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- Ensayo clínico NCT07709585
Befotertinib Plus Chemotherapy With an MRD-guided Adaptive Strategy for Treatment Escalation and Response Optimization in EGFR-mutated NSCLC Patients (BE-MASTER)
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 2
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Xiaoshu Chai, MD
- Número de teléfono: +8613570301605
- Correo electrónico: chaixiaoshu@126.com
Copia de seguridad de contactos de estudio
- Nombre: Yanjuan Zhu, MD
- Número de teléfono: +8613902260217
- Correo electrónico: zyjsophy@gzucm.edu.cn
Ubicaciones de estudio
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Guangdong
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Guangzhou, Guangdong, Porcelana, 510120
- Guangdong Provincial Hospital of Chinese Medicine
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Contacto:
- Xiaoshu Chai, MD
- Correo electrónico: chaixiaoshu@126.com
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
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 de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: 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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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Progression-Free Survival (PFS)
Periodo de tiempo: 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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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.
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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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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Median Overall Survival (OS)
Periodo de tiempo: 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.
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Defined as the time from first dose of study treatment to death from any cause.
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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.
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Objective response rate (ORR)
Periodo de tiempo: including at least 24 months of follow-up after the last participant is enrolled.
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Defined as the proportion of participants achieving confirmed complete response (CR) or partial response (PR) per RECIST version 1.1.
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including at least 24 months of follow-up after the last participant is enrolled.
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Disease control rate (DCR)
Periodo de tiempo: including at least 24 months of follow-up after the last participant is enrolled.
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defined as the proportion of participants achieving confirmed complete response (CR), partial response (PR) or stable disease (SD) per RECIST version 1.1.
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including at least 24 months of follow-up after the last participant is enrolled.
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Time to intolerable toxicity
Periodo de tiempo: Including at least 24 months of follow-up after the last participant is enrolled.
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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.
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Including at least 24 months of follow-up after the last participant is enrolled.
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Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Xiaoshu Chai, MD, Guangdong Provincial Hospital of Traditional Chinese Medicine
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Procesos Patológicos
- Neoplasias
- Procesos Neoplásicos
- Condiciones Patológicas, Signos y Síntomas
- Neoplasia Residual
- Aminoácidos, péptidos y proteínas
- Químicos orgánicos
- Compuestos heterocíclicos
- Compuestos heterocíclicos, 2 anillos
- Compuestos heterocíclicos, anillo fusionado
- Químicos inorgánicos
- Compuestos de cloro
- Compuestos de nitrógeno
- Complejos de coordinación
- Guanina
- Hipoxantino
- Purinones
- Purinas
- Glutamatos
- Aminoácidos, ácido
- Aminoácidos
- Aminoácidos, dicarboxílico
- Compuestos de platino
- Pemetrexed
- Carboplatino
- Cisplatino
Otros números de identificación del estudio
- ZF2026-214
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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