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ORIGINAL RESEARCH article

Front. Med., 23 September 2021
Sec. Hematology

Trends Analysis of Non-Hodgkin Lymphoma at the National, Regional, and Global Level, 1990–2019: Results From the Global Burden of Disease Study 2019

\nWenwen Cai,&#x;Wenwen Cai1,2Qingle Zeng&#x;Qingle Zeng3Xingxing Zhang,Xingxing Zhang1,2Weiqing Ruan
Weiqing Ruan1*
  • 1Huiqiao Medical Center, Nanfang Hospital, Southern Medical University, Guangzhou, China
  • 2School of Nursing, Southern Medical University, Guangzhou, China
  • 3Department of Interventional Radiology, Nanfang Hospital, Southern Medical University, Guangzhou, China

Background: Non-Hodgkin lymphoma is a common hematologic malignancy. This article aimed to estimate the trends of non-Hodgkin lymphoma (NHL) globally from 1990 to 2019.

Methods: Data on the NHL burden were explored from the Global Burden of Disease study 2019. The trends of NHL burden were estimated using age-standardized rate (ASR) and estimated annual percentage change (EAPC).

Results: The ASR of NHL incidence showed an increasing trend worldwide from 1990 to 2019, with an EAPC of.56 [95% CI: 0.45–0.66]. Meanwhile, increasing trends were observed in both sexes and in most geographic regions, particularly East Asia (EAPC = 3.57, 95% CI: 3.29–3.86). The most pronounced increasing trends were seen in Georgia (EAPC = 4.7, 95% CI: 4.20–5.21), followed by Belarus and Uzbekistan. However, death and disability-adjusted life years (DALYs) caused by NHL showed decreasing trends globally, in which the respective EAPCs were −0.09 (95% CI: −0.17 to −0.02) and −0.28 (95% CI: −0.35 to −0.22). Decreasing trends were mainly seen in high and high-middle sociodemographic index (SDI) areas. At the national level, the largest increasing trends of death and DALYs were observed in Georgia, in which the respective EAPCs were 4.54 (95% CI: 4.01–5.07) and 4.97 (95% CI: 4.42–5.52).

Conclusions: Decreasing trends of death and DALYs caused by NHL were observed worldwide from 1990 to 2019, but NHL remains a substantial challenge globally. The findings would inform the strategies for reducing the burden of NHL.

Introduction

Non-Hodgkin lymphoma is a kind of lymphoma characterized by a wide range of morbid features and difficulties in diagnosis (1) and accounts for 90% of all lymphoma incidences (2).

According to the Global Cancer Statistics 2018, the burden of non-Hodgkin lymphoma (NHL) aggravated in many regions, and reached 509,590 incidences and 248,724 deaths in 2018, accounting for 2.8 and 2.6%, respectively, of the total incidence and mortality of 36 cancers involved (3). In the United States, for example, the incidence of NHL has increased significantly over the past few decades, and now accounts for ~4% of total cancer incidence (4). Conversely, improved survival in NHL was commonly reported in recent years. In the 1970s, just over one-fifth of people with NHL survived more than 10 years, but now the proportion has increased to almost two-thirds (5). Of these, survival in the UK has seen a 3-fold increase in the last 40 years (5). The reasons for the increasing NHL incidence involve many social factors. The major risk factors for the development of NHL are various, including AIDS infection, immunosuppressive drugs, occupational exposures, pesticide contiguity, and smoking (69). In terms of the typologies of NHL, it has been studied that most NHL evolved from mature B lymphocytes, with a few from T lymphocytes or natural killer (NK) cells (10). In Western countries, the majority of NHL cases are B-cell lymphomas (~85%), but T-cell lymphoma is less common (~15%), while the reversed proportion occurs in developing regions (5, 11), which probably explains the significant geographic heterogeneity in the distribution of NHL burden.

The Global Burden of Disease study (GBDs) comprehensively assessed the burden caused by cancers globally (12, 13), which facilitated the tracking of the temporal trends of the disease burden. Strategies such as adjusting causes of death to compensate for incomplete data, developing maps to adjust study data, reassigning garbage codes, refining age groupings, and developing criteria to exclude outliers are used to ensure data quality and improve comparability (14). Therefore, this article aimed to estimate the trends of NHL burden from 1990 to 2019 using the data derived from the GBDs 2019 to provide information on health strategies.

