Abstract
Background
Breast cancer (BC) incidence and mortality vary significantly across countries, highlighting the need to update the global burden of female BC, including current trends and future projections.
Methods
Data were sourced from GLOBOCAN 2022, including estimated new cases and deaths from BC across 21 United Nation (UN) regions and 185 countries, the age-standardized incidence rate (ASIR) and mortality rate (ASMR), the estimated annual percentage changes (EAPC), and demographic projections through 2050. The region-specific and country-specific BC burden for women of all ages and for young women (< 40 years old) was reorganized and re-plotted to highlight subgroup differences. Linear regression was used to explore the link between ASIR/ASMR and the human development index (HDI). Transitioning countries referred to those with low or medium HDI, while transitioned countries were those with high or very high HDI.
Results
In 2022, an estimated 2.3 million new BC cases and 666,000 BC-related deaths occurred globally, accounting for 23.8 % and 15.4 % of all cancer cases and deaths in women, respectively. Regionally, Eastern Asia reported the highest number of cases (480,019, ASIR: 37.54/100,000), while South-Central Asia had the highest number of deaths (135,348, ASMR: 13.41/100,000). At the country level, China had the highest number of cases due to its large population, whereas India reported the highest number of deaths. ASIR for both overall and early-onset BC increased with HDI, while ASMR for early-onset BC decreased with HDI (P < 0.05). Overall BC showed an increasing trend in ASIR during 2003–2015 (EAPC: 0.92 %) and a decreasing trend in ASMR during 2006–2016 (EAPC:-1.06 %). Early-onset BC showed a more significant rise in ASIR (EAPCs: 1.4 %) and a slight increase in ASMR (EAPCs: 0.16 %). If national rates remain stable, BC cases and deaths will increase by 54.7 % and 70.9 %, respectively, by 2050. Notably, increased early-onset BC cases are only observed in transitioning countries, while decreased cases are seen in transitioned countries.
Conclusions
Breast cancer remains the leading cancer burden in women, particularly in transitioning countries. Addressing this growing burden requires urgent integration of primary prevention, early detection and high-quality treatment through multi-sectoral collaboration.
Keywords: Breast cancer, Mortality, Incidence, Trend: early onset, Human development index
1. Introduction
Female breast cancer (BC) has been the leading cause of cancer morbidity and mortality among women in the majority of countries for decades. In 2020, there were an estimated 2.3 million new cases and 685,000 deaths from female BC worldwide, which accounted for one in four cancer cases and one in six cancer deaths among women.1 According to the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2021, BC is the leading cancer in terms of disability adjusted life years (DALYs) for women of all ages, with BC death burden ranking second only to lung cancer. The forecasted BC DALYs increased from 238.6 (223.2–254.2) per 100,000 in 2022 to 239.5 (186.9–300.6) per 100,000 in 2050.2 Globally, about 30 % of BC cases are attributable to modifiable risk factors, such as excess body weight, physical inactivity, and alcohol consumption, thus may be preventable.3, 4, 5 Elevated incidence supported that female-specific factors related to reproductive characteristics, including early age at menarche, later age at menopause, advanced age at first birth, fewer number of children, less breastfeeding, hormonal menopausal therapy, oral contraceptive, and breast density, also collectively contributed a large proportion of BC cases.1,6, 7, 8, 9 High-quality randomized trials further suggested that mammography screening for BC can reduce nearly 20 % of BC mortality.9 Alongside the benefits of effective prevention and mammography screening, advances in treatment can further prevent death and substantially reduce BC mortality. Given the marked difference in exposure to modifiable risk factors and female reproductive characteristics, coverage of mammography screening and levels of effective treatment across different countries, it is vitally important to update the global landscape of BC burden, including the current status, temporal trend and future projections, according to the latest global estimates of female BC.
Moreover, despite a series of measures that have been taken in several countries (especially in transitioned countries) based on the above effective interventions, regional and country-specific studies suggested that both incidence and mortality of BC would continue to increase in the future decades worldwide,10 especially regarding the burden of early-onset BC, diagnosed at or before the age of 40.11, 12, 13, 14 The excessive BC cases would largely reflect the dramatic changes in female reproductive characteristics associated with socioeconomic development, the rapid increase in aging and growth of the population, as well as the delayed introduction of effective BC screening programs in the vast majority of transitioning countries.8,15,16 Extensive research has been conducted in the past using GLOBOCAN 2020 or earlier data to investigate the global burden of breast cancer. However, there are currently few analyses based on the latest GLOBOCAN 2022 data to assess the most recent disease burden. Furthermore, there is limited research exploring the global distribution patterns of early-onset breast cancer, trends over the past decades, and its associations with national socioeconomic development levels.
Therefore, based on the latest data from GLOBOCAN 2022 released by the International Agency for Research on Cancer (IARC), this study aimed to provide a description of the global incidence and mortality of overall and early-onset female BC, as well as to assess the geographic difference. Specifically, we used the burden of BC in representative countries as examples to support decision-making for global BC prevention and control strategies. Then we tried to describe the temporal trend of overall and early-onset female BC burden over the available data and end with a description of future female BC burden up to 2050 based on global demographic projections.
2. Materials and methods
2.1. Data sources
All data were obtained from the GLOBOCAN 2022 database (https://gco.iarc.fr/), including estimated new cases and deaths, the age-standardized incidence rate (ASIR) and mortality rate (ASMR), the estimated annual percentage changes (EAPC), and demographic projections up to 2050. In brief, country-specific raw data on cancer burden released by countries around the world are aggregated and combined by the IARC under the World Health Organization (WHO) according to uniform standards to form the GLOBOCAN database. Until 2022, the GLOBOCAN database has covered the estimated burden of 36 cancer diseases across 185 countries and 21 regions worldwide, including the current, past, and future incidence, mortality and prevalence of cancer by site and sex. Particularly, the Cancer Today database was extracted to present the current estimated cases and deaths from BC in 2022.17 Cancer incidence refers to the number of new cancer cases diagnosed in a specific population during a defined period of time, while cancer mortality represents the number of deaths attributed to cancer within a specified population during a given period. Incidence data are regularly gathered by national or subnational population-based cancer registries, while cause-specific mortality data are routinely compiled by national vital registration systems. The Cancer Over Time database was used to present temporal trends in cancer-specific incidence and mortality rates over the available period based on the Cancer Incidence in Five Continents (CI5 plus) database and the WHO mortality.18 The Cancer Tomorrow database provided the estimated new cancer cases and deaths up to 2050 based on the estimates in 2022.19
2.2. Selected regions and the human development index (HDI)
In this study, both incidence and mortality of BC were majorly presented according to 21 aggregated regions defined by the United Nations Population Division. Based on the United Nation (UN) Development Program's Human Development Report 2021–22,20 the HDI was used to present the difference in BC burden across countries with different levels of socioeconomic development, and it was calculated based on life expectancy, education level and gross domestic income per capita. All countries were reclassified into four levels on the basis of HDI: low HDI (< 0.55), medium HDI (0.55–0.70), high HDI (0.70–0.79) and very high HDI (≥ 0.80).10,21 According to the UN Development Program report, a transitioning HDI country, which included countries with low or medium HDI, typically refers to a nation undergoing significant changes in its HDI ranking over recent years, including improvements or declines in any of the HDI components mentioned above. A transitioned HDI country, namely those with high or very high HDI, refers to nations that have moved from one category of the HDI to another over a period of time, after experienced significant changes in their HDI rankings due to improvements or declines in factors such as life expectancy, education attainment, and income per capita.
