VEGF表达与舒尼替尼治疗胃肠道间质瘤患者的良好反应和较长的无进展生存期有关。

Youngil Koh, Hee Eun Lee, Seock-Ah Im, Se-Hyung Kim, Tae Min Kim, Sae-Won Han, Do-Youn Oh, Jee Hyun Kim, Se-Hoon Lee, Dong-Wan Kim, Tae-You Kim, Woo-Ho Kim, Dae Seog Heo, Yung-Jue Bang
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引用次数: 4

摘要

我们打算在接受舒尼替尼治疗的晚期胃肠道间质瘤患者中寻找预测标志物。韩国患者在伊马替尼治疗晚期胃肠道间质瘤失败后接受舒尼替尼治疗。进行KIT和PDGFRA基因分型。对PDGFR-α、PDGFR-β和血管内皮生长因子(VEGF)进行免疫组化染色。共分析22例患者。年龄中位数为55.1岁,男女比例为12:10。舒尼替尼的缓解率为30.4%,中位无进展生存期(PFS)为10.1个月。在单因素分析中,舒尼替尼治疗中,VEGF表达与良好的疗效(P=0.002)和较长的PFS (P=0.020)相关。单因素分析中,CD34 (P=0.023)和PDGFR (P=0.022)表达也与长舒尼替PFS相关。然而,基因型对舒尼替尼的应答率和PFS均无影响。综上所述,VEGF、PDGFR和CD34的表达可能对舒尼替尼治疗有预测价值。
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VEGF expression is related to good response and long progression-free survival in gastrointestinal stromal tumor patients treated with Sunitinib.

We intended to find predictive markers in advanced gastrointestinal stromal tumor patients treated with sunitinib. Korean patients who received sunitinib after imatinib failure for advanced gastrointestinal stromal tumor were studied. Genotyping for KIT and PDGFRA were performed. An immunohistochemical stain for PDGFR-α, PDGFR-β, and vascular endothelial growth factor (VEGF) was performed. A total of 22 patients were analyzed. Their median age was 55.1 years, and the male to female ratio was 12:10. The response rate of sunitinib was 30.4% and the median progression-free survival (PFS) was 10.1 months. In the sunitinib treatment, VEGF expression was related to a favorable response (P=0.002) and long PFS (P=0.020) in univariate analysis. CD34 (P=0.023) and PDGFR (P=0.022) expressions were also related to long sunitinib PFS in univariate analysis. However, the genotype did not affect either response rate or the PFS of sunitinib. In conclusion, expressions of VEGF, PDGFR, and CD34 may have predictive value in sunitinib treatments.

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期刊介绍: Diagnostic Molecular Pathology focuses on providing clinical and academic pathologists with coverage of the latest molecular technologies, timely reviews of established techniques, and papers on the applications of these methods to all aspects of surgical pathology and laboratory medicine. It publishes original, peer-reviewed contributions on molecular probes for diagnosis, such as tumor suppressor genes, oncogenes, the polymerase chain reaction (PCR), and in situ hybridization. Articles demonstrate how these highly sensitive techniques can be applied for more accurate diagnosis.
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