Targeted therapy moves to earlier stages of non-small-cell lung cancer: emerging evidence, controversies and future challenges.

ALK EGFR NSCLC ROS1 adjuvant afatinib alectinib crizotinib early-stage erlotinib gefitinib localized NSCLC neoadjuvant non-small-cell lung cancer oncogenic driver osimertinib targeted therapy

Journal

Future oncology (London, England)
ISSN: 1744-8301
Titre abrégé: Future Oncol
Pays: England
ID NLM: 101256629

Informations de publication

Date de publication:
Oct 2021
Historique:
pubmed: 3 8 2021
medline: 8 2 2022
entrez: 2 8 2021
Statut: ppublish

Résumé

Lung cancer continues to be the leading cause of cancer mortality and a serious health problem despite the numerous advances made in the last decade and the rapid advance of research in this field. In recent years, there has been a decrease in mortality from lung cancer coinciding with the approval times of targeted therapy. To date, targeted therapy has been used in the context of advanced disease in clinical practice, with great benefits in survival and quality of life. The next step will be to incorporate targeted therapy into the treatment of earlier stages of non-small-cell lung cancer, and there is already a randomized trial showing a disease-free survival benefit. However, there are many questions that need to be resolved first. In the present review, the authors discuss the findings of published reports and ongoing clinical trials assessing the role of targeted therapies in nonmetastatic disease. Lay abstract Despite major therapeutic advances over the last decade, lung cancer continues to present the highest mortality rate of all cancers. Precision and personalized therapy directed at specific alterations in the genetic material of the tumor as well as immunotherapy has significantly improved survival in metastatic non-small-cell lung cancer. The next step will be to incorporate precision medicine into the treatment of earlier stages of non-small-cell lung cancer. The recent publication of the results of the ADAURA phase III trial showing a significant improvement in disease-free survival in patients with resected EGFR-mutated non-small-cell lung cancer who received an adjuvant EGFR-directed tyrosine kinase inhibitor called osimertinib has opened the doors to the incorporation of this novel agent into routine clinical practice. However, there are many questions that need to be resolved first. In the present review, the authors discuss the findings of published reports and ongoing clinical trials assessing the role of precision medicine in nonmetastatic disease.

Autres résumés

Type: plain-language-summary (eng)
Lay abstract Despite major therapeutic advances over the last decade, lung cancer continues to present the highest mortality rate of all cancers. Precision and personalized therapy directed at specific alterations in the genetic material of the tumor as well as immunotherapy has significantly improved survival in metastatic non-small-cell lung cancer. The next step will be to incorporate precision medicine into the treatment of earlier stages of non-small-cell lung cancer. The recent publication of the results of the ADAURA phase III trial showing a significant improvement in disease-free survival in patients with resected EGFR-mutated non-small-cell lung cancer who received an adjuvant EGFR-directed tyrosine kinase inhibitor called osimertinib has opened the doors to the incorporation of this novel agent into routine clinical practice. However, there are many questions that need to be resolved first. In the present review, the authors discuss the findings of published reports and ongoing clinical trials assessing the role of precision medicine in nonmetastatic disease.

Identifiants

pubmed: 34337973
doi: 10.2217/fon-2020-1255
doi:

Substances chimiques

ErbB Receptors EC 2.7.10.1

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

4011-4025

Auteurs

Xabier Mielgo-Rubio (X)

Department of Medical Oncology, Hospital Universitario Fundación Alcorcón, Budapest 1 Alcorcón, Madrid, 28922, Spain.

Margarita Martín (M)

Department of Radiation Oncology, Ramón y Cajal University Hospital, M-607, km. 9, 100, Madrid, 28034, Spain.

Jordi Remon (J)

Department of Medical Oncology, Centro Integral Oncológico Clara Campal, Hospital HM Delfos, HM Hospitales, Barcelona, Spain.

Oliver Higuera (O)

Department of Medical Oncology, Hospital Universitario La Paz, Paseo de la Castellana 261, Madrid, 28046, Spain.

Virginia Calvo (V)

Department of Medical Oncology, Puerta de Hierro Hospital, Joaquín Rodrigo 1, Majadahonda, Madrid, 28222, Spain.

José Ramón Jarabo (JR)

Department of Thoracic Surgery, Hospital Clínico San Carlos, Calle del Profesor Martín Lagos, s/n, Madrid, 28040, Spain.

Esther Conde (E)

Department of Pathology, Hospital Universitario 12 de Octubre, Madrid, 28041, Spain.

Javier Luna (J)

Department of Radiation Oncology, Fundación Jiménez Díaz, Oncohealth Institute, Avda. Reyes Católicos 2, Madrid, 28040, Spain.

Mariano Provencio (M)

Department of Medical Oncology, Puerta de Hierro Hospital, Joaquín Rodrigo 1, Majadahonda, Madrid, 28222, Spain.

Javier De Castro (J)

Department of Medical Oncology, Hospital Universitario La Paz, Paseo de la Castellana 261, Madrid, 28046, Spain.

Fernando López-Ríos (F)

Department of Pathology, Hospital Universitario 12 de Octubre, Madrid, 28041, Spain.

Florentino Hernando-Trancho (F)

Department of Thoracic Surgery, Hospital Clínico San Carlos, Calle del Profesor Martín Lagos, s/n, Madrid, 28040, Spain.

Felipe Couñago (F)

Department of Radiation Oncology, Hospital Universitario Quirónsalud Madrid, Madrid, 28223, Spain.
Department of Radiation Oncology, Hospital La Luz, Madrid, 28003, Spain.
Medicine Department, School of Biomedical Sciences, Universidad Europea de Madrid, Villaviciosa de Odón, 28670, Spain.

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