Impact Factor 3.675

The 2nd most cited open-access journal in Endocrinology & Metabolism

Review ARTICLE

Front. Endocrinol., 04 June 2013 | https://doi.org/10.3389/fendo.2013.00065

Descriptive epidemiology of human thyroid cancer: experience from a regional registry and the “volcanic factor”

Pasqualino Malandrino1, Claudia Scollo1, Ilenia Marturano1, Marco Russo1, Martina Tavarelli1, Marco Attard2, Pierina Richiusa3, Maria Antonia Violi4, Gabriella Dardanoni5, Riccardo Vigneri1 and Gabriella Pellegriti1*
  • 1Endocrinology, Department of Clinical and Molecular Biomedicine, University of Catania, Garibaldi-Nesima Medical Center, Catania, Italy
  • 2Endocrinology, “Ospedali Riuniti Villa Sofia – Cervello” Hospital, Palermo, Italy
  • 3Endocrinology, Diabetology and Metabolism, Department of Internal and Specialistic Biomedicine, University of Palermo, Palermo, Italy
  • 4Endocrinology, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy
  • 5Sicilian Regional Epidemiology Observatory, Palermo, Italy

Thyroid cancer (TC), the most common endocrine tumor, has steadily increased worldwide due to the increase of the papillary histotype. The reasons for this spread have not been established. In addition to more sensitive thyroid nodule screening, the effect of environmental factors cannot be excluded. Because high incidences of TC were found in volcanic areas (Hawaii and Iceland), a volcanic environment may play a role in the pathogenesis of TC. In January 2002, the Regional Register for TC was instituted in Sicily. With a population of approximately five million inhabitants with similar genetic and lifestyle features, the coexistence in Sicily of rural, urban, industrial, moderate-to-low iodine intake, and volcanic areas provides a conducive setting for assessing the environmental influences on the etiology of TC. In Sicily, between 2002 and 2004, 1,950 new cases of TC were identified, with an age-standardized rate (world) ASR(w) = 17.8/105 in females and 3.7/105 in males and a high female/male ratio (4.3:1.0). The incidence of TC was heterogeneous within Sicily. There were 2.3 times more cases in the Catania province (where most of the inhabitants live in the volcanic area of Mt. Etna): ASR(w) = 31.7/105 in females and 6.4/105 in males vs. 14.1 in females and 3.0 in males in the rest of Sicily. Multivariate analysis documented that residents in the volcanic area of Mt. Etna had a higher risk of TC, compared to the residents in urban, industrial, and iodine deficient areas of Sicily. An abnormally high concentration of several chemicals was found in the drinking water of the Mt. Etna aquifer, which provides water to most of the residents in the Catania province. Our data suggest that environmental carcinogen(s) of volcanic origin may promote papillary TC. Additional analyses, including cancer biological and molecular features, will allow a better understanding of risk factors and etiopathogenetic mechanisms.

Introduction: Thyroid Cancer Epidemiology and Trend

Thyroid cancer (TC) is the most frequent endocrine neoplasm (Curado et al., 2007), which occurs two to four times more frequently in females than in males (Parkin et al., 2005). Its incidence has continuously increased worldwide in recent decades. This increase has occurred in many regions, with variable entity and independent of initial recorded levels, as indicated by data from population-based cancer registries, particularly in the Western world, such as the United States (Davies and Welch, 2006), Canada, and in many European Countries (Leenhardt et al., 2004; Yu et al., 2010) (Table 1).

TABLE 1
www.frontiersin.org

Table 1. Age-adjusted thyroid cancer incidence rates from different population-based cancer registries.

Based on data from 1999 through 2008, TC represents the fastest growing cancer, in terms of prevalence, in the United States among men and women of every racial and ethnic background (except American Indian or Alaska Native men) (Simard et al., 2012).

The epidemiological data of Surveillance Epidemiology and End Results (SEER) reported an annual incidence of TC of 5.9/105 individuals in men and 17.3/105 in women from 2005 through 2009 and an age-adjusted death rate of 0.5/105 in both men and women per year (Howlader et al., 2012).

The reasons for the continuously increasing incidence of TC are unclear and controversial. The increase in TC might be attributed to more intensive and sensitive thyroid nodule diagnostic procedures (thyroid ultrasound and fine-needle aspiration biopsies) and the results of improved diagnosis of subclinical cancers (Davies and Welch, 2006; Kent et al., 2007). Methodologies for the pathological examination of the excised thyroid gland could also explain this phenomenon. Recently, pathologists have begun to dissect thinner slices of the gland (less than 2 mm) and frequently sample not only macroscopically evident lesions but also the entire thyroid gland (Pazaitou-Panayiotou et al., 2007; Boucek et al., 2009). The increased microcarcinoma prevalence and the rising number of incidentally discovered TCs are consistent with these hypotheses (Leenhardt et al., 2004; Davies and Welch, 2006). Recently, it has been hypothesized that environmental factors (or chemical agents) might explain this increasing incidence (Leenhardt and Grosclaude, 2011) and, consequently, that a more accurate screening cannot explain the (likely) multifactorial mechanisms that might account for this increase.

