Oldenhuis C N A M, Oosting S F, Gietema J A, de Vries E G E
Department of Medical Oncology, University Medical Centre Groningen, PO Box 30.001, 9700 RB Groningen, The Netherlands.
Eur J Cancer. 2008 May;44(7):946-53. doi: 10.1016/j.ejca.2008.03.006. Epub 2008 Apr 7.
Numerous options are currently available for tumour typing. This has raised intense interest in the elucidation of prognostic and predictive markers. A prognostic biomarker provides information about the patients overall cancer outcome, regardless of therapy, whilst a predictive biomarker gives information about the effect of a therapeutic intervention. A predictive biomarker can be a target for therapy. Amongst the genes that have proven to be of relevance are well-known markers such as ER, PR and HER2/neu in breast cancer, BCR-ABL fusion protein in chronic myeloid leukaemia, c-KIT mutations in GIST tumours and EGFR1 mutations in NSCLC. Several reasons for the difficult elucidation of new markers will be addressed including the involvement of cellular pathways in tumour biology instead of single genes and interference in disease outcome as a result of anticancer therapies. Future perspectives for the development of prognostic and predictive markers will be given.
目前有多种肿瘤分型方法。这引发了人们对阐明预后和预测标志物的浓厚兴趣。预后生物标志物提供有关患者总体癌症结局的信息,无论治疗情况如何,而预测生物标志物则提供有关治疗干预效果的信息。预测生物标志物可以成为治疗靶点。已被证明具有相关性的基因包括乳腺癌中众所周知的标志物,如雌激素受体(ER)、孕激素受体(PR)和人表皮生长因子受体2/neu(HER2/neu),慢性髓性白血病中的BCR-ABL融合蛋白,胃肠道间质瘤(GIST)中的c-KIT突变以及非小细胞肺癌(NSCLC)中的表皮生长因子受体1(EGFR1)突变。将探讨难以阐明新标志物的几个原因,包括肿瘤生物学中细胞通路而非单个基因的参与以及抗癌治疗对疾病结局的干扰。还将给出预后和预测标志物开发的未来展望。