| Literature DB >> 26686298 |
Cike Peng1,2, Markus Wallwiener3,4, Anja Rudolph5, Katarina Ćuk1,2, Ursula Eilber5, Muhabbet Celik5, Caroline Modugno3,4, Andreas Trumpp6,7, Jörg Heil3, Frederik Marmé2, Dharanija Madhavan1,2, Juliane Nees3,4, Sabine Riethdorf8, Sarah Schott3, Christof Sohn3, Klaus Pantel8, Andreas Schneeweiss3,4, Jenny Chang-Claude5, Rongxi Yang1,2, Barbara Burwinkel1,2.
Abstract
Conventional tumor markers have limited value for prognostication and treatment monitoring in metastatic breast cancer (MBC) patients and novel circulating tumor markers therefore need to be explored. Hyaluronic acid (HA) is a major macropolysaccharide in the extracellular matrix and is reported to be associated with tumor progression. In our study, we investigated plasma HA level with respect to progression free survival (PFS) and overall survival (OS), as well as the treatment monitoring value in MBC patients. The prognostic value of plasma HA level was investigated in a discovery cohort of 212 MBC patients with 2.5-year follow-up and validated in an independent validation cohort of 334 patients with 5-year follow-up. The treatment monitoring value of plasma HA level was investigated in 61 MBC patients from discovery cohort who had been radiographically examined after first complete cycle of chemo therapy. We found a robust association between high plasma HA level and poor prognosis of MBC patients in both discovery (pPFS = 7.92 × 10(-6) and pOS = 5.27 × 10(-5)) and validation studies (pPFS = 3.66 × 10(-4) and pOS = 1.43 × 10(-4)). In the discovery cohort, the plasma HA level displayed independent prognostic value after adjusted for age and clinicopathological factors, with respect to PFS and OS. Further, the decrease of plasma HA level displayed good concordance with treatment response evaluated by radiographic examination (AUC = 0.79). Plasma HA level displays prognostic value, as well as treatment monitoring value for MBC patients.Entities:
Keywords: biomarker; hyaluronic acid; metastatic breast cancer; plasma; prognosis
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Year: 2016 PMID: 26686298 DOI: 10.1002/ijc.29975
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396