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. 2011 Jan 6;119(4):514–518. doi: 10.1289/ehp.1002845

Global Magnitude of Reported and Unreported Mesothelioma

Eun-Kee Park 1, Ken Takahashi 1,, Tsutomu Hoshuyama 1, Tsun-Jen Cheng 2, Vanya Delgermaa 1, Giang Vinh Le 1, Tom Sorahan 3
PMCID: PMC3080934  PMID: 21463977

Abstract

Background

Little is known about the global magnitude of mesothelioma. In particular, many developing countries, including some with extensive historical use of asbestos, do not report mesothelioma.

Objectives

We estimated the global magnitude of mesothelioma accounting for reported and unreported cases.

Methods

For all countries with available data on mesothelioma frequency and asbestos use (n = 56), we calculated the 15-year cumulative number of mesotheliomas during 1994–2008 from data available for fewer years and assessed its relationship with levels of cumulative asbestos use during 1920–1970. We used this relationship to predict the number of unreported mesotheliomas in countries for which no information on mesothelioma is available but which have recorded asbestos use (n = 33).

Results

Within the group of 56 countries with data on mesothelioma occurrence and asbestos use, the 15-year cumulative number of mesothelioma was approximately 174,300. There was a statistically significant positive linear relation between the log-transformed national cumulative mesothelioma numbers and the log-transformed cumulative asbestos use (adjusted R2 = 0.83, p < 0.0001). Extrapolated to the group of 33 countries without reported mesothelioma, a total of approximately 38,900 (95% confidence interval, 36,700–41,100) mesothelioma cases were estimated to have occurred in the 15-year period (1994–2008).

Conclusions

We estimate conservatively that, globally, one mesothelioma case has been overlooked for every four to five reported cases. Because our estimation is based on asbestos use until 1970, the many countries that increased asbestos use since then should anticipate a higher disease burden in the immediate decades ahead.

Keywords: asbestos, frequency, mesothelioma, mortality, prediction


Malignant mesothelioma is a major public health concern, because this rare form of cancer—caused specifically by exposure to asbestos—is difficult to diagnose, has extremely poor prognosis, and is on the increase. Epidemics of mesothelioma have been reported nationally (Centers for Disease Control and Prevention 2009; Hodgson et al. 2005; Kjellstrom and Smartt 2000; Murayama et al. 2006) and regionally (Pelucchi et al. 2004; Peto et al. 1999), but available information is biased toward developed countries and regions (referred to hereafter as “countries”) with the resources to diagnose asbestos-related diseases (ARDs) and with known historical use of asbestos. At present, mesothelioma is grossly underreported in many developing countries (LaDou 2004; Takahashi and Karjalainen 2003), including some with known extensive use of asbestos.

Few attempts have been made to quantify the global incidence of mesothelioma. In a study of the total burden of occupational carcinogens, Driscoll et al. (2005) reported 43,000 mesothelioma deaths/year, based on an estimated proportion of exposed workers and levels of exposure, combined with absolute risk measures. This number, endorsed in a World Health Organization (WHO) document on the elimination of ARDs (WHO 2006a), is widely quoted to guide preventive activities. However, there has been no validation or reassessment of this 2005 estimate, possibly because the indices that were used are difficult to access and reproduce. Commonly available statistics should be used to address the shortage of information, which may also improve estimates of the disease burden.

In a previous study (Lin et al. 2007), we calculated the volume of asbestos consumed per head (per-capita asbestos use) from a report by the U.S. Geological Survey (USGS) (Virta 2006) and used this value as a surrogate for population exposure level. Our results indicated that rates of past asbestos use can predict recent death rates from four types of ARDs at national levels and explained the bulk of the variance (Lin et al. 2007). This relationship, albeit ecological, is likely to reflect a causal relationship. Other researchers have used this surrogate indicator to estimate or predict ARDs in different populations (Antao et al. 2009; Tse et al. 2010).

Information related to mesothelioma frequency is accumulating in relation to the growing number of national and regional registries (Leigh and Driscoll 2003; Marinaccio et al. 2007). In the present study, we estimated the magnitude of mesothelioma in the world accounting for both reported and unreported numbers by using a global database and extending our previous ecological model. We incorporated updated data from the widest possible sources of information, assuming that mortality reflects incidence for this fatal form of cancer. We employed cumulative indicators of asbestos use and number of mesothelioma cases, hypothesizing that recent national burden of mesothelioma is a consequence of historical cumulative use of asbestos. This relationship was then applied to countries that lack relevant health data.

