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An observational study to evaluate the impact of the gene panel test FoundationOne CDx or FoundationOne Liquid CDx on treatment decision-making in metastatic and recurrent breast cancer throughout Japan as a whole.

Not Applicable
Recruiting
Conditions
Patients with stage IV or recurrent breast cancer who have distant metastases at registration
Registration Number
JPRN-UMIN000038065
Lead Sponsor
Japan Breast Cancer Research Group
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
600
Inclusion Criteria

Not provided

Exclusion Criteria

Patients with active invasive double cancer within 5 years or patients with active invasive double cancer that currently needs treatment.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate the accessibility to matched therapies and the access rate to clinical trials that were recommended by FoundationOne CDx or FoundationOne Liquid CDx genome profiling results The matched therapy is defined as the therapy determined by the expert panel according to the results of the F1CDx or F1LCDx Clinical trials include either single arm development studies or clinical trials
Secondary Outcome Measures
NameTimeMethod
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