Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Chrysotile fibers in tissue adjacent to laryngeal squamous cell carcinoma in cases with a history of occupational asbestos exposure


Asbestos describes a group of naturally occurring fibrous silicate mineral compounds that have been associated with a number of respiratory maladies, including mesothelioma and lung cancer. In addition, based primarily on epidemiologic studies, asbestos has been implicated as a risk factor for laryngeal and pharyngeal squamous cell carcinoma (SCC). The main objective of this work was to strengthen existing evidence via empirical demonstration of persistent asbestos fibers embedded in the tissue surrounding laryngeal and pharyngeal SCC, thus providing a more definitive biological link between exposure and disease. Six human papillomavirus (HPV)-negative laryngeal (n = 4) and pharyngeal (n = 2) SCC cases with a history working in an asbestos-exposed occupation were selected from a large population-based case–control study of head and neck cancer. A laryngeal SCC case with no history of occupational asbestos exposure was included as a control. Tissue cores were obtained from adjacent nonneoplastic tissue in tumor blocks from the initial primary tumor resection, and mineral fiber analysis was performed using a scanning electron microscope equipped with an energy dispersive X-ray analyzer (EDXA). Chrysotile asbestos fiber bundles were identified in 3/6 of evaluated cases with a history of occupational asbestos exposure. All three cases had tumors originating in the larynx. In addition, a wollastonite fiber of unclear significance was identified one of the HPV-negative pharyngeal SCC cases. No mineral fibers were identified in adjacent tissue of the case without occupational exposure. The presence of asbestos fibers in the epithelial tissue surrounding laryngeal SCC in cases with a history of occupational asbestos exposure adds a key line of physical evidence implicating asbestos as an etiologic factor.


According to the most recent global cancer statistics, pharyngeal and laryngeal cancer accounted for an estimated 350,917 global incident cancer diagnoses and 180,770 deaths in 2018 [1]. Of these, more than 90% are squamous cell carcinoma (SCC) [2], with smoking, alcohol consumption, and human papillomavirus (HPV) infection, particularly for oropharyngeal SCC, being widely recognized as the primary risk factors [3]. While those risk factors have garnered the majority of attention in etiologic research—deservingly so since they are attributed to the vast majority of these tumors—there is evidence that occupational exposures are also risk factors [4, 5].

Asbestos describes a group of naturally occurring fibrous silicate mineral compounds. Its use dates back thousands of years, but became widespread in the late 19th century through the late 20th century [6] due to its favorable industrial properties, including its strength, flexibility, and thermal properties, with peak use in the United States occurring in the 1970s. Asbestos has been associated with a number of chronic respiratory diseases [7], including malignancy, and was linked to mesothelioma [8, 9] and lung cancer [10] in the early to mid-20th century. Despite the known health risks, asbestos is not universally banned, and is still in use in many countries (including the United States), with an estimated 125 million occupationally exposed individuals worldwide [11].

In addition to mesothelioma and lung cancer, asbestos has also been implicated as a risk factor for cancers involving the upper airway, in particular laryngeal and pharyngeal SCC [4, 12,13,14]; however, the evidence thus far has been primarily based on epidemiologic data from observational studies. Therefore, the goal of this study was to strengthen the existing evidence implicating asbestos as a risk factor for pharyngeal and/or laryngeal SCC via confirmation of persistent asbestos fibers in epithelial tissue surrounding laryngeal and pharyngeal SCC in cases with a history of occupational asbestos exposure.

Materials and methods

Study population

Six cases with incident, HPV-negative pharyngeal (n = 2) and laryngeal (n = 4) SCC (ICD-9: 146, 148, 149.0, 149.1, and 161) with self-reported occupational exposure to asbestos were selected from a large population-based case–control study of head and neck cancer, plus one laryngeal SCC case with no occupational exposure history as a control, matched to the sex, race/ethnicity, and median age (±3 years) and smoking pack-years (±3 pack-years) of the asbestos-exposed cases. Briefly, detailed occupational history was available for 1056 head and neck cancer cases enrolled through major teaching hospitals located in Boston, Massachusetts [15,16,17]. Occupational history was systematically reviewed to verify that cases with self-reported occupational history worked in an occupation at high risk for asbestos exposure. All cases selected had archival tumor and adjacent normal tissue available at Massachusetts General Hospital.