Materials and Methods

Data Sources

Data on the NHL burden, such as incidence, death, and DALYs, were explored using the Global Health Data Exchange query tool (http://ghdx.healthdata.org/gbd-2019). According to the instruction of GBD online tools, data were extracted by sex, age group, geographic region, and country/territory from 1990 to 2019. The data were available in 21 geographic regions (e.g., East Asia, Australia, and the Caribbean) and 204 countries/territories (e.g., Slovenia, Thailand, and Germany) worldwide. The sociodemographic index (SDI) is a compound measure of social development and health outcomes. According to the SDI, these regions and countries/territories were classified into low, low-middle, middle, high-middle, and high. The human development index (HDI) is a compound measure reflecting the level of economy and human well-being, which was acquired from the United Nations Development Program (http://hdr.undp.org/en/data).

Statistical Analysis

When comparing the disease distribution of several different age structures or the same population over a period of time with different age structures, age standardization is necessary to adjust for potential age structure confusion. Age-standardized rate (ASR) (/100,000 people) is calculated using the following formula:

ASR=i=1Aaiwii=1Awi×100,000

Age-standardized rate is equal to the sum of the products of ai (the age-specific rates, where i denotes the ith age class) and wi(the number of persons or weight) in the same age group i of the chosen reference standard population, then divided by the sum of standard population weights.

The estimated annual percentage change is equal to the annual change over the specified range and is calculated on a linear scale. The natural logarithm of the regression-line is fitted to ASR with the following formula: y = α + β x + ε, where y = ln (ASR), and x = calendar year. Estimated annual percentage change (EAPC) and its 95% CI were calculated as 100 × [exp(β)−1] with the linear regression model (15, 16). The trends were determined as follows: when both the EAPC and its lower limit of 95% CI were >0, it meant there was an increasing trend; when both the EAPC and its upper 95% CI were <0, it meant there was a decreasing trend; others meant that ASR was stable over time. In order to explore the influencing factors of EAPC, the relationships between EAPCs and ASR in 1990 and EAPCs and HDI in 2019 were estimated by a Pearson correlation analysis. Data were analyzed using R v3.6.2 (Institute for Statistical Computing, Vienna, Austria), and a value of p < 0.05 was considered to be statistically significant.

Results

Trends in Incidence of NHL

Globally, the incident number of NHL was 457.08 × 103 [95% uncertainty interval (UI): 416.89 × 103 to 498.78 × 103] in 2019, with an increase of 139.65% since 1990. The age-standardized incidence rate (ASIR) showed an increasing trend worldwide from 1990 to 2019 (EAPC = 0.56, 95% CI: 0.45– 0.66) (Table 1, Figure 1). Compared with female patients, an increasing trend in ASIR was more pronounced in male patients (EAPC = 0.78, 95% CI: 0.69– 0.87) (Table 1). The highest incident number was seen in group aged above 80 in 2019 (91.33 × 103), and an increasing percentage in incident number was found in all age groups except for the group aged below 5 years old from 1990 to 2019 (Supplementary Table 1, Figure 2A). Increasing trends in ASIR were observed in four SDI areas, particularly in the middle ones (EAPC = 2.42, 95% CI: 2.26–2.58); whereas a decreasing trend was seen in high SDI areas (EAPC = −0.37, 95% CI: −0.56 to −0.18). At the regional level, East Asia was the region with the highest incident cases (95.93 × 103) in 2019, with an increasing percentage of 343.84% since 1990. Increasing trends in ASIR were observed in 17 regions, and the most pronounced ones were in East Asia and Andean Latin America, in which the respective EAPCs were 3.57 (95% CI: 3.29–3.86) and 2.41 (95%CI: 2.24–2.57). Downward trends in ASIR were only seen in high-income North America and Australasia, whose EAPCs were −1.2 (95% CI: −1.43 to −0.97) and −1.12 (95% CI: −1.39 to −0.85), respectively (Table 1, Figures 1, 2B,C). At the national level, the ASIR in 2019 varied from 0.68/100,000 in Mali to 14.86/100,000 in Andorra. During the period 1990–2019, the largest growing percentages of incident number occurred in Qatar (965.24%) and the United Arab Emirates (782.81%), but the lowest one was in Zimbabwe (4.72%). One hundred fifty countries/territories showed varying degrees of increase in ASIR, particularly Georgia and Belarus, in which the respective EAPCs were 4.7 (95% CI: 4.20–5.21) and 3.96 (95% CI: 3.47–4.44); whereas 28 countries/territories showed decreasing trends, with the lowest EAPCs occurring in Zimbabwe (EAPC = −2, 95% CI: −2.31 to −1.69), followed by Kazakhstan and the United States of America (Supplementary Table 2, Figures 3A–C).

TABLE 1
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Table 1. Number and age-standardized rate of non-Hodgkin lymphoma incidence on a global scale by sex, SDI areas, and geographic regions in 1990 and 2019, and the percentage change of absolute number and the EAPCs from 1990 to 2019.

FIGURE 1
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Figure 1. Trends in the incidence, death, and DALYs of non-Hodgkin lymphoma in the globe, SDI areas, and geographic regions from 1990 to 2019. SDI, sociodemographic index; DALYs, disability-adjusted life years.

