Osimertinib più chemioterapia vs Osimertinib nel NSCLC EGFRm con ctDNA EGFRm di persistenza alla settimana 3 dopo 1 litro di osimertinib (FLAME)
The Efficacy and Safety of Osimertinib Plus Carboplatin and Pemetrexed Versus Osimertinib Monotherapy in Locally Advanced or Metastatic EGFRm NSCLC Patients With EGFRm Persistence in ctDNA at 3 Weeks After 1L Osimertinib: A Multicenter, Randomized Controlled Study
This is a prospective, randomised, open-label, positive-controlled study to investigate the efficacy and safety of Osimertinib plus Carboplatin/Pemetrexed versus Osimertinib monotherapy in locally advanced or metastatic EGFRm NSCLC patients with EGFRm persistence in ctDNA at 3 weeks after first-line therapy with Osimertinib.
Panoramica dello studio
Stato
Stato
Condizioni
Condizioni
Intervento / Trattamento
Intervento / Trattamento
Tipo di studio
Tipo di studio
Iscrizione (Effettivo)
Iscrizione
Fase
Fase
- Fase 2
Contatti e Sedi
Luoghi di studio
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Beijing, Cina
- Cancer Hospital Chinese Academy of Medical Sciences
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Criteri di partecipazione
Criteri di ammissibilità
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Provision and signed of informed consent prior to any study specific procedures;
- Male or female, aged at least 18 years;
- Eastern Cooperative Oncology Group (ECOG) performance-status score of 0 or 1;
- Newly diagnosed, and histologically documented locally advanced or metastatic non-squamous NSCLC with sensitizing EGFR mutations positive (either Exon 19 deletion or 21 L858R, confirmed by histology or cytology ), and classified as stage IIIB, IIIC, IV or recurrent NSCLC which are not amenable to curative surgery or radiotherapy;
- Life expectancy of at least 3 months at recruitment;
- Only the patients receiving osimertinib as 1L treatment and meeting the following criteria will be considered:
A. Prior to 1L osimertinib:
- History of EGFRm (exon 19 deletion or exon 21 L858R) in the plasma ctDNA by the local testing methods.
- No previous systemic treatment. Adjuvant therapies, or definitive radiation/chemoradiation are permitted as long as treatment was completed at least 6 months prior to receiving 1L treatment.
- Patients with asymptomatic and stable CNS metastases for at least 2 weeks will be allowed, including leptomeningeal metastases.
B. Prior to randomization: Patients after 3 weeks of 1L osimertinib treatment who have persistence ctDNA EGFRm by SuperARMS at 3 weeks will be considered to be enrolled. They will need to further meet the criteria below before randomization:
- Patients without disease progression by RECIST 1.1 evaluation;
- At least 1 measurable extracranial lesion according to RECIST 1.1 .
- Female subjects should be using highly effective contraceptive measures, and must have a negative pregnancy test and not be breast-feeding prior to start of dosing if of child-bearing potential, or must have evidence of non-child-bearing potential.
- Male subjects should be willing to agreement to remain abstinent (refrain from heterosexual intercourse) or use contraceptive measures and agreement to refrain from donating sperm.
Exclusion Criteria:
- Involvement in the planning and/or conduct of the study;
- History of hypersensitivity to active or inactive excipients of Osimertinib and/or Pemetrexed and/or Carboplatin or drugs with a similar chemical structure or class to Osimertinib and/or Pemetrexed and/or Carboplatin;
- For patients, inability to collect plasma samples at baseline and disease progression;
- QT prolongation or any clinically important abnormalities in rhythm;
- Any evidence of severe or uncontrolled systemic diseases;
- Currently receiving medications or herbal supplements known to be strong inducers of CYP3A4;
- Any unresolved toxicities from prior therapy greater than CTCAE 5.0 grade 1 at the time of starting study treatment.
- Refractory nausea and vomiting, chronic gastrointestinal diseases, inability to swallow the formulated product or previous significant bowel resection that would preclude adequate absorption of osimertinib.
- Inadequate bone marrow reserve or organ function;
- Past medical history of interstitial lung disease, drug-induced interstitial lung disease, radiation pneumonitis which required steroid treatment, or any evidence of clinically active interstitial lung disease.
- Judgment by the investigator that the patient should not participate in the study if the patient is unlikely to comply with study procedures, restrictions and requirements.
- Contraindication for osimertinib, pemetrexed and carboplatin according to China approved label.
