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Optimization of preoperative chemotherapy for breast cancer using whole genome sequencing -prediction of pathological complete response and exploration of a novel target for patients with non-pathological complete response

Not Applicable
Recruiting
Conditions
Breast Cancer
Registration Number
JPRN-UMIN000051093
Lead Sponsor
West Japan Oncology Group
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
240
Inclusion Criteria

Not provided

Exclusion Criteria

1. Patients with a history of invasive malignancy within the past 3 years from the time consent was obtained. 2. Have an active infection requiring systemic treatment. 3. Have poorly controlled diabetes mellitus or hypertension. 4. Patients with unstable angina, myocardial infarction within 6 months, or clinically significant arrhythmia requiring treatment. 5. Congestive heart failure, poorly controlled valvular heart disease, dilated cardiomyopathy, or hypertrophic cardiomyopathy consistent with New York Heart Association (NYHA) Classification II or higher. 6. Receiving continuous systemic administration of steroids " exceeding 10mg/day of prednisolone equivalent"or immunosuppressive agents. 7. Other cases deemed inappropriate by the physician in charge.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Identify genomic and immunological factors that correlate with pCR in preoperative treatment
Secondary Outcome Measures
NameTimeMethod
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