ArticleESMO real world data and digital oncology2025
Advancing breast cancer research through real-world data from the Singapore Joint Breast Cancer Registry.
Article in ESMO real world data and digital oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
3 citing papers in PubMed.
- Synthesis and multilevel evaluation of benzimidazole-based anticancer compounds: DNA/serum albumin interaction, and in-depth theoretical insights.Molecular and cellular biochemistry · 2026Article
- Retrospective Cohort Study: Extracting Coexisting Background Breast-Lesion Features from Stage I-III Invasive Breast Cancer.Cancers · 2026Article
- Outcomes of a prospective cohort study of PREoperative therapy and supportive care in early & locally advanced breast cancers-PreSCella study.NPJ breast cancer · 2026Article
Corrections and comments
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Authors and funding
27 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: The Joint Breast Cancer Registry (JBCR) was established to collect comprehensive real-world data on patients with breast cancer treated across multiple institutions in Singapore. We present an overview of the registry, its structure, processes, and research findings. Patients and methods: JBCR includes all breast cancer patients aged ≥21 years old, treated in Singapore from 1980 onwards. Information on patient demographics, tumour characteristics, treatment, toxicity, and clinical outcomes is collected. We integrate data collection into clinical workflows, use automation, such as text-mining, and implement quality control processes to improve the accuracy and completeness of the registry. We further describe data security and governance processes that safeguard patients' privacy and allow for data sharing for research purposes. Results: A diverse cohort of over 35 000 patients have been enrolled in the registry from participating institutions across Singapore. The median age at diagnosis is 54 years with a median follow-up time of 7.6 years. About a quarter of the 8883 deaths were attributed to breast cancer. Analyses of JBCR data have revealed findings such as the impact of tumour subtypes on survival, disparities in treatment responses, and the novel role of radiomics in predicting chemotherapy response. We have also identified significant ethnic and socioeconomic disparities in breast cancer outcomes, emphasizing the need for targeted interventions. Conclusion: By leveraging real-world data, JBCR provides insights into the treatment trends and long-term outcomes of breast cancer in Singapore. We provide value to various stakeholders in clinical care, research, and policy-making. Future initiatives seek to address current limitations, including expanding the collection of genetic and molecular data, increasing patient-reported quality-of-life measures, and enhancing international collaborations.
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