Plasma matrix metalloproteinases 7 and 9 in patients with metastatic breast cancer treated with marimastat or placebo: Eastern cooperative oncology group trial E2196

被引:6
|
作者
Zucker, Stanley
Wang, Molin
Sparano, Joseph A.
Gradishar, William J.
Ingle, James N.
Davidson, Nancy E.
机构
[1] Montefiore Med Ctr, Albert Einstein Canc Ctr, Weiler Div, Bronx, NY 10461 USA
[2] Vet Affairs Med Ctr, Northport, NY USA
[3] SUNY Stony Brook, Stony Brook, NY 11794 USA
[4] Dana Farber Canc Inst, Boston, MA 02115 USA
[5] Northwestern Univ, Chicago, IL 60611 USA
[6] Mayo Clin, Rochester, MN USA
[7] Johns Hopkins, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
关键词
matrix metalloproteinase inhibitors; phase III trials; survival;
D O I
10.3816/CBC.2006.n.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The purpose of this study was to evaluate the prognostic and predictive utility of measuring plasma levels of matrix metalloproteinase (MMP)-7 and MMP-9 in patients with metastatic breast cancer (MBC) treated with the oral MMP inhibitor (MMPI) marimastat or a placebo. Patients and Methods: We measured plasma levels of MMP-7 and MMP-9 using an enzyme-linked immunoassay method in 140 evaluable patients with MBC enrolled on a multicenter clinical trial that compared the MMPI marimastat with placebo. Specimens were collected after completion of first-line chemotherapy in patients who had responding or stable disease and 3, 6, and 12 months after initiation of marimastat (10 mg orally twice daily) or placebo. Results: Baseline plasma MMP-7 and MMP-9 levels did not correlate with each other or with progression-free or overall survival. In addition, serial evaluation of plasma MMP-7 and MMP-9 levels revealed no significant changes over time in the marimastat or placebo groups or any correlation with trough plasma marimastat level. Conclusion: We conclude that measurement of plasma MMP-7 or MMP-9 levels, as performed in our trial, was not a useful prognostic or predictive factor in patients with MBC or in patients treated with an MMPI.
引用
收藏
页码:525 / 529
页数:5
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