An enzyme immunoassay for NuMA was evaluated in a retrospective clinical st
udy for its potential utility in the detection of colorectal cancer. The co
ncentrations of NuMA and CEA (Abbott IMx) were measured in sera from 86 pat
ients (presurgical) with colorectal cancer, 72 subjects with benign gastroi
ntestinal diseases, 80 subjects with risk factors for colorectal cancer, an
d 141 age-matched healthy subjects. Reference values for NuMA and CEA were
calculated by two methods: 95% cumulative distribution and ROC analyses ver
sus healthy subjects. By the first method, NuMA and CEA both had approximat
ely 20% sensitivity for colorectal cancel: By the second method (which gene
rated lower reference values), NuMA was more sensitive than CEA for colorec
tal cancer. This improved sensitivity was most evident in Dukes B subjects.
By either analysis method, NuMA was more sensitive than CEA for subjects a
t risk for developing colorectal cancer whereas CEA was more specific for b
enign gastrointestinal diseases.