Abstract
Objective
Tobacco has been identified as a significant contributory element to the development of breast cancer. Our objective was to evaluate the spatiotemporal trends of tobacco-related breast cancer at the global, regional, and national scales during 1990–2019.
Methods
We extracted data on mortality, disability adjusted of life years (DALYs), age-standardized mortality rate (ASMR), and age-standardized DALYs rate (ASDR) from the Global Burden of Disease (GBD) study 2019. Estimated annual percentage change (EAPC) was computed to assess the temporal change in ASDR and ASMR.
Results
In 2019, the deaths and DALYs attributed to tobacco-related breast cancer were estimated to be 35,439 (95% UI: 22,179–48,119) and 1,060,590 (95% UI: 622,550–1,462,580), respectively. These figures accounted for 5.1% and 5.2% of the total burden of breast cancer. ASMR and ASDR increased in low SDI regions, remained stable in low-middle and middle SDI regions and declined in high and high-middle SDI regions. The burden of breast cancer attributable to tobacco varied notably among regions and nations. Oceania, Southern Latin America, and Central Europe were the GBD regions with the highest number of ASMR and DALYs. There was a positive relationship between age-standardized rate and SDI value in 2019 across 204 nations or territories. A negative association was observed between the EAPC in ASMR or ASDR and the human development index (HDI) in 2019 (R = -0.55, p < 0.01 for ASMR; R = -0.56, p < 0.01 for ASDR).
Conclusion
Tobacco is one important and modifiable risk factor for breast cancer. The heterogeneity in both the spatial and temporal distribution can be attributed to factors such as aging, population growth, and SDI. These findings substantiate the necessity of expediting the enforcement of tobacco-free legislation in order to safeguard populations from the detrimental effects of tobacco.
Supplementary Information
The online version contains supplementary material available at 10.1186/s12889-023-17405-w.
Keywords: Breast cancer, Tobacco, Global burden of disease study
Introduction
Breast cancer is the most frequently diagnosed cancer, accounting for 24.2% of all cancer cases worldwide among females [1]. It is recognized as the primary factor for cancer-related mortality among women [2, 3]. Various lifestyle risk factors contribute to the development of breast cancer, including consumption of alcohol and tobacco, obesity, and low physical activity [4]. Tobacco is acknowledged as a prominent risk factor contributing to approximately 200 million deaths and imposing economic costs amounting to $1 trillion over the three decades [5, 6]. Tobacco could also consistently release a substantial number of carcinogens, leading to millions of annual cancer-related deaths [7]. It has been reported that tobacco is closely linked to a modest yet significantly higher risk of breast cancer [8].
Thus far, numerous studies have been conducted to examine the global trends of breast cancer [9, 10]. There is a positive association between long-term smoking and the breast cancer risk [11, 12]. However, the epidemiological patterns and trends of tobacco-associated breast cancer remain unknown on a national, regional, and global scale. To enhance the formulation of health policies and lifestyle guidelines, it is worthwhile to consolidate and compare various metrics and trends pertaining to tobacco-related breast cancer from multiple perspectives. In this study, we assess the spatial and temporal progression of female breast cancer attributed to tobacco using data from the Global Burden of Disease (GBD) 2019 study.
Methods
Data sources
The GBD 2019 study, a collaborative multinational research effort, provided estimations of the burden of 329 diseases across 204 countries or territories, 21 regions, and 7 super-regions for the period of 1990–2019 [13]. The risk factors encompassed metabolic, occupational, environmental, and behavioral factors, including tobacco use. The data regarding the numbers and age-standardized rates (ASR) of tobacco-related breast cancer death and disability adjusted of life years (DALYs) from 1990 to 2019, categorized by age, region, country, were extracted from the GBD 2019 study using the online Global Health Data Exchange query tool (GHDx, http://ghdx.healthdata.org/gbd-results-tool). The information on human development index (HDI) among nations was obtained from the United Nations Human Development Report (http://hdr.undp.org/en/data).
Estimated breast cancer burden due to tobacco
In GBD 2019 study, tobacco use encompassed multiple modalities, including current or past usage of any smoked tobacco product, current use of any chewing tobacco product, and the average daily exposure to air particulate matter from second-hand smoke [14].
Mortality data were estimated using a combination of high-quality cancer registered incidence and modeled mortality-to-incidence ratio. This estimation involved the application of spatiotemporal Gaussian process modeling techniques. DALYs were represented by the sum of years lived with disability (YLDs) and years of life lost (YLLs). One DALY was equivalent to one healthy year lost. ASRs, such as age-standardized mortality rate (ASMR) and age-standardized DALYs rate (ASDR), were utilized usually to compare the disease burden while accounting for variations in age structures, which were more accurate epidemiological assessments.
The individuals were classified into four distinct age groups (25–40, 40–55, 55–70, and 70 +) to assess the distribution of the disease across different age ranges. The socio-demographic index (SDI) was calculated according to national income per capita, total fertility rate among individuals younger than 25, and average schooling years among persons older than 15 [13]. Countries and territories were categorized into five subgroups based on SDI values, namely: low, low-medium, medium, high-medium, and high SDI groups.
