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Clinical Trials/NCT05217381
NCT05217381
Completed
N/A

Retrospective Observational Study With Real-World Data to Assess Demographic and Clinicopathological Profiles, and Management of Breast Cancer Patients With Positive, Low or Negative Expression of HER2 in Spain

MedSIR7 sites in 1 country18,533 target enrollmentFebruary 22, 2022

Overview

Phase
N/A
Intervention
Not specified
Conditions
Early Breast Cancer
Sponsor
MedSIR
Enrollment
18533
Locations
7
Primary Endpoint
Prevalence of HER2 expression change between initial diagnosis versus any of the subsequent BC relapses
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

This is a data-driven, retrospective, longitudinal, population- based, observational, multi-centered study using secondary data captured from congruent electronic health records (EHRs).

Detailed Description

Patients with pathologically documented an initial breast cancer diagnostic (early breast cancer (BC) or locally advanced BC or de novo metastatic BC) with documented human epidermal growth factor receptor 2 (HER2) and estrogen receptor (ER)/progesterone receptor (PgR) expression status at the time of diagnosis. Data to determine the primary endpoint is estimated to be derived from the EHRs of over 2,000 patients that have an initial diagnosis of early BC, or locally advanced BC, or de novo metastatic BC (mBC) between the 1st of January 2005 and the 31st of December 2021, and who had at least one subsequent relapse until the 31st of December 2021 in at least 10 clinical centers. The secondary endpoints utilize a larger collection of data from over 30,000 patients that have an initial diagnosis of early BC, or locally advanced BC, or de novo mBC between the 1st of January 2005 and the 31st of December 2021.

Registry
clinicaltrials.gov
Start Date
February 22, 2022
End Date
September 20, 2023
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
MedSIR
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Male or female patients who have at least 18 years of age at enrollment.
  • Patients with initial diagnosis of early BC or locally advanced BC or de novo mBC between the 1st of January 2005 and the 31st of December 2021
  • Pathologically documented BC for:
  • HER2 receptor expression with a validated assay according to American Society of Clinical Oncology - College of American Pathologists (ASCO/CAP) recommendations at the time of diagnosis. HER2 receptor expression can be: o HER2-positive expression: defined as immunohistochemistry (IHC) 3+ or concurrent IHC 2+ with in situ hybridization (ISH) positive or HER2-low expression: defined as IHC 2+ with ISH-negative or IHC 1+ with ISH-negative or untested) or HER2-negative expression: defined as IHC:
  • Estrogen receptor \[ER\]- and/or progesterone receptor \[PgR\] with a validated assay according to ASCO/CAP guidelines at the time of diagnosis during early and/or advanced setting. ER/PgR expression can be: positive: ER or PgR ≥1% or negative: ER and PgR \<1%
  • Electronic Health Records (EHRs), with guaranteed data to meet requisites, about clinicopathological characteristics, type of surgery, treatment management, disease outcomes, and genomic profile. Centers that agree to participate must commit to include all subjects who meet the inclusion criteria, in order to reduce possible selection bias.
  • Exclusion criteria:
  • Medical charts at Hospital that cannot guarantee reliable and congruent EHRs.
  • If sufficient data cannot be obtained from EHRs.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Prevalence of HER2 expression change between initial diagnosis versus any of the subsequent BC relapses

Time Frame: 180 months

Change in HER2 expression between initial diagnosis of early BC or locally advanced BC or de novo mBC and any of subsequent BC relapses by IHC and/or ISH validated assays.

Secondary Outcomes

  • Prevalence of changes in HER2 expression among different lines of treatment(180 months)
  • Description of the clinicopathological characteristics(180 months)
  • Evaluation of the disease management(180 months)
  • Description of genomic profile(180 months)
  • Efficacy (CBR)(180 months)
  • Efficacy (OS)(180 months)
  • Efficacy (ORR)(180 months)
  • Efficacy (PFS)(180 months)
  • Efficacy (DoR)(180 months)

Study Sites (7)

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