Advertisement for orthosearch.org.uk
Orthopaedic Proceedings Logo

Receive monthly Table of Contents alerts from Orthopaedic Proceedings

Comprehensive article alerts can be set up and managed through your account settings

View my account settings

Visit Orthopaedic Proceedings at:

Loading...

Loading...

Full Access

1.P.13 THE PROGNOSTIC ROLE OF THE EXTRACELLULAR DOMAIN OF HER-2 AND ITS USEFULNESS FOR TREATMENT MONITORING IN OSTEOSARCOMA



Abstract

Serum level of the extracellular domain of HER-2 (ECD/HER2) has been suggested to be a tumor marker in breast cancer. The aim of this study was to assess the prognostic value of baseline level of ECD/HER2 and changes in levels over time in children and adults with osteosarcoma during chemotherapy.

Materials and methods: We analysed 33 newly-diagnosed osteosarcoma patients treated at the Department of Paediatric Oncological Surgery of the Institute of Mother and Child, Warsaw, Poland between 2005–2008. Patients characteristics: age 8–18 years (median 15); staging at diagnosis: disease localised (18) and dissemination (15); disease progression (13); deaths (6). Follow-up: 8–37 months (median 19). ECD/HER2 was measured in 118 serum samples using a validated ELISA kit: at the time of diagnosis (1), after preoperative chemotherapy (2), 2 weeks after surgery (3) and 3–6 moths after surgery (4).

Results: The baseline level of ECD/HER-2 in serum ranged 3.8–34.4 ng/mL (median 5). The elevated baseline ECD/HER2 was associated with decreased progression free survival (ECD/HER2 ng/mL> 5 vs ECD/HER2 ng/mL≤5: 44% vs 77%; p=0.039) and decreased overall survival (ECD/HER2 ng/mL> 5 vs ECD/HER2 ng/mL≤5: 69% vs 94%, p=0.115). The concentration of ECD/HER2> 6 ng/ml during treatment (specially postoperative chemotherapy) was associated with early disease progression (p=0.095).

Conclusions: The high level of ECD/HER2 at the time of diagnosis may be a marker of poor prognosis in osteosarcoma. Additionally, we suggest that changes of this marker concentration over time could be helpful for treatment monitoring.

Correspondence should be addressed to Professor Stefan Bielack, Olgahospital, Klinikum Stuttgart, Bismarkstrasse 8, D-70176 Stuttgart, Germany. Email: s.bielack@klinikum_stuttgart.de