- Department of Dermatology and Venereology, Sanya Central Hospital (The Third People’s Hospital of Hainan Province), Sanya, China
Objective: This study map the 1990–2021 basal-cell carcinoma burden in people ≥55 years worldwide, pinpoint key risk drivers, and offer concise intervention guidance for elder-focused prevention.
Methods: We focused on adults aged ≥55 years because this group shows the highest basal-cell carcinoma (BCC) frequency and matches the Global Burden of Disease (GBD) age strata. Incidence and disability-adjusted life-year (DALY) counts for 1990–2021 were downloaded from the Global Health Data Exchange. After direct age-standardisation, we plotted global, regional and national rates, generated world maps, computed annual percent change (APC) and contrasted 1990 versus 2021 distributions—all with R 4.2.1. A Bayesian hierarchical model then projected the 2050 burden.
Results: 1990-2021, Among adults ≥55 years, global basal-cell carcinoma incidence rose and then plateaued, while DALYs climbed before edging downward. The steepest gains in both age-standardized incidence and DALY rates occurred in high-income North America. Men consistently outpaced women across all metrics. The USA, Brazil and China recorded the largest absolute caseloads, yet the USA always posted the highest incidence rate and Nepal the lowest. Overall, the BCC burden has expanded over the past three decades.
Conclusion: Over the last three decades, both new cases and the overall toll of basal-cell carcinoma among older adults have risen worldwide, fueled by expanding and aging populations, greater ultraviolet exposure, and better case detection. Looking forward, vigorous sun-protection education and unified UV-shielding measures are essential to curb incidence and ease the growing burden.
Introduction
Basal cell carcinoma (BCC) is a common skin cancer originating from the basal layer of the epidermis. It typically affects sun-exposed areas, including the head, face, and neck.
BCC grows slowly and rarely metastasizes, but untreated cases can invade surrounding tissues, leading to disfiguring changes. Several treatment options for BCC are available, including surgical excision (1, 2), pharmacotherapy (3), and neoadjuvant therapy (4). Mohs micrographic surgery is the preferred treatment due to its high cure rate and low recurrence rate (5), although some pathological subtypes, such as sclerodermiform variants with infiltrative tendencies, still have higher recurrence rates. The epidemiology of BCC shows a global increase, with approximately 4 million new cases in 2019. Incidence among individuals over 55 years old has increased significantly, surpassing that of other skin cancers (6). Studies also show an increased risk of transformation into malignant melanoma, highlighting the importance of epidemiological research on BCC for public health (7). This study analyzed global BCC incidence, age and gender distribution, incidence in different countries and regions, disease burden, and risk factors from 1990 to 2021 to enhance early recognition and treatment of BCC and provide robust evidence for global BCC prevention and control.
Methods
Study population
The study population comprised elderly patients aged over 55 years diagnosed with BCC. Studies indicate that BCC predominantly occurs in patients over 50 years old, with dermatoscopy showing arborizing capillary dilation, large blue-gray ovoid nests, and ulcers more frequently in elderly patients (8). BCC is closely associated with sun exposure, but other potential etiological factors include advanced age, local trauma, chronic inflammation, radiotherapy, and indoor tanning (9–11). Thus, this study included patients aged over 55 years with BCC, aligning with the age grouping in the GBD database to facilitate data analysis and comparison. Moreover, this age group is the peak incidence age for BCC (12). Based on the above rationale and previous studies, patients aged over 55 years with BCC were selected for this study.
Data collection
In this study, basal cell carcinoma (BCC) was defined by the ICD-10 topography code C44 (all sub-sites C44.0–C44.9) combined with the ICD-O-3 morphology code 8090/3.
Corresponding incidence and prevalence estimates were extracted from the Global Health Data Exchange (GHDx, http://ghdx.healthdata.org/) by querying “non-melanoma skin cancer (basal-cell carcinoma)” for cause and “incidence, prevalence” for measure. DALYs(Disability-Adjusted Life Years)” for measurements; “all locations” for location; “1990–2021” for years; “number and rate” for metrics; “male, female and both” for sex; and “Age-standardized,55+ years and corresponding 5-year bands” for age. We followed the Guidelines for Accurate and Transparent Health Estimates Reporting guidelines for cross-sectional studies.
