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Breast Cancer Tumor Heterogeneity

Does Breast Tumor Heterogeneity Necessitate Additional HER2 Testing on the Surgical Specimens?

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02108561
Enrollment
110
Registered
2014-04-09
Start date
2014-04-30
Completion date
2018-12-31
Last updated
2018-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

Breast Cancer Heterogeneity Her2

Brief summary

Breast cancer biomarkers are usually performed on core needle biopsy (CNB) specimens and are not routinely repeated on surgical specimens (SS). However, preliminary data suggests that testing these biomarkers, on SS when compared to CNB samples can lead to different results. Our hypothesis is that The aim of this study is to identify a group of women with invasive breast cancer who may benefit from additional HER2 testing on their SS to ensure that areas of HER2 amplification are not missed. Another aim is to determine whether further HER2 testing on the SS in select patients would lead to changes in breast cancer treatment options.

Interventions

OTHERPost Surgical Her2 testing

Eligible patients will have post surgical Her2 testing on the primary tumor, a satellite lesion and a tumor positive node. The results will be provided to medical oncologist, who will comment as to whether the additional testing will prompt treatment recommendation changes

Sponsors

Genentech, Inc.
CollaboratorINDUSTRY
Anne Arundel Health System Research Institute
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

1. Women \> age 18 with capacity to consent 2. Invasive breast cancer identified on CNB at AAMC within 45 days of study consent 3. IHC biomarkers performed on original CNB (including HER2) 4. Tumors with greater than 2cm of invasive disease (measured radiographically prior to resection or microscopically after resection), or 5. Multifocal or multicentric tumors

Exclusion criteria

1. Men 2. Women with HER2 positive tumors detected on CNB specimens 3. Women receiving neoadjuvant chemotherapy 4. Women whose CNB or surgical resection was performed at a hospital other than AAMC. If the CNB prior to resection was repeated at AAMC and new tumor biomarkers were performed, then the patient is eligible for enrollment 5. Women whose IHC marker results were inconclusive on CNB or not performed -

Design outcomes

Primary

MeasureTime frameDescription
Benefit of additional Her2 testing2 yearsTo identify a subset of women with invasive breast cancer who may benefit from additional Her2 testing (by immunochemistry and FISH) on their surgical specimen to ensure that areas of Her2 amplification are not missed due to sampling error of the core needle biopsy.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026