Efficacy of bevacizumab-containing chemotherapy for non-squamous non-small cell lung cancer with bone metastases
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  • 作者:Takaaki Tokito (1)
    Takehito Shukuya (1)
    Hiroaki Akamatsu (1)
    Tetsuhiko Taira (1)
    Akira Ono (1)
    Hirotsugu Kenmotsu (1)
    Tateaki Naito (1)
    Haruyasu Murakami (1)
    Toshiaki Takahashi (1)
    Masahiro Endo (2)
    Nobuyuki Yamamoto (1)
  • 关键词:Bone metastases ; Skeletal ; related event ; Bevacizumab ; Chemotherapy
  • 刊名:Cancer Chemotherapy and Pharmacology
  • 出版年:2013
  • 出版时间:June 2013
  • 年:2013
  • 卷:71
  • 期:6
  • 页码:1493-1498
  • 全文大小:180KB
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  • 作者单位:Takaaki Tokito (1)
    Takehito Shukuya (1)
    Hiroaki Akamatsu (1)
    Tetsuhiko Taira (1)
    Akira Ono (1)
    Hirotsugu Kenmotsu (1)
    Tateaki Naito (1)
    Haruyasu Murakami (1)
    Toshiaki Takahashi (1)
    Masahiro Endo (2)
    Nobuyuki Yamamoto (1)

    1. Division of Thoracic Oncology, Shizuoka Cancer Center Hospital, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka, 411-8777, Japan
    2. Division of Diagnostic Radiology, Shizuoka Cancer Center, Nagaizumi-cho, Sunto-gun, Shizuoka, Japan
  • ISSN:1432-0843
文摘
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.

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