首页> 外文期刊>Journal of Clinical Oncology >Immunoglobulin G fragment C receptor polymorphisms and clinical efficacy of trastuzumab-based therapy in patients with HER-2eu-positive metastatic breast cancer.
【24h】

Immunoglobulin G fragment C receptor polymorphisms and clinical efficacy of trastuzumab-based therapy in patients with HER-2eu-positive metastatic breast cancer.

机译:免疫球蛋白G片段C受体多态性与基于曲妥珠单抗的治疗在HER-2 / neu阳性转移性乳腺癌患者中的临床疗效。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

PURPOSE: The anti-HER-2eu monoclonal antibody trastuzumab has been shown to engage both activatory (fragment C receptor [Fc gamma R]IIIa; Fc gamma RIIa) and inhibitory (Fc gamma RIIb) antibody receptors and Fc gamma R polymorphisms have been identified that may affect the antibody-dependent cell-mediated cytotoxicity (ADCC) of natural-killer cells/monocytes. In this study, we tested whether Fc gamma R polymorphisms are associated with clinical outcome of patients with breast cancer who received trastuzumab. PATIENTS AND METHODS: Fifty-four consecutive patients with HER-2eu-amplified breast cancer receiving trastuzumab plus taxane for metastatic disease were evaluated for genotype for the Fc gamma RIIIa-158 valine(V)/phenylalanine(F), Fc gamma RIIa-131 histidine(H)/arginine(R), and Fc gamma RIIb-232 isoleucine(I)/threonine(T) polymorphisms. Trastuzumab-mediated ADCC of patients' peripheral blood mononuclear cells (PBMCs) was measured by chromium-51 release using a HER-2eu-expressing human breast cancer cell line as a target. Controls comprised thirty-four patients treated with taxane alone. RESULTS: Our population was in Hardy-Weinberg equilibrium except for the Fc gamma RIIb polymorphism. The Fc gamma RIIIa-158 V/V genotype was significantly correlated with objective response rate (ORR) and progression-free survival (PFS). Also, there was trend significance in ORR and PFS for the Fc gamma RIIa-131 H/H genotype. The combination of the two favorable genotypes (VV and/or H/H) was independently associated with better ORR and PFS compared with the other combinations. The ADCC analysis showed that V/V and/or H/H PBMCs had a significantly higher trastuzumab-mediated cytotoxicity than PBMCs harboring different genotypes. CONCLUSION: These data support for the first time the hypothesis that Fc gamma R-mediated ADCC plays an important role in the clinical effect of trastuzumab. Prospective studies are needed to confirm the role of Fc gamma R polymorphisms in predicting clinical outcome of patients with breastcancer treated with trastuzumab-based therapy.
机译:用途:抗HER-2 / neu单克隆抗体曲妥珠单抗已被证明与激活性(片段C受体[FcγR] IIIa; FcγRIIa)和抑制性(FcγRIIb)抗体受体结合,FcγR多态性具有已经鉴定出可能影响天然杀伤细胞/单核细胞的抗体依赖性细胞介导的细胞毒性(ADCC)。在这项研究中,我们测试了FcγR多态性是否与接受曲妥珠单抗的乳腺癌患者的临床结局相关。病人和方法:对连续连续接受转移性疾病接受曲妥珠单抗加紫杉烷治疗的HER-2 / neu扩增乳腺癌的54例患者进行了FcγRIIIa-158缬氨酸(V)/苯丙氨酸(F),FcγRIIa的基因型分析。 -131组氨酸(H)/精氨酸(R)和FcγRIIb-232异亮氨酸(I)/苏氨酸(T)多态性。曲妥珠单抗介导的患者外周血单核细胞(PBMC)的ADCC通过以表达HER-2 / neu的人类乳腺癌细胞系为靶标的铬51释放进行测量。对照组包括仅用紫杉烷治疗的34名患者。结果:除FcγRIIb多态性外,我们的人群处于Hardy-Weinberg平衡状态。 FcγRIIIa-158 V / V基因型与客观应答率(ORR)和无进展生存期(PFS)显着相关。同样,对于FcγRIIa-131H/ H基因型,ORR和PFS也具有趋势意义。与其他组合相比,两种有利基因型(VV和/或H / H)的组合与更好的ORR和PFS独立相关。 ADCC分析表明,与具有不同基因型的PBMC相比,V / V和/或H / H PBMC具有显着更高的曲妥珠单抗介导的细胞毒性。结论:这些数据首次支持了FcγR介导的ADCC在曲妥珠单抗的临床作用中起重要作用的假说。需要进行前瞻性研究来证实FcγR多态性在预测接受曲妥珠单抗治疗的乳腺癌患者的临床结局中的作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号