Materials and Methods

We extracted all data on asbestos use from a report by the USGS (Virta 2006, 2009). We adopted the USGS definition of use (production plus import minus export), the data for which are available by country, in 10-year intervals from 1920 to 1970, in 5-year intervals from 1970 to 1995, and annually from 1995 to 2007. We treated a reported negative value of asbestos use (caused by storage, for example) as zero in this analysis. Using linear interpolation, cumulative asbestos use was calculated independently for two periods (1920–1970 and 1971–2007) to allow a sufficient lag time from the earlier period to that of mesothelioma observation (1994–2008). When necessary, we interpolated values for asbestos use for the calendar year lacking data.

The cumulative numbers of all types of mesothelioma [code C45; International Classification of Diseases, 10th Revision (ICD-10; WHO 2006a b] were obtained from the WHO Mortality Database (WHO 2010a) and tallied by country. Note that the WHO data comprise deaths registered in national civil registration systems, with underlying cause of death as coded by the relevant national authority (WHO 2010b). Data were extracted for countries with at least 3 years of data coded as C45 (ICD-10) or any of its subcategories. To maximize use of available data, we separately counted numbers recorded for malignant neoplasm of the pleura (code 163; International Classification of Diseases, 9th Revision (ICD-9; WHO 1977)]. To investigate countries that did not report data to the WHO, we used PubMed (National Center for Biotechnology Information 2010) and other sources to search for national frequency data published in English (Lee et al. 2010; Rüegger 2008). Data were prioritized for analysis in that order, and overlapping information was evaluated once only. For a number of countries, national counts of mesothelioma deaths were reported for intermittent years or did not span the entire period. For each country, the 15-year cumulative number was estimated by first calculating the annual mean of reported mesothelioma deaths from data available for fewer years, which was then multiplied by 15.

National population data were obtained from the WHO (2010a) and the U.S. Census Bureau (2010), and prioritized for use in that order.

Of the 89 analyzed countries, 12 warranted special treatment of asbestos use data because of political transition (e.g., disintegration, unification) or combined treatment with other countries/entities by the USGS. We used historical information in an unbiased manner to the extent possible to give continuity with data of countries existing today:

  • Data on asbestos use for the Soviet Union during 1920–1990 in the USGS database represented those of Russia and Kazakhstan combined (Virta 2006). We thus apportioned data recorded by the Soviet Union during 1920–1990 between Russia and Kazakhstan during 1920–1990 according to the ratio of use recorded by Russia and Kazakhstan during 1995–2007.

  • Data on asbestos use for West and East Germany during 1950–1985 were combined into one entity (i.e., Germany).

  • To account for the disintegration of Czechoslovakia in 1993 (United Nations 2010), data on asbestos use for Czechoslovakia during 1920–1990 were apportioned to the level of use during 1995–2007 between Czech Republic and Slovakia.

  • To account for the disintegration of Yugoslavia in 1991 (Duffield 2003), data on asbestos use for Yugoslavia during 1930–1990 were apportioned to the level of use during 1995–2007 among Bosnia and Herzegovina, Croatia, Serbia and Montenegro, the former Yugoslav Republic of Macedonia, and Slovenia (we treated Serbia and Montenegro as one entity).

  • Data on asbestos use for Belgium and Luxembourg were combined during 1930–2001 in the USGS database (Virta 2006). We apportioned these data to Belgium and Luxembourg according to the size of the respective populations during this period.

We compiled all data and performed descriptive statistics using Microsoft Excel (Microsoft Corporation, Redmond, WA, USA). We then conducted the regression analyses using SAS, version 9.1 (SAS Institute Inc., Cary, NC, USA). Because of the extremely wide dispersion of data for both asbestos and mesothelioma, data were log-transformed to construct the regression model: log10 (mortality) = B0 + [B1 × log10 (asbestos)], where B0 is the intercept and B1 is the coefficient. We applied PROC REG (SAS Institute Inc.) to obtain the parameters and their confidence limits, the adjusted R2, and p-values of the regression model. The size of the national populations was used as weights. To further obtain the confidence limits for the mean predicted value for each observation, we added the confidence limits for the mean option. This accounted for the variation due to estimating the parameters only. All the aforementioned processes were accomplished in one run of PROC REG.

After predicted values were obtained, based on the principle that if Yi ~ N(mi, si2) is the measurement for the ith cluster then Y = sum(Yi) ~ N[sum(mi), sum(si2)], the confidence limits for the sum of predicted values were calculated from the square root of the sum of the variance.

