M. Degardin et al., HYPERCALCEMIA AND SQUAMOUS-CELL CARCINOMA OF THE HEAD AND NECK - FREQUENCY AND PROGNOSIS, Bulletin du cancer, 82(11), 1995, pp. 975-980
We performed a retrospective analysis on all head and neck cancers wit
h hypercalcemia seen between January 1988 and June 1993 at the Centre
Oscar-Lambret, cancer center of northern France. Hypercalcemia, non al
bumin-corrected, higher than 2.60 mmol/l was obsserved in 173 of 3,394
consecutive patients (5%). Median age of patients with hypercalcemia
was 53 years and 97% of these patients were males. All patients with h
ypercalcemia had advanced or recurrent and/or metastatic squamous cell
carcinoma of head and neck (SCCHN); 31 of them were not pretreated. T
here was no significant difference in histology between patients with
or without hypercalcemia, but hypercalcemia was most commonly associat
ed with lesions of the oropharynx (p = 0.00001). The median of calcemi
a was of 2.83 mmol/l (2.61-4.70). Gastrointestinal and neurologic symp
toms respectively occurred in 24% and in 14% of patients and bone meta
stases in 25% of patients. Median survival after the first determinati
on of hypercalcemia was of 7 weeks (0-128) for the overall group of 17
3 patients and of 12 weeks (1-128) for those 31 patients with hypercal
cemia at initial diagnosis. Prognosis associated factors were: efficac
y of antitumour treatment performance status and hypercalcemia superio
r or not to 3 mmol/l. We concluded that hypercalcemia in head and neck
cancer is usually a late manifestation associated with advanced, recu
rrent and/or metastatic disease and carries a poor prognosis. The prol
ongation of survival can be obtained in some patients if an effective
antitumour treatment is feasible.