Musolino Antonino, Naldi Nadia, Bortesi Beatrice, Pezzuolo Debora, Capelletti Marzia, Missale Gabriele, Laccabue Diletta, Zerbini Alessandro, Camisa Roberta, Bisagni Giancarlo, Neri Tauro Maria, Ardizzoni Andrea
Medical Oncology Unit, University Hospital of Parma, via Gramsci 14, 43100 Parma, Italy.
J Clin Oncol. 2008 Apr 10;26(11):1789-96. doi: 10.1200/JCO.2007.14.8957. Epub 2008 Mar 17.
The anti-HER-2/neu 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.
Fifty-four consecutive patients with HER-2/neu-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-2/neu-expressing human breast cancer cell line as a target. Controls comprised thirty-four patients treated with taxane alone.
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.
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 breast cancer treated with trastuzumab-based therapy.
抗HER-2/neu单克隆抗体曲妥珠单抗已被证明可与激活型(C片段受体[FcγR]IIIa;FcγRIIa)和抑制型(FcγRIIb)抗体受体结合,并且已鉴定出可能影响自然杀伤细胞/单核细胞的抗体依赖性细胞介导的细胞毒性(ADCC)的FcγR多态性。在本研究中,我们测试了FcγR多态性是否与接受曲妥珠单抗治疗的乳腺癌患者的临床结局相关。
对54例连续接受曲妥珠单抗加紫杉烷治疗转移性疾病的HER-2/neu扩增乳腺癌患者进行了FcγRIIIa-158缬氨酸(V)/苯丙氨酸(F)、FcγRIIa-131组氨酸(H)/精氨酸(R)和FcγRIIb-232异亮氨酸(I)/苏氨酸(T)多态性的基因分型评估。使用表达HER-2/neu的人乳腺癌细胞系作为靶标,通过51铬释放法测量患者外周血单核细胞(PBMC)的曲妥珠单抗介导的ADCC。对照组包括34例仅接受紫杉烷治疗的患者。
除FcγRIIb多态性外,我们的研究人群处于哈迪-温伯格平衡。FcγRIIIa-158 V/V基因型与客观缓解率(ORR)和无进展生存期(PFS)显著相关。此外,FcγRIIa-131 H/H基因型在ORR和PFS方面也有趋势性意义。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,V/V和/或H/H PBMC的曲妥珠单抗介导的细胞毒性明显高于具有不同基因型的PBMC。
这些数据首次支持了FcγR介导的ADCC在曲妥珠单抗的临床疗效中起重要作用这一假设。需要进行前瞻性研究以证实FcγR多态性在预测接受曲妥珠单抗治疗的乳腺癌患者临床结局中的作用。