Yaziji Hadi, Goldstein Lynn C, Barry Todd S, Werling Robert, Hwang Harry, Ellis Georgiana K, Gralow Julie R, Livingston Robert B, Gown Allen M
PhenoPath Laboratories, Seattle, Wash 98103, USA.
JAMA. 2004 Apr 28;291(16):1972-7. doi: 10.1001/jama.291.16.1972.
Testing for HER-2 oncogene in breast cancer has increased because of its role as a prognostic and predictive factor. Some advocate gene testing by fluorescence in situ hybridization (FISH) vs protein testing by immunohistochemistry as the method which most accurately evaluates and predicts response to the anti-HER-2 antibody, trastuzumab. However, critical examination of FISH on a screening basis has yet to be performed.
To determine the correlation between FISH and immunohistochemistry results by determining HER-2/neu gene status on tumor sections with indeterminate immunohistochemistry results (2+ score), confirm gene amplification on tumor sections with positive results (3+ score), and verify gene status on tumor sections with negative results (0 or 1+ score).
DESIGN, SETTING, AND PATIENTS: A quality control and quality assurance program for HER-2 testing by FISH, which used tumor specimens from 2963 patients (median age, 56 years) with breast cancer received from 135 hospitals and cancer centers in 29 states, was performed at a reference laboratory from January 1, 1999, to May 15, 2003. Every specimen evaluated by FISH was parallel tested with immunohistochemistry tests.
With FISH as the presumed standard testing method, the positive and negative predictive values and sensitivity and specificity of immunohistochemistry were calculated.
A total of 3260 clinical HER-2 tests by FISH were performed on 2963 serially referred breast cancer specimens. Of these, 2933 tests were successful and 2913 breast cancer specimens had both FISH and immunohistochemistry results available. With FISH as the standard testing method, the positive predictive value of positive immunohistochemistry score (3+) was 91.6%, and the negative predictive value of negative immunohistochemistry score (0 or 1+) was 97.2%. The sensitivity of immunohistochemistry tests, including tumor sections with scores of 2+ or 3+, was 92.6% and the specificity of immunohistochemistry tests with scores of 3+ was 98.8%. The FISH test had a significantly higher failure rate (5% vs 0.08%) and reagent cost (140 dollars vs 10 dollars), and longer testing (36 hours vs 4 hours) and interpretation times (7 minutes vs 45 seconds) vs immunohistochemistry tests.
A testing algorithm for HER-2 determination is most efficient by using immunohistochemistry as the method of choice, with FISH performed for cancers with indeterminate results (2+ score). Successful quality control and quality assurance programs are a prerequisite for such approaches.
由于HER-2癌基因作为一种预后和预测因子的作用,乳腺癌中对其进行检测的情况有所增加。一些人主张通过荧光原位杂交(FISH)进行基因检测,而非通过免疫组织化学进行蛋白质检测,认为前者是最准确评估和预测抗HER-2抗体曲妥珠单抗反应的方法。然而,尚未对基于筛查的FISH进行严格审查。
通过确定免疫组织化学结果不确定(评分为2+)的肿瘤切片上的HER-2/neu基因状态、确认免疫组织化学结果为阳性(评分为3+)的肿瘤切片上的基因扩增情况以及验证免疫组织化学结果为阴性(评分为0或1+)的肿瘤切片上的基因状态,来确定FISH与免疫组织化学结果之间的相关性。
设计、地点和患者:1999年1月1日至2003年5月15日,在一家参考实验室开展了一项针对通过FISH进行HER-2检测的质量控制和质量保证项目,该项目使用了从29个州的135家医院和癌症中心接收的2963例乳腺癌患者(中位年龄56岁)的肿瘤标本。每个通过FISH评估的标本都同时进行了免疫组织化学检测。
以FISH作为假定的标准检测方法,计算免疫组织化学的阳性和阴性预测值以及敏感性和特异性。
对2963例连续送检的乳腺癌标本共进行了3260次FISH临床HER-2检测。其中,2933次检测成功,2913例乳腺癌标本同时有FISH和免疫组织化学结果。以FISH作为标准检测方法,免疫组织化学阳性评分(3+)的阳性预测值为91.6%,免疫组织化学阴性评分(0或1+)的阴性预测值为97.2%。免疫组织化学检测的敏感性(包括评分为2+或3+的肿瘤切片)为92.6%,评分为3+的免疫组织化学检测的特异性为98.8%。与免疫组织化学检测相比,FISH检测的失败率显著更高(5%对0.08%)、试剂成本更高(140美元对10美元)、检测时间更长(36小时对4小时)以及解读时间更长(7分钟对45秒)。
HER-2检测的算法以免疫组织化学作为首选方法最为高效,对于结果不确定(评分为2+)的癌症进行FISH检测。成功的质量控制和质量保证项目是此类方法的前提条件。