Evaluation of Trastuzumab Anti-Tumor Efficacy and its Correlation with HER-2 Status in Patient-Derived Gastric Adenocarcinoma Xenograft Models

被引:5
作者
Chen, Hao [1 ]
Ye, Qingqing [2 ]
Lv, Jing [2 ]
Ye, Peng [2 ]
Sun, Yun [2 ]
Fan, Shuqiong [2 ]
Su, Xinying [2 ]
Gavine, Paul [2 ]
Yin, Xiaolu [2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Ren Ji Hosp, Dept Gen Surg, Shanghai 200127, Peoples R China
[2] AstraZeneca R&D, Dept Translat Sci Asia & Emerging Market iMed, Shanghai 201203, Peoples R China
关键词
HER2; Gastric carcinoma; Trastuzumab; Xenograft model antitumor assays; Fluorescence in situ hybridization; Immunohistochemistry; IN-SITU HYBRIDIZATION; GENE AMPLIFICATION; PROTEIN EXPRESSION; CANCER; EPIDEMIOLOGY; ESOPHAGEAL; MANAGEMENT; THERAPY; BIOLOGY; MOUSE;
D O I
10.1007/s12253-015-9909-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of the study was to investigate trastuzumab anti-tumor efficacy and its correlation with HER-2 status in primary xenograft models derived from Chinese patients with gastric adenocarcinoma. Patient-derived gastric adenocarcinoma xenograft (PDGAX) mouse models were firstly generated by implanting gastric adenocarcinoma tissues from patients into immune deficient mice. A high degree of histological and molecular similarity between the PDGAX mouse models and their corresponding patients' gastric adenocarcinoma tissues was shown by pathological observation, HER-2 expression, HER-2 gene copy number, and mutation detection. Based on Hoffmann's criteria in gastric cancer, three models (PDGAX001, PDGAX003 and PDGAX005) were defined as HER-2 positive with fluorescence in situ hybridization (FISH) amplification or immunohistochemistry (IHC) 2+/ 3+, while two models (PDGAX002, PDGAX004) were defined as HER-2 negative. Upon trastuzumab treatment, significant tumor regression (105 % TGI) was observed in model PDGAX005 (TP53 wt), while moderate sensitivity (26 % TGI) was observed in PDGAX003, and resistance was observed in PDGAX001, 002 and 004. A significant increase in HER-2 gene copy number was only observed in PDGAX005 (TP53 wt). Interestingly, trastuzumab showed no efficacy in PDGAX001 (HER2 IHC 3+ and FISH amplification, but with mutant TP53). Consistent with this finding, phosphor-HER2 modulation by trastuzumab was observed in model PDGAX005, but not in PDGAX001.
引用
收藏
页码:947 / 955
页数:9
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