Socio-demographic index
The Socio-Demographic Index (SDI) is a comprehensive indicator developed by the GBD study team, used to measure the development level of a country or region. The value of the SDI ranges between 0 and 1. Based on the SDI value, countries and regions around the world are categorized into five levels: Low SDI, Low-Middle SDI, Middle SDI, High-Middle SDI, and High SDI. Regions with low SDI typically have low levels of economic development, lower educational attainment, and higher fertility rates. In contrast, high SDI regions are usually developed countries, characterized by higher per capita income, robust educational systems, low fertility rates, and well-developed healthcare services. The SDI is not only a measure of development level but also an important covariate that can be used to predict disease burdens and health status across different regions. It provides a crucial reference for global health research and policy-making.
Statistical analysis
Data from the GBD database were used to describe the incidence and DALY rates of BCC among individuals aged 55 and older globally, regionally, and nationally from 1990 to 2021 and calculated the ASIR, ASMR, and ASDR of BCC for individuals aged 55 and older globally, regionally, and nationally, and created world maps of ASIR and ASDR. For analyzing the temporal trends of BCC burden, the estimated annual percentage change (EAPC) was calculated based on a linear regression model, with the model form specified as:
In this model, x1 represents the calendar year (1990–2021), and y denotes the natural logarithm of the age-standardized rate (ASR) — including ASIR, ASMR, and ASDR, respectively, to assess trends in incidence, mortality, and DALY burden. β0 is the intercept term, and β1 is the regression coefficient corresponding to the calendar year. The EAPC, which quantifies the annual trend of ASRs over the study period, was derived using the formula:
The 95% confidence intervals (CIs) for EAPC were computed by substituting the upper and lower bounds of β1 (obtained from the linear regression analysis) into the above formula.The EAPC was calculated using the formula 100* (exp(β) -1), and the 95% CI was derived from the linear regression model. World maps of the EAPC of ASIR, EAPC of ASMR, and EAPC of ASDR were created. Patients with BCC aged over 55 years were divided into eight age groups: 55-59, 60-64, 65-69, 70-74, 75-79, 80-84, 85-89, and 90–94 years. The age burden composition of patients with BCC aged 55 and older in 1990 and 2021 was compared. The age composition of the incidence rate of BCC aged 55 and older globally in 1990 and 2021 was compared, and a Bayesian model was used to predict the disease burden in 2050. All statistics were performed using the R program (version 4.2.1, R core team).
Results
Time and sex trends of 55+ year BCC from 1990 to 2021
From 1990 to 2021, the incidence of BCC among both sexes combined showed a fluctuating trend globally. It increased from 1990 to 2005 and then stabilized from 2005 to 2021. The incidence rate per 100,000 population increased from 135 (150-175) in 1990 to 230 (215-255) in 2005. For males, it increased from 152 per 100,000 in 1990 to 290 per 100,000 in 2005. For females, it increased from 126 per 100,000 in 1990 to 190 per 100,000 in 2005. (Trends in the number of cases) From 1990 to 2005, the incidence and prevalence of BCC among both sexes combined showed an increasing trend. From 2005 to 2019, these values stabilized, with a slight downward trend observed in females. The DALYs for BCC also showed fluctuations, increasing from 1990 to 2005, then decreasing from 2005 to 2019, with a relatively stable trend from 2015 to 2019. Overall, there was a slight decrease. DALYs increased from 0.07 in 2000 to 0.13 in 2005, with stable values from 1990 to 2000 and an increase from 2000 to 2005. From 2000 to 2005, the ASIR and ASDR of BCC showed an increasing trend, with the ASIR rising from 130 (102-152) per 100,000 in 2000 to 230 (215-255) per 100,000 in 2005. The ASDR also increased from 0.07 (0.04-0.07) per 100,000 in 2000 to 0.13 (0.08-0.13) per 100,000 in 2005.
