Oral mucositis is a dose-limiting toxicity of 5-fluorouracil (5-FU). This p
rospective cohort study investigated factors associated with mucositis in p
atients receiving 5-FU for cancer of the digestive tract. Sixty-three patie
nts (mean age 65 years) completed self-administered questionnaires and had
interviews, oral examinations and unstimulated whole salivary flow measurem
ents at baseline and follow-up appointments. The duration of follow-up was
2 months. Predictor variables included sociodemographic data, body surface
area, diabetes, smoking, alcohol consumption, salivary flow, oral hygiene,
presence of prostheses, performance status, regimen of cytotoxic drugs, hem
atological data, and herpes simplex virus antibody titer. Forty-six per cen
t of patients developed at least one episode of oral mucositis during cytot
oxic treatment. Pearson's chi-square analysis showed that mucositis was sig
nificantly associated with xerostomia at baseline, xerostomia during chemot
herapy, and lower baseline neutrophil counts (P less than or equal to 0.05)
. Multiple logistic regression analysis indicated that xerostomia at baseli
ne (odds ratio, OR = 10.0), or baseline neutrophil level under 4000 cells/m
m(3) (OR = 3.9) were significant predictors of mucositis. Taking into accou
nt the effect of neutrophil level at baseline, xerostomia during chemothera
py (OR = 4.5) was also a significant predictor of mucositis. The results sh
owed that xerostomia and lower baseline neutrophil levels are significantly
associated with oral mucositis. These variables should be taken into consi
deration in the design of intervention studies to reduce the frequency and
severity of mucositis. More research is required to investigate the role of
saliva and neutrophils in the pathogenesis of chemotherapy-induced mucosit
is. (C) 1998 Elsevier Science Ltd. All rights reserved.