Serum uric acid as a surrogate marker of favorable response to bevacizumab treatment in patients with metastatic colon cancer

Yükleniyor...
Küçük Resim

Tarih

2016

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

Springer

Erişim Hakkı

info:eu-repo/semantics/openAccess

Özet

Bevacizumab is a monoclonal antibody which is a vascular endothelial growth factor inhibitor. It obscures vascularization of tumor tissue and damages intratumoral microcirculation. The damaged intratumoral microcirculation leads to tissue hypoxia and results in increase of uric acid level. The main aim of our study was to investigate the relationship between uric acid change and response to bevacizumab therapy. This study included a total of 158 patients with metastatic colorectal cancer who had received bevacizumab therapy. The number of male patients was 100 (63.3 %) while female patients number was 58 (37.7 %). The median age was 61 (29-83). There was relationship between increase of uric acid level of third month uric acid level and stable disease (p < 0.001). There was a significant overall survival increased in the group with increased uric acid level (p < 0.001). The decline of CEA level was related to uric acid level (p < 0.022). In conclusion, this study is the first showing significant increases of serum uric acid in patients with metastatic colorectal cancer who favorably responded to chemotherapy with bevacizumab. But further studies are justified to test whether monitoring uric acid levels might predict clinical outcomes of patients with metastatic colorectal cancer.

Açıklama

WOS: 000385182500005
PubMed ID: 26781472

Anahtar Kelimeler

Bevacizumab, Uric Acid, Hypoxia, Metastatic Colorectal Cancer, Carcinoembryonic Antigen, Survival

Kaynak

Clinical & Translational Oncology

WoS Q Değeri

Q3

Scopus Q Değeri

Q2

Cilt

18

Sayı

11

Künye

Selçukbiricik, F., Kanbay, M., Solak, Y., Bilici, A., Kanıtez, M., Balık, E. ... Mandel, N. M. (2016). Serum uric acid as a surrogate marker of favorable response to bevacizumab treatment in patients with metastatic colon cancer. Clinical & Translational Oncology, 18(11), 1082-1087. https://dx.doi.org/10.1007/s12094-016-1485-1