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Dacomitinib versus erlotinib in patients with EGFR-mutated advanced nonsmall-cell lung cancer (NSCLC): pooled subset analyses from two randomized trials
- Source :
- Annals of oncology : official journal of the European Society for Medical Oncology. 27(7)
- Publication Year :
- 2016
-
Abstract
- Background The irreversible epidermal growth factor receptor (EGFR) inhibitors have demonstrated efficacy in NSCLC patients with activating EGFR mutations, but it is unknown if they are superior to the reversible inhibitors. Dacomitinib is an oral, small-molecule irreversible inhibitor of all enzymatically active HER family tyrosine kinases. Methods The ARCHER 1009 (NCT01360554) and A7471028 (NCT00769067) studies randomized patients with locally advanced/metastatic NSCLC following progression with one or two prior chemotherapy regimens to dacomitinib or erlotinib. EGFR mutation testing was performed centrally on archived tumor samples. We pooled patients with exon 19 deletion and L858R EGFR mutations from both studies to compare the efficacy of dacomitinib to erlotinib. Results One hundred twenty-one patients with any EGFR mutation were enrolled; 101 had activating mutations in exon 19 or 21. For patients with exon19/21 mutations, the median progression-free survival was 14.6 months [95% confidence interval (CI) 9.0–18.2] with dacomitinib and 9.6 months (95% CI 7.4–12.7) with erlotinib [unstratified hazard ratio (HR) 0.717 (95% CI 0.458–1.124), two-sided log-rank, P = 0.146]. The median survival was 26.6 months (95% CI 21.6–41.5) with dacomitinib versus 23.2 months (95% CI 16.0–31.8) with erlotinib [unstratified HR 0.737 (95% CI 0.431–1.259), two-sided log-rank, P = 0.265]. Dacomitinib was associated with a higher incidence of diarrhea and mucositis in both studies compared with erlotinib. Conclusions Dacomitinib is an active agent with comparable efficacy to erlotinib in the EGFR mutated patients. The subgroup with exon 19 deletion had favorable outcomes with dacomitinib. An ongoing phase III study will compare dacomitinib to gefitinib in first-line therapy of patients with NSCLC harboring common activating EGFR mutations (ARCHER 1050; NCT01774721). Clinical trials number ARCHER 1009 (NCT01360554) and A7471028 (NCT00769067).
- Subjects :
- 0301 basic medicine
Oncology
Adult
Male
medicine.medical_specialty
Lung Neoplasms
medicine.drug_class
Antineoplastic Agents
Pharmacology
Tyrosine-kinase inhibitor
Disease-Free Survival
03 medical and health sciences
chemistry.chemical_compound
Erlotinib Hydrochloride
0302 clinical medicine
Gefitinib
Internal medicine
Carcinoma, Non-Small-Cell Lung
medicine
Mucositis
Humans
Epidermal growth factor receptor
Protein Kinase Inhibitors
Aged
Quinazolinones
Aged, 80 and over
biology
business.industry
Hazard ratio
Hematology
Middle Aged
medicine.disease
Dacomitinib
ErbB Receptors
030104 developmental biology
chemistry
030220 oncology & carcinogenesis
Mutation
biology.protein
Female
Erlotinib
business
Tyrosine kinase
medicine.drug
Subjects
Details
- ISSN :
- 15698041
- Volume :
- 27
- Issue :
- 7
- Database :
- OpenAIRE
- Journal :
- Annals of oncology : official journal of the European Society for Medical Oncology
- Accession number :
- edsair.doi.dedup.....a9aa211e4c16a5f08263a4445a345c80