Study of Chemotherapy With Adoptive Cellular Therapy With DC-CIK Cells in Triple Negative Breast Cancer Patients
DCCIK
Study of Chemotherapy Combined With Adoptive Cellular Therapy With Dendritic and Cytokine-induced Killer Cells in Triple Negative Breast Cancer Patients
1 other identifier
observational
23
1 country
1
Brief Summary
To access the effectiveness of cyclophosphamide combined thiotepa and carboplatin chemotherapy combined with adoptive cellular therapy with dendritic and cytokine-induced killer cells in triple negative metastatic breast cancer patients
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Jul 2011
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2011
CompletedFirst Submitted
Initial submission to the registry
July 14, 2011
CompletedFirst Posted
Study publicly available on registry
July 15, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2015
CompletedJuly 22, 2015
July 1, 2015
3.4 years
July 14, 2011
July 20, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
progression-free survival
progression-free survivalis measured from the date therapy is initiated to the date of documented disease progression or death
six months to two year
Secondary Outcomes (1)
clinical benefit response and overall survival
six months to two year
Eligibility Criteria
female patients with metastatic breast cancer
You may qualify if:
- Failure to anthracycline and/or taxol chemotherapy;
- metastatic tumor is histologically confirmed by immunohistochemical staining to be ER-negative and PR-negative. FISH testing for her-2-negative;
- Metastatic tumor can not be removed through surgery procedure;
- An Eastern Cooperative Oncology Group (ECOG) performance status of 0-2;
- Normal cardiac, hepatic, renal and bone marrow functions;
- Life expectancy ≥3 months.
You may not qualify if:
- Central nervous system metastases;
- Serious or uncontrolled concurrent medical illness;
- History of other malignancies;
- Having been enrolled in some other clinal trials within a month;
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Beijing Cancer Hospital
Beijing, 100142, China
Biospecimen
about 4ml peripheral vein blood,paraffin section on metastatic tissue,
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jing Yu, MD, PhD
Peking University Cancer Hospital & Institute
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Director of the Medical Oncology
Study Record Dates
First Submitted
July 14, 2011
First Posted
July 15, 2011
Study Start
July 1, 2011
Primary Completion
December 1, 2014
Study Completion
June 1, 2015
Last Updated
July 22, 2015
Record last verified: 2015-07