Osimertinib Combined With Anlotinib in EGFR T790M Mutated NSCLC Patients With Progression on Osimertinib Treatment

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Zhejiang University

Status and phase

Phase 2


Non Small Cell Lung Cancer


Drug: osimertinib mesylate tablets and anlotinib hydrochloride capsules

Study type


Funder types




Details and patient eligibility


EGFR T790M gatekeeper mutation accounts for approximately 60% of acquired resistance to the first- or second-generation EGFR-TKI treatment. Osimertinib, a third-generation EGFR TKI, has become the standard therapy for NSCLC patients with acquired EGFR T790M mutation. However, acquired resistance to osimertinib is still inevitable and there is no established targetable agent currently. Thus, treatment strategy for patients with acquire resistance to osimertinib remains an urgent issue. In this study, we aimed to evaluate the efficacy of osimertinib combined with anlotinib in acquired EGFR T790M mutated NSCLC patients with gradual progression on osimertinib treatment.

Full description

In current clinical practice, acquired resistance to osimertinib can be divided into three clinical modes: dramatic progression, gradual progression and local progression. For patients with gradual progression,there are various clinical explorations,including the continuation of osimertinib with chemotherapy or radiotherapy, osimertinib combined with antiangiogenic agents. In preclinical studies, an overactive vascular endothelial growth factor/vascular endothelial growth factor receptor (VEGF/VEGFR) pathway and tumour angiogenesis plays a crucial role in the resistance to EGFR-TKIs, and the dual targeting of both the VEGF and EGFR pathways may prevent resistance. Anlotinib (AL3818) is an inhibitor targeting multiple receptor tyrosine kinases involved in tumour progression, especially VEGFR 2/3, PDGFRα/β and c-Kit. We suppose that the combination treatment of osimertinib and anlotinib may ameliorate acquired resistance to osimertinib.This is a multi-center, open, single-arm, exploratory phase 2 trial evaluating osimertinib combined with anlotinib in acquired EGFR T790M mutated NSCLC patients with gradual progression on osimertinib treatment.


3 patients




18 to 75 years old


No Healthy Volunteers

Inclusion criteria

  • Ability to provide informed consent, complete all study assessments and have complete medical record.
  • Age:18-75 years.
  • Histologically or cytologically confirmed diagnosis of local advanced or metastatic NSCLC.
  • Patients should be confirmed acquired EGFR T790M mutation and received osimertinib as the second line treatment, and they should have the following: (1) benefit from treatment with osimertinib initially ;(2) gradual progression on osimertinib treatment as defined by minor increment of tumor burden (≥10% but <20% in the sum of target lesions).
  • At least one measurable lesion as defined by lesions ≥10mm in long axis according to RECIST 1.1.

Exclusion criteria

  • Patients who will be or were involved in any other interventional antitumour clinical studies for locally advanced/metastatic NSCLC currently or previously.
  • Small cell lung cancer (including small lung cancer mixed with non-small cell lung cancer).
  • Patients at risk of bleeding.
  • Patients with renal dysfunction.
  • Uncontrolled severe hypertension.
  • Any concomitant condition evaluated by physicians which is not suitable for osimertinib or anlotinib treatment.

Trial design

3 participants in 1 patient group

osimertinib combined with anlotinib
Experimental group
Drug: osimertinib mesylate tablets and anlotinib hydrochloride capsules

Trial contacts and locations



Data sourced from clinicaltrials.gov

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