Thor A
Department of Pathology, Northwestern University Medical School, Chicago, Illinois, USA.
Ann Oncol. 2001;12 Suppl 1:S101-7. doi: 10.1093/annonc/12.suppl_1.s101.
HER2 (neu, erbB-2), a receptor related to the human epidermal growth factor receptor, has now become more important as a predictive marker of treatment response. While the value and direction of the treatment/HER2 interaction may vary, depending on the agents, dose, or schedule of drug administration, there is little disagreement that HER2 testing is an important part of breast cancer evaluation. In 1998, trastuzumab (Herceptin) was approved for the treatment of HER2-positive metastatic breast cancer patients by the Food and Drug Administration of the USA. Patients with abnormal HER2 in their breast cancer cells (generally 2 or 3+ with the HercepTest, overexpression by other immunohistochemical assays or amplification by fluorescence in situ hybridization [FISH] assay) have demonstrated the greatest response to trastuzumab treatment. It is unclear which test (method, reagent, cut-off points, etc.) is best to use to evaluate HER2 for this purpose because parallel testing of the same cancers from patients who received trastuzumab has only recently been initiated and the data are limited. It is widely believed that breast cancers without HER2 alterations will not be responsive to trastuzumab, although a clinical trial to test this specific hypothesis has not been initiated. There are also concerns that clonal heterogeneity for HER2 within a tumor, or between primary and metastatic cancer foci, may affect treatment response; yet we do not currently evaluate these parameters. Consensus regarding the best methods, reagents, or cut-off points to define HER2 status for determining trastuzumab responsivity has not yet been reached. HER2 testing for other prognostic or predictive purposes, e.g. to determine whether patients are likely to respond to other agents, such as dose-intensive doxorubicin, may be less. Data from the Cancer and Leukemia Group B trial 8541 (companion 8869) suggest that, with proper controls in high-volume laboratories, many of the available methods produce comparable results.
HER2(neu,erbB-2)是一种与人类表皮生长因子受体相关的受体,如今作为治疗反应的预测标志物变得愈发重要。虽然治疗与HER2相互作用的价值和方向可能因药物、剂量或给药方案而异,但几乎没有人会反对HER2检测是乳腺癌评估的重要组成部分。1998年,曲妥珠单抗(赫赛汀)被美国食品药品监督管理局批准用于治疗HER2阳性转移性乳腺癌患者。乳腺癌细胞中HER2异常的患者(使用赫赛汀检测通常为2+或3+,通过其他免疫组织化学检测为过表达或通过荧光原位杂交[FISH]检测为扩增)对曲妥珠单抗治疗反应最为显著。目前尚不清楚用于评估HER2的最佳检测方法(方法、试剂、临界值等)是什么,因为对接受曲妥珠单抗治疗患者的同一癌症进行平行检测才刚刚开始,且数据有限。人们普遍认为,没有HER2改变的乳腺癌对曲妥珠单抗无反应,尽管尚未开展针对这一特定假设的临床试验。也有人担心肿瘤内或原发性和转移性癌灶之间HER2的克隆异质性可能会影响治疗反应;然而我们目前并未评估这些参数。关于确定曲妥珠单抗反应性的最佳HER2状态定义方法、试剂或临界值尚未达成共识。用于其他预后或预测目的的HER2检测,例如确定患者是否可能对其他药物(如意向性密集阿霉素)有反应的检测可能较少。癌症与白血病B组试验8541(配套试验8869)的数据表明,在大容量实验室进行适当对照的情况下,许多现有方法可产生可比的结果。