2.3. Statistical analysis
The region-specific and country-specific BC burden for women of all ages and for young women (< 40 years old) was reorganized and re-plotted to highlight subgroup differences. Specifically, the statistical descriptive analysis method was mainly used to present the UN regional and country-specific incidence and mortality of overall and early-onset BC in this study. The ASIR and mortality rate ASMR of BC were calculated based on the population originally proposed by Segi (1960) and later modified by Doll et al (1966).22 The early-onset BC was defined as patients who were diagnosed as BC before 40 years old. The linear regression model was used to characterize the relationship between ASIR or ASMR and HDI, and log-transformed correlation coefficient (r) was used to measure the magnitude of the correlation. The estimated annual percentage change (EAPC) was calculated using a generalized linear model used to characterize the temporal trend in ASIR and ASMR over the time period selected with a Gaussian distribution considered.18 The projections for BC incidence and mortality in 2050 presented in the analysis were sourced from the Cancer Tomorrow website. Demographic projections of BC cases and deaths were predicted to 2050 after assuming that the national projected changes in population growth and aging would not change in the forecast period between 2022 and 2050.19 The change percentage in the future estimated burden of BC was calculated as the predicted estimates in 2050 minus the corresponding estimates in 2022 and then divided by the estimates in 2022. The change percentages were further grouped by HDI.
All statistical analyses were performed with R software (version 4.2.3), Microsoft Excel (version 4.2.3) and the Global Cancer Observatory online, and P < 0.05 was considered statistically significant.
3. Results
3.1. Global and regional breast cancer burden in 2022
In 2022, an estimated 2,296,840 new cases of female BC were reported globally, with an ASIR of 46.8 per 100,000. BC accounted for approximately 23.8 % of all cancer cases in women worldwide (Supplementary Fig. 1). Regionally, Eastern Asia had the highest number of incident cases (480,019 cases, ASIR: 37.54/100,000), followed by Northern America (306,307 cases, ASIR: 95.12/100,000). At the country level, China reported the most BC cases due to its large population (16 % of global cases), followed by the United States (12 %) and India (8 %) (Fig. 1). South Central Asia had the highest number of early-onset BC cases across different regions (44,266), with China (13 %), India (11 %), the USA (7 %) leading in this category across different countries (Fig. 1). Australia-New Zealand had the highest ASIR for overall BC (100.28/100,000) (Table 1), while South Central Asia recorded the lowest (26.70/100,000) (Table 1). For early-onset BC, Southern Europe had the highest ASIR (15.82/100,000), while Micronesia had the lowest (4.45/100,000) (Table 1).
Fig. 1.
Country-level proportion of estimated cases and deaths from female breast cancer worldwide in 2022. (A, B) Proportion of overall (A) and early-onset (B) breast cancer cases. (C, D) Proportion overall (C) and early-onset (D) breast cancer deaths.
Table 1.
The estimated burden of breast cancer for different regions in 2022.
| World regions | Incidence |
Mortality |
||||||
|---|---|---|---|---|---|---|---|---|
| All ages |
< 40 years old |
All ages |
< 40 years old |
|||||
| Numbers | ASR (per 100,000) |
Numbers | ASR (per 100,000) |
Numbers | ASR (per 100,000) |
Numbers | ASR (per 100,000) |
|
| World | 2,296,840 | 46.80 | 246,060 | 8.10 | 666,103 | 12.70 | 48,700 | 1.60 |
| Region | ||||||||
| Northern America | 306,307 | 95.12 | 18,096 | 13.14 | 49,744 | 12.32 | 1391 | 1.00 |
| Eastern Asia | 480,019 | 37.54 | 42,048 | 6.81 | 97,389 | 6.52 | 3935 | 0.62 |
| Eastern Africa | 47,300 | 31.94 | 11,747 | 7.12 | 25,330 | 17.58 | 5342 | 3.25 |
| Middle Africa | 16,856 | 29.97 | 4456 | 7.24 | 9142 | 16.82 | 2043 | 3.33 |
| Northern Africa | 64,977 | 53.17 | 13,703 | 13.69 | 23,186 | 19.00 | 3562 | 3.52 |
| Southern Africa | 15,815 | 46.16 | 1912 | 6.12 | 5693 | 16.57 | 548 | 1.74 |
| Western Africa | 53,605 | 41.63 | 11,350 | 8.19 | 27,901 | 22.25 | 5085 | 3.68 |
| Caribbean | 14,862 | 49.57 | 1768 | 10.55 | 5953 | 18.17 | 410 | 2.39 |
| Central America | 39,835 | 38.28 | 6010 | 7.96 | 10,670 | 10.05 | 830 | 1.08 |
| South-Eastern Asia | 168,536 | 41.73 | 23,109 | 8.39 | 61,228 | 14.85 | 4693 | 1.68 |
| South Central Asia | 273,902 | 26.70 | 44,266 | 5.27 | 135,348 | 13.41 | 12,063 | 1.43 |
| Western Asia | 63,360 | 45.40 | 10,958 | 9.56 | 21,344 | 15.11 | 2514 | 2.16 |
| Eastern Europe | 163,474 | 58.30 | 11,911 | 10.19 | 49,973 | 14.44 | 1419 | 1.15 |
| Northern Europe | 89,324 | 90.80 | 4675 | 12.03 | 18,629 | 13.70 | 409 | 1.04 |
| Southern Europe | 124,621 | 81.76 | 7543 | 15.82 | 31,450 | 13.81 | 503 | 1.00 |
| Western Europe | 180,113 | 89.81 | 10,067 | 15.27 | 44,387 | 15.37 | 805 | 1.19 |
| Australia-New Zealand | 25,786 | 100.28 | 1601 | 13.31 | 4152 | 12.81 | 109 | 0.88 |
| Melanesia | 2294 | 49.21 | 446 | 10.55 | 1179 | 26.77 | 180 | 4.26 |
| South America | 165,427 | 57.16 | 20,354 | 11.30 | 43,253 | 13.80 | 2853 | 1.54 |
| Micronesia | 133 | 43.88 | 9 | 4.45 | 53 | 16.74 | 0 | 0 |
| Polynesia | 294 | 76.89 | 31 | 12.43 | 99 | 25.26 | 6 | 2.34 |
| HDI | ||||||||
| Very HDI country | 1,092,663 | 75.63 | 74,665 | 12.54 | 245,043 | 13.21 | 7025 | 1.15 |
| High HDI country | 737,959 | 38.79 | 87,293 | 7.88 | 195,347 | 9.50 | 13,420 | 1.18 |
| Medium HDI country | 331,089 | 29.71 | 51,744 | 5.67 | 153,835 | 13.96 | 15,259 | 1.67 |
| Low HDI country | 134,122 | 34.10 | 32,255 | 7.75 | 71,458 | 18.99 | 12,965 | 3.12 |
Abbreviations: ASIR, age-standardized incidence rate; ASMR, age-standardized mortality rate; HDI, human development index.
