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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06125314
Other study ID # D133FR00197
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 5, 2024
Est. completion date December 31, 2024

Study information

Verified date May 2024
Source AstraZeneca
Contact AstraZeneca Clinical Study Information Center
Phone 1-877-240-9479
Email information.center@astrazeneca.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

HER2-low Breast cancer (BC) has emerged as a new subtype of BC with distinct clinical, pathological, and prognostic features. Little is known about the prevalence of the HER2-low subtype in HER2-negative patients, and previous reports showed variations in the criteria used to define the HER2-low subtype. Besides, data on the clinical features and prognosis of HER2-low patients are limited, and it is still unclear whether HER2-low BC has a prognostic value. Identifying the prevalence and clinical features of HER2-low BC can help establish a more accurate and reproducible definition of HER2-low BC. In the Gulf Cooperation Council (GCC) region, BC is the most common malignancy in women and still poses a significant burden on healthcare resource utilization, moreover, there is only one record for reimbursed HER2 IHC status, categorized as HER2-positive and HER2-negative. It is important to understand the prevalence, clinical features, and outcomes of HER2-low in BC patients from the GCC In this retrospective, non-interventional, multicenter study, the aim to describe the prevalence of HER2-low BC among the current HER2-negative BC population using rescored HER2 IHC samples. The local treatment patterns and the outcomes will be analyzed using the information abstracted from the corresponding medical chart review. The study will cover the GCC region countries (United Arab Emirates [UAE], Saudi Arabia, Qatar, Kuwait, and Oman)


Recruitment information / eligibility

Status Recruiting
Enrollment 385
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria: - women = 18 years of age at date of diagnosis - Patients must have a histological or cytological confirmed diagnosis of Unresectable or/and mBC between 01st January 2018 and 31st December 2022. - Patients with at least 12 months of follow-up data (from the index date) in the medical records at the participating site unless patient died. - Patients must have been diagnosed as HER2-negative (HER2 IHC 0, 1+, 2+/ISH-), regardless of hormone status. - Patients who are diagnosed and/or progressed on at least one prior systemic anticancer therapy (e.g., ET, chemotherapy, CDK4/6i, targeted therapies other than anti- HER2, or immunotherapy) in the metastatic setting. - Patients must have historical HER2 fixed tissue IHC stained slides in acceptable quality to allow retesting of HER2 expression only in case of the absence of accurate scoring of IHC/ISH in pathology report. Exclusion Criteria: - Have a history of other malignancies other than basal cell carcinoma of the skin and squamous cell carcinoma of the skin. - Patients who are HER2 positive (with historical HER2 status of IHC 2+/ISH+ or 3+, or HER2 amplified.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Kuwait Research Site Kuwait
Qatar Research Site Doha
Saudi Arabia Research Site Makkah
Saudi Arabia Research Site Riyadh
Saudi Arabia Research Site Riyadh
United Arab Emirates Research Site Abu Dhabi
United Arab Emirates Research Site Al Ain
United Arab Emirates Research Site Dubai
United Arab Emirates Research Site Dubai

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Countries where clinical trial is conducted

Kuwait,  Qatar,  Saudi Arabia,  United Arab Emirates, 

Outcome

Type Measure Description Time frame Safety issue
Primary HER2-low prevalence based on rescoring of historical HER2 fixed tissue slides among HER2-negative Unresectable or/and metastatic Breast Cancer patients. 1st January 2018 to 31st December 2022
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