Tumor type M2 pyruvate kinase expression in advanced breast cancer

Citation
D. Luftner et al., Tumor type M2 pyruvate kinase expression in advanced breast cancer, ANTICANC R, 20(6D), 2000, pp. 5077-5082
Citations number
17
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
ANTICANCER RESEARCH
ISSN journal
02507005 → ACNP
Volume
20
Issue
6D
Year of publication
2000
Pages
5077 - 5082
Database
ISI
SICI code
0250-7005(200011/12)20:6D<5077:TTMPKE>2.0.ZU;2-B
Abstract
Background: Recently, a high validity correlation of the tumor M2 pyruvate kinase (Tu M2-PK) isoenzyme in comparison to standard tumor markers has bee n demonstrated in solid tumors. We investigated this markers in 67 patients with advanced breast cancer (ABC) in comparison to healthy controls. Mater ials and Methods: Plasma Tu M2-PK was measured using an ELISA assay (ScheBo (R) Tech Giessen, Germany) while serum CA27.29 was determined using a chemi luminescent immunoassay (Bayer Diagnostics Tarrytown, USA). Results: In a R OC analysis, the art-off to discriminate patients from controls was establi shed at 15 U/ml for Tu M2-PK (specificity 85%; positive predictive value 81 %) and 30 U/ml for CA27.29 (specificity 91%; positive predictive value 92%) . Median ABC baseline levels (ranges) in patients with ABC Sol Ttl M2-PK an d CA27.29 were 12.8 U/ml (4.8-252495) and 130 U/ml (13.3-8130), respectivel y. Response assessment was done in 45 chemotherapy courses of 35 pts. In 13 out of 19 blocks (68.4%) with PD (progressive disease), an elevated level of Tu M2-PK at baseline ol in the follow-lip was found In 17 out of 20 bloc k (85%) with SD (stable disease), the Tn M2-PK level was normal at baseline ol normalised within 4 week of treatment. All 6 patients with disease remi ssion had a normal baseline Tn M2-PK level or the levels decreased promptly . Conclusion: Tu M2-PK gives additional information about ABC, indicating d isease activity and sensitivity to chemotherapy while CA27.29 reflects tumo r burden.