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NCT06131424Completed

NIS Study Determining Prevalence of HER2-low in Metastatic Breast Cancer Patients

Multicentre NIS Retrospective Study to Know the Prevalence of HER2- Low,Clinical Characteristics,Treatment Patterns,Associated Outcome in Patient With HER2-negative in Metastatic Breast Cancer Who Progressed on Systemic Anticancer Therapy

Source: ClinicalTrials.gov · Last updated 18 Sept 2025

Brief summary (registry, in English)

This noninterventional, multicenter,retrospective study has been proposed to estimate the prevalence, clinicopathological characteristics,treatment patterns and clinical outcomes of human epidermal growth factor receptor 2 -(HER2)low locally-advanced or metastatic breast cancer(mBC) by accurate rescoring of archived IHC-stained formalin-fixed paraffin-embedded (FFPE) slides for HER2 in patients previously identified as HER2-negative from emerging markets of international regions (non-US and non-European region) with largely unknown prevalence estimates of HER2 low mBCs. Patients with a confirmed diagnosis of HER2-negative, locally-advanced or mBC regardless of Hormone receptor (HR)status between 01 January 2019 and 31 December 2022 who progressed on any systematic anticancer therapy (eg, ET, chemotherapy, CDK4/6 inhibitor, targeted therapies other than anti-HER2, or immunotherapy) in advanced disease with availability of atleast 12 months of follow-up data (from the index date) in the medical records at the participating site, unless patient died within the first 12 months of diagnosis of locally-advanced or mBC will be enrolled in the study. The HR positive patients will be considered eligible for the study if they have received ET as adjuvant therapy in the early BC setting and progressed within 24 months. This scenario will be considered as progression on systematic treatment in the advanced or metastatic setting.

Status (registry)
Completed
Study type
Observational
Enrollment
1151 (actual)
First submitted
9 Nov 2023
Start date
23 Apr 2024
Primary completion date
19 May 2025
Lead sponsor
AstraZeneca
NCT number
NCT06131424

What you commit to

  • Study type: Observational
  • Participants enrolled: 1151
  • From 23 Apr 2024 to the primary completion date, 19 May 2025
  • 23 sites in 13 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Who the study is looking for

  • \-

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (23)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
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RosarioArgentinaUnknown status
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São PauloBrazilUnknown status
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Santo DomingoDominican RepublicUnknown status
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Hong KongHong Kong SAR ChinaUnknown status
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JakartaIndonesiaUnknown status
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BengaluruIndiaUnknown status
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BhubaneswarIndiaUnknown status
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DelhiIndiaUnknown status
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HyderabadIndiaUnknown status
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KochiIndiaUnknown status
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MohaliIndiaUnknown status
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MumbaiIndiaUnknown status
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VaranasiIndiaUnknown status
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Mexico CityMexicoUnknown status
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Kaula LumpurMalaysiaUnknown status
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Subang JayaMalaysiaUnknown status
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Panama CityPanamaUnknown status
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Quezon CityPhilippinesUnknown status
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SingaporeSingaporeUnknown status
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BangkokThailandUnknown status
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HanoiVietnamUnknown status
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Ho Chi Minh CityVietnamUnknown status
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HuếVietnamUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.