Adjuvant Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors (TKIs) in Resected Non-Small Cell Lung Cancer (NSCLC): A Systematic Review and Meta-analysis.


Journal

American journal of clinical oncology
ISSN: 1537-453X
Titre abrégé: Am J Clin Oncol
Pays: United States
ID NLM: 8207754

Informations de publication

Date de publication:
05 2019
Historique:
pubmed: 27 3 2019
medline: 11 2 2020
entrez: 27 3 2019
Statut: ppublish

Résumé

The role of adjuvant tyrosine kinase inhibitors (TKIs) in non-small cell lung cancer (NSCLC) is not well defined. Recent randomized controlled trials showed a disease-free survival (DFS) benefit in patients harboring an epidermal growth factor receptor (EGFR) mutation. Yet, older trials on patients with any EGFR status did not demonstrate the same benefit. We aimed to assess the efficacy and safety of adjuvant TKIs in NSCLC patients. The electronic databases Medline (PubMed) and EMBASE were searched for relevant randomized controlled trials. Random effect models were used. The primary outcome was DFS measured as hazard ratio (HR). The secondary outcomes were overall survival (OS) measured as HR, 2-year DFS and toxicity expressed as risk ratio and odds ratio (OR), respectively. Subgroup analyses assessed DFS by trial design. Six trials incorporating 1860 patients were included. In patients harboring an EGFR mutation, adjuvant TKIs decreased the risk of disease recurrence by 48% (HR: 0.52, 95% confidence interval [CI]: 0.35-0.78), improved 2-year DFS (HR: 0.53, 95% CI: 0.43-0.66) but did not improve OS (HR: 0.64, 95% CI: 0.22-1.89). The risk of developing ≥grade 3 skin toxicity (OR: 6.07, 95% CI: 4.34-8.51) and diarrhea (OR: 4.05; 95% CI: 2.44-6.74) was increased. In subgroup analyses, the DFS benefit was more pronounced in trials using TKIs over chemotherapy compared with trials using TKIs postchemotherapy. In conclusion, adjuvant TKIs decrease the risk of recurrence in NSCLC patients harboring an EGFR mutation but do not improve OS. Longer follow-up is needed for a definitive assessment of OS and to define the role of adjuvant TKI for NSCLC in the clinical practice.

Identifiants

pubmed: 30913091
doi: 10.1097/COC.0000000000000533
doi:

Substances chimiques

Protein Kinase Inhibitors 0
EGFR protein, human EC 2.7.10.1
ErbB Receptors EC 2.7.10.1
Receptor Protein-Tyrosine Kinases EC 2.7.10.1

Types de publication

Journal Article Meta-Analysis Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

440-445

Auteurs

Jacques Raphael (J)

London Regional Cancer Program, Department of Oncology, Division of Medical Oncology.
Institute of Health Policy, Management and Evaluation, University of Toronto.

Mark Vincent (M)

London Regional Cancer Program, Department of Oncology, Division of Medical Oncology.

Gabriel Boldt (G)

London Regional Cancer Program, Department of Oncology, Division of Medical Oncology.

Prakesh S Shah (PS)

Institute of Health Policy, Management and Evaluation, University of Toronto.
Department of Pediatrics, Mount Sinai Hospital, Toronto, ON, Canada.

George Rodrigues (G)

London Regional Cancer Program, Department of Oncology, Division of Radiation Oncology, Western University, London.

Phillip Blanchette (P)

London Regional Cancer Program, Department of Oncology, Division of Medical Oncology.

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Classifications MeSH