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Tumor-microenvironment Spatial Interaction to Identify Markers of Resistance to Therapy in HER2+ Breast Cancer Patients

G

Giampaolo Bianchini

Status

Not yet enrolling

Conditions

HER2-positive Breast Cancer

Study type

Observational

Funder types

Other

Identifiers

NCT06518382
TaME-HER2BrCa

Details and patient eligibility

About

This retrospective observational study aims at the comparison of the tumour-microenvironment tissue architecture before and after neo-adjuvant therapy in samples from HER2-positive (HER2+) breast cancer (BrCa) patients that display residual invasive disease in the breast/lymph node at surgery after standard-of-care combined chemotherapy and trastuzumab treatment.

The working hypothesis of the investigators is that:

Therapy imposes a selective pressure on tumour-microenvironment features promoting resistance to treatment.

Participant that have already undergone neo-adjuvant treatment as part of their regular medical care for HER2-positive breast cancer will provide access to formalin-fixed paraffin-embedded (FFPE) samples taken before and after therapy.

Tumoral, peri-tumoral and stromal regions of each specimen will be analyzed with the ultimate goal to identify new biomarkers (and putative targets) of resistance to therapy.

Enrollment

10 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Participant is willing and able to give informed consent for participation in the study.
  2. Patient underwent the following procedure before surgery: biopsy, sequential chemotherapy comprising treatment with antracyclines (AC/EC q21, 4 cycles) followed by taxanes (paclitaxel 1,8,15 q21 for 12 weeks) in combination with the anti-HER2 antibody trastuzumab.
  3. Specimen collected at surgery display residual invasive disease in the breast/lymph node.

Exclusion criteria

  1. pre-existing conditions or concurrent diagnoses;
  2. concomitant use of other medications during neo-adjuvant treatment;
  3. quality of stored specimen does not meet the standard for Imaging Mass Cytometry analysis.

Trial contacts and locations

1

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Central trial contact

Tiziana Daniele, PhD

Data sourced from clinicaltrials.gov

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