z-logo
Premium
The liberated domain I of urokinase plasminogen activator receptor – a new tumour marker in small cell lung cancer
Author(s) -
Almasi Charlotte E.,
Drivsholm Lars,
Pappot Helle,
HøyerHansen Gunilla,
Christensen Ib J.
Publication year - 2013
Publication title -
apmis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.909
H-Index - 88
eISSN - 1600-0463
pISSN - 0903-4641
DOI - 10.1111/j.1600-0463.2012.02955.x
Subject(s) - urokinase receptor , hazard ratio , lung cancer , proportional hazards model , medicine , supar , oncology , receptor , cancer research , urokinase , confidence interval
The prognosis of small cell lung cancer ( SCLC ) remains poor with a 5‐year survival rate of 4–6%. In non‐small cell lung cancer ( NSCLC ), high levels of intact and cleaved forms of the receptor for urokinase plasminogen activator ( uPAR ) are significantly associated with short overall survival. Our aim was therefore to determine the prognostic value of the different uPAR forms in blood from SCLC patients. Serum samples from 92 treatment naive SCLC patients were analysed. Intact uPAR , uPAR (I–III), intact and cleaved uPAR , uPAR (I–III) +  uPAR (II–III) and the liberated domain I, uPAR (I) were measured using time‐resolved fluorescence immunoassays ( TR ‐ FIA 1–3). Assessment of association of the uPAR forms to overall survival ( OS ) was done using Cox regression analysis adjusted for clinical covariates [age, gender, stage, lactate dehydrogenase ( LDH ), WHO performance status ( PS )]. Multivariate survival analysis demonstrated that high levels of uPAR (I) were significantly (p = 0.009) associated with short overall survival ( OS ). Patients with uPAR (I) levels above the second tertile had a hazard ratio ( HR ) of 1.9 (95% confidence interval ( CI ): 1.1–3.3), compared to patients with levels below the first tertile. High serum uPAR (I) levels are associated with short OS in SCLC patient, independent of LDH and PS .

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here