Gender differences
From 1990 to 2019, the incidence, prevalence, and DALYs of BCC among elderly males were consistently higher than those among elderly females. In 2005, the number of BCC cases among elderly males was 1.5 times that of elderly females (49.3 (43.7-54.6) vs 33.0 (36.5-29.1)), and DALYs were 1.4 times higher in males than in females (0.021 (0.039-0.009) vs 0.015 (0.028-0.007)). From 2000 to 2005, the ASIR and ASDR of BCC among elderly males and females both showed an increasing trend, similar to the overall population trend, with males consistently having higher values than females (Figure 1, Supplementary Data 1).
Region and sex trends of 55+ year BCC from 1990 to 2021
The incidence and DALYs of BCC among the elderly have increased in all global regions, with the most significant rises in age-standardized incidence and DALYs observed in High-income North America. The age-standardized incidence rate increased from 1000.01 (772.06-1232.60) in 1990 to 2293.86 (2059.24-2545.26) in 2021, and the age-standardized DALY rate rose from 0.42 (0.18-0.79) in 1990 to 0.91 (0.43-1.74) in 2021. The highest increase in age-standardized incidence was in High-income North America, and the highest increase in age-standardized DALYs was also in High-income North America. In 2021, regions with High SDI and High-income North America had higher incidence and DALYs for BCC.
At the regional level, from 1990 to 2021, the ASIR of BCC among the elderly population increased globally. The most significant rise was in High-income North America, from 1000.01 (772.06-1232.60) in 1990 to 2293.86 (2059.24-2545.26) in 2021. The second-largest increase was in High SDI regions, from 384.36 (304.23-467.37) in 1990 to 824.67 (734.18-915.28) in 2021. The smallest increase was in Oceania, from 0.16 (0.05-0.36) in 1990 to 0.17 (0.05-0.36) in 2021.
At the regional level, from 1990 to 2021, the incidence rates of BCC increased across the SDI quintiles, from Low SDI to High SDI regions. The highest incidence rate was in High SDI regions, at 824.67 (734.18-915.28) in 2021. Similarly, the DALY rates increased with higher SDI levels, with the highest DALY rate in High SDI regions at 0.34 (0.16-0.66) in 2021. Among the 21 regions, High-income North America had the highest incidence and DALY rates, followed by Western Europe. The smallest increases were in Oceania, followed by South Asia.
Globally, the age-standardized DALYs for BCC among the elderly have shown an increasing trend, with the most significant rise in High-income North America, from 0.42 (0.18-0.79) in 1990 to 0.91 (0.43-1.74) in 2021. The smallest increase was in Oceania, from 0.0001 (0.00002-0.0002) in 1990 to 0.0001 (0.000025-0.00027) in 2021, followed by South Asia, from 0.0024 (0.00100-0.0049) in 1990 to 0.0027 (0.00111-0.00534) in 2021. In all regions, the DALYs for males were consistently higher than those for females (Table 1).
Trends in national burden of 55+ year BCC from 1990 to 2021
In 1990, the highest number of BCC cases among the elderly were reported in the United States of America (572,530 cases, range 442,328–705,463), Brazil (42,195 cases, range 36,167–48,281), and France (34,021 cases, range 30,344–37,645). In 2021, the highest number of BCC cases were reported in the United States of America (2,562,722 cases, range 2,301,511–2,842,198), China (511,566 cases, range 416,717–611,458), and Brazil (68,793 cases, range 54,410–84,605). In 1990, the highest age-standardized incidence rates (ASIR) were in the United States of America (1,091 per 100,000, range 843–1,345), Ireland (385 per 100,000, range 342–425), and Switzerland (350 per 100,000, range 335–365). The lowest ASIRs were in Bhutan (0.03 per 100,000, range 0.008–0.06), Nepal (0.03 per 100,000, range 0.008–0.058), and Bangladesh (0.03 per 100,000, range 0.009–0.059). In 2021, the highest age-standardized incidence rates (ASIR) were in the United States of America (2,556 per 100,000, range 2,296–2,835), Sweden (271 per 100,000, range 219–333), and Greenland (264 per 100,000, range 197–333). The lowest ASIRs were in Nepal (0.03 per 100,000, range 0.009–0.058), Bangladesh (0.03 per 100,000, range 0.009–0.058), and Bhutan (0.03 per 100,000, range 0.009–0.057).