To the best of our knowledge, there are no available data in the recent literature, but we can hypothesize that the more diffuse use of sensitive diagnostic procedures has reached a plateau in many countries because of standardized diagnostic protocols. The incidence of TC has not been steady, as reported in the case of prostate cancer, according to data from the SEER registries (annual percentage change of −1.5 in the period 2000–2009) (Howlader et al., 2012).

The relevant increase of TC generally refers to papillary cancer less than 1 cm in diameter (microcarcinoma), which leads to an “epidemic of micropapillary TC” (How and Tabah, 2007). A recent article emphasized that the most common type of TC in patients older than 45 years is microcarcinoma (Hughes et al., 2011). Nevertheless, the incidence of TCs of all sizes (including the large ones, ≥4 cm in diameter) increased in the 1988–2005 period in the United States (Chen et al., 2009) as well as in other countries (Rego-Iraeta et al., 2009).

Furthermore, the increased incidence of TC is nearly exclusively due to the papillary histotype, with no significant change in the other histotypes. This finding suggests that specific carcinogens might favor the molecular abnormalities typical of papillary cancer.

Controversy has emerged regarding the differences in the incidence of TC in different ethnic groups. In addition to the possible effect of genetic factors, variable access to medical care has been hypothesized to be a contributing to this incidence. Although the incidence of TC is lower among Hispanics and Afro-Americans compared to Caucasians (Simard et al., 2012), very recent data report the greatest acceleration in incidence rate of papillary TC among black females (Aschebrook-Kilfoy et al., 2013).

At present, carcinogens that may trigger TC or contribute to its progression have not been established. The risk factors for TC include exposure to ionizing radiations (Nikiforov, 2006), a history of goiter or thyroid nodules or a family history of TC. In addition, dietary factors (Markaki et al., 2003), westernized lifestyle and obesity (Kitahara et al., 2011), or anthropogenic pollution (i.e., caused by human activities) cannot be excluded as factors. Concerning dietary factors, several studies have investigated the impact of iodine intake on the risk of TC onset. Whether adequate iodine consumption has a protective role against thyroid carcinogenesis has not been determined. These studies concur with the observation that the ratio of papillary to follicular TCs is higher in geographical areas with adequate iodine intake than in areas with moderate-to-severe iodine deficiency (Peterson et al., 2012).

Some of the highest incidences of TC were found in Hawaii (Goodman et al., 1988; Kolonel et al., 1990) and Iceland (Arnbjornsson et al., 1986), both volcanic areas. A comparison of the same ethnic groups living in Hawaii or in other geographical areas indicated that the incidence of TC was significantly higher in the first group, which suggests that environmental factors might play a role (Goodman et al., 1988).

Large population-based cancer registries are appropriate for studying the incidence of cancer and genetic factors in relation to the environment. These registries require a close cooperation between clinicians, epidemiologists, and environment specialists.

Creating such a registry was the aim of our research; the study began planning early in 2000 on the Mediterranean island of Sicily.

The Sicilian Regional Registry for TC

Sicily, with approximately five million inhabitants, offers the opportunity to study different environmental factors that can influence the incidence of TC. Sicily has a homogeneous population in terms of genetics and lifestyle, with similar access to medical assistance and, as an island, is very well geographically delimited. In Sicily, there is the concomitant presence of rural and urban areas, industrial and non-industrial areas, and areas of low or adequate iodine intake. Sicily also hosts Mt. Etna, the highest and most active volcano in Europe.

Data collection was organized through the institution of the Sicilian Regional Registry for Thyroid Cancer (SRRTC). Patients were identified by a systemic survey (three to four times each year) of all Sicilian (public and private) morbid pathology services. Data were recorded in a computerized archive and were correlated with population data (Italian National Institute of Statistics, 2001) (Pellegriti et al., 2009).

