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NCT Number: NCT05203458

Prevalence and Clinicopathologic Features of Different HER2 Level in Chinese Breast Cancer Patients

This retrospective study aims to estimate the prevalence of different HER2 expression levels (HER2+, HER2-low, HER2 Ø) in approximately 200 breast cancer patients at FUSCC through the year of 2015 and 3000 breast cancer patients from about 10 medical centres in China between July 2021 and July 2022

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Research Site, Shanghai, Shanhai, China

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About this study

This is a multicenter, retrospective study to estimate the prevalence of different HER2 expression levels (HER2+, HER2-low, HER2 Ø) in approximately 200 breast cancer patients at FUSCC through the year of 2015 and 3000 breast cancer patients from about 10 medical centres in China between July 2021 and July 2022.

This study will be divided into two parts: The first part will include 200 subjects who were pathologically diagnosed with breast cancer at FUSCC between Jan 2015 and Dec 2015 (PART 1).This part will collect rescored HER2 expression level results based on the archived HER2 IHC slides and re-staining and re-scoring HER-2 IHC while relative demographic, treatment, and clinicopathologic data will be extracted from the FUSCC Breast Cancer Single Disease Database.

The second part will include 3000 patients from all sites in China who were pathologically diagnosed with breast cancer between July 2021 and July 2022 (PART 2). This part will collect re-assessed HER2 expression level results based on the archived HER2 IHC slides. The general information of patients, diagnosis, clinicopathological information were collected from medical records, Hospital Information System (HIS) and Laboratory Information Management System (LIS).

In PART 2, among 3000 patients, 270 from all participating sites except FUSCC should have enough tumor tissue for re-staining and re-scoring HER-2 IHC at FUSCC to analyse the concordance between leading site and other centers.

In PART 2, among 3000 patients, 800 HER-2 IHC samples will be selected for the validation through AI-assisted HER2 assessment system

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Patients fulfilling all of the following criteria will be eligible for this study:

  • Male and female patients must have a histological confirmed diagnosis of BC
  • The patients must be ≥18 years old at the diagnosis.
  • In PART 1, all patients should be diagnosed at FUSCC between Jan 2015 and Dec 2015.
  • In PART 2, all patients should be diagnosed at all participating sites between July 2021 and July 2022.
  • Provision of at least 1 archived HER2 IHC slides associated with confirmed diagnosis of BC, which are in good condition for rescoring.
  • FISH result is available for HER2 IHC2+ in primary scoring.

Exclusion criteria

Patients who meet any of the following criteria will be disqualified from entering the study:

  • Absence of all demographic, histopathologic, clinicopathologic information .
  • Have a history of other malignancies, other than basal cell carcinoma of the skin and squamous cell carcinoma of the skin.

Treatment and study plan

Primary outcomes

  1. The Prevalence of different HER2 expression levels

    Time frame: Within one year

    To estimate the prevalence of different HER2 expression levels (HER2+, HER2-low(defined as IHC 1+,2+/ISH-), HER2 Ø) in Chinese breast cancer patients in PART 2.

Secondary outcomes

  1. Tumor size of histopathological

    Time frame: Within one year

    Tumor size of Histopathological characteristic by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2

  2. Positive lymph node number of the histopathological

    Time frame: Within one year

    Positive lymph node number of histopathological characteristic by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2

  3. TNM stage by different HER2 expression levels

    Time frame: Within one year

    TNM stage by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2

  4. Pathological type of histopathological

    Time frame: Within one year

    Pathological type by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2

  5. Histological grade of histopathological

    Time frame: Within one year

    Histological grade by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2

  6. Multi-focal of histopathological

    Time frame: Within one year

    Multi-focal by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2

  7. ER status of histopathological

    Time frame: Within one year

    ER status by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2

  8. ER percentage by different HER2 expression levels.

    Time frame: Within one year

    ER percentage by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2

  9. PR status of histopathological

    Time frame: Within one year

    PR status by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2

  10. PR percentage by different HER2 expression levels.

    Time frame: Within one year

    PR(Progesterone Receptor) percentage by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2

  11. Ki-67 percentage by different HER2 expression levels.

    Time frame: Within one year

    Histopathological and clinicopathological characteristics by different HER2 expression level (Ø /Low/High) including: Ki-67 percentage,in PART 1 and PART 2

  12. HER2 IHC score of histopathological

    Time frame: Within one year

    HER2 IHC score by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2

  13. FISH status of histopathological

    Time frame: Within one year

    FISH status by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2

  14. The concordance between historical scoring and reassess scoring in each IHC score category (IHC score Ø, 1+, 2+and 3+)

    Time frame: Within one year

    To estimate the concordance between historical scoring and reassess scoring in each IHC score category (IHC score Ø, 1+, 2+and 3+) in PART 2

  15. The concordance of HER2 expression between manual and AI assisted HER2 interpretation

    Time frame: Within one year

    To estimate the concordance of HER2 expression between manual and AI assisted HER2 interpretation among 800 patients in PART 2

  16. The concordance of HER2 expression between leading site (FUSCC) and other centers

    Time frame: Within one year

    To estimate the concordance of HER2 expression between leading site (FUSCC) and other centers among 270 patients in PART 2

Other outcomes

  1. The prevalence of HER2 IHC0 and HER2 IHC >0<1+

    Time frame: Within one year

    To estimate the prevalence of HER2 IHC0 and HER2 IHC >0<1+ in PART 2

  2. Age at diagnosis of patients' demographic at baseline

    Time frame: At baseline

    Age at diagnosis of patients' demographic at baseline by different HER2 expression level in PART 1

  3. BMI of patients' demographic at baseline

    Time frame: At baseline

    BMI of patients' demographic at baseline by different HER2 expression level in PART 1

  4. Menopause or not of patients' demographic at baseline

    Time frame: At baseline

    Menopause or not of patients' demographic at baseline by different HER2 expression level in PART 1

  5. The baseline treatment patterns across patients with different HER2 expression levels

    Time frame: At baseline

    Patients' treatment patterns at baseline, by different HER2 expression level in PART 1

Sponsors and collaborators

Lead sponsor

AstraZeneca

Industry

Registry information

Official study title

HER2 Retrospective Epidemiology Study Prevalence and Clinicopathologic Features of Different HER2 Level in Chinese Breast Cancer Patients (HER2 PATH)

Acronym: HER2 PATH

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Jan 24, 2022
Registry last updated
May 16, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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