2003
DOI: 10.1016/s0002-9270(03)00128-x
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Usefulness of gastric cancer screening using the serum pepsinogen test method

Abstract: The pepsinogen test method can be used as a screening test for high-risk subjects with atrophic gastritis, rather than as a tool for cancer itself. Systemic endoscopic surveillance of this group is also useful.

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Cited by 67 publications
(112 citation statements)
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“…[15] In a cohort study, mass screening for gastric cancer was performed using both serum PG measurements and X-ray methods; 23.6% of those screened by serum PG measurements, and 11.7% screened by X-ray, required further endoscopic screening. [16] In total, 10 gastric cancers were detected. The measurement of serum PG showed a higher rate of gastric cancer detection (0.18%) than the X-ray method (0.05%).…”
Section: Discussionmentioning
confidence: 99%
“…[15] In a cohort study, mass screening for gastric cancer was performed using both serum PG measurements and X-ray methods; 23.6% of those screened by serum PG measurements, and 11.7% screened by X-ray, required further endoscopic screening. [16] In total, 10 gastric cancers were detected. The measurement of serum PG showed a higher rate of gastric cancer detection (0.18%) than the X-ray method (0.05%).…”
Section: Discussionmentioning
confidence: 99%
“…One study showed that when pepsinogen-I <50 ng/ml and the pepsinogen-I/II ratio <3 were taken to indicate extensive atrophic gastritis, the percentage of those screened who needed further examination was 19.5%. The cancer detection rate was 0.28%, and 83% of the cancers detected by the pepsinogen test were of the intestinal type [30]. Thus, the pepsinogen test is extremely useful for detecting the well-differentiated histological type (very similar to the intestinal type) of gastric carcinoma in asymptomatic subjects with small, early, intestinal-type cancers, particularly in Japan, where the incidence of gastric atrophy is extremely high.…”
Section: Discussionmentioning
confidence: 99%
“…In addition, fasting pepsinogen (PG) I and II levels were assayed using the chemiluminescence enzyme immunoassay for determination of serum atrophy in patients who did not have a history of use of antacids within the previous 2 weeks [21]. Serum samples were collected before ESD.…”
Section: Methodsmentioning
confidence: 99%