We used Sigmaplot (version 9.01; Systat Software Inc., San Jose, CA, USA) to draw the figure; the size of the bubbles is proportionate to the size of national populations of the year 2000. p-Values < 0.05 were deemed statistically significant in all analyses.

Results

Globally, 89 countries had available information on frequency of mesothelioma and/or use of asbestos at the national level. These countries represented 82.6% of the global population in the year 2000. Of these countries, 56 had data for both mesothelioma frequency and asbestos use, and 33 had no mesothelioma frequency data but had data for asbestos use (Table 1).

Table 1.

Baseline characteristics of the 89 analyzed countries/entities with available data for asbestos and/or mesothelioma.

Data category Both asbestos and mesothelioma (n = 56) Asbestos only (n = 33) Total (n = 89)
Asbestos, recorded cumulative use (million metric tons)
 During 1920–1970 51.2 14.2 65.4
 During 1971–2007 52.8 71.3 124.1
Mesothelioma, reported cumulative mortality during 1994–2008 [No. of cases (no. of countries)]
 ICD-10, code C45 90,929 (50) 0a (NA) NA
 ICD-9, code 163 336 (4) 0a (NA) NA
 Other data sourceb 868 (2) 0c (NA) NA
 Total 92,133 (56) 0 (33) NA

NA, not applicable.

a

No record in WHO mortality database.

b

Published articles in English identified via Pubmed or other source of national data (see References; Lee et al. 2010; Rüegger 2008).

c

Data cannot be identified.

The cumulative asbestos use during 1920–1970 was 51.2 million metric tons in the 56 countries having data on both mesothelioma frequency and asbestos use and 14.2 million metric tons in the 33 countries having data on asbestos use only, totaling 65.4 million metric tons in all 89 analyzed countries. This volume represented 100% of the global asbestos use during 1920–1970. By individual country, cumulative asbestos use was highly skewed, led by the United States, Russia, United Kingdom, Germany, and Japan, with volumes at 21.8, 8.4, 4.8, 4.1, and 3.2 million metric tons, respectively (Tables 2 and 3). The 56 countries with mesothelioma data reported a total of 92,133 deaths during 1994–2008 (336 of which were coded as ICD-9 163 by four countries) (Table 1).

Table 2.

Reported and extrapolated 15-year cumulative mortality of mesothelioma during 1994–2008 in 56 countries/entities with data for mesothelioma mortality and use of asbestos.

