Abstract 1586P
Background
According to GLOBOCAN's 2024 report breast cancer (BC) is the second leading cause of cancer, posing a significant health challenge in both developed (DE) and developing countries (DC) (Bray F., 2024). Among women, BC is the most commonly diagnosed cancer and the leading cause of cancer deaths, with an estimation of 2.3 million new cases and 666,000 deaths in 2022.
Methods
We performed a critical review of the disparities in BC between DE and DC countries using data from the GLOBOCAN and the North American Association of Central Cancer Registries databases, alongside pertinent literature.
Results
DE countries show substantially higher incidence rates (54.1 vs 30.8 per 100,000), peaking in France, Australia/New Zealand, North America and Northern Europe. Conversely, mortality rates are significantly higher in DC countries (15.3 vs 11.3 per 100,000) (Bray F., 2024). Compared with the risk factors for age-standardized death rate (ASDR) in 1990, smoking and alcohol consumption decreased. In contrast, high plasma glucose and body mass index were ranked as significant contributors to increased ASDR in 2019 (Lv L., 2023). In DE countries, BC incidence increased until 2000, then stabilized and rised again since 2005 (Breen N., 2011). Meanwhile, the mortality rate declined in recent years (Bray F., 2024; Cronin KA., 2022). In contrast, DC countries are witnessing rapid increases in both incidence and mortality rates, driven by socioeconomic transitions, urbanization, obesity, changes in female reproductive patterns and challenges of healthcare systems (Lv L., 2023; Ginsburg O., 2017). Early detection and treatment improve survival rates, but DC countries often face late-stage diagnosis due to limited screening and cancer care (Brand NR., 2019). The WHO’s 2021 Global Initiative aims to lower mortality by 2.5% yearly through enhanced health promotion, early detection and comprehensive management of the disease (WHO., 2023).
Conclusions
BC remains a global challenge with pronounced disparities between DE and DC countries in incidence, mortality and survival. These differences highlight the need for a coordinated global response that addresses risk factors, early detection and ensures access to treatment, regardless of the geographical location.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The author.
Funding
Has not received any funding.
Disclosure
The author has declared no conflicts of interest.
Resources from the same session
1501P - Sex-specific variation in symptoms presentation: Experience of an outpatient clinic integrated model between radiotherapy and palliative care
Presenter: Luca Tontini
Session: Poster session 10
1502P - Sexual dysfunction and quality of life in rectal cancer
Presenter: Fatih Kus
Session: Poster session 10
1503P - Spiritual needs in cancer patients: A cross-sectional study
Presenter: Diego Toloi
Session: Poster session 10
1546P - Use of ESMO-MCBS Scorecards in supporting funding decisions in private insurance
Presenter: Samantha Field
Session: Poster session 10
1547P - Time from approval to reimbursement of new cancer and non-cancer drugs: A comparative analysis between the US, England, Germany, and Switzerland (2011-2022)
Presenter: Camille Glaus
Session: Poster session 10
1548P - Real-world impact of the platinum chemotherapy shortage on advanced cancer patients
Presenter: Jacob Reibel
Session: Poster session 10
1549P - Accelerating access to innovative oncology drugs: Insights from France's early access reform
Presenter: Tess Martin
Session: Poster session 10
1550P - Addressing uncertainties of clinical value and improving access for newly authorised indications through DRUG-Access Protocol (DAP)-like platforms: Joint collection and evaluation of real-world evidence
Presenter: Sahar van Waalwijk van Doorn-Khosrovani
Session: Poster session 10
1551P - Breakthrough therapy cancer drugs and indications with FDA approval: Development time, innovation, trials, clinical benefit, epidemiology, and price
Presenter: Christoph Michaeli
Session: Poster session 10
1552P - Regulatory approval of novel immunotherapy for lymphoid neoplasm in the US, EU, and Japan
Presenter: Kensuke Matsuda
Session: Poster session 10