We evaluated the age-standardized incidence rate for the world population (ASRw) in each of the nine provinces in Sicily in the 3-year period of 2002–2004. We found a more than twofold increased incidence of TC in the province of Catania (ASRw F = 31.7/105; M = 6.4/105), where approximately 80% of the residents live in the volcanic area of Mt. Etna, in contrast to the rest of Sicily (ASRw F = 14.1/105; M = 3.0/105) (Table 2). The incidence of TC was not different between the industrial and the non-industrial areas nor between the areas of sufficient and deficient iodine intake. A higher ASRw was observed in urban areas compared to rural areas. A similar finding was reported by Sassolas et al. (2009), who documented in France a higher incidence of TC in the urban cantons of the Rhône-Alpes region than in the non-urban areas of the same region. A non-uniform presence of medical specialists between the urban and non-urban areas may explain this difference. Although a different access to medical assistance between the urban and rural areas is reasonable, this variable access is not likely to explain the difference between the Catania province and the other eight Sicilian provinces. The Catania province includes the Catania metropolitan area (approximately 650,000 inhabitants) and a large rural area with approximately 350,000 inhabitants. A similar urban/rural ratio is present for the provinces of Palermo and Messina, where the incidence of TC is much lower than in Catania. In Sicily, a similar access to medical assistance is indicated by the number of routine biochemical laboratory tests per inhabitant: 6.89, 7.42, and 6.18 in 2007 in the provinces of Catania, Messina, and Palermo, respectively (Sicilian Public Health Report 2008, Appendix 1, www.gurs.regione.sicilia.it). These three provinces include the largest Sicilian cities, approximately 60% of the Sicilian population, as well as the largest medical schools and major hospitals. Moreover, the Poisson regression analysis adjusted for all environmental characteristic confirmed that, compared with residents of urban, industrial, and iodine deficient areas, living in the volcanic area of the province of Catania was an independent risk factor of TC in both females (odds ratio = 2.242, 95% C.I. = 2.020–2.488) and males (odds ratio = 2.052, 95% C.I. = 1.652–2.565) inhabitants (Table 3).

TABLE 2
www.frontiersin.org

Table 2. Thyroid cancer incidence in Sicily: age-standardized rates for the world population (ASRw) for the entire island and by environmental characteristic.

TABLE 3
www.frontiersin.org

Table 3. Thyroid cancer incidence in Sicily: odds ratio by environmental characteristic.

The mean age of the patients at the time of diagnosis and the female/male ratio were similar between the Catania province and the other Sicilian provinces. Most of TCs in the Catania province were papillary (94%), whereas in Sicily, excluding the Catania province, the percentage of papillary TC was lower (86%) (p < 0.0001). Although the mean tumor size at the time of diagnosis was slightly but significantly higher in Sicily, excluding Catania, with respect to the Catania province (1.50 ± 0.04 vs. 1.30 ± 0.05 cm; p = 0.002), the occurrence of both extrathyroid extension and lymph node metastases and the stage classification of tumors were not different between the two areas. Curiously, a higher percentage of multifocal TC was observed in the Catania province; i.e., 32 vs. 25% in the rest of Sicily (p = 0.001).

Volcanic Activity: A Possible Risk Factor for TC

The presence of a high incidence of TC in volcanic areas in different parts of the world suggests that factors are present in the volcanic environment that may act as endocrine disruptors and carcinogens.

Several studies analyzed the incidence of TC among people living in the volcanic areas of Iceland (Hrafnkelsson et al., 1989), Hawaii (Kolonel et al., 1990), New Caledonia (Truong et al., 2007), and French Polynesia (Curado et al., 2007) and documented some of the highest occurrence rates reported in the literature. In French Polynesians, for example, the ASRw are 5.4/105 for males and 37.4/105 for females. How the volcanic environment may influence thyroid carcinogenesis is not known, but non-anthropogenic carcinogens of volcanic origin may be responsible (Kung et al., 1981; Duntas and Doumas, 2009). The geologic processes of volcanism produce various elements and metals in abnormal concentrations in the soil, water, and atmosphere. Mt. Etna continuously delivers, and has for many decades, suspended particulate matter and gases: sulfur dioxide, hydrogen chloride, hydrogen fluoride, hydrogen sulfide, hydrochloric acid, sulfuric acid, ammonium sulfate, helium, and radon. These substances were detected in various volcanic eruptions (Hansell and Oppenheimer, 2004). Many of these potentially toxic compounds may become concentrated the environment (Kusky, 2008) and contaminate cultivated fields, including cultured vegetables and the animal food chain (Hogan and Burstein, 2007).