Country (abbreviation) Cumulative use of asbestos, (tons), 1920–1970 Years with available data (n) Reported cumulative mortality (cases) Annual average of reported mortality (cases) Extrapolated 15-year cumulative mortality (cases)
1 USA (USA) 21,840,583 7 17,062 2,437 36,561
2 UK (GBR) 4,829,517 7 13,239 1,891 28,369
3 Germany (DEU) 4,144,825 9 9,569 1,063 15,948
4 Japan (JPN) 3,210,349 14 11,212 801 12,013
5 France (FRA) 2,352,646 8 6,608 826 12,390
6 Canada (CAN) 1,955,347 5 1,603 321 4,809
7 Italy (ITA) 1,934,558 3 3,706 1,235 18,530
8 Australia (AUS) 1,152,776 8 3,747 468 7,026
9 Belgium (BEL) 1,110,214 3 467 156 2,335
10 Spain (ESP) 701,565 7 1,840 263 3,943
11 Poland (POL) 581,013 10 957 96 1,436
12 Brazil (BRA) 577,333 10 955 96 1,433
13 Romania (ROU) 550,799 10 581 58 872
14 Slovakia (SVK) 548,874 12 154 13 193
15 Denmark (DNK) 447,590 13 918 71 1,059
16 Mexico (MEX) 422,645 10 1,513 151 2,270
17 Sweden (SWE) 414,601 11 1,348 123 1,838
18 Netherlands (NLD) 411,989 13 5,141 395 5,932
19 Austria (AUT) 410,249 7 563 80 1,206
20 Argentina (ARG) 338,870 11 1,065 97 1,452
21 Finland (FIN) 299,695 13 970 75 1,119
22 Switzerland (CHE) 267,302 4 568 142 2,130
23 Republic of Korea (KOR) 244,802 12 339 28 424
24 Hungary (HUN) 235,442 13 451 35 520
25 South Africa (ZAF) 203,566 12 2,322 194 2,903
26 Colombia (COL) 196,345 9 323 36 538
27 Croatia (HRV) 165,011 14 547 39 586
28 Norway (NOR) 158,017 12 648 54 810
29 New Zealand (NZL) 147,197 7 513 73 1,099
30 Cyprus (CYP) 145,745 4 21 5 79
31 Czech Republic (CZE) 140,920 15 611 41 611
32 Egypt (EGY) 124,908 4 7 2 26
33 Chile (CHL) 103,780 9 331 37 552
34 Greece (GRC)a 101,021 15 128 9 128
35 Malaysia (MYS) 94,540 6 20 3 50
36 Slovenia (SVN) 94,114 12 270 23 338
37 Venezuela (VEN) 93,210 11 124 11 169
38 Portugal (PRT)a 90,605 8 152 19 285
39 Israel (ISR) 78,122 10 262 26 393
40 Taiwan (TWN) 67,670 12 300 25 375
41 Philippines (PHL) 41,132 5 51 10 153
42 Luxembourg (LUX) 38,749 9 39 4 65
43 Serbia and Montenegro (SRB & MNE) 34,222 12 313 26 391
44 Uruguay (URY) 33,914 6 38 6 95
45 Bulgaria (BGR) 33,576 4 35 9 131
46 Latvia (LVA) 22,189 13 112 9 129
47 Costa Rica (CRI) 11,718 9 24 3 40
48 Iceland (ISL) 6,417 12 28 2 35
49 Lithuania (LTU) 5,396 11 135 12 184
50 Guatemala (GTM)a 3,757 5 9 2 27
51 Panama (PAN) 3,506 7 14 2 30
52 Singapore (SGP)a 3,150 13 47 4 54
53 Estonia (EST) 2,300 12 45 4 56
54 Hong Kong (HKG) 616 7 79 11 169
55 Netherlands Antilles (ANT) 335 4 5 1 19
56 Nicaragua (NIC) 316 4 4 1 15
Total 51,229,638 NA 92,133 NA 174,300

NA, not applicable.

a

Number of cases represents malignant neoplasm of the pleura (ICD-9 code 163).

Table 3.

Predicted 15-year cumulative mortality of mesothelioma in 33 countries/entities with data only for use of asbestos.

Country (abbreviation) Cumulative use of asbestos (tons), 1920–1970 Predicted 15-year cumulative mortality (cases) 95% CI
1 Russia (RUS) 8,443,923 21,308 15,026–30,218
2 Kazakhstan (KAZ) 2,301,286 6,500 5,006–8,440
3 China (CHN) 1,767,086 5,107 3,976–6,558
4 India (IND) 688,015 2,158 1,700–2,739
5 Thailand (THA) 152,378 545 400–741
6 Zimbabwe (ZWE) 122,595 447 323–617
7 Algeria (DZA) 90,005 337 238–477
8 Swaziland (SWZ) 87,868 329 232–468
9 Iran (IRN) 68,437 262 181–380
10 Turkey (TUR) 60,345 234 159–343
11 Morocco (MAR) 55,697 217 147–321
12 Former Yugoslav Republic of Macedonia (MKD) 48,829 193 129–288
13 Lebanon (LBN) 47,718 189 126–283
14 Nigeria (NGA) 34,443 140 91–216
15 Peru (PER)a 32,645 133 86–207
16 Indonesia (IDN) 29,920 123 79–193
17 Democratic Republic of the Congo (COD) 22,579 95 59–153
18 Uganda (UGA) 18,139 78 47–128
19 Iraq (IRQ) 16,202 70 42–117
20 Zambia (ZMB) 15,607 68 41–113
21 Mozambique (MOZ) 14,566 64 38–107
22 Angola (AGO) 14,378 63 37–106
23 Jamaica (JAM) 10,698 48 28–83
24 Myanmar (MMR) 10,632 48 28–83
25 Tunisia (TUN) 9,724 44 25–77
26 Bolivia (BOL) 8,959 41 23–72
27 El Salvador (SLV)a 6,545 31 17–56
28 Kenya (KEN) 3,153 16 8–31
29 Botswana (BWA) 1,163 6 3–14
30 Senegal (SEN) 799 5 2–10
31 Libya (LBY) 540 3 1–7
32 Bosnia and Herzegovina (BIH) 387 2 1–6
33 Madagascar (MDG)b 16 NA NA
Total 14,185,272 38,900 36,700–41,100

NA, not applicable.

a

Treated as lacking data on mesothelioma frequency because only 2 years of data were available in the WHO mortality database and no other information could be identified (see “Materials and Methods”).

b

Out of range of the regression model.