Among 198 countries and territories, the age-standardized incidence rate (ASIR) of BCC in the elderly population has shown an increasing trend. The most significant increase was in the United States of America, rising from 1091.3 per 100,000 (843.1–1344.7) in 1990 to 2556.4 per 100,000 (2835.2–2295.8) in 2021. Sweden also saw an increase from 185.1 per 100,000 (141.3–238.9) in 1990 to 271.4 per 100,000 (219.3–333.0) in 2021. The smallest increase was in Nepal, rising from 0.025 per 100,000 (0.009–0.058) in 1990 to 0.03 per 100,000 (0.009–0.057) in 20 (Figure 2, Supplementary Data 2).
Figure 2. Country trends of 55+ year BCC from 1990 to 2021. (A) ASIR in basal-cell carcinoma(1990); (B) ASIR in basal-cell carcinoma(2021); (C) ASDR in basal-cell carcinoma(1990); (D) ASDR in basal-cell carcinoma(2021); (E) Incidence rate in basal-cell carcinoma(1990 to 2021); (F) DALYs rate in basal-cell carcinoma(1990 to 2021).
The burden trend by age group from1990 to 2021
Comparison of age-standardized incidence rates (ASIR), DALYs, and age-standardized DALY rates (ASDR) for BCC globally in 1990 and 2021. The ASIR and DALYs for BCC increased with age, with the highest proportion of patients in the 70–74 years age group. In 2021, the number of new BCC cases, DALYs, ASIR, and ASDR were all higher than in 1990 (Figure 3, Supplementary Data 3).
Figure 3. Differences by age group of 55+ year BCC (A) 55+ age burden of incidence cases; (B) 55+ age burden of ASIR; (C) 55+ age burden of DALYs cases; (D) .55+ age burden of ASDR.
The burden trend by SDI group at different time periods
From 1990 to 2021, the number of new cases of BCC among individuals aged 55 and older increased globally, rising from approximately 500,000 cases in 1990 to nearly 1.5 million cases in 2021. In different SDI countries, the increase in the number of new cases among 55+ BCC patients was smaller in high SDI countries and larger in low SDI countries. In terms of relative proportion, the proportion of 55+ BCC patients remained relatively stable globally but varied among different SDI countries. For example, in high SDI countries, the relative proportion of 55+ BCC patients was about 15% in 2021, while in low SDI countries, it was close to 50%. In terms of DALYs for BCC, the number of 55+ BCC patients also increased globally from approximately 20,000 in 1990 to nearly 60,000 in 2021. In different SDI countries, the increase in DALYs among 55+ BCC patients was smaller in high SDI countries and larger in low SDI countries. In terms of relative proportion, the proportion of DALYs for 55+ BCC patients remained relatively stable globally but varied among different SDI countries. For example, in high SDI countries, the relative proportion of DALYs for 55+ BCC patients was about 10% in 2021, while in low SDI countries, it was close to 40% (Figure 4, Supplementary Data 4).
Figure 4. Distribution of disease burden of Basal cell carcinoma from 1990 to 2021 (A) Temporal changes in the absolute number of BCC incidences by age group from 1990 to 2021; (B) Temporal changes in the relative proportion of BCC incidences by age group from 1990 to 2021; (C) Temporal changes in the absolute number of BCC DALYs by age group from 1990 to 2021; (D) Temporal changes in the relative proportion of BCC DALYs by age group from 1990 to 2021.
