PRECAMA: Molecular Subtypes of Premenopausal Breast Cancer in Latin American Women

NCT03144648 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 3000

Last updated 2025-05-06

No results posted yet for this study

Summary

Breast cancer has become a major public health problem in Latin America, as it is the most common form of cancer among women. Women are more likely to develop breast cancer at younger age, and to be diagnosed at an advanced stage compared to western women. Over the past twenty years, the mortality from breast cancer in Latin America has also been increasing very rapidly, and is currently the leading cause of cancer mortality. Little is known on specific risk factors for premenopausal breast cancer in general, and in Latin America in particular. There is a lack of specific knowledge on tumor molecular and pathological characteristics of breast cancer in Latin America premenopausal women, and this has major consequences on cancer treatment and survival.

To improve our understanding on determinants of breast cancer incidence and mortality in young Latin America women and support preventive actions, we implemented an international, population-based multi-center study in Latin America: the PRECAMA study (Molecular Subtypes of Premenopausal Breast Cancer in Latin American Women (PRECAMA): a multicenter population-based case-control study).

PRECAMA is coordinated by the International Agency for Research on Cancer (IARC), and is conducted within 4 Latin American countries: Mexico, Costa Rica, Colombia and Chile. Major aims of the project are the following:

1. To develop a multi-centric population-based case-control study on breast cancer in premenopausal women in several countries in Latin America with structured collection of individual, clinical, pathological information and biological specimens, according to strictly controlled protocols
2. To characterize, in these populations, the subtypes of premenopausal breast cancer on the basis of their molecular and pathological phenotypes
3. To improve the identification of specific endogenous/exogenous factors, and disentangle the interplay of these different factors with regard to breast tumor subtypes.
4. Provide advanced training, induce a structuring effect on the breast cancer research community in Latin America and influence the public health agenda regarding the management of breast cancer.

The results of our study will be of utmost importance to understand the etiology of breast cancer in Latin America countries, and would provide important information on the role of modifiable exposures for breast cancer prevention.

Conditions

  • Breast Cancer Female

Interventions

OTHER

lifestyle

Observational study

Sponsors & Collaborators

  • University of Chile

    collaborator OTHER
  • Fundación Inciensa

    collaborator OTHER
  • Instituto Nacional de Salud Publica, Mexico

    collaborator OTHER
  • Universidad de Antioquia

    collaborator OTHER
  • Barretos Cancer Hospital

    collaborator OTHER
  • International Agency for Research on Cancer

    lead OTHER

Principal Investigators

  • Sabina Rinaldi, PhD · International Agency for Research on Cancer, Lyon, France

  • Maria Luisa Garmendia, PhD · INTA, Universidad de Chile, Santiago, Chile

  • Carolina Porras, PhD · Proyecto Epidemiológico Guanacaste, Fundación INCIENSA, Costa Rica

  • Gabriela Torres-Mejía, PhD · Instituto Nacional de Salud Pública, Cuernavaca, Mexico

  • Gloria I Sánchez, PhD · Grupo Infección y Cáncer, Universidad de Antioquía, Medellín, Colombia

  • Fabiana Vazquez · Barretos Cancer Hospital

Eligibility

Min Age
20 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-10-12
Primary Completion
2025-12-30
Completion
2025-12-30

Countries

  • Brazil
  • Chile
  • Colombia
  • Costa Rica
  • Mexico

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03144648 on ClinicalTrials.gov