Molekulární patologie plicních karcinomů pro rutinní praxi - update 2017
[Molecular pathology of lung cancer in routine diagnostic practice: 2017 update]
Jazyk čeština Země Česko Médium print
Typ dokumentu časopisecké články, přehledy
PubMed
29227119
PII: 62335
- Klíčová slova
- NSCLC - lung adenocarcinoma - EGFR - ALK - BRAF - KRAS - RET - MET - PD-L1 - ROS1.,
- MeSH
- adenokarcinom * diagnóza genetika terapie MeSH
- lidé MeSH
- molekulární patologie MeSH
- mutace MeSH
- nádory plic * diagnóza genetika terapie MeSH
- nemalobuněčný karcinom plic * diagnóza genetika terapie MeSH
- protoonkogenní proteiny MeSH
- tyrosinkinasy MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- Názvy látek
- protoonkogenní proteiny MeSH
- tyrosinkinasy MeSH
The group of non-small cell lung carcinomas includes tumors that are variable at the clinical, histopathological and molecular levels. Advances in the understanding of molecular pathology of lung adenocarcinomas in particular led to changes in their histopathological classification and treatment. Patients diagnosed with lung adenocarcinoma harboring specific mutations benefit from the administration of specific targeted therapy. Analysis of EGFR gene mutations and ALK rearrangement in lung adenocarcinomas are already routinely performed and are closely related to the indication for the administration of tyrosinkinase inhibitors. Besides EGFR mutations and ALK rearrangement there are also available other potential markers for analyzing, e.g. b-raf - BRAF, ROS1. Moreover, immunotherapy needs standardization of detection of crucial molecules, namely PD-L1. The aim of this review is to summarize the role of the most relevant molecules that could also serve as the therapeutic target for practicing pathologists.