Several studies reported that various elements and chemicals (including HCO3, SO4, calcium, selenium, fluoride, chloride, magnesium, boron, manganese, iron, and vanadium and their salts and 222 radon) are often increased in water samples from various sources of Mt. Etna’s volcanic aquifer (Giammanco et al., 1996; Brusca et al., 2001; Aiuppa et al., 2002; D’Alessandro and Vita, 2003). Similar findings were reported in studies of water samples from other volcanic areas (Tilling and Jones, 1996; Martin-Del Pozzo et al., 2002). Mt. Etna is a large basaltic volcano with fissured and highly permeable lava layers interbedded with discontinuation layers of scarcely permeable pyroclastics. The main aquifers of Mt. Etna (overall calculated as 1.7 million cubic meters of water) lie between the volcanic rocks and the underlying impermeable sediments. A magmatic-type interaction occurs between the water and the volcanic soil; an enormous amount of CO2 produced by the volcanic degasification leads to the acidification of water and chemicals leaching from the basalt rock, especially in the lower south-southwestern and eastern flanks of the volcano (Brusca et al., 2001). Vanadium, for instance, is classified by the International Agency for Research on Cancer (IARC) as a possible human carcinogen (Group 2B) (IARC, 2006), which may influence thyroid function and cell proliferation. Experiments on rats documented the role of vanadium in affecting iodine metabolism and thyroid function by decreasing the thyroid peroxidase activity (Uthus and Nielsen, 1990). Vanadium may have a mitogen effect by stimulating the action of an unknown growth factor (Zhang et al., 2001; Ingram et al., 2003). Approximately 700,000 residents in the province of Catania receive water from the volcanic aquifer, and large agricultural areas are irrigated with water originating from the Mt. Etna aquifer. The role of water can explain why the increased cancer incidence is not related to the distance from the top of Mt. Etna. Messina (ASRw F = 16.2/105; M = 4.2/105) and Enna (ASRw F = 15.9/105; M = 2.8/105), which are adjacent to the Catania province, despite their proximity to Mt. Etna, do not have an increased incidence of TC. Messina and Enna provinces, however, receive most of their water from different aquifers (Peloritani Mountains for Messina and Erei Mountains for Enna) (Pellegriti et al., 2009).

However, the role of the different aquifer systems of the eastern Sicilian provinces has not been confirmed. The role of volcanic water as the vehicle for carcinogenic trace elements in initiating and promoting TC requires additional research.

The population’s exposure to one or more carcinogens of volcanic origin can occur in other ways, such as atmosphere, soil, or contaminated foods. The preliminary data indicate that the resident population is exposed to an abnormal concentration of trace elements that are increased in biological fluids. Mt. Etna (and other volcanoes) is a large emitter of trace elements; metals, separated from magma during degassing, are transported by rising gases, and as they approach the surface, they condense to small particles that are dispersed throughout the atmosphere. Because of the constant degassing and recurrent lava flow eruptions, atmospheric emissions of particulate Cd, Hg, Se, Cu, and Zn by Mt. Etna are equivalent to the amount of these elements released in the Mediterranean area by all of the anthropogenic activities (Buat-Ménard and Arnold, 1978). Most common winds in the Mt. Etna region blow from the north-northwest (Favalli et al., 2004). The Mt. Etna plume, therefore, moves mainly south-east, and Catania province inhabitants mostly live in the downwind areas of the ash fallout. Therefore, these individuals are exposed to high levels of these particulates. Moreover, vegetables and plants may accumulate various trace elements dispersed in the atmosphere. Several studies documented an increased amount of heavy metals in plants grown in volcanic areas. For instance, a significantly enhanced Hg content was found in Pinus of the Mt. Etna area (Barghiani et al., 1987). Other researchers found high levels of different trace elements (As, Sb, Bi, Cd, Cr, Pb, Zn) in vegetables grown in areas characterized by volcanic activity (Queirolo et al., 2000; Jung et al., 2002; Abiye et al., 2011). Vegetable contamination may occur not only through the atmospheric pollution but also by the presence of heavy metals in the irrigation water (Dahal et al., 2008).

Finally, environmental carcinogens of volcanic origin could be responsible for gene mutations favoring the thyroid carcinogenesis. In a recent paper, our group reported a higher rate of BRAF(V600E) in eastern Sicily (hosting the Mt. Etna), compared to western Sicily (Frasca et al., 2008).

Table 4 provides a summary of the principal studies quoted in the present manuscript.

TABLE 4
www.frontiersin.org

Table 4. Summary of the principal studies quoted in the manuscript.

Conclusion

The rising number and the diffusion of sensitive diagnostic procedures may justify only part of the continuous increase of TC incidence. Additional studies are necessary to investigate the role of environmental factors, which may include the volcanic environment. Population-based cancer registries may allow a better understanding of the different agents and mechanisms underlying this increase.

