Serum sialyl lewis X-i antigen levels in non-small cell lung cancer: correlation with distant metastasis and survival
To evaluate the correlation between serum levels of sialyl Lewis X-i antigen and distant metastasis and survival in patients with non-small cell lung cancer (NSCLC), we measured the serum levels of the tumor marker in 371 patients with untreated NSCLC. The sialyl Lewis X-i antigen level was measured...
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Published in | Clinical cancer research Vol. 3; no. 4; pp. 495 - 499 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Philadelphia, PA
American Association for Cancer Research
01.04.1997
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Subjects | |
Online Access | Get full text |
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Summary: | To evaluate the correlation between serum levels of sialyl Lewis X-i antigen and distant metastasis and survival in patients
with non-small cell lung cancer (NSCLC), we measured the serum levels of the tumor marker in 371 patients with untreated NSCLC.
The sialyl Lewis X-i antigen level was measured using a RIA kit. In patients with adenocarcinoma or other NSCLC subtypes,
there was a correlation between serum sialyl Lewis X-i antigen and stage of the disease (P = 0.0001 and P = 0.0015, respectively).
Levels of the marker varied significantly depending on the number of metastatic organs in adenocarcinoma (P = 0.0089) and
in other NSCLC subtypes (P = 0.002). Univariate analysis showed that survival of NSCLC patients with high (more than 100 units/ml)
sialyl Lewis X-i antigen levels was significantly poorer than that of patients with low antigen levels (P = 0.0001). Multivariate
analysis using Cox's proportional hazard model showed that high sialyl Lewis X-i antigen levels correlated significantly with
poor survival (P = 0.004). Our data suggest that a high serum level of sialyl Lewis X-i antigen seems to be an indicator of
the presence of metastasis and might indicate the need for a careful investigation of all putative metastatic sites. The serum
levels of sialyl Lewis X-i antigen may reflect the extension of metastasis and would be helpful in considering treatment options. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1078-0432 1557-3265 |