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Dacomitinib + Pemetrexed for Patients With Advanced Non-squamous Non-small Cell Lung Cancer (NSCLC)

12 de diciembre de 2019 actualizado por: Central European Cooperative Oncology Group

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)

To identify a dose of dacomitinib in combination with pemetrexed that is safe and tolerated as determined by the incidence of DLTs (dose limiting toxicities).

Descripción general del estudio

Estado

Terminado

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

Intervencionista

Inscripción (Actual)

5

Fase

  • Fase 1

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

      • Graz, Austria
        • Medizinische Universität Graz Klinische Abteilung für Onkologie
      • Innsbruck, Austria
        • Universitätsklinik für Innere Medizin I

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

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:

    1. Adequate bone marrow reserve: absolute neutrophil count (ANC) should be ≥ 1500 cells/mm3, platelets should be ≥ 100.000 cells/mm3
    2. Creatinine clearance ≥ 45 mL/min
    3. Total bilirubin ≤ 1.5 x upper normal limit (ULN)
    4. Aspartate Aminotransferase (AST) (SGOT) ≤ 3 x ULN (≤ 5.0 x ULN if hepatic metastases)
    5. 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:

    1. Myocardial infarction within 12 months
    2. Uncontrolled angina within 6 months
    3. Congestive heart failure within 6 months
    4. Diagnosed or suspected congenital long QT syndrome
    5. Any history of clinically significant ventricular arrhythmias (such as ventricular tachycardia, ventricular fibrillation, or Torsades de pointes)
    6. 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
    7. Any history of second or third degree heart block (may be eligible if currently have a pacemaker)
    8. Heart rate <50/minute on baseline electrocardiogram
    9. 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

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿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
Experimental: Dacomitinib, Pemetrexed
Pemetrexed 500mg/m2 (i.v) q21d Dacomitinib 45mg/ orally (continuous)
Pemetrexed 500mg/m2 i.v (q21d) Dacomitinib 45mg orally (continuous)
Otros nombres:
  • Alimata

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
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.
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).
From start of treatment to end of treatment or death, whichever occurs first. The study was suspended after 36 months.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
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
Overall Response Rate (ORR) is defined as the proportion of patients with complete Response (CR) or partial Response (PR).
Until progression of disease (PD) or 24 month after end of treatment for participants with no PD. The study was suspended after 36 months
Overall Survival
Periodo de tiempo: until date of death. The study was suspended after 36 months.
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.
until date of death. The study was suspended after 36 months.
Progression-free Survival
Periodo de tiempo: Up to progression or death due to any cause. The study was suspended after 36 months
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.
Up to progression or death due to any cause. The study was suspended after 36 months

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

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

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio

30 de julio de 2013

Finalización primaria (Actual)

15 de septiembre de 2016

Finalización del estudio (Actual)

15 de septiembre de 2016

Fechas de registro del estudio

Enviado por primera vez

27 de mayo de 2013

Primero enviado que cumplió con los criterios de control de calidad

7 de agosto de 2013

Publicado por primera vez (Estimar)

8 de agosto de 2013

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

30 de diciembre de 2019

Última actualización enviada que cumplió con los criterios de control de calidad

12 de diciembre de 2019

Última verificación

1 de enero de 2018

Más información

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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