Cyclophosphamide, Paclitaxel, and Trastuzumab in Treating Stage I-II HER2/Neu Positive Breast Cancer After Surgery
NCT02654119
Breast Diseases, Breast Neoplasms
Norfolk, Nebraska, United States
View Trial DetailsNCT Number: NCT05203458
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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Observational
Research Site, Shanghai, Shanhai, China
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
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:
Exclusion criteria
Patients who meet any of the following criteria will be disqualified from entering the study:
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.
Time frame: Within one year
Tumor size of Histopathological characteristic by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2
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
Time frame: Within one year
TNM stage by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2
Time frame: Within one year
Pathological type by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2
Time frame: Within one year
Histological grade by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2
Time frame: Within one year
Multi-focal by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2
Time frame: Within one year
ER status by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2
Time frame: Within one year
ER percentage by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2
Time frame: Within one year
PR status by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2
Time frame: Within one year
PR(Progesterone Receptor) percentage by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2
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
Time frame: Within one year
HER2 IHC score by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2
Time frame: Within one year
FISH status by different HER2 expression level (Ø /Low/High) in PART 1 and PART 2
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
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
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
Time frame: Within one year
To estimate the prevalence of HER2 IHC0 and HER2 IHC >0<1+ in PART 2
Time frame: At baseline
Age at diagnosis of patients' demographic at baseline by different HER2 expression level in PART 1
Time frame: At baseline
BMI of patients' demographic at baseline by different HER2 expression level in PART 1
Time frame: At baseline
Menopause or not of patients' demographic at baseline by different HER2 expression level in PART 1
Time frame: At baseline
Patients' treatment patterns at baseline, by different HER2 expression level in PART 1
AstraZeneca
Industry
HER2 Retrospective Epidemiology Study Prevalence and Clinicopathologic Features of Different HER2 Level in Chinese Breast Cancer Patients (HER2 PATH)
Acronym: HER2 PATH
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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