In 2022, there were an estimated 666,103 BC-related deaths globally (ASMR of 12.70/100,000), accounting for approximately 15.4 % of all cancer deaths in women (Supplementary Fig. 1). Regionally, South-Central Asia recorded the highest number of deaths (135,348, ASMR: 13.41/100,000), followed by Eastern Asia (97,389, ASMR: 6.52/100,000). At the country level, India reported the highest number of BC-related deaths (15 % of global deaths), followed by China (11 %), the USA (6 %), Indonesia (3 %), Brazil (3 %), Russia (3 %), Germany (3 %) and Japan (3 %) (Fig. 1). South-Central Asia also had the highest number of early-onset BC deaths (12,063, ASMR: 1.43/100,000), with India (16 %), China (7 %), Ethiopia (5 %), and Nigeria (5 %) leading in the category across different countries (Fig. 1). Melanesia has the highest ASMR for overall BC (26.77/100,000) (Table 1), while Eastern Asia had the lowest (6.52/100,000) (Table 1). For early-onset BC, Melanesia again had the highest ASMR (4.26/100,000), followed by Western Africa (3.68/100,000) (Table 1).
3.2. Link between HDI and BC incidence and mortality
Countries with very high HDI reported the highest number of female BC cases (1,092,663, ASIR: 75.63/100,000), much higher than those with high HDI (737,959, ASIR: 38.79/100,000), medium HDI (331,089, ASIR: 29.71/100,000), and low HDI (134,122, ASIR: 34.10/100,000). The same pattern was observed for early-onset BC, with countries of very high HDI having the highest ASIR (12.54 /100,000), and medium HDI countries having the lowest (5.67/100,000, Table 1). In contrast, countries with low HDI had the highest ASMR for both overall (18.99/100,000) and early-onset BC (3.12/100,000). High HDI countries had the lowest ASMR for overall BC (9.50/100,000), while very high HDI countries had the lowest ASMR for early-onset BC (1.15/100,000, Table 1).
As shown in Fig. 2, ASIRs for overall, early-onset and post-40 BC consistently increased with HDI. The correlation between HDI and overall BC ASIR (r = 0.689, P < 0.001) was stronger than the correlation between HDI and early-onset BC ASIR (r = 0.307, P < 0.001) (Fig. 2A and B), and slightly weaker than the correlation for post-40 BC (r = 0.703, P < 0.001) (Fig. 2C). The correlation between HDI and ASMR for overall BC (r = −0.044, P = 0.559, Fig. 2D) and post-40 BC (r = 0.046, P = 0.548, Fig. 2F) were non-significant. However, the correlation between HDI and early-onset BC ASIR was significant (r = −0.629, P < 0.001, Fig. 2E).
Fig. 2.
Link between HDI and ASIR and ASMR of female breast cancer. (A-C) Link between HDI and ASIR of overall (A), early-onset (B) breast cancer and post-40 breast cancer (C). (D-F) Link between HDI and ASMR of overall (D), early-onset (E) breast cancer and post-40 breast cancer (F). ASIR, age-standardized incidence rate; ASMR, age-standardized mortality rate; HDI, human development index.
3.3. Temporal trends in breast cancer incidence and mortality
Based on continuous data from registries, the ASIR of overall BC showed an upward trend in most countries. Notable examples include the Republic of Korea (1999–2017, EAPC: 5.5893 %), Thailand (1993–2017, EAPC: 3.5683 %), Japan (1978–2015, EAPC: 3.4873 %), Qatar (2003–2017, 3.1281 %), Uganda (1993–2017, 2.6998 %), Kuwait (1998–2017, 2.6449 %), and France (Martinique) (1993–2017, 2.5390 %) (Fig. 3A). When analyzing data within the continuous monitoring period covered by all countries (2006–2015), the global average EAPC for overall BC ASIR was 1 % (Supplementary Fig. 2A). The Republic of Korea exhibited the highest country-specific EAPC (4.5721 %) (Supplementary Fig. 2A). Globally, the ASIR of early-onset BC in most countries also showed an increased trend, with an average EAPC of 1.6 % between 2006 and 2015 (Supplementary Fig. 2B), which was higher than the EAPC for overall ASIR. In China, the EAPC of early-onset BC ASIR (4.7014 %, 2002–2017, Fig. 3B) was higher than that for overall BC ASIR (2.0032 %, 2002–2017, Fig. 3A), and a similar trend was observed in the UK (Wales) and France (metropolitan). Conversely, countries like the Republic of Korea, Japan, and India showed an opposite trend, with a higher EAPC in overall BC than early-onset BC (Fig. 3B).
Fig. 3.
EAPC of ASIR and ASMR of breast cancer in different countries. (A, B) EAPC of overall (A) and early-onset (B) breast cancer ASIR. (C, D) EAPC of overall (C) and early-onset (D) breast cancer ASMR. ASIR, age-standardized incidence rate; ASMR, age-standardized mortality rate; EAPC, estimated annual percentage change.
The ASMR for overall BC declined in most countries, with the global EAPC for ASMR at ˗1.06 % during 2006–2016 (Fig. 3C). At the country level, Malaysia showed an upward trend in ASMR during 2000–2020 (EAPC: 3.9825 %, Fig. 3C), while countries such as the UK, USA, and Germany reported a downward trend (Fig. 3C). For early-onset BC, the ASMR showed a downward trend in most countries, but globally, the average EAPC for early-onset BC ASMR showed a slightly upward trend during 2006–2016 (0.16 %) (Fig. 3D).