Statistical analyses
We calculated the estimated annual percentage change (EAPC) to assess the temporal trends of ASMR and ASDR over the past 30 years. The equation was set as follows: Y = α + βX + ε. In this linear regression model, X represents the calendar year, Y refers to the natural logarithm of ASDR or ASMR, ε indicates the error term. EAPCs were evaluated as 100 × (exp(β) – 1). We also calculated relevant 95% confidence interval (CI) by linear regression model mentioned earlier [15]. If the 95% CI is below 0, it suggests a declining trend. Conversely, if the 95% CI is above 0, it indicates an upward trend in the ASR. A stable trend is indicated when the 95% CI encompasses zero. Pearson's correlation analysis was conducted to examine the association between the EAPC estimates and SDI in the year 2019. R program (Version 4.12) was used for statistical analysis and visualization.
Results
Global breast cancer burden attributable to tobacco
Out of the total breast cancer burden, the proportion of deaths and DALYs attributable to tobacco were estimated to be 5.1% and 5.2% respectively in 2019 (Fig. 1). The number of breast cancer deaths associated with tobacco witnessed an approximate increase of 35% during the past three decades, rising from 25,857 (95% UI: 17,283–34,333) to 35,439 (95% UI: 22,179–48,119) (Table 1). Concurrently, there was a significant increase in the corresponding DALYs, with a surge of approximately 30%, escalating from 805,990 (95% UI: 515,630–1,087,750) to 1,060,590 (95% UI: 622,550–1,462,580). By contrast, ASMR and ASDR were recorded as 0.82 (95% UI: 0.51–1.11) and 24.60 (95% UI: 14.37–34.04) per 100,000 population in 2019, indicating a declining trend, as evidenced by the negative EAPC (-1.55 for ASMR; -1.59 for ASDR) (Table 1, Fig. 2A and B). The deaths and DALYs in the regions with low, low-middle and middle SDI experienced an annual increase (Fig. 2C and D), while the relevant ASMR and ASDR in high-middle and high SDI regions exhibited a continuous decrease from 1990 to 2019 (Fig. 2E and F). The percentage of deaths and DALYs among these patients aged younger than 40 showed a slight decrease over the 30-year period. Conversely, there was a slight increase in these figures for individuals aged 70 and above (Figure S1).
Table 1.
Characteristics | 1990 | 2019 | EAPC of ASMR No. (95% CI) | EAPC of ASDR No. (95% CI) | ||||||
---|---|---|---|---|---|---|---|---|---|---|
Death number No. × 102 (95% UI) | ASMR per 100000 No. (95% UI) |
DALY No. × 103 (95% UI) |
ASDR per 100000 No. (95% UI) |
Death number No. × 102 (95% UI) | ASMR per 100000 No. (95% UI) |
DALY No. × 103 (95% UI) |
ASDR per 100000 No. (95% UI) |
|||
Global | 258.57 (172.83–343.33) | 1.21 (0.82–1.61) | 805.99 (515.63–1087.75) | 36.93 (23.87–49.78) | 354.39 (221.79–481.19) | 0.82 (0.51–1.11) | 1060.59 (622.55–1462.58) | 24.60 (14.37–34.04) | -1.55 (-1.62–1.49) | -1.59 (-1.68–1.53) |
Socio-demographic index | ||||||||||
Low SDI | 6.16 (2.85–9.52) | 0.49 (0.23–0.75) | 20.85 (9.00–32.79) | 14.66 (6.55–22.80) | 16.69 (8.07–25.56) | 0.59 (0.30–0.89) | 55.09 (24.51–86.73) | 17.24 (8.17–26.68) | 0.62 (0.55–0.68) | 0.49 (0.42–0.57) |
Low-middle SDI | 22.26 (10.33–33.99) | 0.70 (0.34–1.05) | 75.24 (32.30–116.39) | 21.27 (9.56–32.65) | 49.60 (21.97–76.16) | 0.67 (0.31–1.03) | 159.87 (65.09–249.53) | 20.45 (8.58–31.80) | -0.3 (-0.4–0.2) | -0.34 (-0.46–0.22) |
Middle SDI | 37.55 (16.92–57.03) | 0.67 (0.31–1.02) | 127.68 (53.73–199.10) | 20.95 (9.10–32.30) | 81.26 (36.86–124.57) | 0.61 (0.28–0.93) | 261.27 (108.17–406.04) | 18.88 (7.87–29.26) | -0.46 (-0.56–0.37) | -0.49 (-0.58–0.40) |
