Dealing with NSCLC EGFR mutation testing and treatment: A comprehensive review with an Italian real-world perspective. (April 2021)
- Record Type:
- Journal Article
- Title:
- Dealing with NSCLC EGFR mutation testing and treatment: A comprehensive review with an Italian real-world perspective. (April 2021)
- Main Title:
- Dealing with NSCLC EGFR mutation testing and treatment: A comprehensive review with an Italian real-world perspective
- Authors:
- Malapelle, Umberto
Pilotto, Sara
Passiglia, Francesco
Pepe, Francesco
Pisapia, Pasquale
Righi, Luisella
Listì, Angela
Bironzo, Paolo
Belluomini, Lorenzo
Tabbò, Fabrizio
Reale, Maria Lucia
Russo, Gianluca
De Luca, Caterina
Novello, Silvia
Troncone, Giancarlo - Abstract:
- Graphical abstract: Highlights: EGFR mutations play a pivotal role as predictive biomarkers in NSCLC. EGFR mutational assessment is critical for adequate management of NSCLC patients. Around 20 % of Italian institutions adopt NGS platforms for EGFR mutation testing. Definition and treatment of uncommon EGFR mutations are quite heterogenous. Implementation of molecular tumor board is critical to support the treatment selection process. Abstract: Since their discovery, relevant efforts have been made to optimize the detection approaches to EGFR mutations as well as the clinical management of EGFR -mutated NSCLC. The recent shift from single gene testing to novel comprehensive detection platforms along with the development of new generation tyrosine kinase inhibitors, targeting both common and uncommon EGFR -mutations, is leading to a progressive increase in the number of patients who may benefit from targeted approaches, with subsequent impact on their long-term survival and quality of life. However, a prompt and adequate implementation of the most recent diagnostic and treatment advances in the routine practice often remains critical to be specifically addressed. In this review we provide a complete and updated overview of the different detection platforms and therapeutic options currently available for the clinical management of advanced EGFR -positive NSCLC, summarizing scientific evidence and describing molecular testing as well as treatment practice in the real-wordGraphical abstract: Highlights: EGFR mutations play a pivotal role as predictive biomarkers in NSCLC. EGFR mutational assessment is critical for adequate management of NSCLC patients. Around 20 % of Italian institutions adopt NGS platforms for EGFR mutation testing. Definition and treatment of uncommon EGFR mutations are quite heterogenous. Implementation of molecular tumor board is critical to support the treatment selection process. Abstract: Since their discovery, relevant efforts have been made to optimize the detection approaches to EGFR mutations as well as the clinical management of EGFR -mutated NSCLC. The recent shift from single gene testing to novel comprehensive detection platforms along with the development of new generation tyrosine kinase inhibitors, targeting both common and uncommon EGFR -mutations, is leading to a progressive increase in the number of patients who may benefit from targeted approaches, with subsequent impact on their long-term survival and quality of life. However, a prompt and adequate implementation of the most recent diagnostic and treatment advances in the routine practice often remains critical to be specifically addressed. In this review we provide a complete and updated overview of the different detection platforms and therapeutic options currently available for the clinical management of advanced EGFR -positive NSCLC, summarizing scientific evidence and describing molecular testing as well as treatment practice in the real-word scenario. … (more)
- Is Part Of:
- Critical reviews in oncology/hematology. Volume 160(2021)
- Journal:
- Critical reviews in oncology/hematology
- Issue:
- Volume 160(2021)
- Issue Display:
- Volume 160, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 160
- Issue:
- 2021
- Issue Sort Value:
- 2021-0160-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-04
- Subjects:
- EGFR -- Common mutations -- Uncommon mutations -- Molecular testing -- Tyrosine kinase inhibitors -- Non-small cell lung cancer
Oncology -- Periodicals
Hematology -- Periodicals
616.994 - Journal URLs:
- http://www.sciencedirect.com/science/journal/10408428 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.critrevonc.2021.103300 ↗
- Languages:
- English
- ISSNs:
- 1040-8428
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3487.479000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 16326.xml