There is a strong association between very high TC incidence and patient residence in volcanic areas. We propose the following considerations: (1) TC registries should be instituted in all volcanic areas with elevated population density because those populations are most likely at high risk for developing TC. However, not all volcanoes are necessarily the same in terms of environmental factors and vehicles for human exposure to carcinogens. (2) A primary aim of the research in this field should be to identify environmental factors and thyroid carcinogens in volcanic areas. These studies will enable us to understand the mechanisms and molecular alterations that might lead to TC. We can then develop specific interventions to prevent the increased risk of TC. (3) It is important to ascertain whether, in addition to TC, other cancers are favored by the volcanic environment. In the Mt. Etna area, an increased incidence of mesothelioma has been reported in the Biancavilla municipality district (Comba et al., 2003). Mesothelioma has been attributed to the increased inhalation of asbestiform fibers, a consequence of the generalized use of building materials from a local quarry. In Africa, endemic Kaposi’s sarcoma has been observed in areas containing volcanic clay minerals (Ziegler, 1993).

More than 500 million people in the world live in volcanic areas. Identifying the potential carcinogens involved in the pathogenesis of TC might help to promote preventive measures and understand the worldwide increase of this disease.

Conflict of Interest Statement

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.

References

Abiye, T. A., Sulaiman, H., and Hailu, A. (2011). Metal concentration in vegetables grown in the hydrothermally affected area in Ethiopia. J. Geogr. Geol. 3, 86–93.

AIRTUM Working Group. (2006). I Tumori in Italia – Rapporto 2006. Incidence and mortality data of the Cancer Registries, 1998–2002. Epidemiol Prev. 30(Suppl. 2), 1–148.

Aiuppa, A., Federico, C., Paonita, A., Pecoraino, G., and Valenza, M. (2002). S, Cl and F degassing as an indicator of volcanic dynamics: the 2001 eruption of Mount Etna. Geophys. Res. Lett. 29, 1559. doi:10.1029/2002GL015032

CrossRef Full Text

Arnbjornsson, E., Arnbjornsson, A., and Olafsson, A. (1986). Thyroid cancer incidence in relation to volcanic activity. Arch. Environ. Health 41, 36–40. doi:10.1080/00039896.1986.9935763

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Aschebrook-Kilfoy, B., Kaplan, E. L., Chiu, B. C., Angelos, P., and Grogan, R. H. (2013). The acceleration in papillary thyroid cancer incidence rates is similar among racial and ethnic groups in the United States. Ann. Surg. Oncol. doi:10.1245/s10434-013-2892-y [Epub ahead of print].

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Barghiani, C., Gloffré, D., and Bargali, R. (1987). “Mercury content in Pinus Sp. of the Mt. Etna volcanic area,” in Proceedings of the Sixth International Conference on Heavy Metals in the Environment, eds S. E. Lindberg, and T. C. Hutchinson (New Orleans: CEP Consultants Publisher), 51.

Biondi, B., Arpaia, D., Montuori, P., Ciancia, G., Ippolito, S., Pettinato, G., et al. (2012). Under the shadow of vesuvius: a risk for thyroid cancer?. Thyroid 22, 1296–1297. doi:10.1089/thy.2012.0002

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Boucek, J., Kastner, J., Skrivan, J., Grosso, E., Gibelli, B., Giugliano, G., et al. (2009). Occult thyroid carcinoma. Acta Otorhinolaryngol. Ital. 29, 296–304.

Pubmed Abstract | Pubmed Full Text

Brusca, L., Aiuppa, A., D’Alessandro, W., Parello, F., Allard, P., and Michel, A. (2001). Geochemical mapping of magmatic gas-water-rock interactions in the acquifer of Mount Etna volcano. J. Volcanol. Geoth. Res. 108, 199–218. doi:10.1016/S0377-0273(00)00286-9

CrossRef Full Text

Buat-Ménard, P., and Arnold, M. (1978). The heavy metal chemistry of atmospheric particulate matter emitted by Mount Etna Volcano. Geophys. Res. Lett. 5, 245–248. doi:10.1029/GL005i004p00245

CrossRef Full Text

Burgess, J. R. (2002). Temporal trends for thyroid carcinoma in Australia: an increasing incidence of papillary thyroid carcinoma (1982–1997). Thyroid 12, 141–149. doi:10.1089/105072502753522374

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Chen, A. Y., Jemal, A., and Ward, E. M. (2009). Increasing incidence of differentiated thyroid cancer in the United States, 1988-2005. Cancer 115, 3801–3807. doi:10.1002/cncr.24416

CrossRef Full Text

Comba, P., Gianfagna, A., and Paoletti, L. (2003). Pleural mesothelioma cases in Biancavilla are related to a new fluoro-edenite fibrous amphibole. Arch. Environ. Health 58, 229–232. doi:10.3200/AEOH.58.4.229-232

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Curado, M., Edwards, B., Shin, H., Storm, H., Ferlay, J., Heanue, M., et al. (2007). Cancer Incidence in Five Continents Vol. IX. IARC Scientific Publication No. 160. Lyon: IARC.

