Institute of Pathology, Charité, University Medicine Berlin, Berlin, Germany.
Oncol Res Treat. 2016;39(12):804-810. doi: 10.1159/000453085. Epub 2016 Nov 25.
The increasing importance of targeting drugs and check-point inhibitors in the treatment of several tumor entities (breast, colon, lung, malignant melanoma, lymphoma, etc.) and the necessity of a companion diagnostic (HER2, (pan)RAS, EGFR, ALK, BRAF, ROS1, MET, PD-L1, etc.) is leading to new challenges for surgical pathology. Since almost all the biomarkers to be specifically detected are tissue based, a precise and reliable diagnostic is absolutely crucial. To meet this challenge surgical pathology has adapted a number of molecular methods (semi-quantitative immunohistochemistry, fluorescence in situ hybridization, PCR and its multiple variants, (pyro/Sanger) sequencing, next generation sequencing (amplicon, whole exome, whole genome), DNA arrays, methylation analyses, etc.) to be applicable for formalin-fixed paraffin-embedded tissue. Reading a patient's tissue as 'deeply' as possible and obtaining information on the morphological, genetic, proteomic and epigenetic background are the tasks of pathologists and molecular biologists and provide the clinicians with information relevant for precision medicine. Intensified cooperation between clinicians and pathologists will provide the basis of improved clinical drug selection and guide development of new cancer gene therapies and molecularly targeted drugs by research units and the pharmaceutical industry.
靶向药物和检查点抑制剂在治疗多种肿瘤实体(乳腺癌、结肠癌、肺癌、恶性黑色素瘤、淋巴瘤等)中的重要性不断增加,以及对伴随诊断(HER2、(泛)RAS、EGFR、ALK、BRAF、ROS1、MET、PD-L1 等)的必要性,这给外科病理学带来了新的挑战。由于几乎所有需要专门检测的生物标志物都是基于组织的,因此精确和可靠的诊断至关重要。为了应对这一挑战,外科病理学已经采用了许多分子方法(半定量免疫组织化学、荧光原位杂交、PCR 及其多种变体、(焦磷酸/Sanger)测序、下一代测序(扩增子、外显子组、全基因组)、DNA 芯片、甲基化分析等),以适用于福尔马林固定石蜡包埋组织。对患者的组织进行尽可能深入的“解读”,并获取有关形态、遗传、蛋白质组学和表观遗传学背景的信息,是病理学家和分子生物学家的任务,为临床医生提供与精准医学相关的信息。临床医生和病理学家之间的加强合作将为改善临床药物选择提供基础,并为研究单位和制药行业指导新的癌症基因治疗和分子靶向药物的开发。