Table 2 shows the 15-year cumulative mortality of mesothelioma extrapolated from numbers reported for fewer years in the 56 countries with mesothelioma data, ranked in order of the cumulative asbestos use. The 15-year cumulative numbers are highly skewed but generally paralleled the level of cumulative asbestos use. Leading countries for the 15-year mesothelioma number are the United States (36,561 cases), the United Kingdom (28,369 cases), Italy (18,530 cases), Germany (15,948 cases), and France (12,390 cases) (Table 2). The total 15-year cumulative mortality was approximately 174,300 deaths.

Figure 1 shows scatterplots of national data for the group of 56 countries. There is a clear positive linear relation between the log-transformed values of the 15-year cumulative mortality of mesothelioma during 1994–2008 and the cumulative use of asbestos during 1920–1970. Cumulative asbestos use was a significant predictor of cumulative mesothelioma mortality, with an adjusted R2 value of 0.83 (p < 0.0001). Similar findings were obtained when data for the four countries reporting deaths coded to the ICD-9 were omitted, with an adjusted R2 value of 0.82 (p < 0.0001).

Figure 1.

Figure 1

Relationship between 15-year cumulative mortality of mesothelioma (1994–2008) and cumulative use of asbestos (1920–1970) weighted by the size of national populations in 56 countries/entities with data for both mesothelioma and asbestos use. Asbestos use for 33 countries/entities without mesothelioma frequency data is indicated along the x-axis. The figure is based on the following regression model: log10(15-year cumulative mortality of mesothelioma) = β0 + β1 × log10(cumulative use of asbestos), where β0 = −1.998 (95% CI, −2.676 to −1.319) and β1 = 0.913 (95% CI, 0.800 to 1.026). Adjusted R2 = 0.827; p < 0.0001.

Table 3 shows the predicted 15-year cumulative mortality of mesothelioma in the group of 33 countries that lacked data on mesothelioma frequency; predictions were obtained from the value of cumulative asbestos use applied to the relationship obtained earlier. The range of cumulative asbestos use of the 33 countries, except for Madagascar, fell within the range reported by the 56 countries. Leading countries for the predicted 15-year mesothelioma number are Russia (21,300 cases), Kazakhstan (6,500 cases), China (5,100 cases), India (2,200 cases), and Thailand (500 cases). In total, an estimated 38,900 [95% confidence interval (CI), 36,700–41,100] mesothelioma cases possibly occurred but were unreported during 1994–2008.

Discussion

It is unlikely that mesothelioma is absent in countries that have used asbestos but do not report mesothelioma frequency. There is increasing evidence that the extent of asbestos use can be used to predict subsequent incidence and mortality of ARDs at national levels (Antao et al. 2009; Lin et al. 2007; Nishikawa et al. 2008; Tse et al. 2010). This is not unexpected, as mesothelioma is almost exclusively attributable to past asbestos exposure. We thus postulated that national experiences would follow reasonably similar patterns where countries lacking mesothelioma data were probably “missing” the disease burden to an extent proportionate to the level of historical cumulative asbestos use. Based on available data of 56 countries, we observed that recent cumulative mortality of mesothelioma is closely related to historical cumulative use of asbestos. Further extrapolation of this relation to the 33 countries with no available data for mesothelioma suggested that one mesothelioma case is unreported for every four to five cases reported worldwide (38,900 unreported vs. 174,300 reported).

Accounting for the reported and unreported numbers, we estimated the global burden of mesothelioma to be 213,200 (15-year cumulative mortality during 1994–2008). This is equivalent to an annual average of approximately 14,200 cases, assuming a flat change rate, or approximately 25,000 cases in the year 2008 assuming a 10% annual increase rate (38,000 cases assuming a 20% annual increase rate). These estimates are larger than the estimated 10,000 mesothelioma deaths proposed by consensus for only the developed regions in the world (Tossavainen 1997) but smaller than the 43,000 mesothelioma deaths estimated for the world by Driscoll et al. (2005). Nevertheless, our values are reasonably close to those of earlier reports, despite the different methods used.