Dahal, B. M., Fuerhacker, M., Mentler, A., Karki, K. B., Shrestha, R. R., and Blum, W. E. (2008). Arsenic contamination of soils and agricultural plants through irrigation water in Nepal. Environ. Pollut. 155, 157–163. doi:10.1016/j.envpol.2007.10.024

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

D’Alessandro, W., and Vita, F. (2003). Groundwater radon measurements in the Mt. Etna area. J. Environ. Radioact. 65, 187–201. doi:10.1016/S0265-931X(02)00096-6

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Davies, L., and Welch, H. G. (2006). Increasing incidence of thyroid cancer in the United States, 1973-2002. JAMA 295, 2164–2167. doi:10.1001/jama.295.18.2164

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Duntas, L. H., and Doumas, C. (2009). The ‘rings of fire’ and thyroid cancer. Hormones (Athens) 8, 249–253.

Pubmed Abstract | Pubmed Full Text

Favalli, M., Mazzarini, F., Pareschi, M. T., and Boschi, E. (2004). Role of local wind circulation in plume monitoring at Mt. Etna volcano (Sicily): insights from a mesoscale numerical model. Geophys. Res. Lett. 31, L09105. doi:10.1029/2003GL019281

CrossRef Full Text

Frasca, F., Nucera, C., Pellegriti, G., Gangemi, P., Attard, M., Stella, M., et al. (2008). BRAF(V600E) mutation and the biology of papillary thyroid cancer. Endocr. Relat. Cancer 15, 191–205. doi:10.1677/ERC-07-0212

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Giammanco, S., Valenza, M., Pignato, S., and Giammanco, G. (1996). Mg, Mn, Fe, and V concentrations in the ground waters of Mount Etna (Sicily). Water Res. 30, 378–386. doi:10.1016/0043-1354(95)00183-2

CrossRef Full Text

Goodman, M. T., Yoshizawa, C. N., and Kolonel, L. N. (1988). Descriptive epidemiology of thyroid cancer in Hawaii. Cancer 61, 1272–1281. doi:10.1002/1097-0142(19880315)61:6<1272::AIDCNCR2820610636>3.0.CO;2-8

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Hansell, A., and Oppenheimer, C. (2004). Health hazards from volcanic gases: a systematic literature review. Arch. Environ. Health 59, 628–639. doi:10.1080/00039890409602947

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Hogan, D. E., and Burstein, J. (2007). “Volcanic eruptions,” in Disaster Medicine, 2nd Edn, eds E. Hogan, and J. Burstein (Philadelphia: Lippincott Williams & Wilkins), 266–276.

How, J., and Tabah, R. (2007). Explaining the increasing incidence of differentiated thyroid cancer. CMAJ 177, 1383–1384. doi:10.1503/cmaj.071464

CrossRef Full Text

Howlader, N., Noone, A. M., Krapcho, M., Neyman, N., Aminou, R., Waldron, W., et al. (2012). SEER Cancer Statistics Review, 1975-2009 (Vintage 2009 Populations). Bethesda, MD: National Cancer Institute.

Hrafnkelsson, J., Tulinius, H., Jonasson, J. G., Olafsdottir, G., and Sigvaldason, H. (1989). Papillary thyroid carcinoma in Iceland. A study of the occurrence in families and the coexistence of other primary tumours. Acta Oncol. 28, 785–788. doi:10.3109/02841868909092308

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Hughes, D. T., Haymart, M. R., Miller, B. S., Gauger, P. G., and Doherty, G. M. (2011). The most commonly occurring papillary thyroid cancer in the United States is now a microcarcinoma in a patient older than 45 years. Thyroid 21, 231–236. doi:10.1089/thy.2010.0137

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

IARC. (2006). “Vanadium pentoxide,” in Cobalt in Hard Metals and Cobalt Sulfate, Gallium Arsenide, Indium Phospide and Vanadium Pentoxide (Lyon: IARC Press), 227–292.

Ingram, J. L., Rice, A. B., Santos, J., Van Houten, B., and Bonner, J. C. (2003). Vanadium-induced HB-EGF expression in human lung fibroblasts is oxidant dependent and requires MAP kinases. Am. J. Physiol. Lung Cell Mol. Physiol. 284, L774–L782.

