Ritka mutációktól a klasszikusig, jelátviteli útvonalak gátlása a nem kissejtes tüdőrákban

Gálffy, Gabriella [Gálffy, Gabriella (Pulmonológia), szerző] Mellkassebészeti Klinika (SE / AOK / K)

Magyar nyelvű Összefoglaló cikk (Folyóiratcikk) Tudományos
Megjelent: MAGYAR ONKOLÓGIA 0025-0244 2060-0399 64 (3) pp. 196-204 2020
  • SJR Scopus - Medicine (miscellaneous): Q4
Azonosítók
Lung cancer is the leading cause of cancer deaths not only in Hungary but also in the world. Within this, women's lung cancer morbidity and mortality have increased significantly in recent years. For many years, we only had a chemotherapy option to treat lung cancer. The year 2005 was a major breakthrough in the treatment of non-small cell lung cancer with the advent of a new treatment strategy, targeted treatments, EGFR-TKI treatments. Since then, we have several years of experience with first-, second-, and even third-generation TKI treatments in lung adenocarcinoma. The second major step in targeted therapy for lung cancer was to learn about ALK mutant lung cancer and the emergence of ALK inhibitor therapies on the therapeutic palette with the advent of first, second and third generation formulations. In recent years, the range of options for targeted therapeutic targets has expanded to include personalized therapeutic options. By recognizing and targeting the ROS1, BRAF, MET, RET, NTRK, HER2 mutations, we can tailor the most optimal treatment to more and more patients.
Hivatkozás stílusok: IEEEACMAPAChicagoHarvardCSLMásolásNyomtatás
2025-04-14 08:09