FIGURE 2
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Figure 2. Incident number of non-Hodgkin lymphoma in age groups, SDI areas, and geographic regions from 1990 to 2019. (A) Incident number in age groups; (B) ASIR in SDI areas; (C) incident number in geographical regions. SDI, sociodemographic index; ASIR, age-standardized incidence rate.

FIGURE 3
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Figure 3. ASIR, percentage changes in the incident number, and EAPCs of non-Hodgkin lymphoma at the national level, 1990–2019. (A) ASIR in 2019; (B) percentage changes in incident numbers between 2000 and 2019; (C) distribution of EAPCs presented in countries/territories. Countries/territories with extreme values were annotated. ASIR, age-standardized incidence rate; EAPC, estimated annual percentage change.

Trends in Death Caused by NHL

Over the past 30 years, deaths due to NHL in the world increased steadily by increased 101.94% and reached up to 254.61 × 103 (95% UI: 237.71 × 103 to 270.35 × 103) in 2019. The overall age-standardized death rate (ASDR) presented a decreasing trend from 1990 to 2019 (EAPC = −0.09, 95% CI: −0.17 to −0.02) (Supplementary Table 3, Figure 1). A slight increasing trend in ASDR was observed in male patients (EAPC = 0.08, 95% CI: 0.01– 0.15), while a downward trend was observed in female patients (EAPC = −0.34, 95% CI: −0.44 to −0.23) (Supplementary Table 3). Among the age groups, the largest number of deaths was seen in the age group with participants over 80 years old in 2019 (58.77 × 103). From 1990 to 2019, the increasing percentages in death were observed in all age groups of above 15 years, with the most notable one showing in the age group of over 80 years (231.1%). However, the percentage declined in patients aged younger than 14 years (Supplementary Table 1, Supplementary Figure 1A). Upward trends were observed in most SDI areas, especially the middle SDI areas, with an EAPC of 0.94 (95% CI: 0.84–1.03). However, a decreasing tendency only occurred in high SDI areas (EACP = −0.98, 95% CI: −1.15 to −0.82). Among 21 regions, the highest death number in 2019 occurred in East Asia (46.45 × 103), while the lowest one was in Oceania (0.13 × 103). During the period 1990–2019, the largest increasing percentage was observed in Andean Latin America (218.58%) and South Asia (210.46%). Increasing trends in ASDR were seen in 12 regions, and the most pronounced one was in South Asia (EAPC = 1.25, 95% CI: 1.18–1.32). On the other hand, decreasing trends were observed in eight regions, particularly in Australasia (EAPC = −1.78, 95%CI: −2.01 to −1.56) (Supplementary Table 3, Figure 1, Supplementary Figures 1B,C). At the national level, the highest ASDR in 2019 occurred in San Marino (9.56/100,000), while the lowest one occurred in Mali (0.7/100,000). During the period 1990–2019, the largest increases in numbers of deaths were in the United Arab Emirates (609.26%) and in Qatar (491.98%), but the pronounced decreasing one was in Niue (−2.86%). Increasing trends in ASDR occurred in 102 countries/territories, with the most significant one occurring in Georgia (EAPC = 4.54, 95% CI: 4.01–5.07), followed by Uzbekistan and Belarus. However, decreasing trends appeared in 75 countries/territories, particularly in the Syrian Arab Republic and Bermuda, in which the EAPCs were −2.46 (95% CI: −3.05 to −1.86) and −2.21 (95% CI: −2.46 to −1.96), respectively (Supplementary Table 4, Supplementary Figures 3A–C).