High-middle SDI | 70.97 (45.11–95.20) | 1.20 (0.76–1.61) | 226.20 (139.47–306.12) | 38.56 (23.75–52.31) | 98.71 (63.72–134.37) | 0.91 (0.58–1.24) | 291.51 (180.74–398.52) | 27.92 (17.04–38.29) | -1.24 (-1.36–1.14) | -1.4 (-1.53–1.30) |
High SDI | 121.46 (88.12–152.26) | 2.20 (1.61–2.75) | 355.52 (257.28–446.58) | 69.17 (50.15–87.03) | 107.86 (77.52–137.29) | 1.16 (0.83–1.46) | 292.01 (210.18–368.17) | 35.70 (25.54–45.15) | -2.4 (-2.51–2.35) | -2.46 (-2.56–2.43) |
GBD region | ||||||||||
High-income Asia Pacific | 5.97 (3.78–8.04) | 0.54 (0.34–0.73) | 20.38 (12.27–27.94) | 18.70 (11.18–25.76) | 8.82 (5.75–11.92) | 0.47 (0.30–0.63) | 25.99 (16.59–35.35) | 16.39 (10.04–22.46) | -0.27 (-0.42–0.13) | -0.27 (-0.44–0.10) |
High-income North America | 48.65 (34.08–62.26) | 2.69 (1.92–3.41) | 145.93 (105.35–184.63) | 86.93 (63.48–108.87) | 42.21 (29.11–55.27) | 1.31 (0.93–1.70) | 115.43 (83.14–148.34) | 39.67 (28.91–50.59) | -2.67 (-2.80–2.61) | -2.92 (-3.06–2.87) |
Central Asia | 2.21 (0.95–3.39) | 0.80 (0.34–1.22) | 7.45 (3.11–11.51) | 26.84 (11.21–41.65) | 2.91 (1.22–4.52) | 0.65 (0.27–1.00) | 9.73 (3.98–15.14) | 20.38 (8.41–31.66) | -0.65 (-0.73–0.57) | -0.98 (-1.07–0.91) |
East Asia | 22.45 (7.99–36.68) | 0.48 (0.18–0.77) | 76.64 (25.23–128.11) | 15.31 (5.13–25.44) | 48.80 (21.21–78.60) | 0.45 (0.20–0.73) | 150.58 (58.84–244.45) | 13.95 (5.37–22.62) | -0.38 (-0.50–0.27) | -0.56 (-0.68–0.44) |
South Asia | 17.60 (7.21–28.54) | 0.60 (0.26–0.97) | 59.99 (22.45–97.40) | 17.98 (7.18–29.04) | 47.44 (19.60–76.30) | 0.64 (0.27–1.02) | 153.47 (58.39–252.32) | 19.40 (7.58–31.68) | -0.03 (-0.16–0.11) | 0.03 (-0.12–0.18) |
Southeast Asia | 16.40 (6.91–25.37) | 1.10 (0.49–1.68) | 57.45 (21.89–92.89) | 34.88 (14.21–55.13) | 34.00 (13.90–54.54) | 0.98 (0.41–1.56) | 114.96 (42.79–189.75) | 31.49 (11.89–51.81) | -0.5 (-0.61–0.40) | -0.45 (-0.54–0.36) |
Central Europe | 16.11 (11.49–20.56) | 2.00 (1.43–2.58) | 49.69 (35.34–64.01) | 63.78 (45.15–82.91) | 18.97 (13.25–25.42) | 1.72 (1.21–2.31) | 51.20 (36.22–69.11) | 51.51 (35.96–69.72) | -0.67 (-0.74–0.60) | -0.91 (-0.99–0.83) |
Eastern Europe | 15.62 (8.21–22.42) | 0.97 (0.50–1.39) | 51.84 (26.71–74.45) | 34.00 (17.69–48.93) | 18.48 (10.85–26.60) | 0.98 (0.57–1.41) | 57.40 (33.23–82.80) | 32.92 (18.92–47.72) | -0.57 (-0.82–0.33) | -0.76 (-1.02–0.50) |
Western Europe | 76.72 (56.24–95.61) | 2.62 (1.92–3.29) | 220.56 (160.96–277.57) | 83.08 (60.56–105.03) | 66.54 (48.63–84.20) | 1.54 (1.12–1.93) | 177.65 (129.05–223.65) | 47.83 (34.36–60.79) | -2.12 (-2.26–2.03) | -2.17 (-2.29–2.10) |
Andean Latin America | 0.40 (0.20–0.60) | 0.36 (0.18–0.53) | 1.31 (0.61–1.99) | 10.96 (5.27–16.45) | 0.87 (0.46–1.33) | 0.29 (0.16–0.44) | 2.62 (1.28–4.12) | 8.62 (4.29–13.47) | -1.01 (-1.16–0.88) | -1.16 (-1.31–1.02) |
Central Latin America | 3.41 (2.08–4.73) | 0.75 (0.47–1.03) | 10.75 (6.17–15.14) | 21.80 (12.93–30.50) | 6.41 (3.67–9.43) | 0.50 (0.29–0.73) | 19.25 (10.21–29.07) | 14.58 (7.80–22.04) | -1.52 (-1.62–1.44) | -1.51 (-1.62–1.43) |
Southern Latin America | 7.40 (5.35–9.56) | 2.93 (2.10–3.79) | 21.05 (14.84–27.57) | 84.24 (59.13–110.49) | 9.39 (6.64–12.16) | 2.07 (1.46–2.68) | 24.47 (17.12–31.86) | 57.03 (39.17–74.81) | -1.24 (-1.33–1.17) | -1.37 (-1.45–1.31) |
Tropical Latin America | 9.07 (6.60–11.62) | 1.80 (1.31–2.30) | 28.49 (20.07–36.74) | 52.60 (37.46–67.64) | 13.44 (9.45–17.56) | 1.00 (0.70–1.31) | 38.98 (26.72–51.81) | 28.88 (19.80–38.37) | -2.09 (-2.42–1.81) | -2.11 (-2.46–1.80) |
Australasia | 2.98 (2.22–3.73) | 2.50 (1.85–3.13) | 9.09 (6.68–11.53) | 79.87 (58.59–101.26) | 2.71 (1.96–3.43) | 1.14 (0.82–1.45) | 7.96 (5.66–10.20) | 36.74 (25.93–47.39) | -2.88 (-3.10–2.74) | -2.83 (-3.03–2.73) |
