Be involved

The Joint Breast Cancer Registry (JBCR) invites internal, external collaborators to engage in high-impact scientific partnerships that leverage our comprehensive, granular database. Containing prospective records since 1990, the registry provides an invaluable resource for studying breast cancer within a uniquely diverse Asian population, characterized by exceptionally long-term and thorough clinical follow-up. This longitudinal data facilitates a broad spectrum of multidisciplinary research, including clinical outcomes analysis, deep learning applications, epidemiology, and the investigation of socio-economic determinants of health.

We specifically welcome partnerships with industry and pharmaceutical companies seeking real-world evidence on treatment modalities, toxicity profiles, and long-term outcomes to advance value-driven care. Similarly, we encourage engagement from government agencies and healthcare policy makers to leverage our longitudinal insights for strategic policy planning, resource allocation, and the optimization of national breast cancer programs.

Study Team Members

The list of our study members and contributors can be found here.

Contact us:

For the following enquiries, please contact the respective email addresses.

Available: Monday-Friday, 10:00am-5pm