Informations générales (source: ClinicalTrials.gov)

NCT04222335 En recrutement
Understanding and Overcoming the Early Adaptive Resistance to EGFR Tyrosine-kinase Inhibitors in Lung Cancer Patients (LUNG-RESIST)
Interventional
  • Carcinome pulmonaire non à petites cellules
  • Tumeurs du poumon
N/A
University Hospital, Toulouse (Voir sur ClinicalTrials)
mars 2021
décembre 2028
06 juillet 2024
Epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKI) are effective therapies for advanced lung cancer patients bearing EGFR-activating mutations, but are not curative due to the invariable apparition of resistances. The investigator team have identified a new phenotype related to drug tolerance after EGFR-TKI treatment that shares several characteristics of a known process of Therapy-Induced Senescence (TIS), which could be a major event of drug tolerance in patients. Using cutting-edge technologies, patient-derived xenografts (PDX) and circulating tumor cells (CTC), the investigator team will perform an exhaustive characterization of the phenotypic and molecular changes associated with this drug-tolerant state in patients. Their results should lead to new therapeutic approaches to eliminate the reservoir of drug-tolerant cells and to prevent emergence of resistance mutations responsible for the relapse of patients.
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Etablissements

Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
Toulouse University Hospital - 31300 - Toulouse - Occitanie - France Sandra BERNARD En recrutement Contact (sur clinicalTrials)

Critères

Tous
Inclusion Criteria:

- Patient with non operable and / or metastatic non-small cell lung cancer documented
histologically.

- Pathological diagnosis of NSCLC carrying an EGFR activating mutation associated with
sensitivity to the tyrosine kinase inhibitors (TKI) (exons 18, 19 and 21).

- Sufficient tissue sample quantity and quality for translational research

- Naïve TKI-treated EGFR patient who can receive first-line treatment with Osimertinib
or second-line after chemotherapy



- Any patient with an exon 20 EGFR mutation.

- Any disease or pathology that recommend not to perform blood samples collection

- Any psychological, family, geographical or social condition that could potentially,
according to the investigator's judgment, prevent the collection of informed consent
or interfere with compliance with the study protocol

- Patient with a resistance mutation of EGFR

- Patient under State Medical Assistance

- Patient deprived of liberty on administrative or judicial decision, or patient under
guardianship, curatorship or safeguard of justice