Journal of Clinical Oncology, Vol 12, 1648-1658, Copyright © 1994 by American Society of Clinical Oncology
Plasminogen activator inhibitor-1 and prognosis in primary breast cancer
JA Foekens, M Schmitt, WL van Putten, HA Peters, MD Kramer, F Janicke and JG Klijn
Department of Medical Oncology, Dr Daniel den Hoed Cancer Center, Rotterdam, The Netherlands.
PURPOSE: Evaluation of the relationship between plasminogen activator
inhibitor-1 (PAI-1) and the metastatic potential of primary breast cancer,
and to compare the prognostic impact of PAI-1 in multivariate analysis with
those of conventional prognostic factors, including steroid-hormone
receptors, and those of urokinase plasminogen activator (uPA), pS2-protein
(PS2), and cathepsin D. PATIENTS AND METHODS: Cell biologic prognostic
factors were analyzed in 657 cytosols routinely prepared from frozen-tissue
biopsies that were submitted to our laboratory for the assessment of
steroid-hormone receptor status. The median duration of follow-up in
patients still alive at the time of analysis was 48 months. Estrogen
receptor (ER) and progesterone receptor (PgR) status were assessed by
radioligand binding assay, PS2, and cathepsin D by radiometric immunoassay,
and uPA and PAI-1 by enzyme- linked immunosorbent assay (ELISA). RESULTS:
PAI-1 levels were found to be strongly positively correlated with the rates
of relapse (P < .0001) and death (P < .001). Relating the levels of
PAI-1 with those of other cytosolic prognostic factors, we found a positive
association with the metastasis-related proteases uPA (P < .0001) and
cathepsin D (P < .0001). On the other hand, PAI-1 levels were found to
be negatively correlated with ER (P < .005) and PgR (P < .001), and
the estrogen- regulated pS2-protein (P < .001), which are proteins
associated with a favorable prognosis. In multivariate regression analysis
for 5-year relapse-free survival, and using an optimized cutoff point for
discrimination between PAI-1-positive and -negative, independent predictors
of the rate of relapse were found to be PAI-1 (P < .0001) and uPA (P =
.01) of the cytosolic parameters, and tumor size, lymph node status, and
premenopausal age of the clinical parameters. In multivariate analysis in
patients with node-negative disease, only PAI- 1 (P < .001) and tumor
size (P = .03) were positively and premenopausal age negatively (P <
.001) associated with the rate of relapse. In patients with node-positive
disease, PAI-1 (P < .001), uPA (P = .02), tumor size (P < .001), and
the number of positive lymph nodes (P < .001) were all positively
associated with the rate of relapse. CONCLUSION: We conclude that the PAI-1
level measured in routinely prepared cytosols is an important parameter to
predict the metastatic potential in both node-negative and node-positive
human primary breast cancer.

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