High-risk HPV testing

Serologic testing was performed for antibodies against E6 and E7 viral oncoproteins for high-risk HPV (HPV16, 18, 31, 33, 45, 52, and 58) using sandwich ELISA assays, as previously described [18,19,20,21,22]. Subjects were considered high-risk HPV seropositive if antibodies were present for either viral oncoprotein.

Asbestos fiber counts

Cores were obtained from adjacent nonneoplastic tissue in tumor blocks from the initial primary tumor resection. A count of asbestos fibers ≥5 μm was performed on the cores from each case at Duke University via scanning electron microscopy [23]. Specimens were deparaffinized in xylene, rehydrated in 95% ethanol, and wet weight was obtained on an analytical balance. The tissue was then digested in sodium hypochlorite solution, and the residue collected on 13 -mm Nuclepore filters with a pore size of 0.4 μm. These were mounted on a carbon stub with colloidal graphite, sputter-coated with platinum, and examined by scanning electron microscopy (SEM) equipped with an energy dispersive X-ray analyzer (EDXA). One hundred consecutive fields were examined at a screen magnification of ×1300 and all fibers ≥5 μm in length counted, and examined by EDXA [23].

Immune assessment

For descriptive purposes, morphologic analysis was performed to assess severity and type of inflammation in the tumor microenvironment. “Global” qualitative assessments of inflammation severity were performed by two board-certified Anatomic Pathologists (each blinded to the other’s assessments), as well as assessments of the presence or absence of dense lymphoid tissue and neutrophilic inflammation. The lymphoid infiltrate in each case was assigned one of three “patterns” depending on whether lymphoid tissue around tumor cells formed a continuous and dense rim (Pattern 1), was present as discontinuous dense patches (Pattern 2), or was limited or absent (Pattern 3) [24]. Neutrophilic inflammation and global qualitative inflammation assessments were also scored as three-tiered variables (0–25%, 25–50%, >50%) and as mild, moderate, and severe, respectively [25].


Study subject characteristics, including occupation(s) and duration spent working in an occupation with asbestos exposure, are presented in Table 1. Briefly, all asbestos-exposed cases were Caucasian males with a median age of 63.5 years (range: 56–77 years). Asbestos-exposed occupations/industries of the cases included automotive mechanic, space shuttle thermal protection applicator (solid-fuel boosters contained asbestos materials [26]), firefighter, Army artillery, school custodian, and metal lather, with a median duration spent in an asbestos-exposed occupation of 34.5 years (range: 5–56 years). The non-asbestos-exposed case was a 64-year-old Caucasian male with an occupational history as a truck driver. With the exception of one of the cases (HN2), all subjects had a smoking history, with a median of 39 packs-years (range: 0–114 pack-years). The reported occupational asbestos exposures for all cases overlapped peak industrial usage in the United States [27] as depicted in Fig. 1.

Table 1 Description of study subject characteristics and occupational history
Fig. 1

Timeframe of occupational asbestos exposure for cases in the context of annual industrial asbestos consumption in the United States. The rows at the bottom of the figure correspond to the occupation with asbestos exposure for the cases, where red boxes represent years working in each occupation. The upper plot shows annual asbestos consumption in the United States from 1900 to 2015

Histopathologic slides were available for the primary tumors of 4/6 cases (Fig. 2). Of those, two distinct patterns of inflammation were noted. Two cases showed prominent lymphoid infiltrates, which were present as a continuous dense rim in one case (HN1) and as discontinuous dense patches in the other (HN6), with each exhibiting minimal to absent neutrophilic inflammation. In contradistinction, the other two cases (HN3 and HN4) contained limited or no lymphoid tissue, but did show prominent neutrophilic inflammation.

Fig. 2

Representative formalin-fixed-paraffin embedded tumor sections stained with hematoxylin and eosin (H&E) from cases with an occupational asbestos exposure history and available tumor tissue, with corresponding immune scores

Chrysotile asbestos fiber bundles were identified by SEM in adjacent nonneoplastic tissue from 3/6 asbestos-exposed cases with spectra confirmed by EDXA, all of which had laryngeal SCC (Fig. 3); neither of the two HPV-negative pharyngeal cancer cases had detectable asbestos fibers. Fibers ranged from 7 to 14 µm in length and 0.2 to 0.5 µm in diameter. It should be noted that, given the archival nature of the tissue, samples for all cases were well below the recommended amount of 0.3 g wet weight for fiber analysis (Table 2). A wollasonite fiber (calcium silicate) was identified in adjacent tissue in one of the two HPV-negative oropharyngeal cases (HN4), although this is of uncertain significance. No mineral fibers were identified in the adjacent tissue of the case without any known occupational exposure (control).

