posted on 2022-03-16, 03:39authored byMatt Shirley, Susan J. Keam
Declarations
Funding The preparation of this review was not supported by any external funding.
Authorship and Conflict of interest M. Shirley and S. Keam are salaried employees of Adis International Ltd/Springer Nature, and declare no relevant conflicts of interest. All authors contributed to the review and are responsible for the article content.
Ethics approval, Consent to participate, Consent to publish, Availability of data and material, Code availability Not applicable.
Additional
information about this Adis Drug Review can be found here.
Abstract
Aumolertinib (formerly almonertinib; Ameile®) is an oral, third-generation
epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (EGFR-TKI) that
is selective for mutant EGFR over wild-type EGFR. It has been developed for the
treatment of advanced EGFR mutation-positive non-small cell lung cancer
(NSCLC). In the phase 3 AENEAS trial conducted in Chinese patients, aumolertinib
as first-line treatment significantly prolonged progression-free survival (PFS)
and duration of response (DoR) compared with gefitinib in patients with advanced
EGFR mutation-positive NSCLC; overall survival (OS) data from this study are
immature. In the phase 1/2 APOLLO trial, aumolertinib showed good clinical
activity (based on objective response rate, PFS, DoR and OS) in Chinese
patients with locally advanced or metastatic EGFR T790M mutation-positive NSCLC
who had progressed on or after prior EGFR-TKI therapy. Aumolertinib has a
generally manageable tolerability profile; adverse events associated with
wild-type EGFR inhibition (e.g. rash and diarrhoea) were less frequent with
aumolertinib than gefitinib in AENEAS. Thus, aumolertinib is a promising new
option for both first-line and second-line treatment in patients with advanced
EGFR mutation-positive NSCLC.