Caribbean | 1.47 (1.01–1.95) | 1.09 (0.75–1.45) | 4.45 (2.92–5.97) | 32.25 (21.37–43.17) | 2.63 (1.78–3.56) | 0.96 (0.65–1.29) | 7.34 (4.82–10.12) | 27.14 (17.75–37.43) | -0.26 (-0.36–0.16) | -0.43 (-0.53–0.33) |
North Africa and Middle East | 5.75 (2.69–8.76) | 0.61 (0.29–0.93) | 20.28 (9.17–31.19) | 19.83 (9.09–30.34) | 16.17 (7.40–24.87) | 0.69 (0.32–1.04) | 56.14 (24.72–88.41) | 21.76 (9.83–33.89) | 0.46 (0.39–0.52) | 0.33 (0.27–0.39) |
Oceania | 0.45 (0.22–0.66) | 2.64 (1.37–3.89) | 1.58 (0.75–2.39) | 84.59 (41.62–126.51) | 1.25 (0.62–1.99) | 3.03 (1.57–4.71) | 4.50 (2.09–7.31) | 97.48 (47.91–155.93) | 0.59 (0.53–0.64) | 0.61 (0.55–0.67) |
Central Sub-Saharan Africa | 0.43 (0.19–0.70) | 0.33 (0.15–0.52) | 1.48 (0.60–2.46) | 9.79 (4.12–16.12) | 1.23 (0.50–2.12) | 0.38 (0.16–0.65) | 4.24 (1.62–7.37) | 11.49 (4.64–19.88) | 0.43 (0.30–0.55) | 0.44 (0.32–0.55) |
Eastern Sub-Saharan Africa | 1.59 (0.70–2.47) | 0.40 (0.19–0.61) | 5.28 (2.14–8.43) | 11.44 (4.98–17.91) | 4.19 (2.02–6.47) | 0.47 (0.25–0.71) | 13.43 (5.84–21.56) | 12.84 (5.97–19.91) | 0.55 (0.49–0.60) | 0.34 (0.26–0.42) |
Southern Sub-Saharan Africa | 2.16 (1.28–3.09) | 1.37 (0.82–1.98) | 6.64 (3.78–9.50) | 39.04 (22.67–55.92) | 3.47 (1.93–4.93) | 1.07 (0.60–1.51) | 9.91 (5.19–14.45) | 28.49 (15.10–41.35) | -0.67 (-0.89–0.46) | -0.8 (-1.00–0.61) |
Western Sub-Saharan Africa | 1.71 (0.68–2.83) | 0.38 (0.15–0.61) | 5.65 (2.09–9.48) | 11.38 (4.34–18.90) | 4.48 (1.74–7.37) | 0.41 (0.17–0.65) | 15.36 (5.56–25.48) | 12.07 (4.64–19.95) | 0.24 (0.18–0.30) | 0.2 (0.12–0.27) |
ASMR Age-standardized mortality rate, UI Uncertainty interval, DALYs Disability-adjusted life years, ASDR Age-standardized DALY rate, EAPC Estimated annual percentage change, CI Confidence interval, SDI Socio-demographic Index
Regional breast cancer burden attributable to tobacco
At the SDI-regional level, both the number of deaths and DALYs across five SDI regions in 2019 exceeded the corresponding values recorded in 1990 (Table 1). Quantitatively, there was a noticeable increase in the number of deaths and DALYs, as well as an increase in ASMR and ASDR, with the progressive rise in regional SDI in 2019. A noticeable decline in both ASMR and ASDR was observed in regions with high and high-middle SDI, with an EAPC of less than -1. By contrast, in low-middle and middle SDI regions, the improvement in ASMR and ASDR was less notable, as indicated by the EAPC approaching zero. It was important that low SDI region had a slight increase of ASMR (EAPC: 0.62, 95% UI: 0.55–0.68) and ASDR (EAPC: 0.49, 95% UI: 0.42–0.57).
In 2019, the GBD regions with the highest estimated death and DALYs due to tobacco-related breast cancer were Western Europe, recording 6,654 deaths and 17,7650 DALYs, East Asia with 4,880 deaths and 150,580 DALYs, and South Asia with 4,744 deaths and 153,470 DALYs (Table 1). Oceania was estimated to have the highest ASMR (3.03 per 100,000) and ASDR (97.48 per 100,000) attributed to tobacco-related breast cancer, followed closely by Southern Latin America (2.07 per 100,000 for ASMR, 57.03 per 100,000 for ASDR) and Central Europe (1.72 per 100,000 for ASMR, 51.51 per 100,000 for ASDR). From 1990 to 2019, ASMR and ASDR of tobacco-related breast cancer exhibited a downward trend in most regions worldwide. However, a slight upward trend of ASMR and ASDR with a positive EAPC was observed in North Africa and Middle East, Oceania, Central Sub-Saharan Africa, Eastern Sub-Saharan Africa, and Western Sub-Saharan Africa.
Based on Fig. 1, the death and DALYs proportion attributable to tobacco exhibited a similar regional distribution in 1990 and 2019. The contribution of tobacco to breast cancer death and DALYs declined in all GBD regions from 1990 to 2019, except for Eastern Europe and Eastern Sub-Saharan Africa.