55+ BCC projections of trends in the burden of disease in 2050
Since 2021, the disease burden of 55+ BCC patients has shown varying upward trends across different genders. Specifically, as age increases, the disease burden of 55+ BCC patients significantly rises in the older age groups (e.g., 85-89, 90-94, 95+ years), indicating a higher concentration of BCC burden in these age groups. Meanwhile, the disease burden of BCC also increases in the middle and lower age groups (e.g., 55-59, 60-64, 65–69 years). By 2050, it is projected that 55+ BCC patients will have a higher disease burden across all age groups, with the most significant increases expected in the 90–94 and 95+ age groups. This suggests that the disease burden of BCC may further increase in the coming decades, with the trend being particularly pronounced in the elderly population. In males, the disease burden of 55+ BCC patients has shown a clear upward trend since 2021. Specifically, the disease burden significantly increases in the older age groups (e.g., 85-89, 90-94, 95+ years), with the ASDR expected to reach a higher level in the 95+ age group by 2050. The disease burden also rises in the middle and lower age groups (e.g., 55-59, 60-64, 65–69 years), but the increase is relatively smaller. In females, the disease burden of 55+ BCC patients has also shown an upward trend since 2021, but compared to males, the increase is more pronounced in the older age groups. Specifically, the ASDR for female BCC patients in the 90–94 and 95+ age groups is expected to reach a higher level by 2050, with a larger increase. Although the disease burden also increases in the middle and lower age groups (e.g., 55-59, 60-64, 65–69 years), the increase is relatively more gradual (Figure 5, Supplementary Data 5).
Figure 5. 55+BCC projections of trends in the burden of disease in 2050; (A) Both sex; (B) Male sex; (C) Female sex.
Discussion
BCC is one of the most common skin malignancies globally, with varying incidence rates reported across different regions. A systematic review analyzing data from 38 different countries between 1955 and 2007 found that Australia had the highest annual incidence rate (>1000 per 100,000 person-years), while some regions in Africa had the lowest incidence rate (<1/100,000 person-years) (13, 14). Over the past 30 years, there has been no literature specifically reporting on the incidence of BCC in the elderly population globally and its distribution across different countries and regions, although there have been reports on the overall incidence of skin cancer (15). Studies on the burden of BCC in the elderly are rare. Therefore, analyzing factors such as the incidence rate, age of onset, gender distribution, incidence rate distribution across different countries and regions, and disease burden comparison for elderly BCC globally from 1990 to 2021 is of significant importance to clinical practice, epidemiology, and public health.
Analysis of temporal trends
From the data presented, we observe that from 1990 to 2021, the number of new cases of BCC among the elderly population globally showed a certain fluctuation, with a continuous increase from 1990 to 2005 and a stabilization from 2005 to 2021. The fluctuations are mainly influenced by changes in lifestyle and environment, ultraviolet (UV) exposure, population aging, genetic factors, and medical resources and diagnostic capabilities. Changes in lifestyle and environment, such as increased use of tobacco, alcohol, overweight, environmental pollution, lack of exercise, and emotional stress, which are cancer risk factors, have significantly increased the risk of cancer. After 2005, as awareness of the hazards of UV exposure increased, people may have adopted more preventive measures, such as using sunscreen and avoiding sun exposure during peak hours, which may have helped stabilize or even reduce the incidence of BCC. Therefore, as public awareness of skin cancer and its association with UV exposure increases, more preventive measures will be taken, which will to some extent reduce the incidence of the disease. In the future, screening for BCC should focus on elderly patients over 60 years old and implement relevant preventive measures.
Analysis of gender trends
According to global BCC data, the incidence rates in males are consistently higher than those in females across different regions. Possible reasons include: First, outdoor work and recreational activities increase exposure to ultraviolet (UV) radiation, which is a major risk factor for BCC. Men are more likely to be exposed to UV radiation due to their higher engagement in outdoor work. Second, men are less likely than women to use sunscreen, hats, and other protective gear, which increases their risk of developing BCC.
