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- Essai clinique NCT07709585
Befotertinib Plus Chemotherapy With an MRD-guided Adaptive Strategy for Treatment Escalation and Response Optimization in EGFR-mutated NSCLC Patients (BE-MASTER)
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Phase
- Phase 2
Contacts et emplacements
Coordonnées de l'étude
- Nom: Xiaoshu Chai, MD
- Numéro de téléphone: +8613570301605
- E-mail: chaixiaoshu@126.com
Sauvegarde des contacts de l'étude
- Nom: Yanjuan Zhu, MD
- Numéro de téléphone: +8613902260217
- E-mail: zyjsophy@gzucm.edu.cn
Lieux d'étude
-
-
Guangdong
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Guangzhou, Guangdong, Chine, 510120
- Guangdong Provincial Hospital of Chinese Medicine
-
Contact:
- Xiaoshu Chai, MD
- E-mail: chaixiaoshu@126.com
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
- Histologically or cytologically confirmed stage IIIB-IV non-small cell lung cancer (NSCLC).
- Age ≥18 years, any gender.
- Confirmed EGFR exon 19 deletion or exon 21 (L858R) substitution mutation by central laboratory or site-validated testing assay.
- No prior systemic anti-tumor therapy.
- ECOG performance status 0-2.
- Expected survival ≥12 weeks.
- Able to swallow oral study medication.
- At least one measurable lesion per RECIST 1.1 criteria.
Adequate organ function as defined below:
- Absolute neutrophil count ≥1.5 × 10^9/L;
- Platelet count ≥100 × 10^9/L;
- Hemoglobin ≥9 g/dL (transfusion allowed);
- Total bilirubin ≤1.5 × ULN;
- ALT/AST ≤2.5 × ULN (≤5 × ULN if liver metastasis);
- Serum creatinine ≤1.5 × ULN, or creatinine clearance ≥45 mL/min by Cockcroft-Gault formula if creatinine >1.5 × ULN.
- Fertile men and women agree to effective contraception during study treatment and for specified time after last dose.
Exclusion Criteria:
- Receiving other systemic anti-tumor therapy, or plan to combine other systemic anti-cancer agents during study.
- Participated in another investigational drug trial within 4 weeks prior to first study drug; major surgery within 4 weeks; unhealed wound, active ulcer or fracture; radiotherapy within 2 weeks without recovery.
- Severe cardiovascular disease: QTcF ≥450 ms or clinically significant ECG abnormality; uncontrolled hypertension (SBP>160 mmHg or DBP>100 mmHg); congestive heart failure, cardiomyopathy, arrhythmia requiring intervention, unstable angina, myocardial infarction, stroke or TIA within 6 months prior to treatment.
- Uncontrolled active infection including active HBV, HCV, HIV, active syphilis infection judged by investigator. Stable infection without safety risk is permitted.
- History of interstitial lung disease, drug-induced interstitial lung disease, radiation pneumonitis requiring steroids, or active interstitial lung disease.
- Active hemorrhage, clinically significant hemoptysis, high thromboembolic risk or prior severe thromboembolic events unsuitable for study treatment.
- Renal dysfunction with creatinine clearance <45 mL/min; prior intolerable toxicity to pemetrexed; severe hypersensitivity to pemetrexed or its excipients.
- Positive serum pregnancy test within 7 days before treatment, pregnant or breastfeeding women; fertile subjects refusing contraception during study and 3 months after last dose.
- Known severe hypersensitivity to befotertinib, cisplatin, carboplatin or their excipients.
