Efficacy and safety of ramucirumab-containing chemotherapy in patients with pretreated metastatic gastric neuroendocrine carcinoma

被引:12
作者
Mishima, Saori [1 ]
Kawazoe, Akihito [1 ]
Matsumoto, Hiroshi [1 ]
Kuboki, Yasutoshi [1 ]
Bando, Hideaki [1 ]
Kojima, Takashi [1 ]
Doi, Toshihiko [1 ]
Ohtsu, Atsushi [1 ]
Yoshino, Takayuki [1 ]
Nonte, Elizabeth M. [2 ]
Chintharlapalli, Sudhakar [3 ]
Nasir, Aejaz [2 ]
Kuwata, Takeshi [4 ]
Shitara, Kohei [1 ]
机构
[1] Natl Canc Ctr Hosp East, Dept Gastrointestinal Oncol, Kashiwa, Chiba, Japan
[2] Eli Lilly & Co, Tailored Therapeut Diagnost & Expt Pathol, Indianapolis, IN 46285 USA
[3] Eli Lilly & Co, Angiogenesis & Tumor Microenvironm Biol, Indianapolis, IN 46285 USA
[4] Natl Canc Ctr Hosp East, Dept Pathol & Clin Labs, Kashiwa, Chiba, Japan
关键词
MULTICENTER; MONOTHERAPY; STOMACH; TUMOR;
D O I
10.1136/esmoopen-2018-000443
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Ramucirumab (RAM), a monoclonal antibody for vascular endothelial growth factor 2 (VEGFR2), has been effective for advanced gastric adenocarcinoma (AC). However, little is known about the efficacy of RAM-containing chemotherapy (RAM-CTx) in gastric neuroendocrine carcinoma (G-NEC). Methods We retrospectively analysed and compared the clinical outcomes of patients (pts) with G-NEC receiving RAM-CTx, G-NEC receiving CTx without RAM and AC receiving RAM-CTx in our hospital. G-NEC was defined by neuroendocrine carcinoma features, regardless of the proportion, based on histology and neuroendocrine markers (synaptophysin, chromogranin A or CD56). VEGFR2 expression in tumour vessels was evaluated in archival primary 6-NEC tissues by immunohistochemistry using the same anti-VEGFR2 primary antibody and scoring scheme (vascular VEGFR2 H-score) as in the REGARD trial. Results Seventeen G-NEC receiving RAM-CTx, 13 G-NEC receiving CTx without RAM and 173 AC pts receiving RAM CTx were analysed. The overall response rate (59% vs 8 % vs 28%), progression-free survival (median 7.7 vs 1.8 vs 3.3 months) and overall survival (median 16.1 vs 8.6 vs 9.6 months) were significantly better in pts with G-NEC receiving RAM-CTx than G-NEC receiving CTx without RAM or AC receiving RAM-CTx. No severe or unexpected adverse events occurred. The median vascular VEGFR2 H-score, based on available G-NEC tissues from 12 pts receiving RAM-CTx, was 220 (range 150-260), which was markedly higher than that reported on AC tissues from the REGARD trial as historical control (median 35, range 0-240). Conclusions RAM-CTx showed a promising activity without severe or unexpected safety profile in pts with G-NEC. This may in part be explained by higher vascular VEGFR2 expression in G-NEC tissues.
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页数:7
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