Pulmonary toxicity is a rare but well described side effect of mitomyc
in C (MMC). We describe 14 cases of MMC pulmonary toxicity that were d
etected in four clinical trials performed at The Mayo Clinic using MMC
-containing regimens for nonsmall cell lung cancer (NSCLC) and by revi
ewing the charts of patients treated at The Mayo Clinic with MMC-conta
ining regimens for NSCLC from 1976 to 1995. The median age was 61 (ran
ge 44-84) years, with an M:F ratio of 1:1. The median number of cycles
of MMC to develop toxicity was four (range two to five) with a median
cumulative dose of MMC of 29 mg/m(2). MMC toxicity occurred despite p
re-medication with corticosteroids in 11 patients. At diagnosis of MMC
lung toxicity, the median diffusing lung capacity (DLCO) was 9 and-Pa
O2 was 49 mm Hg. Of those having bronchoscopy, four patients had pulmo
nary histologic changes consistent with lung injury. Two patients had
bronchioalveolar lavages that were nondiagnostic. All patients respond
ed initially to corticosteroids, but approximately 40% had progressive
pulmonary insufficiency despite high doses of corticosteroids. This c
hronic, progressive phase of MMC lung toxicity is a largely underestim
ated sequelae of MMC.