Pubmed Abstract | Pubmed Full Text

Italian National Institute of Statistics. (2001). Available at: http://dawinci.istat.it/pl/index_eng.html

Jung, M. C., Thornton, I., and Chon, H. T. (2002). Arsenic, Sb and Bi contamination of soils, plants, waters and sediments in the vicinity of the Dalsung Cu-W mine in Korea. Sci. Total Environ. 295, 81–89. doi:10.1016/S0048-9697(02)00042-6

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Kent, W. D., Hall, S. F., Isotalo, P. A., Houlden, R. L., George, R. L., and Groome, P. A. (2007). Increased incidence of differentiated thyroid carcinoma and detection of subclinical disease. CMAJ 177, 1357–1361. doi:10.1503/cmaj.061730

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Kitahara, C. M., Platz, E. A., Freeman, L. E., Hsing, A. W., Linet, M. S., Park, Y., et al. (2011). Obesity and thyroid cancer risk among U.S. men and women: a pooled analysis of five prospective studies. Cancer Epidemiol. Biomarkers Prev. 20, 464–472. doi:10.1158/1055-9965.EPI-10-1220

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Kolonel, L. N., Hankin, J. H., Wilkens, L. R., Fukunaga, F. H., and Hinds, M. W. (1990). An epidemiologic study of thyroid cancer in Hawaii. Cancer Causes Control 1, 223–234. doi:10.1007/BF00117474

CrossRef Full Text

Kung, T. M., Ng, W. L., and Gibson, J. B. (1981). Volcanoes and carcinoma of the thyroid: a possible association. Arch. Environ. Health 36, 265–267. doi:10.1080/00039896.1981.10667635

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Kusky, T. M. (2008). Volcanoes: Eruption and Other Volcanic Hazards. New York: Facts on File, Inc.

Leenhardt, L., Bernier, M. O., Boin-Pineau, M. H., Conte Devolx, B., Marechaud, R., Niccoli-Sire, P., et al. (2004). Advances in diagnostic practices affect thyroid cancer incidence in France. Eur. J. Endocrinol. 150, 133–139. doi:10.1530/eje.0.1500133

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Leenhardt, L., and Grosclaude, P. (2011). Epidemiology of thyroid carcinoma over the world. Ann. Endocrinol. (Paris) 72, 136–148. doi:10.1016/j.ando.2011.03.025

CrossRef Full Text

Markaki, I., Linos, D., and Linos, A. (2003). The influence of dietary patterns on the development of thyroid cancer. Eur. J. Cancer 39, 1912–1919. doi:10.1016/S0959-8049(03)00432-5

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Martin-Del Pozzo, A. L., Aceves, F., Espinasa, R., Aguayo, A., Inguaggiato, S., Morales, P., et al. (2002). Influence of volcanic activity on spring water chemistry at Popocatepetl Volcano, Mexico. Chem. Geol. 190, 207–229. doi:10.1016/S0009-2541(02)00117-1

CrossRef Full Text

Netea-Maier, R. T., Aben, K. K., Casparie, M. K., den Heijer, M., Grefte, J. M., Slootweg, P., et al. (2008). Trends in incidence and mortality of thyroid carcinoma in The Netherlands between 1989 and 2003: correlation with thyroid fine-needle aspiration cytology and thyroid surgery. Int. J. Cancer 123, 1681–1684. doi:10.1002/ijc.23678

CrossRef Full Text

Nikiforov, Y. E. (2006). Radiation-induced thyroid cancer: what we have learned from Chernobyl. Endocr. Pathol. 17, 307–317. doi:10.1007/s12022-006-0001-5

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Parkin, D. M., Bray, F., Ferlay, J., and Pisani, P. (2005). Global cancer statistics, 2002. CA Cancer J. Clin. 55, 74–108. doi:10.3322/canjclin.55.2.74

CrossRef Full Text

Pazaitou-Panayiotou, K., Capezzone, M., and Pacini, F. (2007). Clinical features and therapeutic implication of papillary thyroid microcarcinoma. Thyroid 17, 1085–1092. doi:10.1089/thy.2007.0005

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Pellegriti, G., De Vathaire, F., Scollo, C., Attard, M., Giordano, C., Arena, S., et al. (2009). Papillary thyroid cancer incidence in the volcanic area of Sicily. J. Natl. Cancer Inst. 101, 1575–1583. doi:10.1093/jnci/djp354

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Peterson, E., De, P., and Nuttall, R. (2012). BMI, diet and female reproductive factors as risks for thyroid cancer: a systematic review. PLoS ONE 7:e29177. doi:10.1371/journal.pone.0029177

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Queirolo, F., Stegen, S., Restovic, M., Paz, M., Ostapczuk, P., Schwuger, M. J., et al. (2000). Total arsenic, lead, and cadmium levels in vegetables cultivated at the Andean villages of northern Chile. Sci. Total Environ. 255, 75–84. doi:10.1016/S0048-9697(00)00450-2