From the observed linear relation between log-transformed values of cumulative mesothelioma and asbestos, y = 10(0.913 * log x − 1.998), where y (cases) is the 15-year cumulative mesothelioma mortality for the period 1994–2008, and x (metric tons) is the cumulative asbestos use during 1920–1970. When values are back-transformed to their original units, there is a linear relation between variables x and y, each dispersed for a very wide range (i.e., to the power of 10). Further, the amount of asbestos use corresponding to one mesothelioma case (asbestos-to-mesothelioma ratio), or x/y, varies depending on the level of x. For example, the asbestos-to-mesothelioma ratio is 182–222 metric tons per case for cumulative use of 1,000–10,000 metric tons, and 271–331 metric tons per case for cumulative use of 100,000–1,000,000 metric tons [see Supplemental Material, Table 1 (doi:10.1289/ehp.1002845)]. The values recorded here for the asbestos-to-mesothelioma ratio should be distinguished from a ratio reported by Tossavainen (2004) and referenced widely (fixed value of 170 metric tons per case); that value was derived using data from 11 developed countries with looser definitions and time frame.

The present study is the first to provide a global estimate of missed mesothelioma cases accounting for the experience of countries with data. We directly compared national asbestos use and mesothelioma frequency using cumulative indicators (the denominator population would be common to all calculations of rates); this method had the advantage of directly estimating the disease burden and maximizing use of sparse data. Asbestos has an extremely long industrial life span, and populations are repeatedly exposed during production, maintenance, and abatement. Smoking is unrelated to mesothelioma and thus does not have to be accounted for as a confounder. These facts supported the assumption that cumulative asbestos use causes health effects that are reflected in the cumulative mesothelioma count in populations.

There are, however, obvious limitations in the methods in the present study, as well as potential sources of errors in the information applied. First and foremost, our findings are based on an ecological relation, and thus we do not know the extent to which the consumed amounts of asbestos reflected actual exposure levels of populations. Second, extrapolating from the collective experience of one group of countries to another may introduce bias, especially because the former group consisted of developed and developing countries, whereas the latter group consisted of predominantly developing countries. Third, we did not have information for consumed fiber types (e.g., amphiboles, chrysotile).

Whether and the extent to which the aforementioned limitations and possible errors collectively caused overestimation or underestimation merits further consideration. One potential source of overestimation (pertaining to the extrapolation of data from one group to another) is that developed countries may incur more mesothelioma cases because of an older age composition. However, this factor is probably offset by several potential sources of disease underestimation: a) a lack of data on the trade of asbestos-containing products could impose additional risk; b) our estimates cannot account for the national experiences of the majority of countries in the world with no information on asbestos use (USGS information on asbestos use may be less complete for the less-developed countries, especially for the earlier years); and c) underdiagnosis and underreporting of mesothelioma is also a major problem in developed countries. Therefore, our values should be viewed as conservative estimates.

It is plausible that the hidden burden is substantial in countries with high cumulative use of asbestos, including asbestos-producing countries such as Russia, Kazakhstan, China, and India. Underdiagnosis and/or underreporting may have occurred in these countries because of lack of awareness, knowledge, and resources. It is also possible that, even if mesothelioma cases are diagnosed domestically, frequency numbers are not actively disclosed to the international community because of the increasing number of countries adopting bans on asbestos use (Kazan-Allen 2005) on grounds of public health. Some countries with vested interest in maintaining the production and trade of asbestos may be poorly motivated to acknowledge ARDs. For example, Russia is known for not recognizing asbestosis in its territory (Walgate 2010).

The world nearly doubled cumulative use of asbestos from 65 million metric tons up until 1970, to 124 million metric tons since then. In particular, the group of 33 countries not reporting mesothelioma frequency quintupled asbestos use (Table 1). Individually, the number of countries exceeding the cumulative use of 3.0 million metric tons have increased from five in 1971 (United States, Russia, United Kingdom, Germany, and Japan) to eight: Russia (36.1 million metric tons), China (11.2), Kazakhstan (9.6), Japan (8.1), the United States (6.9), Brazil (5.3), Germany (5.2), India (4.5), and Thailand (3.6) (data not shown). Thus, even with the expected hygienic improvements to reduce exposure over time, and particularly since 1970 onward, these countries should anticipate the need to deal with a very high burden of mesothelioma in the immediate decades ahead.

Developed countries should share experience and technology to enable developing countries to promote accurate diagnosis, reporting, and management of ARDs (Takahashi 2008), including mesothelioma. Moreover, political will is essential to ensure that asbestos use ceases globally.