Trends in DALYs Caused by NHL

Globally, the DALYs number of NHL has increased by 68.59% since 1990, and it went by up to 6991.3 × 103 (95% UI: 6570.14 × 103 to 7450.47 × 103) in 2019. The overall ASR of DALYs declined from 1990 to 2019, with an EAPC of −0.28 (95% CI: −0.35 to −0.22). Trends in the ASR of DALYs had a minor increase in male patients but had a decrease in female patients (EAPC = −0.34, 95% CI: −0.44 to −0.23) (Supplementary Table 5, Figure 1). Among the age groups, the largest number of DALYs in 2019 was seen in patients aged 65–69 years (733.13 × 103). During the period 1990–2019, the percentage of DALYs number decreased in age groups younger than 14 years, but decreased in the rest, particularly in the age group of above 80 years (226.13%) (Supplementary Table 1; Supplementary Figure 2A). Increasing trends in the ASR of DALYs were observed in all the SDI areas, except the high SDI area (EACP = −1.48, 95% CI: −1.65 to −1.31). Among 21 geographic regions, the highest DALYs number in 2019 was seen in East Asia (1362.18 × 103), and the lowest one was seen in Oceania (5.08 × 103). During the period 1990–2019, the largest increasing percentage was observed in Andean Latin America (138.6%) and South Asia (149.70%). Increasing trends in the ASR of DALYs were found in 11 regions, especially South Asia and Central Asia, with EAPCs of 1.01 (95% CI:0.94 to 1.09) and.81 (95% CI:0.62–1.01), respectively. However, decreasing trends were demonstrated in six regions, particularly in high-income North America (EAPC = −2.04, 95%CI: −2.27 to −1.82) (Supplementary Table 5, Figure 1, Supplementary Figures 2B,C). Among the 204 countries/territories, the ASR of DALYs in 2019 ranged from 23.53/100,000 in Mali to 409.87/100,000 in Monaco. From 1990 to 2019, the largest increases in DALYs were in the United Arab Emirates (561.34%) and in Qatar (471.66%), but the pronounced decreasing one was in Mali (−39.28%). Increasing trends in the ASR of DALYs were observed in 80 countries/territories, and the most pronounced ones were in Georgia (EAPC = 4.97, 95% CI: 4.42 to 5.52), followed by Uzbekistan and Lesotho. On the other hand, decreasing trends were seen in 90 countries/territories, particularly Kazakhstan and Malawi, with EAPCs of −2.92 (95%CI: −3.59 to −2.25) and −2.71 (95%CI: −2.95 to −2.47) (Supplementary Table 6, Supplementary Figures 4A–C), respectively.

Analysis on the Influential Factors of EAPC

For the period 1990–2019, EAPCs had negative relationships with the ASR of incidence, death, and DALYs attributable to NHL (ρ = −0.34, p < 0.01; ρ = −0.44, p < 0.01; ρ = −0.43, p < 0.01, respectively) (Figures 4A–C). In addition, EAPC was also negatively correlated with HDI in 2019 in DALYs attributable to NHL (ρ = −0.2, p = 0.005) (Supplementary Figure 5).

FIGURE 4
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Figure 4. Correlation between EAPCs and ASR in 1990 at the national level. (A) EAPCs of incidence, (B) death, and (C) DALYs had negative associations with ASR in 1990. The association was calculated by a Pearson correlation analysis. The size of the circle is increased with the numbers in 1990. EAPC, estimated annual percentage change; ASR, age-standardized rate. DALYs, disability-adjusted life years.

Discussion

In this article, increasing trends in the ASIR of NHL were observed worldwide and in most regions and countries from 1990 to 2019, which were due to population growth and aging, diagnostic improvements, the AIDS epidemic, and environmental pollution such as organic matter and heavy metals caused by urban industrialization (1721). The significantly increasing burden was observed in old patients with NHL, and was probably related with age, which is a strong negative factor in all lymphoma subtypes (2224). In part, it is also affected by various co-morbidities (17), such as cancer, cardiovascular disease, and stroke (6). The decline in mortality and DALYs for children aged below 14 years compared with adults may be due to biological differences across the age groups. For example, in the case of diffuse large B-cell lymphoma (DLBCL) and anaplastic large cell lymphoma (ALCL), pediatric patients are more likely to have GCB disease (a main subtype of DLBCL) and anaplastic lymphoma kinase (+) ALCL (ALK+ ALCL), both of which have superior prognostic features of NHL (2527). Thus, comparing pathogenesis patterns by NHL subtypes may provide key clues for future etiologic investigations (28). Meanwhile, the lower burden of NHL in female patients was similar to the previous epidemiological studies, in which 5- and 10-year survival was demonstrated to be generally higher in women (3, 29). However, the difference in survival is independent of race, ethnicity, year of diagnosis, or NHL subtypes (24), and this may be caused by different lifestyles between sexes or hormonal influences (22).

In recent years, the improved survival in NHL has been largely attributed to medical advances, such as the development and clinical application of effective treatments like rituximab (a monoclonal antibody)(30). However, the heterogeneity in NHL burden between regions and countries was deeply influenced by local economic development, disease prevalence (11), and local health systems (24). Interestingly, we observed a significant increase in the disease burden in some countries of the former Soviet Union, where Georgia showed the most pronounced trends in its increases in incidence, death, and DALYs, which may reflect the insufficient level of early HIV diagnosis; although medical and economic conditions have improved in recent years, more than half of the cases still do not receive timely and effective treatment (31, 32). The late-stage diagnoses of HIV also occurred in Europe, especially in cases of co-morbid NHL, where HIV detection rates are lower than in other diseases (33). In addition, the increased morbidity in Belarus may also be related to the high prevalence of HIV and the rapid spread of HIV variants in recent years (32). Nevertheless, the explanations still need to be supported by more in-depth studies because of the sparse data in the epidemiological literature on NHL in Eastern Europe and Central Asia. However, the incidence of NHL has significantly declined in developed countries, such as Australia and the United States, because of highly active antiretroviral therapy (HAART) (34, 35). Meanwhile, we also note an interesting point: the relative risk of HIV-associated NHL in whites is twice that of blacks in countries such as the United States, which may be due to differences in immune system regulatory genes caused by racial distinguishments (36). It is also certain that the decline in trend in Zimbabwe is also associated with the widespread availability of antiretroviral therapy or possibly with the loss of public health data (37).

