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Dasatinib in Treating Patients With Stage IIIB, Stage IV, or Recurrent Non-Small Cell Lung Cancer

8 februari 2019 bijgewerkt door: National Cancer Institute (NCI)

Phase II Study of Dasatinib in Non Small Cell Lung Cancer

Dasatinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. This phase II trial is studying how well dasatinib works in treating patients with stage IIIB, stage IV, or recurrent non-small cell lung cancer.

Studie Overzicht

Gedetailleerde beschrijving

PRIMARY OBJECTIVES:

I. Determine the progression-free survival at 12 weeks in patients with stage IIIB or IV or recurrent non-small cell lung cancer treated with dasatinib.

SECONDARY OBJECTIVES:

I. Determine the rate of response in patients treated with this drug. II. Examine the relationship between clinical response to this drug and epidermal growth factor receptor (EGFR) mutational status, EGFR copy number, and (phosphorylated Src) pSrc expression levels in pre-treatment tumor biopsies.

III. Determine the toxicity of this drug.

OUTLINE:

Patients received oral dasatinib twice daily on days 1-21. Treatment repeats every 21 days in the absence of disease progression or unacceptable toxicity.

Previously obtained paraffin-embedded tumor tissue samples are analyzed by polymerase chain reaction and fluorescent in situ hybridization (FISH) for epidermal growth factor receptor and by immunohistochemistry for pSrc expression.

Studietype

Ingrijpend

Inschrijving (Werkelijk)

35

Fase

  • Fase 2

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

    • Texas
      • Houston, Texas, Verenigde Staten, 77030
        • M D Anderson Cancer Center

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:

  • Platelet count >= 100,000/mm^3
  • Histologically or cytologically confirmed non-small cell lung cancer meeting 1 of the following criteria:

    • Stage IV disease
    • Stage IIIB disease with pleural effusion
    • Recurrent disease after surgery or radiotherapy
  • Measurable disease, defined as >= 1 lesion that can be accurately measured in at least 1 dimension (longest diameter to be recorded) >= 20 mm by conventional techniques OR >= 10 mm by spiral CT scan
  • Previously treated brain metastasis allowed, provided there is no bleeding, no midline shift, no need for steroids or anti-convulsants, and no symptoms
  • Must agree to obtain residual tumor tissue available from the existing diagnostic biopsy tumor tissue
  • Eastern cooperative oncology group (ECOG) performance status (PS) 0-1 OR Karnofsky PS 60-100%
  • Life expectancy > 12 weeks
  • White blood cell (WBC) >= 3,000/mm^3
  • Absolute neutrophil count >= 1,500/mm^3
  • Bilirubin =< 1.5 times upper limit of normal (ULN)
  • Aspartate aminotransferase (AST) and ALT =< 2.5 times ULN
  • Creatinine =< 3 times ULN OR Creatinine clearance >= 60 mL/min
  • No uncontrolled congestive heart failure or potentially life-threatening arrhythmia
  • No angina at rest
  • No neuropathy >= grade 2
  • No chronic diarrhea or history of inflammatory bowel disease
  • No history of pulmonary fibrosis (other than in an irradiated field)
  • No other concurrent serious medical illness
  • O2 saturation > 92% on room air
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception
  • No history of allergic reactions to compounds of similar chemical or biological composition to dasatinib
  • No heart rate-corrected QT interval (QTc) prolongation (i.e., QTC >= 480 msec) or other significant ECG abnormalities that could lead to adverse effects if the QTc interval were prolonged
  • No medical condition that impairs the ability to swallow, retain, or absorb dasatinib including, but not limited to, any of the following:

    • Gastrointestinal tract disease resulting in an inability to take oral medication, requirement for IV alimentation, prior surgical procedures affecting absorption, active peptic ulcer disease
  • No myocardial infarction or ventricular tachyarrhythmia within the past 6 months
  • left ventricular ejection fraction (LVEF) normal
  • No major conduction abnormality (unless cardiac pacemaker is present)
  • No ongoing or active infection
  • No history of significant bleeding disorder (congenital [von Willebrand's disease] or acquired [antifactor VIII antibodies])
  • No psychiatric illness or social situation that would preclude study compliance
  • No prior chemotherapy or biologic therapy for recurrent or metastatic non-small cell lung cancer
  • Adjuvant cytotoxic chemotherapy after surgical resection or chemotherapy with radiation for locally advanced disease (curative intent) allowed provided disease recurrence >= 3 months after completion of last chemotherapy dose
  • Measurable disease must be outside the radiotherapy port OR clearly growing inside the port
  • No prior radiotherapy to >= 25% of the marrow-containing skeleton
  • At least 7 days since prior and no concurrent medications that are inhibitors or inducers of CYP3A4
  • At least 7 days since prior and no concurrent agents with proarrhythmic potential
  • No other concurrent investigational agents
  • No other concurrent anticancer agents or therapies
  • No concurrent antiretroviral therapy for HIV-positive patients
  • No concurrent systemic antacids (H2 receptor antagonists and proton pump inhibitors)
  • Locally acting antacids allowed except for 2 hours before and after dasatinib administration

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: Arm I
Patients received oral dasatinib twice daily on days 1-21. Treatment repeats every 21 days in the absence of disease progression or unacceptable toxicity.
Mondeling gegeven
Andere namen:
  • BMS-354825
  • Sprycel

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Number of Participants With Objective Response (Complete Response (CR) or Partial Response (PR))
Tijdsspanne: 12 weeks
Objective response defined as participants with Complete Response (CR) or Partial Response (PR) evaluated using the Response Evaluation Criteria in Solid Tumors (RECIST) criteria. RECIST definitions are Complete Response (CR): Disappearance of all target lesions; Partial Response (PR): At least a 30% decrease in sum of the longest diameter (LD) of target lesions, taking as reference the baseline sum LD; Progressive Disease (PD): At least a 20% increase in the sum of the LD of target lesions, taking as reference the smallest sum LD recorded since the treatment started or the appearance of one or more new lesions; Stable Disease (SD): Neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD, taking as reference the smallest sum LD since the treatment started. Response measured by tumor size on computed tomography scans and by metabolic activity on positron emission tomography scans.
12 weeks
Progression-free Survival (PFS)
Tijdsspanne: Time from start of treatment to time of progression or death, assessed at 2 months
Progression-free survival (PFS) is defined as the duration of time from start of treatment to time of progression or death.
Time from start of treatment to time of progression or death, assessed at 2 months

Andere uitkomstmaten

Uitkomstmaat
Tijdsspanne
Time to Progression (TTP)
Tijdsspanne: Time from start of treatment to time of progression or death, assessed radiographically every 6 weeks
Time from start of treatment to time of progression or death, assessed radiographically every 6 weeks
Epidermal Growth Factor Receptor (EGFR) Mutational Status
Tijdsspanne: Baseline
Baseline
Epidermal Growth Factor Receptor (EGFR) Copy Number
Tijdsspanne: Baseline
Baseline
Phospho-Src (pSrc) Expression
Tijdsspanne: Baseline
Baseline

Medewerkers en onderzoekers

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

Onderzoekers

  • Hoofdonderzoeker: Faye Johnson, M.D. Anderson Cancer Center

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

1 maart 2007

Primaire voltooiing (Werkelijk)

1 april 2012

Studie voltooiing (Werkelijk)

1 april 2012

Studieregistratiedata

Eerst ingediend

9 april 2007

Eerst ingediend dat voldeed aan de QC-criteria

9 april 2007

Eerst geplaatst (Schatting)

11 april 2007

Updates van studierecords

Laatste update geplaatst (Werkelijk)

5 maart 2019

Laatste update ingediend die voldeed aan QC-criteria

8 februari 2019

Laatst geverifieerd

1 februari 2019

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • NCI-2009-00225 (Register-ID: CTRP (Clinical Trial Reporting Program))
  • P30CA016672 (Subsidie/contract van de Amerikaanse NIH)
  • N01CM62202 (Subsidie/contract van de Amerikaanse NIH)
  • 7798 (Andere identificatie: CTEP)
  • CDR0000538668
  • 2006-0593 (Andere identificatie: M D Anderson Cancer Center)

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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