Conclusions

We estimated the 15-year cumulative frequency of mesothelioma during 1994–2008 in the 56 countries reporting mesothelioma to be 174,300. Using cumulative asbestos use to predict cumulative mesothelioma frequency at national levels, we predicted the 15-year cumulative frequency of mesothelioma during 1994–2008 in the 33 countries that do not report mesothelioma to be 38,900 (95% CI, 36,700–41,100). Thus, globally, for every four to five reported cases of mesothelioma, one case has been overlooked. These estimates support the need for countermeasures at national, regional, and international levels.

Footnotes

Supplemental Material is available online (doi:10.1289/ehp.1002845 via http://dx.doi.org/).

We thank K. Cho (School of Medicine, Yale University) and M. Ohtaki (Department of Environmetrics and Biometrics, Research Institute for Radiation Biology and Medicine, Hiroshima University, Japan) for their valuable advice.

This work was supported in part by the Japan Society for the Promotion of Sciences (JSPS) Asia Africa (AA) Science Platform Program.

References

  1. Antao VC, Pinheiro GA, Wassell JT. Asbestosis mortality in the USA: facts and predictions. Occup Environ Med. 2009;66:335–338. doi: 10.1136/oem.2008.039172. [DOI] [PubMed] [Google Scholar]
  2. Centers for Disease Control and Prevention. Malignant mesothelioma mortality—United States, 1999–2005. MMWR Morb Mortal Wkly Rep. 2009;58:393–396. [PubMed] [Google Scholar]
  3. Driscoll T, Nelson DI, Steenland K, Leigh J, Concha-Barrientos M, Fingerhut M, et al. The global burden of disease due to occupational carcinogens. Am J Ind Med. 2005;48:419–431. doi: 10.1002/ajim.20209. [DOI] [PubMed] [Google Scholar]
  4. Duffield JS. Regional conflict management in Europe. In: Diehl PF, Lepgold J, editors. Regional Conflict Management. Lanham, MD: Rowman and Littlefield Publishers; 2003. pp. 239–268. [Google Scholar]
  5. Hodgson JT, McElvenny DM, Darnton AJ, Price MJ, Peto J. The expected burden of mesothelioma mortality in Great Britain from 2002 to 2050. Br J Cancer. 2005;92:587–593. doi: 10.1038/sj.bjc.6602307. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Kazan-Allen L. Asbestos and mesothelioma: worldwide trends. Lung Cancer. 2005;49((suppl 1)):S3–S8. doi: 10.1016/j.lungcan.2005.03.002. [DOI] [PubMed] [Google Scholar]
  7. Kjellstrom T, Smartt P. Increased mesothelioma incidence in New Zealand: the asbestos-cancer epidemic has started. N Z Med J. 2000;113:485–490. [PubMed] [Google Scholar]
  8. LaDou J. The asbestos cancer epidemic. Environ Health Perspect. 2004;112:285–290. doi: 10.1289/ehp.6704. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Lee LJ, Chang YY, Wang JD. Impact of malignant mesothelioma in Taiwan: a 27-year review of population-based cancer registry data. Lung Cancer. 2010;68:16–19. doi: 10.1016/j.lungcan.2009.05.016. [DOI] [PubMed] [Google Scholar]
  10. Leigh J, Driscoll T. Malignant mesothelioma in Australia, 1945–2002. Int J Occup Environ Health. 2003;9:206–217. doi: 10.1179/oeh.2003.9.3.206. [DOI] [PubMed] [Google Scholar]
  11. Lin RT, Takahashi K, Karjalainen A, Hoshuyama H, Wilson D, Kameda T, et al. Ecological association between asbestos-related diseases and historical asbestos consumption: an international analysis. Lancet. 2007;369:844–849. doi: 10.1016/S0140-6736(07)60412-7. [DOI] [PubMed] [Google Scholar]
  12. Marinaccio A, Binazzi A, Cauzillo G, Cavone D, Zotti RD, Ferrante P, et al. Analysis of latency time and its determinants in asbestos related malignant mesothelioma cases of the Italian register. Eur J Cancer. 2007;43:2722–2728. doi: 10.1016/j.ejca.2007.09.018. [DOI] [PubMed] [Google Scholar]
  13. Murayama T, Takahashi K, Natori Y, Kurumatani N. Estimation of future mortality from pleural malignant mesothelioma in Japan based on an age-cohort model. Am J Ind Med. 2006;49:1–7. doi: 10.1002/ajim.20246. [DOI] [PubMed] [Google Scholar]
  14. National Center for Biotechnology Information. PubMed. 2010. [[accessed 22 February 2011]]. Available: http://www.ncbi.nlm.nih.gov/pubmed.
