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首页> 外文期刊>The oncologist >Commercialized multigene predictors of clinical outcome for breast cancer.
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Commercialized multigene predictors of clinical outcome for breast cancer.

机译:乳腺癌临床结果的商业化多基因预测因子。

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摘要

In the past 5 years, a number of commercialized multigene prognostic and predictive tests have entered the complex and expanding landscape of breast cancer companion diagnostics. These tests have used a variety of formats ranging from the familiar slide-based assays of immunohistochemistry and fluorescence in situ hybridization to the nonmorphology-driven molecular platforms of quantitative multiplex real-time polymerase chain reaction and genomic microarray profiling. In this review, 14 multigene assays are evaluated as to their scientific validation, current clinical utility, regulatory approval status, and estimated cost-benefit ratio. Emphasis is placed on two tests: oncotype DX and MammaPrint. Current evidence indicates that the oncotype DX test has the advantages of earlier commercial launch, wide acceptance for payment by third-party payors in the U.S., ease of use of formalin-fixed paraffin-embedded tissues, recent listing by the American Society of Clinical Oncology Breast Cancer Tumor MarkersUpdate Committee as recommended for use, continuous scoring system algorithm, ability to serve as both a prognostic test and predictive test for certain hormonal and chemotherapeutic agents, demonstrated cost-effectiveness in one published study, and a high accrual rate for the prospective validation clinical trial (Trial Assigning Individualized Options for Treatment). The MammaPrint assay has the advantages of a 510(k) clearance by the U.S. Food and Drug Administration, a larger gene number, which may enhance further utility, and a potentially wider patient eligibility, including lymph node-positive, estrogen receptor (ER)-negative, and younger patients being accrued into the prospective trial (Microarray in Node-Negative Disease May Avoid Chemotherapy). A number of other assays have specific predictive goals that are most often focused on the efficacy of tamoxifen in ER-positive patients, such as the two-gene ratio test and the cytochrome P450 CYP2D6 genotyping assay.
机译:在过去的5年中,许多商业化的多基因预后和预测性测试已进入复杂且不断扩大的乳腺癌伴随诊断领域。这些测试使用了多种格式,从熟悉的基于幻灯片的免疫组织化学和荧光原位杂交分析到定量多重实时聚合酶链反应和基因组微阵列分析的非形态学驱动分子平台。在这篇综述中,评估了14种多基因测定的科学有效性,当前临床效用,法规批准状态以及估计的成本效益比。重点放在两个测试上:癌型DX和MammaPrint。当前证据表明,癌型DX测试具有以下优势:较早的商业推出,美国第三方付款人对付款的广泛接受,福尔马林固定的石蜡包埋组织的易用性,美国临床肿瘤学会最近列出的优点推荐使用乳腺癌肿瘤标记物更新委员会,连续评分系统算法,对某些激素和化学治疗剂既能进行预后测试又能进行预测测试的能力,在一项已发表的研究中证明具有成本效益,并且对前瞻性研究的应计率很高验证临床试验(分配个体化治疗方案的试验)。 MammaPrint测定法的优点是,美国食品药品监督管理局(FDA)清除了510(k),更大的基因数量(可能会进一步增强用途)以及潜在的更广泛的患者资格(包括淋巴结阳性,雌激素受体(ER)) -阴性,且年轻患者被纳入前瞻性试验(Node阴性疾病中的微阵列可避免化学疗法)。许多其他测定具有特定的预测目标,这些目标通常侧重于他莫昔芬在ER阳性患者中的功效,例如双基因比率测试和细胞色素P450 CYP2D6基因分型测定。

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