Back to Search Start Over

Efficacy of bevacizumab-containing chemotherapy for non-squamous non-small cell lung cancer with bone metastases.

Authors :
Tokito, Takaaki
Shukuya, Takehito
Akamatsu, Hiroaki
Taira, Tetsuhiko
Ono, Akira
Kenmotsu, Hirotsugu
Naito, Tateaki
Murakami, Haruyasu
Takahashi, Toshiaki
Endo, Masahiro
Yamamoto, Nobuyuki
Source :
Cancer Chemotherapy & Pharmacology. Jun2013, Vol. 71 Issue 6, p1493-1498. 6p.
Publication Year :
2013

Abstract

Purpose: Skeletal-related events (SREs) negatively affect the quality of life of patients with cancer. Vascular endothelial growth factor receptor (VEGFR)-targeted therapy is effective against bone metastasis in animal models, but the clinical efficacy of anti-VEGFR inhibitors against bone metastases remains unclear. Therefore, we aimed to investigate the efficacy of chemotherapy with bevacizumab, an anti-VEGF antibody, against bone metastases. Methods: We retrospectively reviewed consecutive patients with non-squamous non-small cell lung cancer who received first-line platinum-based chemotherapy with zoledronic acid at Shizuoka Cancer Center between 2007 and 2011. Results: Of 25 patients, 13 received bevacizumab-based chemotherapy (BEV group) and 12 received chemotherapy without bevacizumab (non-BEV group). The overall response (54 vs. 8 %, p = 0.01) and disease control (100 vs. 50 %, p = 0.01) rates were higher in the BEV group than in the non-BEV group. The bone-specific response (23 vs. 0 %, p = 0.038) and disease control (100 vs. 67 %, p = 0.01) rates were also higher in the BEV group. The median time to progression (TTP) for bone metastases was higher in the BEV group (13.7 vs. 4.3 months, p = 0.06), whereas that for overall disease was similar between the groups (5.7 vs. 2.6 months, p = 0.17). The proportions of patients with SREs were 23 and 50 % in the BEV and non-BEV groups, respectively ( p = 0.16). Conclusion: Bevacizumab might potentiate the antitumor activity of chemotherapy against systemic disease and bone metastases, prolonging bone-specific TTP and reducing the incidence of SRE. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03445704
Volume :
71
Issue :
6
Database :
Academic Search Index
Journal :
Cancer Chemotherapy & Pharmacology
Publication Type :
Academic Journal
Accession number :
87846483
Full Text :
https://doi.org/10.1007/s00280-013-2148-3