Analysis of global trends
From 1990 to 2021, the incidence and DALYs of BCC among the elderly population globally showed an upward trend, with a significant increase from 1990 to 2005 and a stabilization from 2005 to 2021. The reasons for this trend are multifaceted, including genetic, environmental, and medical factors. The occurrence of BCC is associated with genetic factors, with certain genetic disorders such as Gorlin syndrome, xeroderma pigmentosum, and ocular albinism increasing the risk of developing BCC (16–21).Abnormalities in the PTCH gene, which controls cell proliferation and differentiation, may be associated with the development of BCC (22, 23). In terms of environmental factors, UV exposure is an extremely important cause of BCC, with long-term sun exposure particularly affecting exposed areas of the body, especially the face (24, 25). UV exposure and genetic mutations play a major role, with the abnormal activation of the Hedgehog (Hh) signaling pathway being considered the most important mechanism in the development of BCC (26, 27). Importantly, the carcinogenic effects of UV radiation are further amplified in the elderly population. Aging is associated with impaired skin barrier function and diminished DNA repair capacity, which compromise the skin’s ability to counteract UV-induced DNA damage. These age-related changes may exacerbate the accumulation of mutations in key regulatory genes such as PTCH, thereby promoting abnormal activation of the Hedgehog signaling pathway and increasing the risk of BCC initiation. Consequently, individuals aged ≥55 years represent a high-risk group for BCC development. This underscores the necessity of targeted sun protection interventions in the elderly, not only to reduce UV exposure but also to mitigate the molecular vulnerabilities associated with aging.Long-term intake of inorganic arsenic or arsenic-rich water and food may also be associated with the development of BCC (28). Medical factors include ionizing radiation, with long-term occupational exposure to low-to-moderate levels of ionizing radiation also increasing the risk of BCC (29). With advancements in pharmacotherapy, the increased use of immunosuppressants has led to a higher risk of BCC in individuals with long-term immune suppression, such as kidney transplant recipients, whose overall incidence of BCC is 7 to 16 times that of the general population (30). Secondly, population aging is a significant factor, as BCC is an indolent skin tumor that typically takes decades to develop, and thus most cases occur in individuals over 60 years old. The incidence of BCC is associated with geographical latitude and negatively correlated with skin pigmentation (31–33).The risk of developing BCC increases with age. The use of dermatoscopy and other imaging techniques has improved diagnostic accuracy, potentially leading to an increase in reported cases (34–37).These factors collectively contribute to the increase in the incidence of BCC among the elderly and changes in age-standardized incidence rates. UV exposure and genetic factors play a significant role in the development of BCC, while population aging and advancements in medical technology also influence the incidence statistics.
Analysis of SDI quintile trends
At the regional level, from 1990 to 2021, the incidence rates across the five SDI quintiles increased progressively from Low SDI to High SDI, with the highest incidence in High SDI regions. The reasons for the high incidence in High SDI regions may include the following: First, people in these regions tend to engage in more outdoor activities and may have less ozone layer protection or stronger sunlight exposure, leading to increased UV exposure and a higher incidence of skin cancers such as BCC (38). Second, High SDI regions typically have higher life expectancy and more severe population aging than other regions, which increases the risk of age-related cancers (39). Additionally, these regions may have more industrial activities, increasing residents’ exposure to various risk factors. Moreover, High SDI regions usually have better medical resources and diagnostic capabilities, which may lead to more cases being detected and reported. Finally, these regions may face more environmental pollution, including cancer risk factors such as tobacco, alcohol, overweight, environmental pollution, lack of exercise, and emotional stress. These factors collectively contribute to the relatively higher cancer incidence in High SDI regions.
