A Prospective Cohort Study to Evaluate Molecular pRognostic Factors and Resistance Mechanisms to Osimertinib in Adjuvant Treatment of Completely Resected pIB-IIIA Non-small Cell Lung Carcinoma With Common EGFR Mutations (L858R and Del19)
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Plasma ctDNA, FFPE blocks.
- Who it may be relevant to
- Registry conditions: Non Small Cell Lung Cancer, EGFR Activating Mutation, EGFR DEL19, EGFR L858R. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
IFCT-2202 ROSIE study aims to incorporate a broad-panel centralized NGS testing at baseline in all patients with completely resected NSCLC with common EGFR mutation after confirmation of an optimal preoperative extension assessment and with a centralized review of the quality of the surgical excision. Furthermore, the IFCT-2202 ROSIE study also aims to study the molecular events associated with relapse on, or after osimertinib exposure, that should result in the opportunity to accede to optimal treatment in case of metastatic relapse.
Interventions
- Other Plasma ctDNA
* Plasma ctDNA before surgery (optional) * Plasma ctDNA post-surgery : 4 to 8 weeks post-surgery, before starting adjuvant chemotherapy (if given) and before starting adjuvant osimertinib (if given) * Plasma ctDNA every 6 months * Plasma ctDNA at relapse - Other FFPE blocks
* Surgery FFPE blocks * FFPE blocks at relapse (optional)
Primary outcome measures
- Feasibility study [Time frame: 18 months]
Secondary outcome measures (1)
- Incidence, nature, and severity of osimertinib-related adverse events (safety) [Time frame: About 3 years]
Eligibility criteria
Inclusion criteria
- Signed Informed consent.
- Age ≥ 18 years.
- Pre-surgical disease evaluation including brain MRI/CT-scan and total body PET-FDG CT-scan prior to surgery.
- Histologically complete anatomical resection (R0) of stage pIB-IIIA (pTNM 8th edition) NSCLC.
- Presence of a common EGFR mutation (Del19 or L858R).
- Archival tumour tissue FFPE blocks from surgery available for centrally molecular analyses.
- Patient eligible to receive osimertinib adjuvant therapy in a 3-year intent to treat decision; patients could receive if necessary adjuvant chemotherapy before starting osimertinib treatment.
- Patient who is capable, according to the investigator, of complying with the study's requirements and restrictions.
- Patient followed in the institution on a regular basis (every 3 to 6 months) according to standard recommendations.
- Estimated life expectancy > 3 years.
- Woman patients who are of childbearing potential are eligible:
- They must have a negative pregnancy test before the first dose of osimertinib.
- They must agree to use effective methods of contraception throughout the course of treatment and should be maintained for 2 months after the end of treatment.
- Male subjects who are sexually active with a woman of childbearing potential are eligible if an efficacious contraception method should be used during the treatment and during the 4 months following the last dose.
Exclusion criteria
- History of cancer, except for the following situations:
Patients with history of cancer for more than 3 years are eligible if they have been treated and considered cured. Patients with history of in situ carcinoma of the cervix or non-melanoma skin carcinoma are eligible.
- Neoadjuvant anti-cancer treatment (osimertinib and/or chemotherapy or other anti-cancer treatment).
- Incompletely resected NSCLC (R1 or R2).
- Any medical condition that would, according to the investigator's judgment, prevent the patient's participation in the clinical study.
- Active infection (e.g. patients receiving treatment for infection) including hepatitis C virus (HCV) and human immunodeficiency virus (HIV), or active uncontrolled hepatitis B infection except for the situations described in APPENDIX I. Screening for chronic conditions is not required.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Diagnostic
Study locations
France · 36 centers
- Angers - CHU — Angers
- Bayonne - CH — Bayonne
- Boulogne - Ambroise Paré — Boulogne
- Lyon - URCOT — Bron
- Caen - CHU — Caen
- Clermont-Ferrand - CHU — Clermont-Ferrand
- Colmar - CH — Colmar
- Créteil - CHI — Créteil
- … and 28 more centers
Identifiers
NCT: NCT06053099 · IFCT-2202