Non-invasive diagnosis of gastric adenocarcinoma (GAC) is usually diff
icult due to the low sensitivity and specificity of serologic markers,
including pepsinogens and gastrin. For the improvement of the diagnos
tic values of these markers, a ''recursive partitioning and amalgamati
on'' algorithm was employed to construct a decision protocol. A total
of 636 subjects including 161 healthy subjects, 163 patients with GAG,
196 with gastric ulcer and 116 with duodenal ulcer were enrolled Seru
m levels of gastrin, pepsinogen I, pepsinogen II, and the ratio of pep
sinogen I / pepsinogen II were determined for each of the subjects. Th
e proposed ''decision tree'' classifies subjects into five subgroups w
ith different risks of GAC and peptic ulcer, based on the information
of age, serum pepsinogen and gastrin levels. Using this novel analysis
system, an expected probability of GAC or ulcers could be obtained Pa
tients with an age > 62 years and a serum level of pepsinogen I less t
han or equal to 33 ng/ml were strongly indicated for further confirmat
ory tests of GAC. This tree-structured analysis is also helpful in cla
rifying the interactions between various serologic markers and demogra
phic factors.