3.4. Demographic projection of breast cancer cases and deaths up to 2050
Based on the stable population growth, aging, and estimates in 2022, the number of BC cases globally is expected to rise to 3,533,037 by 2050, with an overall increase of 54.7 %. Similarly, BC-related deaths are projected to reach 1,138,155, representing a 70.9 % increase. When grouped by HDI, the increase in BC cases is projected to range from 19.9 % in countries with very high HDI to 145.4 % in countries with low HDI (Fig. 4A). Similarly, the increase in BC-related deaths is projected to range from 40.3 % in high HDI countries to 150.0 % in low HDI countries (Fig. 4C). The predicted burden of early-onset BC differs significantly from the overall BC burden. Estimated early-onset BC cases are expected to increase in countries with low and medium HDI (by 108.2 % and 16.1 %, respectively), but decrease in countries with high and very high HDI (˗13.0 % and ˗9.9 %) (Fig. 4B). A similar trend is anticipated for early-onset BC-related deaths (Fig. 4D).
Fig. 4.
Estimated new cases and deaths from female breast cancer up to 2050 by HDI. (A, B) New cases of overall (A) and early-onset (B) breast cancer. (C, D) Deaths of overall (C) and early-onset (D) breast cancer. HDI, human development index.
Among the top 19 countries with the highest number of BC cases in 2022, most are expected to see an increase in BC cases by 2050, with Japan being the only country projected to experience a decrease in cases. Specifically, China is projected to have the highest total number of BC cases, while India is expected to see the largest increase in cases (Fig. 5A). India is also predicted to have the highest number of early-onset BC cases, while China is expected to experience a significant decrease in early-onset cases (Fig. 5B). Similar trends are projected for country-specific deaths from both overall (Fig. 5C) and early-onset BC (Fig. 5D).
Fig. 5.
Estimated new cases and deaths from female breast cancer up to 2050 in selected countries with top 19 numbers of cases in 2022. (A, B) New cases of overall (A) and early-onset (B) breast cancer. (C, D) Deaths of overall (C) and early-onset (D) breast cancer.
4. Discussion
This study not only provided a valuable global landscape of BC burden, including the current status, temporal trend and future projections, but also enabled comparisons of BC burden across different populations. Globally, BC remains the leading cause of cancer morbidity and mortality in women, irrespective of the HDI level. Both incidence and mortality of BC vary widely by region. Moreover, BC incidence showed an upward trend worldwide, while mortality showed a decreasing trend. Both of these two trends were more obvious for early-onset BC. Given the increased burden of BC faced by most countries, this situation not only presented a great challenge for health services in different countries, but also provided a series of potential opportunities for creating innovative health service models and breakthroughs in treatment.
Countries with high ASIR of BC are predominantly located in Western Europe, including France, Cyprus, Belgium, and The Netherlands. These countries are mainly developed countries with a relatively high prevalence of risk factors, such as high-fat diets, physical inactivity, delayed marriage and childbearing, limited breastfeeding history, and prolonged use of hormone replacement therapy.23 Many of these countries have high-quality screening systems.24 With the exception of the Russian Federation, Bulgaria, Greece, the Czech Republic, and Slovakia, nearly all European countries have population-based BC screening programs. These screening initiatives not only contribute to higher rates of early diagnosis but also play a crucial role in maintaining lower mortality rates.25 On the other hand, countries with high ASMR, such as Fiji, Jamaica, and the Bahamas, are mostly middle- or low-income countries. These resource-limited countries bear a high percentage of advanced-stage BC, poor BC prognosis and short disease-free survival.26,27 In addition to organized screening, the gap in treatment availability represents another significant factor in explaining the discrepancies between BC ASMR across countries.28 Specifically, the inability to provide consistent and complete treatment is a major challenge in low- and middle-income countries. Additionally, the struggle of healthcare systems with inadequate resources and infrastructure is another key factor contributing to poor prognosis in these regions. Cultural beliefs and the stigma surrounding BC treatment would further discourage women from seeking timely medical care or participating in screenings.29,30
BC ASIR significantly increased with the HDI for both older and younger women, however, the link appear to be more pronounced in older women. The absence of obvious economic and regional differences in early-onset BC incidence suggests that the risk is likely closely associated with unmodifiable genetic risks across counties with varying economic levels. Approximately half of early-onset BC in young women under 30 carry germline mutations in BRCA1, BRCA2, or TP53.31,32 In contrast, the stronger relationship between ASIR and HDI for older women is more likely attributed to higher rates of mammographic screening in high-income countries, as well as the influence of changes in hormone exposure or lifestyle factors linked to socioeconomic development.33 With improvements in living standards and changes in lifestyles, the prevalence of overweight and obesity has generally increased in several countries,34 potentially elevating the risk of BC in these regions. Declining fertility rates lead to fewer pregnancies and later childbearing, which increases exposure to estrogen.35 Additionally, the broader adoption of screening programs has facilitated earlier detection of BC.36 Therefore, the higher BC ASIR in transitioned countries compared to transitioning countries reflects not only a relatively higher prevalence of modifiable risk factors (such as excess body weight, physical inactivity, and alcohol consumption),3,4 but also reflects a longstanding higher prevalence of reproductive and hormonal risk factors (such as early menarche, later menopause, older age at first birth, fewer children), as well as increased detection through organized or opportunistic screening.7,35,37,38 Further studies have found that increasing BC incidence is confined to estrogen receptor (ER)-positive BC but not ER-negative cancers, which would be supported by the link between excess body weight and ER-positive cancer and present the preferential detection slow-growing ER-positive cancers by the mammographic screening.39, 40, 41, 42 Although efforts to decrease excess body weight and alcohol consumption and to encourage physical activity and breastfeeding are expected to lead to a reduction of BC incidence worldwide,43 establishing primary prevention programs for BC remains challenging. A generally uniform upward trend in BC incidence during 1980–2000 has been followed by stable or downward trends during 2001–2010 in several transitioned countries and regions (such as Northern America, Oceania, and Europe).44,45 This downward trend in BC incidence would largely link to the reduced use of menopausal hormone replacement therapy after the Women's Health Initiative in July 2002,46,47 though it would also reflect a plateauing in screening participation.44,45 Therefore, the focus of BC control has gradually shifted towards screening, improved treatment, and other effective prevention strategies.
