Institute for Pathology, Hubertus Wald Tumorzentrum-University Cancer Center Hamburg, University Medical Center Hamburg-Eppendorf, Martinistr. 52, 20246 Hamburg, Germany.
Hum Pathol. 2010 Nov;41(11):1577-85. doi: 10.1016/j.humpath.2010.02.018. Epub 2010 Jul 24.
HER-2 is the molecular target for antibody-based treatment of breast cancer (trastuzumab). The potential benefit of anti-HER-2 therapy is currently investigated in several other HER-2 amplified cancers. For example, trastuzumab was recently shown to be effective in HER-2 positive gastric cancer. To address the potential applicability of anti-HER-2 therapy in colorectal cancer, tissue microarray sections and colorectal resection specimens of 1851 colorectal cancers were analyzed for HER-2 overexpression and amplification using FDA approved reagents for immunohistochemistry and fluorescence in situ hybridization. HER-2 amplification was seen in 2.5% and HER-2 overexpression in 2.7% of 1439 interpretable colorectal cancers. Amplification was often high level with HER-2 copies ranging from 4 to 60 per tumor cell and was strongly related to protein overexpression. HER-2 amplification and overexpression were unrelated to histological tumor type, tumor localization, grading, pT, pN, pM or survival. As heterogeneity of drug target expression could represent a major drawback for targeted cancer therapy we next studied HER-2 heterogeneity in selected cases. Extensive evaluation of all available large sections from patients with HER-2 positive colorectal cancer revealed heterogenous findings in 3 of 4 cases. In summary, high-level HER-2 amplification occurs in a small fraction of colorectal cancers. Heterogeneity of amplification may limit the utility of anti- HER-2 therapy in some of these tumors and therefore, adequate clinical trials are needed to further evaluate this approach.
HER-2 是乳腺癌(曲妥珠单抗)抗体治疗的分子靶点。目前正在研究其他几种 HER-2 扩增癌症中的抗 HER-2 治疗的潜在益处。例如,曲妥珠单抗最近已被证明对 HER-2 阳性胃癌有效。为了解决抗 HER-2 治疗在结直肠癌中的潜在适用性,使用美国食品和药物管理局批准的免疫组织化学和荧光原位杂交试剂分析了 1851 例结直肠癌的组织微阵列切片和结直肠切除标本,以检测 HER-2 过表达和扩增。在 1439 例可解释的结直肠癌中,有 2.7%存在 HER-2 过表达,2.5%存在 HER-2 扩增。扩增通常为高水平,HER-2 拷贝数范围为每个肿瘤细胞 4 至 60 个,并且与蛋白过表达强烈相关。HER-2 扩增和过表达与组织学肿瘤类型、肿瘤定位、分级、pT、pN、pM 或生存无关。由于药物靶标表达的异质性可能是靶向癌症治疗的主要缺点,因此我们接下来在选定病例中研究了 HER-2 异质性。对 4 例 HER-2 阳性结直肠癌患者所有可用大切片的广泛评估显示,其中 3 例存在异质性发现。总之,高水平的 HER-2 扩增发生在一小部分结直肠癌中。扩增的异质性可能会限制某些肿瘤中抗 HER-2 治疗的效用,因此需要进行充分的临床试验来进一步评估这种方法。