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EGFR-TKI re-administration after osimertinib failure in T790M mutation loss cases with re-biopsy
Shinsuke Ogusu1,2, Ryo Ariyasu1, Takahiro Akita1
1Department of Thoracic Medical Oncology, the Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Abstract:
Data on the re-administration of epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) after osimertinib failure in patients with T790M-positive non-small cell lung cancer (NSCLC) is limited. EGFR-TKI re-administration efficacy may vary between patients with T790M loss and those with T790M persistent with re-biopsy after osimertinib treatment. Patients who received EGFR-TKI re-administration (gefitinib, erlotinib, afatinib, dacomitinib, and osimertinib) after osimertinib failure were identified from our database. T790M mutation status before EGFR-TKI re-administration was analyzed via repeat biopsy. We retrospectively evaluated the efficacy of EGFR-TKI re-administration, especially differences according to the T790M mutation status, via repeat biopsy. Until June 2020, 28 patients received EGFR-TKI re-administration and 17 underwent repeat biopsy after osimertinib failure. Patients were divided into three groups, including the T790M loss group, where active mutation persisted and T790M was lost (13/17); T790M remaining group, where both the active mutation and T790M persisted (3/17); and active mutation loss group where both the active mutation and T790M were lost (1/17). The overall response rate (ORR) of EGFR-TKI re-administration in the T790M loss group was 31% and the disease control rate (DCR) was 54%, which were higher than the ORR of 21% and DCR of 43% in the entire patient population. ORR and DCR of the not re-biopsy group were low (9% and 27%, respectively). The therapeutic effect of EGFR-TKI re-administration in patients with T790M-positive NSCLC after osimertinib failure is limited. EGFR-TKI re-administration may be considered in cases of T790M loss after repeat biopsy.
Insights
Re-administering epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) after osimertinib failure in T790M-positive non-small cell lung cancer (NSCLC) shows limited efficacy. However, re-administration may benefit patients with T790M loss identified via repeat biopsy.
Area of Science:
- Oncology
- Medical Genetics
- Pharmacology
Background:
- Limited data exists on re-administering epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) after osimertinib failure in T790M-positive non-small cell lung cancer (NSCLC).
- Efficacy of EGFR-TKI re-administration may differ based on T790M mutation status (loss vs. persistence) after osimertinib treatment, necessitating repeat biopsy.
Purpose of the Study:
- To retrospectively evaluate the efficacy of EGFR-TKI re-administration in patients with T790M-positive NSCLC after osimertinib failure.
- To compare the efficacy of EGFR-TKI re-administration based on T790M mutation status determined by repeat biopsy.
Main Methods:
- Retrospective analysis of 28 patients who received EGFR-TKI re-administration (gefitinib, erlotinib, afatinib, dacomitinib, osimertinib) post-osimertinib failure.
- Analysis of T790M mutation status via repeat biopsy in 17 patients to categorize them into T790M loss, T790M remaining, or active mutation loss groups.
Main Results:
- The T790M loss group (13/17) showed a higher overall response rate (ORR) of 31% and disease control rate (DCR) of 54% compared to the entire patient population (ORR 21%, DCR 43%).
- Patients without repeat biopsy had significantly lower ORR (9%) and DCR (27%).
- The T790M remaining group (3/17) and active mutation loss group (1/17) had limited responses.
Conclusions:
- The overall therapeutic effect of EGFR-TKI re-administration in T790M-positive NSCLC after osimertinib failure is limited.
- EGFR-TKI re-administration may be a viable option for patients with confirmed T790M loss following repeat biopsy.
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