The upward trends in BC ASIR in transitioning countries would further reflect changes in above risk determinants associated with socioeconomic development48,49 (such as increasing prevalence of overweight,50, 51, 52 declining age at menarche,53 postponement of childbearing and falling fertility rate,35,54 increasing use of estrogen and progesterone,47,55 decreasing breastfeeding),56 aging and growth of the population,15,16 as well as changes in increased detection through mammographic screening in these countries.36 The mean age at menarche decreased by approximately two years between women born in 1930 and those born in 1974 in China.53 Additionally, fertility rates have steadily fallen in all countries since 1950 and are projected to continue declining worldwide. By 2050, less than one-quarter of countries are expected to have fertility rates above replacement level, and by 2100, only six are projected to do so.54 Alongside the falling fertility rates and longer life expectancy, the multifaceted impact of rapid aging on economic development and health services has been deeply perceived by China and will continue to present great challenges to public health.15,16 Other populous countries, such as India, Nigeria, the USA, and Pakistan, will also suffer from the increasing demand for health services and social support associated with the increasing aging population.49 Additionally, after the widespread use of mammography in the United States, the detection rate of ductal carcinoma in situ ascended from 10/100,000 (1975–1979) to 79/100,000 during 2008–2012,57 and the age at diagnosis of BC shifted from an elder age to a younger age at the onset of the disease and reached a plateau.58 This situation was also observed in countries that had implemented or planned to initiate organized mammography screening,59,60 and it would be another explanation for the increased estimates of BC in these countries.61 How to turn the above challenges into cancer control opportunities would be a global hot topic in public health in the near future. These not only require support from local health policies, but also urgently need innovative healthcare models and treatment breakthroughs to respond to the soaring demand for health services.
The higher ASMR in transitioning countries compared to transitioned countries largely reflects the combined impacts of lack of high-quality screening, late-stage cancer diagnosis and unavailability of effective treatment due to limited health resources (including adjuvant chemotherapy and hormone therapy since the 1980s and targeted therapy since the 1990s).10,48,62 Notably, due to better and more targeted treatments as well as early detection through screening, BC mortality had fallen by nearly 43 % during 1989–2020 in the United States.35 Similar reductions in BC mortality were also reported in Europe and would continue to decline.63, 64, 65 The Chinese government has launched nationwide BC screening in high-risk areas since 2008.66 Although no obvious decline in the mortality of female BC appeared in China, a slower increase in mortality versus incidence had been observed in the past decade, which would also partially be attributed to the current screening.67 Due to the late introduction of screening, the proportion of BC diagnosed at stage I was 27.6 % in China, which was much lower than that of the USA (51.2 %).68 Alongside the lower early-stage BC at diagnosis, the five-year survival rate of BC was 82.0 % in China during 2012–2015 and 66 % in 12 sub-Saharan African countries during 2008–2015,69,70,71 which was sharply contrasted with 85 % to 90 % in transitioned countries during 2010–2014.72,73 Educational and cultural barriers, including lack of awareness of BC, an incorrect belief that cancer is incurable or contagious, the stigma of having a mastectomy and fear of rejection by their partner or community, would also collectively contribute to the higher mortality of BC in transitioning countries.74 Expanding screening coverage, raising awareness of breast health, and promoting high-quality and effective treatment will be keys to reversing the upward trend in BC mortality in transitioning countries. Notably, expanding screening does not mean screening at an earlier age, before 50 years old. As highlighted by the IARC's comprehensive analysis,75 the evidence supports the efficacy of mammographic screening primarily for women aged 50–69, with limited or inadequate evidence for younger women.
The strengths of the study included its comprehensive global scope, the use of the most recent GLOBOCAN 2022 data, and the detailed regional and country-specific analysis of BC burden. However, there were certain limitations worth noting. First, although this study provided a valuable global landscape of BC burden, it's important to note that high quality local data remained sparse in many countries, especially for transitioning countries, which would unavoidably affect the robustness of the BC estimates presented in these countries. Second, the current country-level BC estimates are not intended as a substitute for the continuous monitoring data collected by high-quality, population-based cancer registries and vital registration systems, which would also bias the estimates in the temporal trend of BC burden. Given the critical importance of continuous monitoring of high-quality data for cancer prevention and control, expanding the coverage of the cancer registry and improving the quality of data will be the basic guarantee for local decisions making on cancer prevention and control. Thirdly, other limitations included lack of male data, inconsistencies between global values and summation of country data, and lack of confidence or uncertainty intervals in the GLOBOCAN database.
5. Conclusions
Based on the latest GLOBOCAN 2022 dataset, this study presents the current status, historical trends, and projected future burden of overall and early-onset BC globally. Additionally, this study also analyzes these trends and burdens of breast cancer in relation to the socioeconomic levels of different countries. In conclusion, BC remains the leading cause of cancer morbidity and mortality in women worldwide, and the global BC burden is expected to increase with socioeconomic development, especially for transitioning countries. To cope with the growing global burden of BC, WHO and international partners launched the Global Breast Cancer Initiative in early 2021, which included three key pillars as an operational approach to achieve final goals, including centering on health promotion and early detection, timely diagnosis, and comprehensive breast cancer management.76 Based on this global initiative, the local government should efficiently integrate the resources of primary prevention, early detection and high-quality treatment for BC to promote collaboration between community stakeholders, advocacy organizations, and health systems, especially under the soaring demand for high-quality health services associated with the increasing aging population.
Declaration of competing interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Acknowledgments
Acknowledgments
Thanks to International Agency for Research on Cancer Registries for providing the qualified public database, and the local cancer registry staff who contributed to the cancer surveillance. This work was supported by the National Key R&D Program of China (grant number: 2021YFC2500400) and Tianjin Health Committee Foundation (grant number: TJWJ2021MS008).
Author contributions
Y.Z., L.Y., H.L., and Y.H. designed the study, guided the writing of the manuscript, and reviewed the manuscript. Y.Z., Y.J., L.W., J.L., X.L., H.D., Q.J., and J.W. collected the data. Y.Z. and Y.J. processed the data, performed the statistical, and drafted the manuscript. Y.Z., Y.J., and J.L. revised the manuscript.
Footnotes
Supplementary material associated with this article can be found, in the online version, at doi:10.1016/j.jncc.2025.02.002.
Contributor Information
Hong Liu, Email: liuhong_submit@tjmuch.com.
Yubei Huang, Email: yubei_huang@163.com.