The burden trend by SDI group at different time periods
Globally, from 1990 to 2021, the number of new cases and DALYs of BCC among individuals aged 55 and older showed an upward trend, with significant differences across countries with different SDI levels. This phenomenon reflects the complex situation of global population structure changes, uneven distribution of medical resources, and the shift in disease burden. First, the intensification of global population aging is an important background factor for the increase in the number of 55+ BCC patients. As life expectancy increases and the proportion of the elderly population rises, the incidence of age-related diseases naturally increases. The increase in BCC cases is closely related to changes in population structure. However, the differences between countries with different SDI levels reveal deeper issues. The increase in the number of cases and DALYs is more significant in low SDI countries, which may be related to the relative scarcity of medical resources and insufficient disease prevention and control capabilities in these countries (39–41). In contrast, although high SDI countries have abundant medical resources, the relative proportion of BCC is still high due to more severe population aging, indicating that even in areas with better medical conditions, age-related diseases remain a significant public health challenge. This is consistent with the findings of spinal cord injury studies, which also show that population growth and aging are the main driving forces behind changes in the burden of spinal cord injuries. From a public health policy perspective, this trend suggests that countries need to develop targeted response strategies based on their SDI levels. Low SDI countries should focus on strengthening basic medical infrastructure, improving disease screening, and early intervention capabilities to slow the rapid growth of age-related diseases such as BCC. High SDI countries need to focus on the long-term management and rehabilitation of age-related diseases, optimize the allocation of medical resources, and address the growing burden of age-related diseases. Moreover, global cooperation and experience sharing are crucial. Efforts by international organizations and non-governmental organizations to promote the sharing of medical technology and resources can help narrow the health gap between countries with different SDI levels and jointly address the challenges posed by global population aging (42).
Projections of trends in the burden of disease for 55+ BCC in 2050
Since 2021, the disease burden of 55+ BCC patients has shown varying upward trends across different genders and age groups, revealing the severe challenges faced by public health in the future. In terms of age distribution, the disease burden of BCC is particularly concentrated in the older age groups (e.g., 85-89, 90-94, 95+ years), with significant increases. This trend may be related to the physiological decline, accumulation of chronic diseases, and increased use of medical resources in the elderly population. As global population aging intensifies and the proportion of the elderly increases, the high burden of BCC is expected to worsen. By 2050, the disease burden of BCC is projected to reach higher levels across all age groups, particularly in the 90–94 and 95+ age groups, posing significant pressure on the healthcare and social security systems. In terms of gender differences, the disease burden of BCC is increasing for both males and females, but the increase is more pronounced in older females. This may be related to the longer average life expectancy of women, longer accumulation of chronic diseases, and the combined effects of physiological and social factors. The increased disease burden in older females highlights the need for future public health policies to pay more attention to the health needs of women, especially in geriatric care and chronic disease management.
Additionally, the disease burden of BCC in middle-aged groups (such as 55-59, 60-64, and 65–69 years) has also shown an upward trend, albeit with smaller increases. This suggests that the age of onset for BCC may be gradually decreasing, which warrants attention. Over the next few decades, changes in population structure and lifestyle are expected to further increase the disease burden of BCC, particularly in the elderly population. In conclusion, future public health policies should focus on the BCC disease burden in the elderly and women, strengthen early screening, prevention, and intervention measures, and optimize the allocation of medical resources to address the ongoing increase in BCC disease burden. Additionally, further research into the pathogenesis and risk factors of BCC is needed to develop more effective treatments and health management strategies.
The 30-year rise in elderly BCC incidence and DALYs is driven not only by ultraviolet exposure, population ageing and immunosuppressant use, but also by heterogenous health-system responses that the GBD lens cannot fully capture: national screening policies range from systematic dermoscopy programmesin Australia to absent formal guidelines in much of sub-Saharan Africa, while high-income countries’ higher recorded rates partly reflect reimbursed skin-clinic visits and pathological confirmation of every excised lesion. Conversely, under- and miscoding of BCC as “other malignant skin” (ICD-10 C44.9, C46.-) remains common where pathology services are scarce; GBD 2021 attempts to separate BCC from SCC and rarer NMSC through a Bayesian meta-regression that redistributes garbage codes and incorporates cancer-registry flag variables, yet this modelling step still depends on the very records that are missing or biased in low-SDI settings. Consequently, the apparent surge in North-West Europe and the relative plateau in parts of South-East Asia may mirror differential detection capacity rather than true epidemiological divergence. Future burden estimates should therefore be triangulated with health-facility audits, claims-data validation studies and geospatial UV-dosimetry, while policy discussions must shift from crude incidence rankings to context-specific prevention packages—shade-planning regulations, opportunistic screening for high-risk outdoor workers, and subsidised topical therapies—that simultaneously reduce under-diagnosis in resource-limited regions and overtreatment in well-served ones.
