S. Atula et al., CANCER OF THE TONGUE IN PATIENTS YOUNGER THAN 40 YEARS - A DISTINCT ENTITY, Archives of otolaryngology, head & neck surgery, 122(12), 1996, pp. 1313-1319
Background: An increase in the incidence of oral cancer among patients
younger than 40 years has been reported worldwide. It has been sugges
ted that the disease behaves more aggressively among young people. Obj
ective: To evaluate the clinical and biologic behavior of tongue cance
r among younger patients. Patients and Methods: Data on all patients y
ounger than 40 years in whom tongue cancer was diagnosed in Finland be
tween 1980 and 1989 (34 cases) were collected; pertinent clinical data
were available for risk factor screening. A follow-up of at least 5 y
ears or until death was available for all 34 patients. Immunocytochemi
cal staining techniques were used to assess the expression of p53 and
bcl-2 proteins, and p53 mutation analysis was performed by using the n
onradioactive single-strand conformation polymorphism technique. Resul
ts: The incidence of tongue cancer in this age group in Finland did no
t change during the study period. The clinical behavior of tongue canc
er in young people was not more aggressive compared with that of older
patients in general, with the overall 5-year survival being as good a
s 70.6%. Altogether, p53 mutations were found in 17 of 33 tumors (51.5
%). The p53 and bcl-2 protein expression was strong or moderate in 33.
3% and 30.3% of the samples, respectively. Intense p53 protein express
ion was associated with the larger tumor size (P<.05). The poorest pro
gnosis was found in patients with tumors greater than 4 cm in diameter
(P=.01) or moderately or poorly differentiated cancer (P=.01). There
was a trend for the adverse prognosis to accumulate in patients with m
oderately or poorly differentiated carcinoma and mutations in p53 (P=.
09). Conclusions: The cause of tongue cancer in patients younger than
40 years seems to be multifactorial. Those patients had a similar clin
ical course, prognosis, and function of p53 as found in the reports of
a normal age variation. Mutations of p53 seemed to be an additional p
rognostic marker that was associated with moderate or poor differentia
tion of the tumors.