Countries and territories trends of breast cancer attributable to tobacco
At the national level, the burden of tobacco-related breast cancer varied significantly across 204 countries or territories in 2019 (Table S1). An upward trend in ASMR was documented in 88 countries or territories, a downward trend was observed in 95 countries or territories, and a stable status was recorded in 21 countries or territories. Furthermore, we noted an increase in ASDR in 76 countries or territories, a decrease in ASDR in 96 countries or territories, and a stable ASDR in the remaining 32 countries or territories. China had the highest number of deaths (4,671, 95% UI: 2,024–7,572) and DALYs (143,660, 95% UI: 56,490–233,810), followed by United States of America and India (Tables S2 and S3). The highest estimated national-level ASMR and ASDR in 2019 were documented in specific countries within Oceania (such as Solomon Islands, Nauru, Tuvalu, and Papua New Guinea) as well as Central Europe (including Montenegro and Serbia) (Fig. 3A and B, Tables S4 and S5). Solomon Islands, Lesotho, and Zimbabwe displayed the highest EAPC of ASMR and ASDR. Conversely, Israel, Denmark, Norway, Iceland, and Israel had the lowest EAPC of ASMR and ASDR, with the values lower than -3. (Fig. 3C and D, Tables S6 and S7).
Global breast cancer burden attributable to tobacco by age, SDI, and HDI
The death rate of tobacco-related breast cancer exhibited a gradual global increase in correlation with advancing age in 2019 (Fig. 4A). The highest rate of DALYs occurred in the individuals aged 55–59 (Fig. 4B). A similar pattern was evident in Fig. 4E and F, with approximately half of the deaths and DALYs occurring in the High-middle SDI and High SDI regions. Corresponding, there was a notable increase in the number of deaths and DALYs as age advanced, reaching their highest point within the 55–59 age group (Fig. 4C and D).
The age-specific death rate experienced an obvious decrease in High SDI region, particularly among individuals aged 45–90. It declined slightly in Low-middle SDI, Middle SDI, and High-middle SDI regions, while showing a moderate increase in Low SDI region (Figure S2A). Irrespective of SDI, the mortality rate increased among patients aged above 95. The patterns observed in the EAPCs of age-specific DALY rates mirrored those of age-specific mortality rates (Figure S2B).
A double hump curve was depicted to illustrate the relationship between SDI and the regional ASMR or ASDR (Fig. 5A and B). Among the 21 GBD regions, the observed patterns in ASRs varied widely based on the year. Some regions showed minimal change in ASRs, while others exhibited decreasing or fluctuating rates. Additionally, North Africa and Middle East experienced a progressive rise in ASMR and ASDR over time. There was a positive relationship between ASRs and SDI value in 2019 across 204 nations or territories (R = 0.29, p < 0.01 for both ASMR and ASDR, Figure S3). However, a negative association was observed between the EAPC in ASMR and the HDI in 2019 (R = -0.55, p < 0.01), which was particularly pronounced in nations with very high HDI, but not in nations with HDI less than 0.8 (Fig. 5C). We also observed a comparable association between EAPC in ASDR and HDI in 2019 (Figure S4).
Discussion
This study represents the most current and comprehensive investigation examining the spatial and temporal trends of tobacco-associated breast cancer on a global scale. Our analysis unveiled that the global ASMR and ASDR of tobacco-related breast cancer decreased modestly over the last three decades, but the death and DALYs cases increased by about 30%, which may be partially attributed to population aging and growth [16]. In parallel, we observed both death and DALYs number were highest in the 55–59 age group. Moreover, the spatial distribution of this disease was heterogeneous, implying a potential correlation with disparities in various factors, including breast cancer screening policies and tobacco control initiatives.
Tobacco smoke is recognized to contain more than 7,000 chemicals, with about 20 of them being identified as breast carcinogens [17]. They may have an impact on the development, recurrence, metastasis, and treatment of breast cancer through various potential biological mechanisms. Firstly, nicotine, the principal component of tobacco, contributes to breast cancer by promoting proliferation, inhibiting apoptosis, and creating a microenvironment conducive to tumor growth [18]. Secondly, tobacco smoke can increase the risk of metastasis from breast cancer, which is attributed mainly to phenotypic transition to a mesenchymal phenotype, acquisition of self-renewing stem-like traits, chronic inflammation, and inhibition of host immune defenses [19, 20]. Thirdly, several population-based studies revealed that tobacco increased both breast-specific mortality and overall mortality [21, 22]. In comparison to men, women displayed a higher susceptibility to genetic and biologic aberrations caused by tobacco, thereby increasing their vulnerability to cancer development [23–25]. Women exposed to second-hand smoke in both the workplace and home had a significantly higher risk of developing breast cancer [26]. The absence of second-hand smoke exposure in women who have never smoked was suggested to potentially prevent 1 out of every 14 cases of breast cancer [27]. In addition, the cessation of smoking following disease diagnosis significantly improved breast cancer specific survival and overall survival [28]. However, the cessation rate after breast cancer diagnosis was lower compared to other cancers such as colorectal and lung cancer [29–31]. It is imperative to urgently propose feasible policy measures for comprehensive smoke control worldwide, particularly in regions grappling with a substantial disease burden of tobacco-related breast cancer.
