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Clinical Trials/NCT06603597
NCT06603597RecruitingNot Applicable

Prospective Evaluation of Outcomes for HER2-positive Breast Cancer (PRO-HER2)

Priyanka Sharma12 sites in 1 country1,000 target enrollmentStarted: September 27, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
1,000
Locations
12
Primary Endpoint
Overall survival rate

Study Overview

Brief Summary

The goal of this observational study is to better understand links between patient or tumor characteristics and outcomes in HER2-positive breast cancer.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Stage I-IV HER2-positive breast cancer

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Overall survival rate

Time Frame: From diagnosis to 5 years after diagnosis

For patients with stage I-III HER2-positive breast cancer, percentage of patients who are alive at 5 years after diagnosis.

Secondary Outcomes

  • Pathologic complete response rate(From start of neoadjuvant systemic treatment until approximately 8 months after start of neoadjuvant systemic treatment)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Priyanka Sharma

Professor of Medicine

University of Kansas Medical Center

Study Sites (12)

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