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

12 december 2019 bijgewerkt door: 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).

Studie Overzicht

Toestand

Beëindigd

Interventie / Behandeling

Gedetailleerde beschrijving

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.

Studietype

Ingrijpend

Inschrijving (Werkelijk)

5

Fase

  • Fase 1

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

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

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar en ouder (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

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)

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Dacomitinib, Pemetrexed
Pemetrexed 500mg/m2 (i.v) q21d Dacomitinib 45mg/ orally (continuous)
Pemetrexed 500mg/m2 i.v (q21d) Dacomitinib 45mg orally (continuous)
Andere namen:
  • Alimta

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Dose Limiting Toxicities (DLTs)
Tijdsspanne: 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.

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Overall Response Rate
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Hoofdonderzoeker: Christoph C Zielinski, Univ. Prof., Univ Clinic for Internal Medicine I, Dep of Oncology, Medical University of Vienna

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start

30 juli 2013

Primaire voltooiing (Werkelijk)

15 september 2016

Studie voltooiing (Werkelijk)

15 september 2016

Studieregistratiedata

Eerst ingediend

27 mei 2013

Eerst ingediend dat voldeed aan de QC-criteria

7 augustus 2013

Eerst geplaatst (Schatting)

8 augustus 2013

Updates van studierecords

Laatste update geplaatst (Werkelijk)

30 december 2019

Laatste update ingediend die voldeed aan QC-criteria

12 december 2019

Laatst geverifieerd

1 januari 2018

Meer informatie

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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