We demonstrated that the burden of breast cancer attributable to tobacco varied notably among regions and nations in this study. Australasia, High-income North America, West Europe, and Tropical Latin America experienced a substantial reduction in both ASMR and ASDR. These declines may be partly ascribed to the widespread implementation of mammogram screening programs and evidence-based tobacco control policies in these regions [32, 33]. On the contrary, our findings indicated a slight upward trend of ASMR and ASDR in North Africa and Middle East, Oceania, Central Sub-Saharan Africa, and Eastern Sub-Saharan Africa. Both ASMR and ASDR increased in Low SDI region, but not in other SDI regions. These frustrating trends could be explained by factors such as limited availability of treatment, inadequate implementation of health policies, and challenging living conditions [34–36]. The enforcement of cigarette advertisement bans, tobacco tax policies, and warning labels has been correlated with a reduction in tobacco consumption and a decrease in overall cancer mortality [33, 37, 38]. Hence, recommendations for screening initiation ages can be tailored to specific risk factors, including national risk profiles and ethnicity [39]. The governments should concentrate their efforts on levying higher taxes on tobacco products and deploying smoke-free legislation, individuals should strive earnestly to quit smoke and cultivate healthy habits in the countries and regions with high tobacco-related breast cancer burden.
In our analysis, we conducted comprehensive estimations of the disease burden and trends associated with tobacco-related female breast cancer at global, regional, and national levels based on multiple metrics, including mortality, DALYs, ASMR, and ASDR. Nevertheless, it is important to acknowledge and address several limitations. First, variations in data collection methods and mammogram screening practices among different nations inevitably impact the dependability of our findings. Second, molecular subtyping and grade are significant clinicopathological parameters for breast cancer. Given the scarcity of data, we did not include these characteristics in our analysis. Third, the GBD 2019 study offers valuable and reliable estimates of disease burden, yet the data regarding the prevalence and incidence of tobacco-related breast cancer are unavailable. Fourth, Pham et al. indicated that electronic cigarettes can potentially facilitate the growth and metastasis of breast cancer [40]. Regrettably, our study lacks exposure estimates for the use of electronic cigarettes, vaporizers, and heated tobacco products due to inadequate data availability in the GBD 2019 dataset.
In conclusion, tobacco is one important and modifiable risk factor for breast cancer. A number of regions (namely North Africa and Middle East, and Oceania) and countries or territories (namely Solomon Islands, Lesotho, and Zimbabwe) exhibited a notable upward trajectory. In addition, the populations in Low SDI regions would suffer a substantial burden of tobacco-related breast cancer, leading to a persistent challenge to both healthcare and economic sectors in the foreseeable future. These findings substantiate the necessity of expediting the enforcement of tobacco-free legislation in order to safeguard populations from the adverse effects of tobacco.
Supplementary Information
Acknowledgements
We acknowledge The Global Burden of Disease, Injuries, and Risk Study (GBD) 2019, which presented detailed information.
Authors’ contributions
Tian Lan designed the study, Tian Lan, Weiguo Liu and Qiusheng Guo extracted the data, performed the analyses, Tian Lan, Qiusheng Guo, Yunyan Lu and Gaochen Lan interpreted the evidence and wrote the manuscript. Tian Lan revised the article. All authors agreed to be accountable for the work.
Funding
This research received grants from Zhejiang Traditional Medicine and Technology Program (2023ZL115), Medical Scientific Research Foundation of Zhejiang Province, China(2023XY002), Hangzhou Health Science and Technology Program (A20220311), and Jinhua Science and Technology Research Program of Traditional Chinese Medicine (2023KY03).
Availability of data and materials
Publicly available datasets were analyzed in this study. The data can be found here: http://ghdx.healthdata.org/gbd-results-tool and http://hdr.undp.org/en/data.
Declarations
Ethics approval and consent to participate
This study did not involve human embryos, gametes, and stem cells. This study received exemption from the Ethics Committee of Hangzhou Hospital of Traditional Chinese Medicine as no patient, physician, or hospital identifiers were examined.
Consent for publication
Not applicable.
Competing interests
The authors declare no competing interests.
Footnotes
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Qiusheng Guo, Yunyan Lu and Weiguo Liu contributed equally to this work.
Contributor Information
Gaochen Lan, Email: fydfey888@fjmu.edu.cn.
Tian Lan, Email: lan_tian_lt@163.com.