Western diet and lifestyle caused by industrial and economic development might be responsible for the increasing NHL burden in East Asia (3840). However, in contrast to the pattern of multiple lymph node disorders in Western countries, Asian countries exhibit intermediate-grade to high-grade diffuse aggressive lymphomas, peripheral T-cell NHL, and extra-lymph node disease more often (41). The poor medical source, misdiagnosis and omission by lacking high quality pathological diagnosis of NHL, and the heavy burden of chemotherapy drugs on the masses had brought the worse prognosis of NHL patients in South Asia (18, 42). In Central Asia, the situation of death, DALYs, and the burden of NHL is far more severe in Uzbekistan than in Kazakhstan, probably because of the fact that HIV genotyping studies have been conducted for a long time in Kazakhstan, while they were just beginning in Uzbekistan (32). In contrast, in South Africa, excluding major changes in society and the lifestyles of the people, scholars hypothesized that the development of NHL was delayed because of the receipt of various anti-infective treatments (4346). Researchers have applied a low-intensity EPOCH (etoposide, prednisolone, vincristine, cyclophosphamide, doxorubicin) infusion regimen in sub-Saharan Africa, which may have contributed to the decline in DALYs in Malawi because the infusion regimen is a treatment that can improve outcomes for adolescents and adults with Burkitt lymphoma (BL) in Malawi and reduce drug toxicity reactions (47). There were several limitations in this study. First, the quality and quantity of data sources determined the accuracy and reliability of GBDs estimates; thus, potential bias probably derived from unreported cases, incomplete testing, miscoding, and misclassification, which were described in detail in the previous GBDs articles (1214). Second, the diagnosis and classifications of NHL had been revised differently in various countries over time, and this has had a significant impact on data estimation, which was an important limitation. Third, the basis of estimating data for most middle- and low-income countries is largely derived from high-income countries with strong cancer registration systems, which still introduces some uncertainty in the veracity of the data due to the heterogeneity across countries. Last but not least, despite the use of tools to correct data, it is impossible for GBDs to fully control biases in data collection, entry, and veracity (14, 48).

Conclusions

In the past three decades, slow decreasing trends in the deaths and DALYs of NHL were observed worldwide. Meanwhile, increasing incident trends in NHL highlighted that NHL burden remained a substantial challenge. Furthermore, the impact of NHL varies widely worldwide and is the result of a combination of factors, such as environmental and genetic, so performing more systematic comparative analyses of NHL by geographic region is warranted (36, 49). The findings also indicated that more effective strategies should be established to improve the management and treatment of patients with NHL.

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

WC: project administration and drafting. QZ: data analysis and validation. XZ: data analysis and visualization. WR: supervision, drafting, and editing. All the authors contributed to the article and approved the submitted version.

Funding

This study was supported by the Science and Technology Planning Project of Guangdong Province of China (Grant Nos: 2015A070707005 and 2020A1414040014).

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.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Acknowledgments

Thanks to the Institute for Health Metrics and Evaluation (IHME) and the Global Burden of Disease study collaborations.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmed.2021.738693/full#supplementary-material

Abbreviations

ASR, age-standardized rate; CI, confidence interval; DALYs, disability-adjusted life years; EAPC, estimated annual percentage change; GBD, Global Burden of Disease; GHDx, Global Health Data Exchange; NHL, non-Hodgkin lymphoma; SDI, sociodemographic index; UI, uncertainty interval.

References

1. Darbà J, Marsà A. Burden of Hodgkin and non-Hodgkin lymphoma in Spain over a 10-year period: productivity losses due to premature mortality. Expert Rev Pharmacoecon Outcomes Res. (2020) 21:87–92. doi: 10.1080/14737167.2020.1769478

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Shankland KR, Armitage JO, Hancock BW. Non-Hodgkin lymphoma. Lancet. (2012) 380:848–57. doi: 10.1016/S0140-6736(12)60605-9

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. (2018) 68:394–424. doi: 10.3322/caac.21492

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Pratap S, Scordino TS. Molecular and cellular genetics of non-Hodgkin lymphoma: diagnostic and prognostic implications. Exp Mol Pathol. (2019) 106:44–51. doi: 10.1016/j.yexmp.2018.11.008

PubMed Abstract | CrossRef Full Text | Google Scholar

5. UK. CR. Non-Hodgkin lYmphoma (NHL) Statistics Key Facts. Available online at: https://www.cancerresearchuk.org/health-professional/cancer-statistics/statistics-by-cancer-type/non-hodgkin-lymphoma#heading-Two (accessed Feb27, 2018).

