Breast Cancer Clinical Trial
Official title:
A Phase III Randomized Controlled Trial of Prophylactic Cranial Irradiation in Patients With Advanced Triple Negative Breast Cancer Who Had a Response to First Line Chemotherapy
Verified date | May 2017 |
Source | Sun Yat-sen University |
Contact | fei Xu |
Phone | 862087342693 |
xufei[@]sysucc.org.cn | |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to compare whether prophylactic cranial irradiation in patients with advanced triple negative breast cancer who had a response to first line chemotherapy could prolong brain-metastasis free survival.
Status | Not yet recruiting |
Enrollment | 326 |
Est. completion date | August 2025 |
Est. primary completion date | August 2025 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: 1. Signed informed consent; 2. Age of 18 to 65 years; 3. Documented advanced breast cancer, clinical and pathological confirmed; 4. Immunohistochemical examination:ER<1%+, progestin receptor (PR)<1%+, HER-2 -/+ or HER-2(++)with negative result of FISH; 5. A response after four to eight cycles of first line chemotherapy; 6. Life expectancy longer than six months evaluated by investigator; 7. A performance status of 0 to 2, according to the criteria of the World Health Organization (with a higher score indicating a poorer performance status) 8. Less than grade 1( Common Terminology Criteria grade version 4.0) of treatment-related toxicities; 9. Adequate baseline organ function. Exclusion Criteria: 1. History of another malignancy. 2. Pregnancy or gestation 3. Definite diagnosed of central nervous system (CNS)or leptomeningeal metastases 4. Serious cardiac illness or medical condition 5. Known history of related central nervous system or leptomeningeal disease 6. Cognition impairment or suffering from mental illness 7. Demand a long-term oral administration of psychotropic drugs 8. Have a concurrent disease or condition that may interfere with study participation, or any serious medical disorder that would interfere with the subject's safety (for example, active or uncontrolled infection, currently active/requiring anti-viral therapy hepatic or biliary disease) |
Country | Name | City | State |
---|---|---|---|
China | State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center | Guangzhou | Guangdong |
Lead Sponsor | Collaborator |
---|---|
wang shusen |
China,
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Saip P, Cicin I, Eralp Y, Karagol H, Kucucuk S, Cosar Alas R, Yavuz E, Dincer M, Saglam E, Topuz E. Identification of patients who may benefit from the prophylactic cranial radiotherapy among breast cancer patients with brain metastasis. J Neurooncol. 2009 Jun;93(2):243-51. doi: 10.1007/s11060-008-9769-0. Epub 2008 Dec 20. — View Citation
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* Note: There are 17 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | brain metastasis-free survival | time from randomization to brain metastasis | eight years | |
Secondary | cumulative risk of brain metastases within 1 year | the percent of subjects occurring brain metastases with 1 year | one year | |
Secondary | progression-free survival | time from randomization to disease progression or death(upon which happen earlier) | eight years | |
Secondary | overall survival | time from randomization to death | eight years | |
Secondary | life quality score | quality of life measured by the EORTC-QLQ-C30 questionnaire score | eight years | |
Secondary | central nervous function score | function of central nervous measured by the EORTC-QLQ-BN20 questionnaire score | eight years |
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