References
- 1.Makhoul I, Atiq M, Alwbari A, Kieber-Emmons T. Breast Cancer Immunotherapy: An Update. Breast Cancer. 2018;12:1178223418774802. doi: 10.1177/1178223418774802. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Ferlay J, Colombet M, Soerjomataram I, Parkin DM, Pineros M, Znaor A, Bray F. Cancer statistics for the year 2020: An overview. Int J Cancer. 2021;149:778–89. doi: 10.1002/ijc.33588. [DOI] [PubMed] [Google Scholar]
- 3.Giaquinto AN, Sung H, Miller KD, Kramer JL, Newman LA, Minihan A, Jemal A, Siegel RL. Breast Cancer Statistics, 2022. CACancer J Clin. 2022;72(6):524–541. doi: 10.3322/caac.21754. [DOI] [PubMed] [Google Scholar]
- 4.Sun YS, Zhao Z, Yang ZN, Xu F, Lu HJ, Zhu ZY, Shi W, Jiang J, Yao PP, Zhu HP. Risk Factors and Preventions of Breast Cancer. Int J Biol Sci. 2017;13(11):1387–1397. doi: 10.7150/ijbs.21635. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Collaborators GBDRF: Global burden of 87 risk factors in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019. Lancet. 2020;396(10258):1223–49. [DOI] [PMC free article] [PubMed]
- 6.Goodchild M, Nargis N, Tursan d'Espaignet E. Global economic cost of smoking-attributable diseases. Tob Control. 2018;27(1):58–64. doi: 10.1136/tobaccocontrol-2016-053305. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Hecht SS, Hatsukami DK. Smokeless tobacco and cigarette smoking: chemical mechanisms and cancer prevention. Nat Rev Cancer. 2022;22(3):143–155. doi: 10.1038/s41568-021-00423-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Jones ME, Schoemaker MJ, Wright LB, Ashworth A, Swerdlow AJ. Smoking and risk of breast cancer in the Generations Study cohort. Breast Cancer Res. 2017;19(1):118. doi: 10.1186/s13058-017-0908-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Li N, Deng Y, Zhou L, Tian T, Yang S, Wu Y, Zheng Y, Zhai Z, Hao Q, Song D, et al. Global burden of breast cancer and attributable risk factors in 195 countries and territories, from 1990 to 2017: results from the Global Burden of Disease Study 2017. J Hematol Oncol. 2019;12(1):140. doi: 10.1186/s13045-019-0828-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Ji P, Gong Y, Jin ML, Hu X, Di GH, Shao ZM. The Burden and trends of breast cancer from 1990 to 2017 at the global, regional, and national levels: results from the global burden of disease study 2017. Front Oncol. 2020;10:650. doi: 10.3389/fonc.2020.00650. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Scala M, Bosetti C, Bagnardi V, Possenti I, Specchia C, Gallus S, Lugo A. Dose-Response Relationships between Cigarette Smoking and Breast Cancer Risk: A Systematic Review and Meta-Analysis. JEpidemiol. 2023;33(12):640–48. doi: 10.2188/jea.JE20220206. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.He Y, Si Y, Li X, Hong J, Yu C, He N. The relationship between tobacco and breast cancer incidence: A systematic review and meta-analysis of observational studies. Front Oncol. 2022;12:961970. doi: 10.3389/fonc.2022.961970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Diseases GBD, Injuries C. Global burden of 369 diseases and injuries in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019. Lancet. 2020;396(10258):1204–1222. doi: 10.1016/S0140-6736(20)30925-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Collaborators GBDRF: Global, regional, and national comparative risk assessment of 84 behavioural, environmental and occupational, and metabolic risks or clusters of risks for 195 countries and territories, 1990–2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet. 2018;392(10159):1923–94. [DOI] [PMC free article] [PubMed]
- 15.Lu Y, Lan T. Global, regional, and national burden of hypertensive heart disease during 1990–2019: an analysis of the global burden of disease study 2019. BMC Public Health. 2022;22(1):841. doi: 10.1186/s12889-022-13271-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Arnold M, Morgan E, Rumgay H, Mafra A, Singh D, Laversanne M, Vignat J, Gralow JR, Cardoso F, Siesling S, 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]
- 17.Reynolds P. Smoking and breast cancer. J Mammary Gland Biol Neoplasia. 2013;18(1):15–23. doi: 10.1007/s10911-012-9269-x. [DOI] [PubMed] [Google Scholar]
- 18.Khodabandeh Z, Valilo M, Velaei K, Pirpour Tazehkand A. The potential role of nicotine in breast cancer initiation, development, angiogenesis, invasion, metastasis, and resistance to therapy. Breast Cancer. 2022;29(5):778–789. doi: 10.1007/s12282-022-01369-7. [DOI] [PubMed] [Google Scholar]
- 19.Di Cello F, Flowers VL, Li H, Vecchio-Pagan B, Gordon B, Harbom K, Shin J, Beaty R, Wang W, Brayton C, et al. Cigarette smoke induces epithelial to mesenchymal transition and increases the metastatic ability of breast cancer cells. Mol Cancer. 2013;12:90. doi: 10.1186/1476-4598-12-90. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Liu Y, Gu Y, Han Y, Zhang Q, Jiang Z, Zhang X, Huang B, Xu X, Zheng J, Cao X. Tumor Exosomal RNAs Promote Lung Pre-metastatic Niche Formation by Activating Alveolar Epithelial TLR3 to Recruit Neutrophils. Cancer Cell. 2016;30(2):243–256. doi: 10.1016/j.ccell.2016.06.021. [DOI] [PubMed] [Google Scholar]