Limitations and future prospects
This study has key limitations to note. First, full dependence on GBD data brings constraints: roughly one-tenth of countries lack non-melanoma skin cancer (NMSC) registries (cross-regional data borrowing may skew BCC counts), variable pathology standards misclassify up to a quarter of BCC cases (only partly corrected by GBD redistribution), 2018-median data misses post-COVID-19 tele-dermatology surges (distorting recent detection trends), and national aggregates hide sub-national extremes (e.g., Queensland’s BCC incidence is 2.3-fold higher than Australia’s national estimate). Second, no primary clinical data limits analysis of BCC subtypes, treatments (cryotherapy, PDT, imiquimod, 5-fluorouracil), or patient outcomes, preventing assessment of treatment’s impact on burden metrics. Third, regional BCC differences may reflect diagnostic/reporting disparities rather than true epidemiology—low SDI countries face under-diagnosis, under-reporting, and poor pathology infrastructure, risking underestimated burden, and emerging studies show some low-SDI regions’ actual incidence may approach high-SDI areas when accounting for under-ascertainment. Fourth, BCC is often grouped with other NMSC in datasets, diluting its trends and biasing case capture/burden assessment amid diverse treatments. Thus, GBD estimates are low-resolution proxies. Future work should integrate clinical cohort data with GBD, audit regional registries (especially low-SDI), conduct sensitivity analyses, advocate for disaggregated NMSC data, and build treatment-stratified models; decision-makers should validate GBD insights with local data (sentinel networks, UV-spatial layers) before resource allocation.
Conclusion
In summary, over the past 30 years, the number of new cases of BCC among the elderly has generally increased globally, which is related to the growth of the global population. The incidence and DALYs of BCC have increased in all global regions, which on one hand reflects the impact of climate and environmental changes on the disease, and on the other hand, highlights the significant role of population aging and the wider use of immunosuppressants. On the other hand, improvements in medical resources have led to earlier diagnosis and treatment of BCC for more patients, especially in developed countries. These high-income regions typically have more advanced medical resources and diagnostic technologies, which may have increased the detection and reporting rates of BCC, thereby raising the incidence data. Meanwhile, the implementation of various treatments and surgeries has also increased the disease burden of BCC, particularly in developed countries. By analyzing the potential causes and disease burden of BCC, we can enhance global preventive measures against BCC in the future, reduce the occurrence and burden of this disease, which is a favorable measure for preventing BCC, and also decrease the use of global health resources.
Data availability statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.
Author contributions
YC: Writing – original draft. MR: Data curation, Writing – review & editing.
Funding
The author(s) declared that financial support was not received for this work and/or its publication.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Generative AI statement
The author(s) declare that no Generative AI was used in the creation of this manuscript.
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Keywords: basal cell carcinoma, burden, risk factors, forecast, global burden of disease
Citation: Cai Y-X and Rong M (2025) Global basal cell carcinoma in 55+ population: 1990– 2021 burden、risk-factor trends and 2050 forecast. Front. Oncol. 15:1702129. doi: 10.3389/fonc.2025.1702129
Received: 09 September 2025; Accepted: 17 November 2025; Revised: 16 November 2025;
Published: 19 December 2025.
Edited by:
Giuseppe Palmieri, University of Sassari, ItalyReviewed by:
Guozhi Zhang, Shaanxi University of Chinese Medicine, ChinaIgnazio Stanganelli, Universita degli Studi di Parma, Skin Cancer Unit, Italy
Copyright © 2025 Cai and Rong. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Yan-Xia Cai, MTU4MTYwOTgyNDhAMTYzLmNvbQ==
Minglei Rong