- Any other medical, metabolic, physical or lab abnormality that may compromise subject safety or interfere with study results per investigator judgment.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Befotertinib with chemotherapy guided by dynamic MRD monitoring
All participants receive oral befotertinib 75 mg once daily for 3 weeks as induction therapy, followed by MRD detection. Treatment is adjusted dynamically based on serial MRD results: MRD-positive patients get 4 cycles of befotertinib plus pemetrexed-platinum chemotherapy; MRD-negative patients continue single-agent befotertinib. Subsequent MRD tests every 12 weeks guide treatment adjustment: patients who have not previously received pemetrexed -platinum chemotherapy and convert to MRD-positive will receive 4 cycles of befotertinib plus pemetrexed-platinum chemotherapy; patients who have previously received pemetrexed-platinum chemotherapy will receive single agent befotertinib if MRD-negative or befotertinib plus pemetrexed maintenance if MRD-positive.Treatment cycles are 21 days, continued until disease progression, intolerable toxicity, withdrawal of consent or death. |
Oral administration, initial dose 75 mg once daily; dose adjusted to 100 mg once daily based on safety and clinical benefit.
Used as induction, single-agent maintenance, or combined with chemotherapy.
This is induction combination chemotherapy for MRD-positive patients after initial befotinib monotherapy.
Pemetrexed at 500 mg/m² is given intravenously on Day 1 of each 21-day cycle, combined with either Cisplatin (75 mg/m² IV Day 1) or Carboplatin (AUC 5 IV Day 1) at investigator's discretion based on patient renal function and tolerability, for up to 4 cycles.
Standard premedication with folic acid, vitamin B12 and dexamethasone is administered per pemetrexed prescribing guidelines.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Progression-Free Survival (PFS)
Délai: Up to 48 months after the last participant enrollment,including at least 24 months of follow-up after the last participant is enrolled.
|
Time from first dose of study treatment to first radiographically confirmed isease progression according to RECIST version 1.1 or death from any cause, whichever occurs first.
|
Up to 48 months after the last participant enrollment,including at least 24 months of follow-up after the last participant is enrolled.
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Median Overall Survival (OS)
Délai: Including at least 24 months of follow-up after the last participant is enrolled.Participants lost to follow-up will be censored at the last date they were known to be alive.
|
Defined as the time from first dose of study treatment to death from any cause.
|
Including at least 24 months of follow-up after the last participant is enrolled.Participants lost to follow-up will be censored at the last date they were known to be alive.
|
|
Objective response rate (ORR)
Délai: including at least 24 months of follow-up after the last participant is enrolled.
|
Defined as the proportion of participants achieving confirmed complete response (CR) or partial response (PR) per RECIST version 1.1.
|
including at least 24 months of follow-up after the last participant is enrolled.
|
|
Disease control rate (DCR)
Délai: including at least 24 months of follow-up after the last participant is enrolled.
|
defined as the proportion of participants achieving confirmed complete response (CR), partial response (PR) or stable disease (SD) per RECIST version 1.1.
|
including at least 24 months of follow-up after the last participant is enrolled.
|
|
Time to intolerable toxicity
Délai: Including at least 24 months of follow-up after the last participant is enrolled.
|
Defined as the time from the first dose of study treatment to the first occurrence of treatment-related intolerable adverse event leading to permanent discontinuation of study therapy.
|
Including at least 24 months of follow-up after the last participant is enrolled.
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Collaborateurs et enquêteurs
Collaborateurs
Les enquêteurs
- Chercheur principal: Xiaoshu Chai, MD, Guangdong Provincial Hospital of Traditional Chinese Medicine
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Processus pathologiques
- Tumeurs
- Processus néoplasiques
- Conditions pathologiques, signes et symptômes
- Tumeur résiduelle
- Acides aminés, peptides et protéines
- Produits chimiques organiques
- Composés hétérocycliques
- Composés hétérocycliques, 2 anneaux
- Composés hétérocycliques, anneau fusionné
- Produits chimiques inorganiques
- Composés de chlore
- Composés d'azote
- Complexes de coordination
- Guanine
- Hypoxanthines
- Purinones
- Purines
- Glutamates
- Acides aminés, acides
- Acides aminés
- Acides aminés, dicarboxylique
- Composés en platine
- Pémétrexed
- Carboplatine
- Cisplatine
Autres numéros d'identification d'étude
- ZF2026-214
Plan pour les données individuelles des participants (IPD)
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Informations sur les médicaments et les dispositifs, documents d'étude
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