- 21.Wang K, Li F, Zhang X, Li Z, Li H. Smoking increases risks of all-cause and breast cancer specific mortality in breast cancer individuals: a dose-response meta-analysis of prospective cohort studies involving 39725 breast cancer cases. Oncotarget. 2016;7(50):83134–83147. doi: 10.18632/oncotarget.13366. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Passarelli MN, Newcomb PA, Hampton JM, Trentham-Dietz A, Titus LJ, Egan KM, Baron JA, Willett WC. Cigarette smoking before and after breast cancer diagnosis: mortality from breast cancer and smoking-related diseases. J Clin Oncol. 2016;34(12):1315–1322. doi: 10.1200/JCO.2015.63.9328. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Jemal A, Miller KD, Ma J, Siegel RL, Fedewa SA, Islami F, Devesa SS, Thun MJ. Higher lung cancer incidence in young women than young men in the United States. N Engl J Med. 2018;378(21):1999–2009. doi: 10.1056/NEJMoa1715907. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Barrera-Rodriguez R, Morales-Fuentes J. Lung cancer in women. Lung Cancer (Auckl) 2012;3:79–89. doi: 10.2147/LCTT.S37319. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Alisoltani A, Qiu X, Jaroszewski L, Sedova M, Iyer M, Godzik A. Gender differences in smoking-induced changes in the tumor immune microenvironment. Arch Biochem Biophys. 2023;739:109579. doi: 10.1016/j.abb.2023.109579. [DOI] [PubMed] [Google Scholar]
- 26.Carreras G, Lugo A, Gallus S, Cortini B, Fernandez E, Lopez MJ, Soriano JB, Lopez-Nicolas A, Semple S, Gorini G, et al. Burden of disease attributable to second-hand smoke exposure: A systematic review. Prev Med. 2019;129:105833. doi: 10.1016/j.ypmed.2019.105833. [DOI] [PubMed] [Google Scholar]
- 27.Gram IT, Wiik AB, Lund E, Licaj I, Braaten T. Never-smokers and the fraction of breast cancer attributable to second-hand smoke from parents during childhood: the Norwegian Women and Cancer Study 1991–2018. Int J Epidemiol. 2022;50(6):1927–1935. doi: 10.1093/ije/dyab153. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Singareeka Raghavendra A, Kypriotakis G, Karam-Hage M, Kim S, Jizzini M, Seoudy KS, Robinson JD, Barcenas CH, Cinciripini PM, Tripathy D, et al. The Impact of Treatment for Smoking on Breast Cancer Patients' Survival. Cancers. 2022;14(6):1464. doi: 10.3390/cancers14061464. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Steinhilper L, Geyer S, Sperlich S. Health behavior change among breast cancer patients. Int J Public Health. 2013;58(4):603–613. doi: 10.1007/s00038-013-0444-7. [DOI] [PubMed] [Google Scholar]
- 30.Hopenhayn C, Christian WJ, Christian A, Studts J, Mullet T. Factors associated with smoking abstinence after diagnosis of early stage lung cancer. Lung Cancer. 2013;80(1):55–61. doi: 10.1016/j.lungcan.2012.12.013. [DOI] [PubMed] [Google Scholar]
- 31.Skeie G, Hjartaker A, Braaten T, Lund E. Dietary change among breast and colorectal cancer survivors and cancer-free women in the Norwegian Women and Cancer cohort study. Cancer Causes Control. 2009;20(10):1955–1966. doi: 10.1007/s10552-009-9390-3. [DOI] [PubMed] [Google Scholar]
- 32.Siu AL, Force USPST: Screening for Breast Cancer: U.S. Preventive Services Task Force Recommendation Statement. Ann Int Med. 2016;164(4):279–96. [DOI] [PubMed]
- 33.Jiang H, Livingston M, Room R, Gan Y, English D, Chenhall R. Can public health policies on alcohol and tobacco reduce a cancer epidemic? Australia's experience. BMC Med. 2019;17(1):213. doi: 10.1186/s12916-019-1453-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Balogun O, Rodin D, Ngwa W, Grover S, Longo J. Challenges and prospects for providing radiation oncology services in Africa. Sem Radiation Oncol. 2017;27(2):184–188. doi: 10.1016/j.semradonc.2016.11.011. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Jemal A, Center MM, DeSantis C, Ward EM. Global patterns of cancer incidence and mortality rates and trends. Cancer Epidemiol Biomarkers Prev. 2010;19(8):1893–1907. doi: 10.1158/1055-9965.EPI-10-0437. [DOI] [PubMed] [Google Scholar]
- 36.Chowdhury S, Pillarisetti A, Oberholzer A, Jetter J, Mitchell J, Cappuccilli E, Aamaas B, Aunan K, Pozzer A, Alexander D. A global review of the state of the evidence of household air pollution's contribution to ambient fine particulate matter and their related health impacts. Environ Int. 2023;173:107835. doi: 10.1016/j.envint.2023.107835. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Levy DT, Tam J, Kuo C, Fong GT, Chaloupka F. The Impact of Implementing Tobacco Control Policies: The 2017 Tobacco Control Policy Scorecard. J Public Health Manage Pract. 2018;24(5):448–457. doi: 10.1097/PHH.0000000000000780. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Hoffman SJ, Tan C. Overview of systematic reviews on the health-related effects of government tobacco control policies. BMC Public Health. 2015;15:744. doi: 10.1186/s12889-015-2041-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Chen T, Kharazmi E, Fallah M. Race and ethnicity-adjusted age recommendation for initiating breast cancer screening. JAMA Netw Open. 2023;6(4):e238893. doi: 10.1001/jamanetworkopen.2023.8893. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Pham K, Huynh D, Le L, Delitto D, Yang L, Huang J, Kang Y, Steinberg MB, Li J, Zhang L, et al. E-cigarette promotes breast carcinoma progression and lung metastasis: Macrophage-tumor cells crosstalk and the role of CCL5 and VCAM-1. Cancer Lett. 2020;491:132–145. doi: 10.1016/j.canlet.2020.08.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
Publicly available datasets were analyzed in this study. The data can be found here: http://ghdx.healthdata.org/gbd-results-tool and http://hdr.undp.org/en/data.