affecting Enrollment in a Randomized Controlled Trial for Japanese Metastatic Breast Cancer Patients (SELECT BC-FEEL)-A Prospective Study

被引:1
|
作者
Ohsumi, Shozo [1 ]
Mukai, Hirofumi [2 ]
Ohashi, Yasuo [3 ]
机构
[1] NHO Shikoku Canc Ctr, Dept Breast Oncol, Matsuyama, Ehime 7910280, Japan
[2] Natl Canc Ctr Hosp East, Div Oncol Hematol, Kashiwa, Chiba, Japan
[3] Univ Tokyo, Sch Hlth Sci & Nursing, Dept Biostat Epidemiol & Prevent Hlth Sci, Tokyo, Japan
关键词
metastatic breast cancer; prospective cohort study; enrollment; informed consent; CLINICAL-TRIALS; PHASE-I; PARTICIPATION; ATTITUDES; ONCOLOGY;
D O I
10.1093/jjco/hyu065
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To examine factors affecting the rates at which informed consent is obtained in randomized controlled trials for Japanese metastatic breast cancer patients, we are conducting prospective studies with a self-administered questionnaire we have developed.To accelerate the completion of clinical trials, it is critical to obtain, at high rates, informed consent to participate from patients who are eligible. It is therefore important to know what factors affect the participation rates of eligible patients. Selection of effective chemotherapy for breast cancer and its successor selection of effective chemotherapy for breast cancer-CONFIRM are randomized controlled trials conducted for Japanese patients with chemotherapy-na < ve metastatic breast cancer. These trials are intended to compare the current standard chemotherapeutic regimens in the first-line setting, which are taxanes for selection of effective chemotherapy for breast cancer and anthracyclines for selection of effective chemotherapy for breast cancer-CONFIRM, respectively, and an oral regimen of TS-1 in terms of overall survival. We are conducting prospective studies to identify the factors affecting the rates at which informed consent is obtained in selection of effective chemotherapy for breast cancer and breast cancer-CONFIRM. We are using a self-administered questionnaire that we have developed to collect information regarding patients' characteristics and attitude to clinical trials.
引用
收藏
页码:696 / 701
页数:6
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