Elsevier

The Annals of Thoracic Surgery

Volume 66, Issue 5, November 1998, Pages 1745-1750
The Annals of Thoracic Surgery

Original Articles
Lewis Y antigen expression and postoperative survival in non–small cell lung cancer

Presented at the Poster session of the Thirty-fourth Annual Meeting of The Society of Thoracic Surgeons, New Orleans, LA, Jan 26–28, 1998.
https://doi.org/10.1016/S0003-4975(98)00937-0Get rights and content

Abstract

Background. In contrast to other Lewis blood group-related antigens, Lewis Y antigen (LeY) has not been fully investigated in non–small cell lung cancer.

Methods. To assess the significance of LeY expression, 236 patients with completely resected pathologic stage 1-3a were reviewed with immunohistochemical analysis.

Results. LeY expression was positive in 179 patients (75.8%). In poorly differentiated cancer, percentage of LeY-positive patients was lower than in moderately to well-differentiated cancer (67.2% versus 81.2%, p = 0.028). Five-year survival rate of LeY-positive patients was 78.2%, significantly higher than that of LeY-negative patients (59.7%, p = 0.001). Combined with p53 status, differences in survival proved to be marked; 5-year survival rate of patients with positive LeY expression and without aberrant p53 expression, was as high as 83.3%, whereas that of patients with negative LeY expression and with aberrant p53 expression was only 38.4% (p < 0.001). Multivariate analysis confirmed that LeY expression was a significant independent factor to predict better survival.

Conclusions. LeY expression is a significant prognostic factor related to grade of cancer differentiation.

Section snippets

Material and methods

A total of 237 consecutive patients with pathologic stage 1–3a NSCLC who underwent complete tumor resection and mediastinal lymph node dissection without chemotherapy nor radiation therapy before operation at the Department of Thoracic Surgery, Chest Disease Research Institute, Kyoto University between January 1, 1985 and December 31, 1990, were reviewed. Complete tumor resection was defined when no microscopic cancers were identified either in the resection margins of the tumor or in the

Expression of LeY

The number of patients for whom the grade of LeY expression was judged (−), (+), (2+), (3+), (4+), or (5+) was 57 (24.2%), 17 (7.2%), 42 (17.8%), 51 (21.6%), 31 (13.1%), and 38 (16.1%), respectively. The 5-year survival rates were 50.2% for (−) group, 79.3% for (1+) group, 80.0% for (2+) group, 74.4% for (3+) group, 76.0% for (4+) group, and 77.6% for (5+) group. The LeY expression (−) group showed significantly worse postoperative prognosis than the other (+), (2+), (3+), (4+), and (5+)

Discussion

During neoplastic transformation, glycosylation may revert to an earlier development form with lung cancer cells reexpressing antigens found on immature embryonic lung cells. The tumor-associated LeY is the focus of the present study and is correlated with postoperative survival.

Several findings have been reported with respect to LeY expression in normal tissue and in cancer tissue since the 1980s, when various kinds of MoAbs against LeY were generated. As for LeY expression in lung cancer,

Acknowledgements

We thank Dr Nobuyuki Hamajima, Division of Epidemiology, Aichi Cancer Institute, Aichi, Japan, for his helpful comment and critical reading of the statistical section of the manuscript.

References (19)

There are more references available in the full text version of this article.

Cited by (29)

  • Fucosyltransferase 4 shapes oncogenic glycoproteome to drive metastasis of lung adenocarcinoma

    2020, EBioMedicine
    Citation Excerpt :

    On the other hand, the clinical significance of fucosyltransferases involved in terminal fucosylation (α1,3- or α1,4- linkage) in lung cancer remains controversial. Past studies have demonstrated aberrant expression of terminal fucosylated epitopes such as Lewis antigens in non-small cell lung cancer tissues [8–10]. Nevertheless, the prognostic values of various Lewis antigens appeared to differ.

View all citing articles on Scopus
View full text