- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT01918761
Dacomitinib + Pemetrexed for Patients With Advanced Non-squamous Non-small Cell Lung Cancer (NSCLC)
Dacomitinib + Pemetrexed for Patients With Advanced Non-squamous Non-small Cell Lung Cancer (NSCLC): a Phase I Trial to Identify a Dose of Dacomitinib in Combination With Pemetrexed That is Safe and Tolerated as Determined by the Incidence of Dose Limiting Toxicities (DLTs)
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
This open label phase Ib trial aims to determine the safety, tolerability, the pharmacokinetic profile, and to identify a dose of dacomitinib in combination with pemetrexed.
Three sites in Austria will participate in this study. Six to nine patients will initially be enrolled to receive the target dose of 45 mg qd dacomitinib (starting from day 2 of first cycle) in combination with pemetrexed (500 mg/m² 10 min infusion, once every 3 weeks). One cycle is defined as 21 days.
The first 3 subjects will be enrolled at a rate of ≤ 1 subject per week. If the target dose regimen is safe based on the incidence of DLT another 3 subjects will be enrolled.
If the dose of 45 mg qd is not safe alternate lower doses will be explored (dose level -1, dose level -2) to identify the maximal tolerated dose (MTD) of dacomitinib in combination of pemetrexed. Six to nine patients per dose level will be enrolled.
Tipo de estudio
Inscripción (Actual)
Fase
- Fase 1
Contactos y Ubicaciones
Ubicaciones de estudio
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Graz, Austria
- Medizinische Universität Graz Klinische Abteilung für Onkologie
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Innsbruck, Austria
- Universitätsklinik für Innere Medizin I
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion criteria:
- Written informed consent
- Histologically or cytologically confirmed stage IV non-squamous NSCLC
- Patients who are candidates to receive pemetrexed monotherapy
- If pemetrexed has been administered as first line therapy there must be a treatment free interval of at least one cycle (21 days)
- Measurable disease by RECIST criteria version 1.1.
- ≥18 years of age
- Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-2
- Adequate left ventricular ejection fraction (LVEF) ≥ 50% by either echocardiogram or multigated acquisition scan (MUGA)
Adequate organ function, including:
- Adequate bone marrow reserve: absolute neutrophil count (ANC) should be ≥ 1500 cells/mm3, platelets should be ≥ 100.000 cells/mm3
- Creatinine clearance ≥ 45 mL/min
- Total bilirubin ≤ 1.5 x upper normal limit (ULN)
- Aspartate Aminotransferase (AST) (SGOT) ≤ 3 x ULN (≤ 5.0 x ULN if hepatic metastases)
- Alanine Aminotransferase (ALT) (SGPT) ≤ 3 x ULN (≤ 5.0 x ULN if hepatic metastases)
- Female patients or their partners must be postmenopausal (defined as 12 months of amenorrhea following last menses), surgically sterile or must agree to use effective contraception while receiving trial treatment and for at least 3 months thereafter (the definition of effective contraception will be based on the judgment of the investigator). Male patients or their partners must be surgically sterile or must agree to use a barrier method of contraception while receiving trial treatment and for at least 3 months thereafter. (In all cases the definition of effective contraception will be based on the judgment of the investigator).
- Able to comply with required protocol procedures and able to receive oral medications
Exclusion criteria:
- Any evidence of mixed histology that includes elements of small cell or carcinoid lung cancer
- Predominantly squamous cell histology
- Patients with symptomatic brain metastases
- Chemotherapy, radiotherapy, biological or investigational agents within two weeks of baseline disease assessments
Patients with uncontrolled or significant cardiovascular disease, including:
- Myocardial infarction within 12 months
- Uncontrolled angina within 6 months
- Congestive heart failure within 6 months
- Diagnosed or suspected congenital long QT syndrome
- Any history of clinically significant ventricular arrhythmias (such as ventricular tachycardia, ventricular fibrillation, or Torsades de pointes)
- Prolonged QTc interval on pre-entry electrocardiogram. QTc must be less than CTC Grade 2 (≤480 msec) using appropriate correction formula with manual read by investigator if required. The echocardiogram (ECG) may be repeated for evaluation of eligibility after management of correctable causes for observed QTc prolongation
- Any history of second or third degree heart block (may be eligible if currently have a pacemaker)
- Heart rate <50/minute on baseline electrocardiogram
- Uncontrolled hypertension
- Prior malignancy: Patients will not be eligible if they have evidence of other malignancy (other than non-melanoma skin cancer or in situ cervical cancer, or localized and presumed cured prostate cancer with prostate specific antigen (PSA) < ULN) within the last 3 years.
- Pregnant or lactating females. Serum pregnancy test to be assessed within 7 days prior to study treatment start. Known hypersensitivity to pemetrexed and/or dacomitinib
- Patients with exposure to other investigational drug therapy
- Previous therapy with an oral tyrosine kinase inhibitor (TKI)
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: Dacomitinib, Pemetrexed
Pemetrexed 500mg/m2 (i.v) q21d Dacomitinib 45mg/ orally (continuous)
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Pemetrexed 500mg/m2 i.v (q21d) Dacomitinib 45mg orally (continuous)
Otros nombres:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Dose Limiting Toxicities (DLTs)
Periodo de tiempo: From start of treatment to end of treatment or death, whichever occurs first. The study was suspended after 36 months.
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The primary objective of this study is to determine the maximal tolerated dose (MTD) of the combination pemetrexed + dacomitinib by the incidence of dose limiting toxicities (DLTs).
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From start of treatment to end of treatment or death, whichever occurs first. The study was suspended after 36 months.
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Overall Response Rate
Periodo de tiempo: Until progression of disease (PD) or 24 month after end of treatment for participants with no PD. The study was suspended after 36 months
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Overall Response Rate (ORR) is defined as the proportion of patients with complete Response (CR) or partial Response (PR).
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Until progression of disease (PD) or 24 month after end of treatment for participants with no PD. The study was suspended after 36 months
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Overall Survival
Periodo de tiempo: until date of death. The study was suspended after 36 months.
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Overall survival (OS) defined as time from start of Dacomitinib to date of death from any cause.
Patients without recorded death were censored at the date the patient was last known to be alive.
Patients were followed up for survival for 24 month after end of Treatment.
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until date of death. The study was suspended after 36 months.
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Progression-free Survival
Periodo de tiempo: Up to progression or death due to any cause. The study was suspended after 36 months
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Progression-free survival (PFS) defined as time from start of Dacomitinib to date of progression or date of death from any cause, whichever occurred first.
Patients without recorded progression or death were censored at the last date they were known to have not progressed.
Patients were followed up for progression-free survival for 24 month after end of Treatment.
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Up to progression or death due to any cause. The study was suspended after 36 months
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Christoph C Zielinski, Univ. Prof., Univ Clinic for Internal Medicine I, Dep of Oncology, Medical University of Vienna
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
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
- Enfermedades de las vías respiratorias
- Neoplasias
- Enfermedades pulmonares
- Neoplasias por sitio
- Neoplasias de las vías respiratorias
- Neoplasias torácicas
- Carcinoma Broncogénico
- Neoplasias Bronquiales
- Neoplasias Pulmonares
- Carcinoma de pulmón de células no pequeñas
- Mecanismos moleculares de acción farmacológica
- Inhibidores de la síntesis de ácidos nucleicos
- Inhibidores de enzimas
- Agentes antineoplásicos
- Antagonistas del ácido fólico
- Pemetrexed
Otros números de identificación del estudio
- CECOG/ NSCLC.1.1.001
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