Fig. 3

Analysis of tissue mineral fiber content. a Scanning electron microscopy (SEM) images of chrysotile asbestos fibers identified in tissue adjacent to laryngeal squamous cell carcinoma tumor in three cases with a history of occupational asbestos exposure: HN2, HN3, and HN6. b The corresponding energy dispersive X-ray analyzer (EDXA) spectrum consistent with chrysotile asbestos fibers

Table 2 Quantity of adjacent tissue for asbestos fiber count analysis


We have identified chrysotile asbestos fibers in nonneoplastic epithelial tissue adjacent to laryngeal SCC in cases with a history of work in an asbestos-exposed occupation, greatly strengthening the causal evidence for asbestos as a risk factor. Up to now, there had only been one other case report identifying mostly amphibole asbestos fibers in nonneoplastic laryngeal tissue in a case with laryngeal SCC [28]. This work significantly adds to these previous reports, quadrupling the number of reported laryngeal SCC cases with detectable asbestos fibers and, importantly represents the first study to identify chrysotile asbestos fibers proximal to laryngeal SCC tumors in the absence of amphibole fibers.

These findings are in agreement with and complementary to existing epidemiological evidence from industrial cohorts and observational studies supporting an association of asbestos exposure and laryngeal SCC [12, 14]. Our observations are also in-line with that from two separate reports of asbestos bodies and/or fibers in laryngeal tissue at autopsy from former asbestos workers with no detectable laryngeal cancer [28, 29]. Of particular interest in our present study is the identification of chrysotile fibers in tissue from a laryngeal SCC case who identified as a never smoker and moderate alcohol user—hardly the prototypical profile of a laryngeal cancer case—but with a high-risk occupational history working as a space shuttle thermal protection system applicator in the 1970s and over two decades as a firefighter (HN2).

Chrysotile fibers were only identified in asbestos-exposed laryngeal SCC cases, with none identified in tissue from either HPV-negative pharyngeal SCC case. However, it bears to be reiterated that the samples in this study ranged 2.7-fold to 3000-fold below the recommended 0.3 g of wet tissue weight that would be used with larger autopsy samples, and therefore samples with no identifiable asbestos fibers should be considered inconclusive rather than negative. To this point, one of the two pharyngeal cases (HN5) had the least amount of tissue available of all of the samples. Wollastonite—an acicular calcium silicate mineral fiber—was identified in the other of the two HPV-negative oropharyngeal cases (HN5). However the significance of this is uncertain, as an IARC working group determined two decades ago that wollastonite cannot be classified as to its carcinogenicity to humans due to insufficient human or experimental models [30], and little to no evidence to the contrary has been surfaced since [31].

There were several strengths to our study, notably use of SEM for fiber analysis with confirmation by EDXA spectra; detailed occupational history and other major risk factor data for the cases; and availability of adjacent nonneoplastic epithelial tissue, which allowed us to avoid a dilution effect that would be encountered by using tumor tissue due to clonal expansion. However, there were also some limitations. Due to labor and resource constraints, including availability of archival tissue materials, we were only able to evaluate a small subset of cases with occupational asbestos exposure in this study [17]. However, despite the small sample size, it is notable that chrysotile fibers were identified in 3/6 of the cases interrogated, and were absent from the cases lacking an occupational asbestos history. Moreover, as we had previously stated, the wet tissue weight for each case was suboptimal for fiber detection, and therefore we cannot rule out the presence of fibers in pharyngeal or laryngeal tissue from the negative cases. Nonetheless, we still were able to identify fibers in a sizeable fraction of interrogated cases.

Despite its known adverse health effects, asbestos continues to be a threat to global health. Although asbestos has been fully banned more than 50 countries, it is still in widespread use among developing nations, and is notably still in use—albeit limited—in the United States [32, 33]. Our identification of chrysotile asbestos fibers in epithelial tissue proximal laryngeal SCC adds a critical empirical link, and bolsters the mounting evidence that asbestos is a risk factor for laryngeal cancer.


