Back to Search Start Over

Pilot Study of Dacomitinib for Patients With Metastatic EGFR -Mutant Lung Cancers With Disease Progression After Initial Treatment With Osimertinib.

Authors :
Choudhury NJ
Makhnin A
Tobi YY
Daly RM
Preeshagul IR
Iqbal AN
Ahn LS
Hayes SA
Heller G
Kris MG
Riely GJ
Yu HA
Source :
JCO precision oncology [JCO Precis Oncol] 2021 Apr 22; Vol. 5. Date of Electronic Publication: 2021 Apr 22 (Print Publication: 2021).
Publication Year :
2021

Abstract

Patients with EGFR- mutant lung cancer have no approved targeted therapies after disease progression on first-line osimertinib, a third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI). Preclinical studies suggest that tumors with both EGFR -sensitizing alteration and acquired second-site EGFR resistance alterations after treatment with osimertinib retain sensitivity to second-generation EGFR TKIs. We hypothesized that dacomitinib, a pan-human epidermal growth factor receptor TKI, may be effective in this setting.<br />Methods: In this phase II study, patients who had progressed on first-line osimertinib were treated with dacomitinib 45 mg orally daily until disease progression or intolerability. The primary end point was objective response rate.<br />Results: We enrolled 12 patients. Two partial responses were documented (17% objective response rate; 95% CI, 5 to 45). The median progression-free survival was 1.8 months (95% CI, 1.6 to not reached). One patient with an original sensitizing EGFR G719A mutation and one patient without molecular testing available had partial responses, whereas 0 of the 3 patients with second-site acquired EGFR resistance mutations (two C797S and one G724S) met the response criteria. The patient with EGFR G719A has an ongoing response at 17 months, which exceeds prior time on osimertinib (11 months).<br />Conclusion: In the first trial evaluating a second-generation EGFR TKI after first-line third-generation osimertinib, we found that dacomitinib after disease progression on osimertinib has limited benefit.<br /> (© 2021 by American Society of Clinical Oncology.)

Details

Language :
English
ISSN :
2473-4284
Volume :
5
Database :
MEDLINE
Journal :
JCO precision oncology
Publication Type :
Academic Journal
Accession number :
34250398
Full Text :
https://doi.org/10.1200/PO.21.00005