ID
45633
Descrição
Principal Investigator: Elaine R. Mardis, PhD, Nationwide Children's Hospital, Columbus, OH, USA MeSH: Breast Neoplasms https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001291 HER2 (ERBB2) gene amplification and overexpression are present in 15-30% of invasive breast cancers. While HER2-targeted agents such as trastuzumab are effective treatments, therapeutic resistance remains a concern in HER2-positive breast cancer with 40-50% of patients having residual disease after neoadjuvant treatment with chemotherapy and trastuzumab. To investigate features that may make it possible to predict at diagnosis which cancers will be responsive to trastuzumab and chemotherapy, 48 tumor/normal DNA pairs extracted from pretreatment tumor biopsies and blood of HER2-positive breast cancer cases treated with neoadjuvant chemotherapy and trastuzumab were sequenced. Whole genome and exome sequence from tumor (average depth 49x and 71x) and normal (average depth 33x and 69x) DNA are included here as well as RNAseq data for 42 of the tumors. The study cohort was equally divided between patients who experienced pathological complete response and those with residual disease. Samples were obtained from the American College of Surgeons Oncology Group Z1041 trial (NCT00513292) and a local single-institution study (NCT00353483).
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Versões (1)
- 09/03/2023 09/03/2023 - Simon Heim
Titular dos direitos
Elaine R. Mardis, PhD, Nationwide Children's Hospital, Columbus, OH, USA
Transferido a
9 de março de 2023
DOI
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Licença
Creative Commons BY 4.0
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dbGaP phs001291 Neoadjuvant Trastuzumab Response in Breast Cancer
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- Subject ID, affection status, and consent group of participants with breast cancer and involved in the "Neoadjuvant Trastuzumab Response in Breast Cancer" project.
- Subject ID, sample ID, and sample use variable of participants with breast cancer and involved in the "Neoadjuvant Trastuzumab Response in Breast Cancer" project.
- Subject ID and gender of participants with breast cancer and involved in the "Neoadjuvant Trastuzumab Response in Breast Cancer" project.
- Sample ID, analyte type, body site, histological type, and tumor status of samples obtained from participants with breast cancer and involved in the "Neoadjuvant Trastuzumab Response in Breast Cancer" project.
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Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- Subject ID, affection status, and consent group of participants with breast cancer and involved in the "Neoadjuvant Trastuzumab Response in Breast Cancer" project.
- Subject ID, sample ID, and sample use variable of participants with breast cancer and involved in the "Neoadjuvant Trastuzumab Response in Breast Cancer" project.
- Subject ID and gender of participants with breast cancer and involved in the "Neoadjuvant Trastuzumab Response in Breast Cancer" project.
- Sample ID, analyte type, body site, histological type, and tumor status of samples obtained from participants with breast cancer and involved in the "Neoadjuvant Trastuzumab Response in Breast Cancer" project.
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