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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05034393
Other study ID # LACOG 0221
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 4, 2022
Est. completion date February 27, 2023

Study information

Verified date October 2023
Source Latin American Cooperative Oncology Group
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims to describe in detail the patient journey from diagnosis to the beginning of treatment and patterns of care of hormone receptor- positive, HER2-negative de novo or recurrent metastatic breast cancer between January 2018 and December 2020 in Brazil.


Recruitment information / eligibility

Status Completed
Enrollment 308
Est. completion date February 27, 2023
Est. primary completion date February 27, 2023
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Women =18 years old - Histologically confirmed hormone receptor-positive HER2-negative invasive breast cancer - Hormone receptor-positive defined as 1% to 100% of tumor nuclei positive for Estrogen - - Receptor and/or Progesterone Receptor, as per ASCO/CAP Guideline 2020 - or Allred score of =3 - HER2-negative defined as IHC result is 0/1+ or 2+ with ISH negative as per ASCO/CAP Guideline 2018 - Diagnosed with de novo or recurrent metastatic breast cancer between January 2018 -and December 2020 - Public health system or private health system Exclusion Criteria: - Male Breast Cancer - First-line treatment for mBC received through clinical trial

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Brazil Instituto do Câncer Brasil - Unidade Andradina Andradina São Paulo
Brazil Hospital Sírio-Libanês DF Brasília Distrito Federal
Brazil IGESDF - Instituto de Gestão Estratégica em Saúde do Distrito Federal Brasília Distrito Federal
Brazil CEPESG - Centro de Pesquisa e Educação da Serra Gaúcha Caxias Do Sul Rio Grande Do Sul
Brazil Instituto do Câncer Brasil - Unidade Pantanal Corumbá Mato Grosso Do Sul
Brazil Instituto de Hematologia e Oncologia Curitiba (Oncoclínicas) Curitiba Paraná
Brazil CRIO - Centro Regional Integrado de Oncologia Fortaleza Ceará
Brazil CPO - Centro Paraibano de Oncologia (Oncoclínicas) João Pessoa Paraíba
Brazil CINPAM - Centro Integrado de Pesquisa da Amazônia Manaus Amazonas
Brazil CPO - Centro de Pesquisa em Oncologia do Hospital São Lucas da PUCRS Porto Alegre Rio Grande Do Sul
Brazil HMV - Hospital Moinhos de Vento Porto Alegre Rio Grande Do Sul
Brazil INCA - Instituto Nacional de Câncer Rio De Janeiro
Brazil CLION - Clínica de Oncologia (Oncoclínicas) Salvador Bahia
Brazil Instituto do Câncer Brasil - Unidade Três Lagoas Três Lagoas Mato Grosso Do Sul
Brazil HINJA - Hospital Jardim Armália Volta Redonda Rio De Janeiro

Sponsors (2)

Lead Sponsor Collaborator
Latin American Cooperative Oncology Group Brazilian Breast Cancer Study Group (GBECAM)

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary The proportion of type of first-line treatment from January 2018 to December 2020
Secondary The PFS, defined as time from treatment start until progression (by image or physical exam) or death from January 2018 to December 2020
Secondary First-line treatment according to the drug name by type of health care coverage (public vs private) from January 2018 to December 2020
Secondary The PFS will be evaluated by type of health care coverage (public vs private). from January 2018 to December 2020
Secondary Timeline from first symptom to diagnosis from January 2018 to December 2020
Secondary Timeline from diagnosis to molecular test from January 2018 to December 2020
Secondary Timeline from diagnosis to the beginning of treatment from January 2018 to December 2020
Secondary Patients' socioeconomic characteristics from January 2018 to December 2020
Secondary Patients' demographics characteristics from January 2018 to December 2020
Secondary BC pathological characterization from January 2018 to December 2020
Secondary Rate of diagnostic tests to define breast cancer molecular subtypes performed from January 2018 to December 2020
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