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Rego-Iraeta, A., Perez-Mendez, L. F., Mantinan, B., and Garcia-Mayor, R. V. (2009). Time trends for thyroid cancer in northwestern Spain: true rise in the incidence of micro and larger forms of papillary thyroid carcinoma. Thyroid 19, 333–340. doi:10.1089/thy.2008.0210

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Sassolas, G., Hafdi-Nejjari, Z., Remontet, L., Bossard, N., Belot, A., Berger-Dutrieux, N., et al. (2009). Thyroid cancer: is the incidence rise abating? Eur. J. Endocrinol. 160, 71–79. doi:10.1530/EJE-08-0624

CrossRef Full Text

Scheiden, R., Keipes, M., Bock, C., Dippel, W., Kieffer, N., and Capesius, C. (2006). Thyroid cancer in Luxembourg: a national population-based data report (1983–1999). BMC cancer 6:102. doi:10.1186/1471-2407-6-102

CrossRef Full Text

Simard, E. P., Ward, E. M., Siegel, R., and Jemal, A. (2012). Cancers with increasing incidence trends in the United States: 1999 through 2008. CA Cancer J. Clin. 62, 118–128. doi:10.3322/caac.20141

CrossRef Full Text

Tilling, R., and Jones, B. F. (1996). Waters associated with an active basaltic volcano, Kilauea, Kawaii: variation in solute sources, 1973-1991. GSA Bull. 108, 562–577. doi:10.1130/0016-7606(1996)108<0562:WAWAAB>2.3.CO;2

CrossRef Full Text

Truong, T., Rougier, Y., Dubourdieu, D., Guihenneuc-Jouyaux, C., Orsi, L., Hemon, D., et al. (2007). Time trends and geographic variations for thyroid cancer in New Caledonia, a very high incidence area (1985-1999). Eur. J. Cancer Prev. 16, 62–70. doi:10.1097/01.cej.0000236244.32995.e1

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Uthus, E. O., and Nielsen, F. H. (1990). Effect of vanadium, iodine and their interaction on growth, blood variables, liver trace elements and thyroid status indices in rats. Magnes. Trace Elem. 9, 219–226.

Pubmed Abstract | Pubmed Full Text

Yu, G. P., Li, J. C., Branovan, D., Mccormick, S., and Schantz, S. P. (2010). Thyroid cancer incidence and survival in the national cancer institute surveillance, epidemiology, and end results race/ethnicity groups. Thyroid 20, 465–473. doi:10.1089/thy.2008.0281

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Zhang, L., Rice, A. B., Adler, K., Sannes, P., Martin, L., Gladwell, W., et al. (2001). Vanadium stimulates human bronchial epithelial cells to produce heparin-binding epidermal growth factor-like growth factor: a mitogen for lung fibroblasts. Am. J. Respir. Cell Mol. Biol. 24, 123–131. doi:10.1165/ajrcmb.24.2.4096

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Ziegler, J. L. (1993). Endemic Kaposi’s sarcoma in Africa and local volcanic soils. Lancet 342, 1348–1351. doi:10.1016/0140-6736(93)92252-O

Pubmed Abstract | Pubmed Full Text | CrossRef Full Text

Keywords: thyroid cancer, epidemiology, registry, incidence, risk factors, papillary, volcanoes

Citation: Malandrino P, Scollo C, Marturano I, Russo M, Tavarelli M, Attard M, Richiusa P, Violi MA, Dardanoni G, Vigneri R and Pellegriti G (2013) Descriptive epidemiology of human thyroid cancer: experience from a regional registry and the “volcanic factor”. Front. Endocrinol. 4:65. doi: 10.3389/fendo.2013.00065

Received: 17 January 2013; Paper pending published: 04 March 2013;
Accepted: 19 May 2013; Published online: 04 June 2013.

Edited by:

Carmelo Nucera, Harvard Medical School, USA

Reviewed by:

Matthew Ringel, The Ohio State University, USA
Caterina Mian, Operative Unit of Endocrinology, Department of Medicine-DIMED, Italy
Mira Milas, Oregon Health and Sciences University, USA

Copyright: © 2013 Malandrino, Scollo, Marturano, Russo, Tavarelli, Attard, Richiusa, Violi, Dardanoni, Vigneri and Pellegriti. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.

*Correspondence: Gabriella Pellegriti, Endocrinology Unit, Department of Clinical and Molecular Biomedicine, University of Catania, Garibaldi-Nesima Medical Center, Via Palermo 636, Catania 95122, Italy e-mail: g.pellegriti@unict.it