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Table 1.

Number of cases of oral (oropharyngeal and oral cavity) squamous cell carcinoma among ages 0–84 between 1973–2012 by race and cancer subsite group.

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Table 1 Expand

Fig 1.

Schematic of the two-stage clonal expansion model with period and cohort dependencies.

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Fig 1 Expand

Fig 2.

Age-adjusted incidence rates of oral squamous cell carcinoma among ages 30–84 by cancer subsite group: (a) HPV-related, (b) HPV-unrelated, and (c) oral tongue.

Please note the change in axes scale for the oral tongue cancer.

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Fig 2 Expand

Fig 3.

Incidence rates of oral squamous cell carcinoma among white males for HPV-related, by cohort (a) and period (b), and HPV-unrelated subsite groups, by cohort (c) and period (d).

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Fig 3 Expand

Fig 4.

Fits of the two-stage clonal expansion model with period and cohort effects on initiation to incidence rates of oral squamous cell carcinoma among white males for HPV-related subsites, by cohort (a) and period (b), and HPV-unrelated subsites, by cohort (c) and period (d).

The dots are SEER data, and lines are model fits.

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Fig 4 Expand

Fig 5.

Hazard, cohort effects, and period effects for the cohort-and-period-effects-on-r APC—TSCE models of oral squamous cell carcinoma by race and cancer subsite group.

(a) HPV-related hazards. (b) HPV-unrelated hazards. (c) Oral tongue hazards. (d) HPV-related cohort effects. (e) HPV-unrelated cohort effects. (f) Oral tongue cohort effects. (g) HPV-related period effects. (h) HPV-unrelated period effects. (i) Oral tongue period effects.

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Fig 5 Expand

Table 2.

Biological parameters for the period-and-cohort-on-r APC—TSCE models of oral squamous cell carcinoma by race and cancer subsite group with 95% Wald confidence intervals.

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Table 2 Expand