  15. Nishikawa K, Takahashi K, Karjalainen A, Wen CP, Furuya S, Hoshuyama T, et al. Recent mortality from pleural mesothelioma, historical patterns of asbestos use, and adoption of bans: a global assessment. Environ Health Perspect. 2008;116:1675–1680. doi: 10.1289/ehp.11272. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Pelucchi C, Malvezzi M, La Vecchia C, Levi F, Decarli A, Negri E. The mesothelioma epidemic in Western Europe: an update. Br J Cancer. 2004;90:1022–1024. doi: 10.1038/sj.bjc.6601638. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Peto J, Decarli A, La Vecchia C, Levi F, Negri E. The European mesothelioma epidemic. Br J Cancer. 1999;79:666–672. doi: 10.1038/sj.bjc.6690105. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Rüegger M. Malignant Mesothelioma Recognized as Occupational Diseases in Switzerland [in German] 2008. [[accessed 15 July 2010]]. Available: http://www.suva.ch/fr/roundtable2008_rueegger.pdf.
  19. Takahashi K. Asbestos-related diseases: time for technology sharing. Occup Med (London) 2008;58:384–385. doi: 10.1093/occmed/kqn086. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Takahashi K, Karjalainen A. A cross-country comparative overview of the asbestos situation in ten Asian countries. Int J Occup Environ Health. 2003;9:244–248. doi: 10.1179/oeh.2003.9.3.244. [DOI] [PubMed] [Google Scholar]
  21. Tossavainen A. Asbestos, asbestosis, and cancer: the Helsinki criteria for diagnosis and attribution. Scand J Work Environ Health. 1997;23:311–316. [PubMed] [Google Scholar]
  22. Tossavainen A. Global use of asbestos and the incidence of mesothelioma. Int J Occup Environ Health. 2004;10:22–25. doi: 10.1179/oeh.2004.10.1.22. [DOI] [PubMed] [Google Scholar]
  23. Tse LA, Yu IT, Goggins W, Clements M, Wang XR, Au JS, et al. Are current or future mesothelioma epidemics in Hong Kong the tragic legacy of uncontrolled use of asbestos in the past? Environ Health Perspect. 2010;118:382–386. doi: 10.1289/ehp.0900868. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. United Nations. Member States of the United Nations. 2010. [[accessed 19 July 2010]]. Available: http://www.un.org/en/members/index.shtml.
  25. U.S. Census Bureau. International Data Base. 2010. [[accessed 20 July 2010]]. Available: http://www.census.gov/ipc/www/idb/
  26. Virta RL. Worldwide Asbestos Supply and Consumption Trends from 1900 through 2003. 2006. [[accessed 11 July 2010]]. Available: http://pubs.usgs.gov/circ/2006/1298/c1298.pdf.
  27. Virta RL. World Asbestos Consumption from 2003 through 2007. 2009. [[accessed 11 July 2010]]. Available: http://minerals.usgs.gov/minerals/pubs/commodity/asbestos/mis-2007-asbes.pdf.
  28. Walgate R. European nations agree to improve environmental health. Lancet. 2010;375:969. doi: 10.1016/s0140-6736(10)60420-5. [DOI] [PubMed] [Google Scholar]
  29. WHO (World Health Organization) Manual of the International Statistical Classification of Diseases, Injuries, and Causes of Death. Vol. 1. Geneva: World Health Organization; 1977. [Google Scholar]
  30. WHO (World Health Organization) Elimination of Asbestos-Related Diseases. Geneva: World Health Organization; 2006a. [[accessed 20 July 2010]]. Available: http://whqlibdoc.who.int/hq/2006/WHO_SDE_OEH_06.03_eng.pdf. [Google Scholar]
  31. WHO (World Health Organization) International Statistical Classification of Diseases and Related Health Problems, 10th Revision; Version for 2007. 2006b. [[accessed 22 February 2011]]. Available: http://apps.who.int/classifications/apps/icd/icd10online/
  32. WHO (World Health Organization) World Health Organization Statistical Information System (WHOSIS): Download the Detailed Data Files of the WHO Mortality Database. 2010a. [[accessed 17 July 2010]]. Available: http://www.who.int/whosis/mort/download/en/index.html.
  33. WHO (World Health Organization) About the WHO Mortality Data. 2010b. [[accessed 3 October 2010]]. Available: http://www.who.int/healthinfo/statistics/mortdata/en/index.html.

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