- Women who are pregnant or breast-feeding.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Numero di armi
Armi e interventi
Gruppo di partecipanti / ArmGruppo di partecipanti / Arm |
Intervento / TrattamentoIntervento / Trattamento |
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Sperimentale: Osimertinib 80 mg QD and platinum-based chemotherapy
Osimertinib 80 mg in combination with pemetrexed (500 mg/m2) plus carboplatin (AUC5) on Day 1 of 21day cycles (every 3 weeks) for up to 6 cycles, followed by Osimertinib daily with pemetrexed maintenance (500 mg/m2) every 3 weeks. |
Pemetrexed (500 mg/m2) plus carboplatin (AUC5) on Day 1 of 21day cycles (every 3 weeks) for up to 6 cycles, followed by Osimertinib daily with pemetrexed maintenance (500 mg/m2) every 3 weeks.
Altri nomi:
Pemetrexed (500 mg/m2) plus carboplatin (AUC5) on Day 1 of 21day cycles (every 3 weeks) for up to 6 cycles, followed by Osimertinib daily with pemetrexed maintenance (500 mg/m2) every 3 weeks. |
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Comparatore attivo: Osimertinib 80mg QD
All patients randomized into this will only receive Osimertinib 80mg. |
Pemetrexed (500 mg/m2) plus carboplatin (AUC5) on Day 1 of 21day cycles (every 3 weeks) for up to 6 cycles, followed by Osimertinib daily with pemetrexed maintenance (500 mg/m2) every 3 weeks.
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
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Progression free survival
Lasso di tempo: The analysis of PFS based on Investigator assessment (according to RECIST 1.1) will occur when approximately 54 progression events have been observed in the 80 randomized patients (approximately 67.5% PFS maturity).
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Progression-free survival (PFS) using Investigator assessment as defined by Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1). |
The analysis of PFS based on Investigator assessment (according to RECIST 1.1) will occur when approximately 54 progression events have been observed in the 80 randomized patients (approximately 67.5% PFS maturity).
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Misure di risultato secondarie
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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OS rate at 18 months
Lasso di tempo: The OS rate at 18 months will be defined as the Kaplan-Meier estimate of OS at 18 months.
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Proportion of patients alive at 18 months |
The OS rate at 18 months will be defined as the Kaplan-Meier estimate of OS at 18 months.
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Objective Response Rate (ORR)
Lasso di tempo: Objective Response Rate analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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ORR (per RECIST 1.1 using Investigator assessments) is defined as the number (percent) of patients with at least 1 visit response of CR or PR. |
Objective Response Rate analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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Disease Control Rate (DCR)
Lasso di tempo: Disease control rate analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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Disease control rate (DCR) is defined as the percentage of subjects who have a best overall response of CR or PR or SD by RECIST 1.1 as assessed by the Investigator. |
Disease control rate analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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Duration of Response (DoR)
Lasso di tempo: Duration of Response analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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DoR is defined as the time from the date of first documented response until the date of documented progression or death in the absence of disease progression. |
Duration of Response analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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Depth of Response
Lasso di tempo: Depth of Response analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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Depth of response by Investigator is defined as the relative change in the sum of the longest diameters of RECIST target lesions at the nadir in the absence of NLs or progression of NTLs when compared to baseline. |
Depth of Response analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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Safety and tolerability: Adverse event
Lasso di tempo: Safety and tolerability analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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All Adverse events/≥grade 3 AE/SAE incidence rate (AE/SAE graded by CTCAE v5); All ADR incidence rate; AESI: ILD/pneumonitis-like event, Cardiac failure |
Safety and tolerability analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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Molecular resistance mechanism
Lasso di tempo: Molecular resistance mechanism analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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To evaluate potential molecular resistance mechanism by biomarker analysis of plasma at baseline and disease progression and tissue samples (if applicable) by next-generation sequencing (NGS). |
Molecular resistance mechanism analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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Collaboratori e investigatori
Sponsor
Sponsor
Collaboratori
Collaboratori
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Inizio studio
Completamento primario (Effettivo)
Completamento primario
Completamento dello studio (Effettivo)
Completamento dello studio
Date di iscrizione allo studio
Primo inviato
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Primo Inserito
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento pubblicato
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Neoplasie per sede
- Neoplasie
- Malattie delle vie respiratorie
- Malattie polmonari
- Neoplasie delle vie respiratorie
- Neoplasie toraciche
- Neoplasie polmonari
- Carcinoma, broncogeno
- Neoplasie bronchiali
- Carcinoma, polmone non a piccole cellule
- Aminoacidi, peptidi e proteine
- Prodotti chimici organici
- Composti eterociclici
- Composti eterociclici, 2 anelli
- Composti eterociclici, anello fuso
- Complessi di coordinamento
- Guanina
- Ipossantine
- Purinoni
- Purine
- Glutammati
- Aminoacidi, acido
- Aminoacidi
- Aminoacidi, dicarbossilico
- Pemetrexed
- Carboplatino
- osimertinib
Altri numeri di identificazione dello studio
Altri numeri di identificazione dello studio
- ESR-19-20439
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