Background. Survival for rhabdomyosarcoma appears to be more favorable
in children and adolescents compared with adults. To determine the si
gnificance of age at diagnosis as a prognostic indicator in rhabdomyos
arcoma, we performed a retrospective analysis of a combined pediatric
and adult rhabdomyosarcoma data base. Methods. Pertinent prognostic va
riables, including age, TNM stage, histopathologic subtype, anatomic s
ite, resectability, radiation to the primary site, and dose intensity
of chemotherapy, were compared in a Cox proportional hazards model wit
h mortality as the outcome variable. Results. Age at diagnosis (P = 0.
0001) and local tumor invasiveness (P < 0.0001), distant parenchymal m
etastases (P < 0.0001), regional lymph node involvement (P = 0.0027),
and histopathologic subtype (P = 0.0446) contributed information to th
e proportional hazards model. Conclusions. Age at diagnosis is an inde
pendent predictor of outcome in patients with rhabdomyosarcoma along w
ith tumor invasiveness, metastases, regional lymph node involvement, a
nd histopathologic subtype.