Appendix. Supplementary materials
References
- 1.Sung H., Ferlay J., Siegel R.L., et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2021;71(3):209–249. doi: 10.3322/caac.21660. [DOI] [PubMed] [Google Scholar]
- 2.GBD 2021 Forecasting Collaborators. Burden of disease scenarios for 204 countries and territories, 2022-2050: a forecasting analysis for the global burden of disease study 2021. Lancet. 2024;403(10440):2204–2256. doi: 10.1016/s0140-6736(24)00685-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.The global burden of cancer attributable to risk factors 2010-19: a systematic analysis for the global burden of disease study 2019. Lancet. 2022;400(10352):563–591. doi: 10.1016/s0140-6736(22)01438-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Chen W., Xia C., Zheng R., et al. Disparities by province, age, and sex in site-specific cancer burden attributable to 23 potentially modifiable risk factors in China: a comparative risk assessment. Lancet Glob Health. 2019;7(2):e257–e269. doi: 10.1016/s2214-109x(18)30488-1. [DOI] [PubMed] [Google Scholar]
- 5.Islami F., Goding Sauer A., Miller K.D., et al. Proportion and number of cancer cases and deaths attributable to potentially modifiable risk factors in the United States. CA Cancer J Clin. 2018;68(1):31–54. doi: 10.3322/caac.21440. [DOI] [PubMed] [Google Scholar]
- 6.Bray F., Laversanne M., Sung H., et al. Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2024;74(3):229–263. doi: 10.3322/caac.21834. [DOI] [PubMed] [Google Scholar]
- 7.Britt K.L., Cuzick J., Phillips K.A. Key steps for effective breast cancer prevention. Nat Rev Cancer. 2020;20(8):417–436. doi: 10.1038/s41568-020-0266-x. [DOI] [PubMed] [Google Scholar]
- 8.Fan L., Strasser-Weippl K., Li J.J., et al. Breast cancer in China. Lancet Oncol. 2014;15(7):e279–e289. doi: 10.1016/s1470-2045(13)70567-9. [DOI] [PubMed] [Google Scholar]
- 9.The benefits and harms of breast cancer screening: an independent review. Lancet. 2012;380(9855):1778–1786. doi: 10.1016/s0140-6736(12)61611-0. [DOI] [PubMed] [Google Scholar]
- 10.Lei S., Zheng R., Zhang S., et al. Global patterns of breast cancer incidence and mortality: a population-based cancer registry data analysis from 2000 to 2020. Cancer Commun (Lond) 2021;41(11):1183–1194. doi: 10.1002/cac2.12207. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Heer E., Ruan Y., Mealey N., Quan M.L., Brenner D.R. The incidence of breast cancer in Canada 1971-2015: trends in screening-eligible and young-onset age groups. Can J Public Health. 2020;111(5):787–793. doi: 10.17269/s41997-020-00305-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Kehm R.D., Yang W., Tehranifar P., Terry M.B. 40 Years of change in age- and stage-specific cancer incidence rates in US women and men. JNCI Cancer Spectr. 2019;3(3):pkz038. doi: 10.1093/jncics/pkz038. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Merlo D.F., Ceppi M., Filiberti R., et al. Breast cancer incidence trends in European women aged 20-39 years at diagnosis. Breast Cancer Res Treat. 2012;134(1):363–370. doi: 10.1007/s10549-012-2031-7. [DOI] [PubMed] [Google Scholar]
- 14.Leclère B., Molinié F., Trétarre B., Stracci F., Daubisse-Marliac L., Colonna M. Trends in incidence of breast cancer among women under 40 in seven European countries: a GRELL cooperative study. Cancer Epidemiol. 2013;37(5):544–549. doi: 10.1016/j.canep.2013.05.001. [DOI] [PubMed] [Google Scholar]
- 15.The L. Population ageing in China: crisis or opportunity? Lancet. 2022;400(10366):1821. doi: 10.1016/s0140-6736(22)02410-2. [DOI] [PubMed] [Google Scholar]
- 16.Gong J., Wang G., Wang Y., et al. Nowcasting and forecasting the care needs of the older population in China: analysis of data from the China Health and Retirement Longitudinal Study (CHARLS) Lancet Public Health. 2022;7(12):e1005–e1013. doi: 10.1016/s2468-2667(22)00203-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Ferlay J.E.M, Lam F., Laversanne M., et al. Global cancer observatory: cancer today (version 1.1). Lyon, France. Int Agen Res Cancer. 2024 https://gco.iarc.who.int/today [Google Scholar]
- 18.Ervik M LF LM, Ferlay J., Bray F. Global cancer observatory: cancer over time. Lyon, France. Int Agen Res Cancer. 2021 https://gco.iarc.fr/overtime [Google Scholar]
- 19.Ferlay J LM EM, Lam F., Colombet M., et al. International Agency for Research on Cancer; Lyon, France: 2024. Global Cancer Observatory: Cancer Tomorrow (version 1.1)https://gco.iarc.fr/tomorrow [Google Scholar]
- 20.2021–22. UNDPHDR. Uncertain Times Unsettled Lives: shaping our future in a transforming world. United Nations; 2022 https://hdr.undp.org/content/human-development-report-2021-22 Accessed April 20, 2024. [Google Scholar]
- 21.Frick C., Rumgay H., Vignat J., et al. Quantitative estimates of preventable and treatable deaths from 36 cancers worldwide: a population-based study. Lancet Glob Health. 2023;11(11):e1700–e1712. doi: 10.1016/s2214-109x(23)00406-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Doll R PP, Waterhouse JAH, Eds. (1966). Cancer Incidence in Five Continents, Vol. I. Geneva: Union Internationale Contre le Cancer.