6. Simard JF, Baecklund F, Chang ET, Baecklund E, Hjalgrim H, Olov AH, et al. Lifestyle factors, autoimmune disease and family history in prognosis of non-hodgkin lymphoma overall and subtypes. Int J Cancer. (2013) 132:2659–66. doi: 10.1002/ijc.27944

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Alexander DD, Mink PJ, Adami HO, Chang ET, Cole P, Mandel JS, et al. The non-Hodgkin lymphomas: a review of the epidemiologic literature. Int J Cancer. (2007) 120(Suppl. 12):1–39. doi: 10.1002/ijc.22719

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Dal Maso L, Franceschi S. Epidemiology of non-Hodgkin lymphomas and other haemolymphopoietic neoplasms in people with AIDS. Lancet Oncol. (2003) 4:110–9. doi: 10.1016/S1470-2045(03)00983-5

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Hartge P, Devesa SS. Quantification of the impact of known risk factors on time trends in non-Hodgkin's lymphoma incidence. Cancer Res. (1992) 52(19 Suppl.):5566s−9s.

PubMed Abstract | Google Scholar

10. Bowzyk AA, Ajithkumar T, Behan S, Hodson DJ. Non-Hodgkin lymphoma. BMJ. (2018) 362:k3204. doi: 10.1136/bmj.k3204

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Perry AM, Diebold J, Nathwani BN, MacLennan KA, Müller-Hermelink HK, Bast M, et al. Non-Hodgkin lymphoma in the developing world: review of 4539 cases from the International Non-Hodgkin Lymphoma Classification Project. Haematologica. (2016) 101:1244–50. doi: 10.3324/haematol.2016.148809

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Fitzmaurice C, Abate D, Abbasi N, Abbastabar H, Abd-Allah F, Abdel-Rahman O, et al. Global, regional, and national cancer incidence, mortality, years of life lost, years lived with disability, and disability-adjusted life-years for 29 cancer groups, 1990 to 2017: a systematic analysis for the global burden of disease Study. JAMA Oncol. (2019) 5:1749–68. doi: 10.1001/jamaoncol.2019.2996

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Fitzmaurice C, Allen C, Barber RM, Barregard L, Bhutta ZA, Brenner H, et al. Global, regional, and national cancer incidence, mortality, years of life lost, years lived with disability, and disability-adjusted life-years for 32 cancer groups, 1990 to 2015: a systematic analysis for the global burden of disease study. JAMA Oncol. (2017) 3:524–48. doi: 10.1001/jamaoncol.2016.5688

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Global regional and national age-sex specific all-cause and cause-specific mortality for 240 causes of death 1990–2013: a systematic analysis for the Global Burden of Disease Study 2013. Lancet. (2015) 385:117–71. doi: 10.1016/S0140-6736(14)61682-2

PubMed Abstract | CrossRef Full Text

15. Ou Z, Yu D, Liang Y, He W, Li Y, Zhang M, et al. Analysis of the Global Burden of Disease study highlights the trends in death and disability-adjusted life years of leukemia from 1990 to 2017. Cancer Commun. (2020) 40:598–610. doi: 10.1002/cac2.12094

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Gao S, Yang WS, Bray F, Va P, Zhang W, Gao J, et al. Declining rates of hepatocellular carcinoma in urban Shanghai: incidence trends in 1976–2005. Eur J Epidemiol. (2012) 27:39–46. doi: 10.1007/s10654-011-9636-8

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Hester LL, Park SI, Wood WA, Stürmer T, Brookhart MA, Lund JL. Cause-specific mortality among Medicare beneficiaries with newly diagnosed non-Hodgkin lymphoma subtypes. Cancer-Am Cancer Soc. (2019) 125:1101–12. doi: 10.1002/cncr.31821

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Nair R, Arora N, Mallath MK. Epidemiology of Non-Hodgkin's Lymphoma in India. Oncology. (2016) 91(Suppl. 1):18–25. doi: 10.1159/000447577

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Ortega-García JA, López-Hernández FA, Cárceles-Álvarez A, Fuster-Soler JL, Sotomayor DI, Ramis R. Childhood cancer in small geographical areas and proximity to air-polluting industries. Environ Res. (2017) 156:63–73. doi: 10.1016/j.envres.2017.03.009

