BACKGROUND. Understanding of prognostic factors in parotid carcinoma has gr
own considerably. In particular, clinical tumor staging and histologic clas
sification have been found to be prognostically important. Univariate and m
ultivariate analyses have indicated that other variables, such as age, pain
, skin invasion, and facial nerve impairment, are important predictors as w
ell. In an actual patient, some of these factors are present and others are
absent. However, a clinical tool incorporating this information, resulting
in an individualized prognosis based on the combined effects of present ad
verse prognostic factors, has never been devised.
METHODS. Of a cohort of 168 patients, 151 were evaluated to assess the prog
nostic Value of clinical and pathologic factors in a multivariate proportio
nal hazards analysis. Follow-up ranged from 1 to 278 months (median, 37 mon
ths). The end point was tumor recurrence. Identified prognostic factors and
their hazard ratios were combined into prognostic scores.
RESULTS. Clinical T classification, clinical N classification, pain, age at
diagnosis, skin invasion, facial nerve dysfunction, perineural growth, and
positive surgical margins acted as major factors predicting recurrence. A
prognostic score (PS), generated by the weighted combination of the factors
present in the individual patient, placed the patient in one of four subgr
oups with markedly different prognoses. In the subgroups based on the preop
erative prognostic score, 5-year recurrence free percentages ranged from 92
% (in the group PS1=1) to 23% (in PS1=4). In the subgroups based on the pos
toperative prognostic score, which took into account the histologic details
of the resected specimen, 5-year recurrence free percentages ranged from 9
5% (in the group PS2=1) to 42% (in PS2=4).
CONCLUSIONS. The proposed subgrouping, which is based on the combined effec
ts of key prognostic preoperative and postoperative factors, provides a pra
ctical prognostic grouping system for the clinician treating patients with
parotid carcinoma. (C) 1999 American Cancer Society.