  1. 1.

    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.

    Article  Google Scholar 

  2. 2.

    Carvalho AL, Nishimoto IN, Califano JA, Kowalski LP. Trends in incidence and prognosis for head and neck cancer in the United States: a site-specific analysis of the SEER database. Int J Cancer. 2005;114:806–16.

    CAS  Article  Google Scholar 

  3. 3.

    Marur S, Forastiere AA. Head and neck cancer: changing epidemiology, diagnosis, and treatment. Mayo Clin Proc. 2008;83:489–501.

    Article  Google Scholar 

  4. 4.

    Paget-Bailly S, Cyr D, Luce D. Occupational exposures to asbestos, polycyclic aromatic hydrocarbons and solvents, and cancers of the oral cavity and pharynx: a quantitative literature review. Int Arch Occup Environ Health. 2012;85:341–51.

    CAS  Article  Google Scholar 

  5. 5.

    Paget-Bailly S, Cyr D, Luce D. Occupational exposures and cancer of the larynx-systematic review and meta-analysis. J Occup Environ Med. 2012;54:71–84.

    Article  Google Scholar 

  6. 6.

    Weiss SH. A call to action: epidemiologists assert themselves with scientific data. Int J Occup Environ Health. 2012;18:167–70.

    Article  Google Scholar 

  7. 7.

    Jamrozik E, de Klerk N, Musk AW. Asbestos-related disease. Intern Med J. 2011;41:372–80.

    CAS  Article  Google Scholar 

  8. 8.

    Gloyne S. Two cases of squamous cell carcinoma of the lung occuring in asbestosis. Tubercle. 1935;17:5–10.

    Article  Google Scholar 

  9. 9.

    Wagner JC, Sleggs CA, Marchand P. Diffuse pleural mesothelioma and asbestos exposure in the North Western Cape Province. Br J Ind Med. 1960;17:260–71.

    CAS  PubMed  PubMed Central  Google Scholar 

  10. 10.

    Doll R. Mortality from lung cancer in asbestos workers. Br J Ind Med. 1955;12:81–6.

    CAS  PubMed  PubMed Central  Google Scholar 

  11. 11.

    WHO. Asbestos: elimination of asbestos-related diseases. 2010. Accessed 28 February 2013.

  12. 12.

    IOM Committee on Asbestos. Asbestos: selected cancers. Institute of Medicine of the National Academies: Washington, DC: The National Academies Press. 2006.

  13. 13.

    Awan KH, Hegde R, Cheever VJ, Carroll W, Khan S, Patil S, et al. Oral and pharyngeal cancer risk associated with occupational carcinogenic substances: systematic review. Head Neck. 2018;40:2724–32.

    Article  Google Scholar 

  14. 14.

    IARC Working Group. Asbestos (chrysotile, amosite, crocidolite, tremolite, actinolyte, and anthophylite). Lyon, France: International Agency for Research on Cancer (IARC); 2012.

    Google Scholar 

  15. 15.

    Fogleman EV, Eliot M, Michaud DS, Nelson HH, McClean MD, Langevin SM, et al. Occupational asphalt is not associated with head and neck cancer. Occup Med. 2015;65:570–3.

    CAS  Article  Google Scholar 

  16. 16.

    Langevin SM, McClean MD, Michaud DS, Eliot M, Nelson HH, Kelsey KT. Occupational dust exposure and head and neck squamous cell carcinoma risk in a population-based case-control study conducted in the greater Boston area. Cancer Med. 2013;2:978–86.

    Article  Google Scholar 

  17. 17.

    Langevin SM, O’Sullivan MH, Valerio JL, Pawlita M, Applebaum KM, Eliot M, et al. Occupational asbestos exposure is associated with pharyngeal squamous cell carcinoma in men from the greater Boston area. Occup Environ Med. 2013;70:858–63.

    Article  Google Scholar 

  18. 18.

    Waterboer T, Sehr P, Michael KM, Franceschi S, Nieland JD, Joos TO, et al. Multiplex human papillomavirus serology based on in situ-purified glutathione s-transferase fusion proteins. Clin Chem. 2005;51:1845–53.

    CAS  Article  Google Scholar 

  19. 19.