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Núñez O, Fernández-Navarro P, Martín-Méndez I, Bel-Lan A, Locutura JF, López-Abente G. Arsenic and chromium topsoil levels and cancer mortality in Spain. Environ Sci Pollut Res Int. (2016) 23:17664–75. doi: 10.1007/s11356-016-6806-y

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Maifredi G, Donato F, Magoni M, Orizio G, Gelatti U, Maiolino P, et al. Polychlorinated biphenyls and non-Hodgkin's lymphoma: a case-control study in Northern Italy. Environ Res. (2011) 111:254–9. doi: 10.1016/j.envres.2010.12.006

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Pfreundschuh M. Age and Sex in Non-hodgkin lymphoma therapy: it's not all created equal, or is it? Am Soc Clin Oncol Educ Journal. (2017) 37:505–11. doi: 10.14694/EDBK_175447

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Sandlund JT, Martin MG. Non-Hodgkin lymphoma across the pediatric and adolescent and young adult age spectrum. Hematology Am Soc Hematol Educ Program. (2016) 2016:589–97. doi: 10.1182/asheducation-2016.1.589

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Crozier JA, Sher T, Yang D, Swaika A, Foran J, Ghosh R, et al. persistent disparities among patients with t-cell non-hodgkin lymphomas and b-cell diffuse large cell lymphomas over 40 years: a SEER database review. Clin Lymphoma Myeloma Leuk. (2015) 15:578–85. doi: 10.1016/j.clml.2015.06.005

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Wood WA, Lee SJ. Malignant hematologic diseases in adolescents and young adults. Blood. (2011) 117:5803–15. doi: 10.1182/blood-2010-12-283093

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Savage KJ, Harris NL, Vose JM, Ullrich F, Jaffe ES, Connors JM, et al. ALK- anaplastic large-cell lymphoma is clinically and immunophenotypically different from both ALK+ ALCL and peripheral T-cell lymphoma, not otherwise specified: report from the International Peripheral T-Cell Lymphoma Project. Blood. (2008) 111:5496–504. doi: 10.1182/blood-2008-01-134270

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Gascoyne RD, Aoun P, Wu D, Chhanabhai M, Skinnider BF, Greiner TC, et al. Prognostic significance of anaplastic lymphoma kinase (ALK) protein expression in adults with anaplastic large cell lymphoma. Blood. (1999) 93:3913–21. doi: 10.1182/blood.V93.11.3913

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Morton LM, Wang SS, Devesa SS, Hartge P, Weisenburger DD, Linet MS. Lymphoma incidence patterns by WHO subtype in the United States, 1992–2001. Blood. (2006) 107:265–76. doi: 10.1182/blood-2005-06-2508

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Monnereau A, Troussard X, Belot A, Guizard AV, Woronoff AS, Bara S, et al. Unbiased estimates of long-term net survival of hematological malignancy patients detailed by major subtypes in France. Int J Cancer. (2013) 132:2378–87. doi: 10.1002/ijc.27889

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Harrison AM, Thalji NM, Greenberg AJ, Tapia CJ, Windebank AJ. Rituximab for non-Hodgkin's lymphoma: a story of rapid success in translation. Clin Transl Sci. (2014) 7:82–6. doi: 10.1111/cts.12111

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Chkhartishvili N, Chokoshvili O, Bolokadze N, Tsintsadze M, Sharvadze L, Gabunia P, et al. Late presentation of HIV infection in the country of Georgia: 2012–2015. PLoS ONE. (2017) 12:e186835. doi: 10.1371/journal.pone.0186835

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Bobkova M. Current status of HIV-1 diversity and drug resistance monitoring in the former USSR. Aids Rev. (2013) 15:204–12.

PubMed Abstract | Google Scholar

33. Raben D, Mocroft A, Rayment M, Mitsura VM, Hadziosmanovic V, Sthoeger ZM, et al. Auditing HIV testing rates across europe: results from the HIDES 2 study. PLoS ONE. (2015) 10:e140845. doi: 10.1371/journal.pone.0140845

PubMed Abstract | CrossRef Full Text | Google Scholar

34. van Leeuwen MT, Vajdic CM, Middleton MG, McDonald AM, Law M, Kaldor JM, et al. Continuing declines in some but not all HIV-associated cancers in Australia after widespread use of antiretroviral therapy. Aids. (2009) 23:2183–90. doi: 10.1097/QAD.0b013e328331d384

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Engels EA, Pfeiffer RM, Goedert JJ, Virgo P, McNeel TS, Scoppa SM, et al. Trends in cancer risk among people with AIDS in the United States 1980–2002. Aids. (2006) 20:1645–54. doi: 10.1097/01.aids.0000238411.75324.59

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Skrabek P, Turner D, Seftel M. Epidemiology of non-Hodgkin lymphoma. Transfus Apher Sci. (2013) 49:133–8. doi: 10.1016/j.transci.2013.07.014

