SAN FRANCISCO—The biologic marker matrix metalloproteinase-9 (MMP-9) has been identified as an important new predictor of disease recurrence and poor outcome in non-small-cell lung cancer (NSCLC). It also offers some insight into the mechanisms by which NSCLC tumors grow and spread.
Eckart Laack, MD, of the University Hospital Hamburg-Eppendorf, Hamburg, Germany, reported the results at the 37th Annual Meeting of the American Society of Clinical Oncology (ASCO abstract 1645). The study involved 118 NSCLC patients (50 with stage I/II disease, 27 with stage IIIA/B disease, and 41 with stage IV disease).
The investigators measured pretreatment serum levels of two factors, both of which play an important role in the angiogenic process: (1) MMP-9, which degrades basement membrane type IV collagen(Drug information on collagen), allowing angiogenesis and, by implication, tumor invasion and metastasis, and (2) vascular endothelial growth factor (VEGF), the most potent growth factor and a positive regulator of angiogenesis in a majority of malignancies.
The study showed that serum levels of MMP-9 were significantly correlated with tumor stage. Patients with early disease had a median MMP-9 level of 910 ng/mL, compared with 1,340 ng/mL for those with locally advanced disease and 1,796 ng/mL for those with metastatic disease (P = .005).
Patients who died during the first year had significantly higher pretreatment levels of MMP-9 (1,796 ng/mL) than those who survived 1 year (989 ng/mL, P = .0005).
The median serum level for MMP-9 for all patients was 1,293 ng/mL. Levels of MMP-9 in excess of 2,300 ng/mL carried a very poor prognostic indication, Dr. Laack said. These patients had a median survival of 278 days vs 587 days for those with levels less than 1,200 ng/mL.
Besides performance status, the only independent prognostic factor in multivariate analysis was the pretreatment serum level of MMP-9. Stage, histologic type, sex, age, and lactate dehydrogenase, hemoglobin, and VEGF levels had no effect on survival.
