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JBCRG-11CPA TR
Translational research for JBCRG-11CPA ("Evaluation of the Usefulness of Pre-operative Exemestane (EXE) Therapy for Treatment of Hormone-Sensitive Breast Cancer in Postmenopausal Patients, and EXE + Low-Dose CPA Combination Therapy for Nonresponders to EXE Therapy.")
- Status
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No Longer Recruiting
- Objectives
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Identification of a molecular marker to predict the therapeutic effect and marker for "Evaluation of the Usefulness of Pre-operative Exemestane (EXE) Therapy for Treatment of Hormone-Sensitive Breast Cancer in Postmenopausal Patients, and EXE + Low-Dose CPA Combination Therapy for Nonresponders to EXE Therapy."
- Subjects
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Among the patients who participated in the "Evaluation of the Usefulness of Pre-operative Exemestane (EXE) Therapy for Treatment of Hormone-Sensitive Breast Cancer in Postmenopausal Patients, and EXE + Low-Dose CPA Combination Therapy for Nonresponders to EXE Therapy." those who submitted tumor tissues and blood samples for this study.
1)Paraffin block 2)Frozen section 3)Serum 4)Blood sample for CEC
- Endpoints
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1)Analysis of paraffin embedded samples, before, after and during treatment. 2)Analysis and immunostaining of frozen section, Expression analysis of mRNA. 3)Analysis of blood samples.
- Trial Period
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2010.Oct~2024.Sep(Entry period:4years, Follow up period :10years from last entry)
- Lead Principal Investigator
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Masakazu Toi(Kyoto University), Hironobu Sasano(Tohoku University), Takayuki Ueno(Kyorin University)
- Target Sample Size
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Patients who agreed to enter JBCRG-11CPA TR
- Regimen
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- Source of Funding
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Japan Breast Cancer Reserch Group
- Conference Presentation
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- Articles and Publications
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- UMIN-ID
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- jRCT
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- Memo
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- COI Disclosure
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