HER-Seq: A Blood-based Screening Study to Identify Patients With HER2 Mutations for Enrollment Into Clinical Research Studies of Neratinib
Stopped early
Conditions studied: Hormone Receptor-Positive, HER2-Negative Metastatic Breast Cancer, Metastatic Cervical Cancer
In brief
This is a multi-center, observational genomic screening protocol to identify participants whose tumors harbor somatic mutations in the ERBB2 (HER2) gene, as measured in circulating tumor DNA (ctDNA) . Participants with histologically confirmed, hormone receptor positive, HER-2 negative, metastatic breast cancer (MBC) or metastatic cervical cancer (MCC) are eligible for screening at 6 months intervals, or if disease progression is suspected/confirmed. Blood samples will be collected from eligible participants and ctDNA will be extracted and sequenced at a central laboratory, using a HER2-targeted next generation sequencing (NGS) test. A certified molecular test report will be issued from the central laboratory and provided to the investigators and the study sponsor. Participants who are identified with HER2 mutations by this screening protocol will subsequently have access to an appropriate neratinib treatment protocol, pending medical eligibility.
Key facts
- Study ID
- NCT03786107
- Run by
- Puma Biotechnology, Inc.
- People needed
- 1583
- Starts
- 2019-03-14
- Expected to finish
- 2021-01-21
- Last updated by the study team
- 2021-05-19
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Women and men who are ≥18 years old at signing of informed consent
- Eastern Cooperative Oncology Group (ECOG) status of 0 to 2
- Provide written informed consent to participate in the study and for circulating tumor DNA screening
- Must be able to provide blood sample(s) for HER2 mutation testing
- Participants with imaging or histologically confirmed, HR-positive, HER2-negative MBC who are presently receiving or have received CDK4/6 inhibitor as a prior therapy in any setting, or participants with imaging or histologically confirmed metastatic cervical cancer
- At least one measurable lesion, as defined by RECIST v1.1
You may not qualify if…
- Participants with breast cancer with known HER2-positive or HER2-amplified tumors
- Participants with breast cancer with HR-negative tumors
- Participants who have received HER2-directed TKI
- Participants with previously documented somatic KRAS activating mutation
Where it is running
- Magee-Womens Hospital of UPMC — Pittsburgh, Pennsylvania, United States
- Institut Curie — Saint-Cloud, France
- Cork University Hospital — Wilton, Cork, Ireland
- St. Vincent's University Hospital — Elm Park, Dublin, Ireland
- Mater Misericordiae University Hospital, Institute for Cancer Research — Dublin, Ireland
- Beaumont Hospital, Cancer Clinical Trials & Research Unit — Dublin, Ireland
- University Hospital Waterford, Department of Medical Oncology — Waterford, Ireland
- Rabin Medical Center, Davidoff Cancer Center — Petah Tikva, Central District, Israel
- Kaplan Medical Center — Rehovot, Central District, Israel
- Sheba Medical Center — Ramat Gan, Israel
- Sourasky Medical Center — Tel Aviv, Israel
- Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale" — Naples, Italy
- Institute for Oncology and Radiology of Serbia — Belgrade, Serbia
- Hospital Universitario Quirónsalud Madrid — Pozuelo de Alarcón, Madrid, Spain
- Instituto Oncológico Dr. Rosell, Hospital Universitario Quirón Dexeus — Barcelona, Spain
- Hospital Universitari Vall D'Hebron — Barcelona, Spain
- Hospital Clinic de Barcelona — Barcelona, Spain
- Hospital Clínico San Carlos — Madrid, Spain
- START Madrid, Hospital Universitario Fundacion Jimenez Diaz — Madrid, Spain
- Hospital Universitario Madrid Sanchinarro — Madrid, Spain
- Fundación Instituto Valenciano de Oncológia — Valencia, Spain
- Hospital Clínico Universitario de Valencia — Valencia, Spain
Full record on ClinicalTrials.gov
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