- 23.Lima S.M., Kehm R.D., Terry M.B. Global breast cancer incidence and mortality trends by region, age-groups, and fertility patterns. EClinicalMedicine. 2021;38 doi: 10.1016/j.eclinm.2021.100985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Zielonke N., Gini A., Jansen E.E.L., et al. Evidence for reducing cancer-specific mortality due to screening for breast cancer in Europe: a systematic review. Eur J Cancer. 2020;127:191–206. doi: 10.1016/j.ejca.2019.12.010. [DOI] [PubMed] [Google Scholar]
- 25.Peintinger F. National breast Screening programs across Europe. Breast Care (Basel) 2019;14(6):354–358. doi: 10.1159/000503715. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Lundqvist A., Andersson E., Ahlberg I., Nilbert M., Gerdtham U. Socioeconomic inequalities in breast cancer incidence and mortality in Europe-a systematic review and meta-analysis. Eur J Public Health. 2016;26(5):804–813. doi: 10.1093/eurpub/ckw070. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Elghazaly H., Aref A.T., Anderson B.O., et al. The first BGICC consensus and recommendations for breast cancer awareness, early detection and risk reduction in low- and middle-income countries and the MENA region. Int J Cancer. 2021;149(3):505–513. doi: 10.1002/ijc.33506. [DOI] [PubMed] [Google Scholar]
- 28.Newman L.A. Breast cancer screening in low and middle-income countries. Best Pract Res Clin Obstet Gynaecol. 2022;83:15–23. doi: 10.1016/j.bpobgyn.2022.03.018. [DOI] [PubMed] [Google Scholar]
- 29.Anyigba C.A., Awandare G.A., Paemka L. Breast cancer in sub-Saharan Africa: the current state and uncertain future. Exp Biol Med (Maywood) 2021;246(12):1377–1387. doi: 10.1177/15353702211006047. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Delpech P.A., Haynes-Smith G. Breast self-examination and health beliefs in Grenadian women. Cancer Nurs. 2015;38(5):E54–E59. doi: 10.1097/ncc.0000000000000218. [DOI] [PubMed] [Google Scholar]
- 31.Lalloo F., Varley J., Moran A., et al. BRCA1, BRCA2 and TP53 mutations in very early-onset breast cancer with associated risks to relatives. Eur J Cancer. 2006;42(8):1143–1150. doi: 10.1016/j.ejca.2005.11.032. [DOI] [PubMed] [Google Scholar]
- 32.Tichy J.R., Lim E., Anders C.K. Breast cancer in adolescents and young adults: a review with a focus on biology. J Natl Compr Canc Netw. 2013;11(9):1060–1069. doi: 10.6004/jnccn.2013.0128. [DOI] [PubMed] [Google Scholar]
- 33.Herbert C., Paro A., Diaz A., Pawlik T.M. Association of community economic distress and breast and colorectal cancer screening, incidence, and mortality rates among US counties. Ann Surg Oncol. 2022;29(2):837–848. doi: 10.1245/s10434-021-10849-7. [DOI] [PubMed] [Google Scholar]
- 34.World Obesity Federation, World obesity atlas 2023. 2023;
- 35.Giaquinto A.N., Sung H., Miller K.D., et al. Breast cancer statistics, 2022. CA Cancer J Clin. 2022;72(6):524–541. doi: 10.3322/caac.21754. [DOI] [PubMed] [Google Scholar]
- 36.Srivastava S., Koay E.J., Borowsky A.D., et al. Cancer overdiagnosis: a biological challenge and clinical dilemma. Nat Rev Cancer. 2019;19(6):349–358. doi: 10.1038/s41568-019-0142-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Maas P., Barrdahl M., Joshi A.D., et al. Breast cancer risk from modifiable and nonmodifiable risk factors among white women in the United States. JAMA Oncol. 2016;2(10):1295–1302. doi: 10.1001/jamaoncol.2016.1025. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.The Lancet O UK pharmaceutical industry under threat. Lancet Oncol. 2014;15(7):667. doi: 10.1016/s1470-2045(14)70252-9. [DOI] [PubMed] [Google Scholar]
- 39.Munsell M.F., Sprague B.L., Berry D.A., Chisholm G., Trentham-Dietz A. Body mass index and breast cancer risk according to postmenopausal estrogen-progestin use and hormone receptor status. Epidemiol Rev. 2014;36(1):114–136. doi: 10.1093/epirev/mxt010. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Suzuki R., Orsini N., Saji S., Key T.J., Wolk A. Body weight and incidence of breast cancer defined by estrogen and progesterone receptor status–a meta-analysis. Int J Cancer. 2009;124(3):698–712. doi: 10.1002/ijc.23943. [DOI] [PubMed] [Google Scholar]
- 41.Gilliland F.D., Joste N., Stauber P.M., et al. Biologic characteristics of interval and screen-detected breast cancers. J Natl Cancer Inst. 2000;92(9):743–749. doi: 10.1093/jnci/92.9.743. [DOI] [PubMed] [Google Scholar]
- 42.Porter P.L., El-Bastawissi A.Y., Mandelson M.T., et al. Breast tumor characteristics as predictors of mammographic detection: comparison of interval- and screen-detected cancers. J Natl Cancer Inst. 1999;91(23):2020–2028. doi: 10.1093/jnci/91.23.2020. [DOI] [PubMed] [Google Scholar]
- 43.Arnold M., Morgan E., Rumgay H., et al. Current and future burden of breast cancer: global statistics for 2020 and 2040. Breast. 2022;66:15–23. doi: 10.1016/j.breast.2022.08.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Breen N., Gentleman J.F., Schiller J.S. Update on mammography trends: comparisons of rates in 2000, 2005, and 2008. Cancer. 2011;117(10):2209–2218. doi: 10.1002/cncr.25679. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Breen N., AC K., Meissner H.I., et al. Reported drop in mammography : is this cause for concern? Cancer. 2007;109(12):2405–2409. doi: 10.1002/cncr.22723. [DOI] [PubMed] [Google Scholar]
- 46.Ravdin P.M., Cronin K.A., Howlader N., et al. The decrease in breast-cancer incidence in 2003 in the United States. N Engl J Med. 2007;356(16):1670–1674. doi: 10.1056/NEJMsr070105. [DOI] [PubMed] [Google Scholar]
- 47.Rossouw J.E., Anderson G.L., Prentice R.L., et al. Risks and benefits of estrogen plus progestin in healthy postmenopausal women: principal results from the Women's Health Initiative randomized controlled trial. JAMA. 2002;288(3):321–333. doi: 10.1001/jama.288.3.321. [DOI] [PubMed] [Google Scholar]
- 48.Torre L.A., Islami F., Siegel R.L., Ward E.M., Jemal A. Global cancer in women: burden and trends. Cancer Epidemiol Biomarkers Prev. 2017;26(4):444–457. doi: 10.1158/1055-9965.Epi-16-0858. [DOI] [PubMed] [Google Scholar]
- 49.Vollset S.E., Goren E., Yuan C.W., et al. Fertility, mortality, migration, and population scenarios for 195 countries and territories from 2017 to 2100: a forecasting analysis for the global burden of disease study. Lancet. 2020;396(10258):1285–1306. doi: 10.1016/s0140-6736(20)30677-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Menarche menopause, and breast cancer risk: individual participant meta-analysis, including 118 964 women with breast cancer from 117 epidemiological studies. Lancet Oncol. 2012;13(11):1141–1151. doi: 10.1016/s1470-2045(12)70425-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Ellingjord-Dale M., Christakoudi S., Weiderpass E., et al. Long-term weight change and risk of breast cancer in the European Prospective Investigation into Cancer and Nutrition (EPIC) study. Int J Epidemiol. 2022;50(6):1914–1926. doi: 10.1093/ije/dyab032. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Gaudet M.M., Carter B.D., Patel A.V., Teras L.R., Jacobs E.J., Gapstur S.M. Waist circumference, body mass index, and postmenopausal breast cancer incidence in the Cancer Prevention Study-II Nutrition Cohort. Cancer Causes Control. 2014;25(6):737–745. doi: 10.1007/s10552-014-0376-4. [DOI] [PubMed] [Google Scholar]