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Chokunonga E, Borok MZ, Chirenje ZM, Nyakabau AM, Parkin DM. Trends in the incidence of cancer in the black population of Harare, Zimbabwe 1991–2010. Int J Cancer. (2013) 133:721–9. doi: 10.1002/ijc.28063

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Chihara D, Ito H, Matsuda T, Shibata A, Katsumi A, Nakamura S, et al. Differences in incidence and trends of haematological malignancies in Japan and the United States. Br J Haematol. (2014) 164:536–45. doi: 10.1111/bjh.12659

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Lee H, Park HJ, Park EH, Ju HY, Oh CM, Kong HJ, et al. Nationwide statistical analysis of lymphoid malignancies in Korea. Cancer Res Treat. (2018) 50:222–38. doi: 10.4143/crt.2017.093

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Liu W, Liu J, Song Y, Zeng X, Wang X, Mi L, et al. Burden of lymphoma in China, 2006–2016: an analysis of the Global Burden of Disease Study 2016. J Hematol Oncol. (2019) 12:115. doi: 10.1186/s13045-019-0785-7

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Müller AM, Ihorst G, Mertelsmann R, Engelhardt M. Epidemiology of non-Hodgkin's lymphoma (NHL): trends, geographic distribution, and etiology. Ann Hematol. (2005) 84:1–12. doi: 10.1007/s00277-004-0939-7

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Montgomery ND, Liomba NG, Kampani C, Krysiak R, Stanley CC, Tomoka T, et al. Accurate real-time diagnosis of lymphoproliferative disorders in Malawi through clinicopathologic teleconferences: a model for pathology services in Sub-Saharan Africa. Am J Clin Pathol. (2016) 146:423–30. doi: 10.1093/ajcp/aqw118

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Buabeng KO, Duwiejua M, Dodoo AN, Matowe LK, Enlund H. Self-reported use of anti-malarial drugs and health facility management of malaria in Ghana. Malar J. (2007) 6:85. doi: 10.1186/1475-2875-6-85

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Maclean KH, Dorsey FC, Cleveland JL, Kastan MB. Targeting lysosomal degradation induces p53-dependent cell death and prevents cancer in mouse models of lymphomagenesis. J Clin Invest. (2008) 118:79–88. doi: 10.1172/JCI33700

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Mbulaiteye SM, Bhatia K, Adebamowo C, Sasco AJ. HIV and cancer in Africa: mutual collaboration between HIV and cancer programs may provide timely research and public health data. Infect Agent Cancer. (2011) 6:16. doi: 10.1186/1750-9378-6-16

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Morgan D, Mahe C, Mayanja B, Whitworth JA. Progression to symptomatic disease in people infected with HIV-1 in rural Uganda: prospective cohort study. BMJ. (2002) 324:193–6. doi: 10.1136/bmj.324.7331.193

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Zuze T, Ellis GK, Kasonkanji E, Kaimila B, Nyasosela R, Nyirenda R, et al. Modified EPOCH for high-risk non-Hodgkin lymphoma in sub-Saharan Africa. Cancer Med. (2020) 9:77–83. doi: 10.1002/cam4.2631

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Mikkelsen L, Phillips DE, AbouZahr C, Setel PW, de Savigny D, Lozano R, et al. A global assessment of civil registration and vital statistics systems: monitoring data quality and progress. Lancet. (2015) 386:1395–406. doi: 10.1016/S0140-6736(15)60171-4

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Fetica B, Achimas-Cadariu P, Pop B, Dima D, Petrov L, Perry AM, et al. Non-Hodgkin lymphoma in Romania: a single-centre experience. Hematol Oncol. (2017) 35:198–205. doi: 10.1002/hon.2266

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: non-Hodgkin lymphoma, global burden of disease, age-standardized rate, estimated annual percentage change, epidemiological trend

Citation: Cai W, Zeng Q, Zhang X and Ruan W (2021) Trends Analysis of Non-Hodgkin Lymphoma at the National, Regional, and Global Level, 1990–2019: Results From the Global Burden of Disease Study 2019. Front. Med. 8:738693. doi: 10.3389/fmed.2021.738693

Received: 13 July 2021; Accepted: 24 August 2021;
Published: 23 September 2021.

Edited by:

Uday Prakash Kulkarni, Christian Medical College and Hospital, India

Reviewed by:

Sushil Selvarajan, Christian Medical College and Hospital, India
Nabhajit Mallik, Post Graduate Institute of Medical Education and Research (PGIMER), India

Copyright © 2021 Cai, Zeng, Zhang and Ruan. 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: Weiqing Ruan, jamela@sina.com

These authors have contributed equally to this work and share first authorship

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