    Kelsey KT, Nelson HH, Kim S, Pawlita M, Langevin SM, Eliot M, et al. Human papillomavirus serology and tobacco smoking in a community control group. BMC Infect Dis. 2015;15:8.

    Article  Google Scholar 

  20. 20.

    Nelson HH, Pawlita M, Michaud DS, McClean M, Langevin SM, Eliot MN, et al. Immune response to HPV16 E6 and E7 proteins and patient outcomes in head and neck cancer. JAMA Oncol. 2017;3:178–85.

    Article  Google Scholar 

  21. 21.

    Michaud DS, Langevin SM, Eliot M, Nelson HH, Pawlita M, McClean MD, et al. High-risk HPV types and head and neck cancer. Int J Cancer. 2014;135:1653–61.

    CAS  Article  Google Scholar 

  22. 22.

    Tan X, Nelson HH, Langevin SM, McClean M, Marsit CJ, Waterboer T, et al. Obesity and head and neck cancer risk and survival by human papillomavirus serology. Cancer Causes Control. 2015;26:111–9.

    Article  Google Scholar 

  23. 23.

    Roggli VL, Sharma A. Analysis of tissue mineral fiber content. In: V.L. R, Oury TD, Sporn TA, editors. Pathology of asbestos-associated diseases. 3rd edn. New York: Springer:; 2014. p. 253–92.

    Google Scholar 

  24. 24.

    Brandwein-Gensler M, Teixeira MS, Lewis CM, Lee B, Rolnitzky L, Hille JJ, et al. Oral squamous cell carcinoma: histologic risk assessment, but not margin status, is strongly predictive of local disease-free and overall survival. Am J Surg Pathol. 2005;29:167–78.

    Article  Google Scholar 

  25. 25.

    Lundqvist L, Stenlund H, Laurell G, Nylander K. The importance of stromal inflammation in squamous cell carcinoma of the tongue. J Oral Pathol Med. 2012;41:379–83.

    Article  Google Scholar 

  26. 26.

    Rogers WP, Armstrong NA, Acheson DC, Covert EE, Feynman RP, Hotz RB, et al. Report of the Presidential Commission on the Space Shuttle Challenger Accident: Washington, DC; 1986.

  27. 27.

    USGS. U.S. Geological Survey, 2017, Asbestos Statistics, [through 2015, last modified January 19, 2017], 2017.

  28. 28.

    Hirsch A, Bignon J, Sebastien P, Gaudichet A. Asbestos fibers in laryngeal tissues. Findings in two patients with asbestosis associated with laryngeal tumors. Chest. 1979;76:697–9.

    CAS  Article  Google Scholar 

  29. 29.

    Roggli VL, Greenberg SD, McLarty JL, Hurst GA, Spivey CG, Heiger LR. Asbestos body content of the larnyx in asbestos workers. A study of five cases. Arch Otolaryngol. 1980;106:533–5.

    CAS  Article  Google Scholar 

  30. 30.

    IARC Working Group. Silica, some silicates, coal dust and para-aramid fibrils. Lyon, France: International Agency for Research on Cancer (IARC); 1997.

    Google Scholar 

  31. 31.

    Maxim LD, McConnell EE. A review of the toxicology and epidemiology of wollastonite. Inhal Toxicol. 2005;17:451–66.

    CAS  Article  Google Scholar 

  32. 32.

    LaDou J, Castleman B, Frank A, Gochfeld M, Greenberg M, Huff J, et al. The case for a global ban on asbestos. Environ Health Perspect. 2010;118:897–901.

    Article  Google Scholar 

  33. 33.

    Joshi TK, Gupta RK. Asbestos in developing countries: magnitude of risk and its practical implications. Int J Occup Med Environ Health. 2004;17:179–85.

    PubMed  Google Scholar 

Download references


This work was supported by the NIH/NIDCR grant R21DE027227 to SML; NIH/NCI grant R01CA100679 to KTK; and NIH/NIEHS supported UC Center for Environmental Genetics (2P30ES006096).

Author information



Corresponding authors

Correspondence to Karl T. Kelsey or Scott M. Langevin.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Additional information

Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Wronkiewicz, S.K., Roggli, V.L., Hinrichs, B.H. et al. Chrysotile fibers in tissue adjacent to laryngeal squamous cell carcinoma in cases with a history of occupational asbestos exposure. Mod Pathol 33, 228–234 (2020).

Download citation


Quick links