- 53.Lewington S., Li L., Murugasen S., et al. Temporal trends of main reproductive characteristics in ten urban and rural regions of China: the China Kadoorie biobank study of 300 000 women. Int J Epidemiol. 2014;43(4):1252–1262. doi: 10.1093/ije/dyu035. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54.Global fertility in 204 countries and territories, 1950-2021, with forecasts to 2100: a comprehensive demographic analysis for the global burden of disease study 2021. Lancet. 2024;403(10440):2057–2099. doi: 10.1016/s0140-6736(24)00550-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Nguyen T.L., Li S., Dite G.S., et al. Interval breast cancer risk associations with breast density, family history and breast tissue aging. Int J Cancer. 2020;147(2):375–382. doi: 10.1002/ijc.32731. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 56.Kobayashi S., Sugiura H., Ando Y., et al. Reproductive history and breast cancer risk. Breast Cancer. 2012;19(4):302–308. doi: 10.1007/s12282-012-0384-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 57.Welch H.G., Prorok P.C., O'Malley A.J., Kramer B.S. Breast-cancer tumor size, overdiagnosis, and mammography screening effectiveness. N Engl J Med. 2016;375(15):1438–1447. doi: 10.1056/NEJMoa1600249. [DOI] [PubMed] [Google Scholar]
- 58.Anderson W.F., Reiner A.S., Matsuno R.K., Pfeiffer R.M. Shifting breast cancer trends in the United States. J Clin Oncol. 2007;25(25):3923–3929. doi: 10.1200/jco.2007.11.6079. [DOI] [PubMed] [Google Scholar]
- 59.Cardoso R., Hoffmeister M., Brenner H. Breast cancer screening programmes and self-reported mammography use in European countries. Int J Cancer. 2023;152(12):2512–2527. doi: 10.1002/ijc.34494. [DOI] [PubMed] [Google Scholar]
- 60.Huang Y., Lyu Z., Zhang Y., et al. Cohort profile: design and methods of the Chinese colorectal, breast, lung, liver, and stomach cancer screening trial (C-BLAST) Cancer Biol Med. 2023;20(10):713–720. doi: 10.20892/j.issn.2095-3941.2023.0278. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 61.Feng R.M., Zong Y.N., Cao S.M., Xu R.H. Current cancer situation in China: good or bad news from the 2018 Global Cancer Statistics? Cancer Commun (Lond) 2019;39(1):22. doi: 10.1186/s40880-019-0368-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 62.Lei S., Zheng R., Zhang S., et al. Breast cancer incidence and mortality in women in China: temporal trends and projections to 2030. Cancer Biol Med. 2021;18(3):900–909. doi: 10.20892/j.issn.2095-3941.2020.0523. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 63.Wojtyla C., Bertuccio P., Wojtyla A., La Vecchia C. European trends in breast cancer mortality, 1980-2017 and predictions to 2025. Eur J Cancer. 2021;152:4–17. doi: 10.1016/j.ejca.2021.04.026. [DOI] [PubMed] [Google Scholar]
- 64.Carioli G., Malvezzi M., Rodriguez T., Bertuccio P., Negri E., La Vecchia C. Trends and predictions to 2020 in breast cancer mortality in Europe. Breast. 2017;36:89–95. doi: 10.1016/j.breast.2017.06.003. [DOI] [PubMed] [Google Scholar]
- 65.Hensing W., CA Santa-Maria, Peterson L.L., Sheng J.Y. Landmark trials in the medical oncology management of early stage breast cancer. Semin Oncol. 2020;47(5):278–292. doi: 10.1053/j.seminoncol.2020.08.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 66.Xia C., Basu P., Kramer B.S., et al. Cancer screening in China: a steep road from evidence to implementation. Lancet Public Health. 2023;8(12):e996–e1005. doi: 10.1016/s2468-2667(23)00186-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 67.Sun K., Lei L., Zheng R., et al. Trends in incidence rates, mortality rates, and age-period-cohort effects of female breast cancer - China, 2003-2017. China CDC Wkly. 2023;5(15):340–346. doi: 10.46234/ccdcw2023.065. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 68.Zeng H., Ran X., An L., et al. Disparities in stage at diagnosis for five common cancers in China: a multicentre, hospital-based, observational study. Lancet Public Health. 2021;6(12):e877–e887. doi: 10.1016/s2468-2667(21)00157-2. [DOI] [PubMed] [Google Scholar]
- 69.Zeng H., Chen W., Zheng R., et al. Changing cancer survival in China during 2003-15: a pooled analysis of 17 population-based cancer registries. Lancet Glob Health. 2018;6(5):e555–e567. doi: 10.1016/s2214-109x(18)30127-x. [DOI] [PubMed] [Google Scholar]
- 70.Joko-Fru W.Y., Miranda-Filho A., Soerjomataram I., et al. Breast cancer survival in sub-Saharan Africa by age, stage at diagnosis and human development index: a population-based registry study. Int J Cancer. 2020;146(5):1208–1218. doi: 10.1002/ijc.32406. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 71.Soerjomataram I., Cabasag C., Bardot A., et al. Cancer survival in Africa, central and south America, and Asia (SURVCAN-3): a population-based benchmarking study in 32 countries. Lancet Oncol. 2023;24(1):22–32. doi: 10.1016/s1470-2045(22)00704-5. [DOI] [PubMed] [Google Scholar]
- 72.Allemani C., Matsuda T., Di Carlo V., et al. Global surveillance of trends in cancer survival 2000-14 (CONCORD-3): analysis of individual records for 37 513 025 patients diagnosed with one of 18 cancers from 322 population-based registries in 71 countries. Lancet. 2018;391(10125):1023–1075. doi: 10.1016/s0140-6736(17)33326-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 73.Siegel R.L., Giaquinto A.N., Jemal A. Cancer statistics, 2024. CA Cancer J Clin. 2024;74(1):12–49. doi: 10.3322/caac.21820. [DOI] [PubMed] [Google Scholar]
- 74.Youlden D.R., Cramb S.M., Dunn N.A., Muller J.M., Pyke C.M., Baade P.D. The descriptive epidemiology of female breast cancer: an international comparison of screening, incidence, survival and mortality. Cancer Epidemiol. 2012;36(3):237–248. doi: 10.1016/j.canep.2012.02.007. [DOI] [PubMed] [Google Scholar]
- 75.Lauby-Secretan B., Scoccianti C., Loomis D., et al. Breast-cancer screening–viewpoint of the IARC Working Group. N Engl J Med. 2015;372(24):2353–2358. doi: 10.1056/NEJMsr1504363. [DOI] [PubMed] [Google Scholar]
- 76.Anderson B.O., Ilbawi A.M., Fidarova E., et al. The Global Breast Cancer Initiative: a strategic collaboration to strengthen health care for non-communicable diseases. Lancet Oncol. 2021;22(5):578–581. doi: 10.1016/s1470-2045(21)00071-1. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.





