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A Study In Patients With Non-Small Cell Lung Cancer Testing If Erlotinib Plus SU011248 (Sunitinib) Is Better Than Erlotinib Alone (SUN1058)

31 stycznia 2013 zaktualizowane przez: Pfizer

Randomized, Double-Blind, Phase 2 Study Of Erlotinib With Or Without SU011248 In The Treatment Of Metastatic Non-Small Cell Lung Cancer

This study will test whether treatment with erlotinib plus SU011248 is better than erlotinib alone in patients with advanced/metastatic lung cancer who have received previous treatment with a platinum-based regimen

Przegląd badań

Status

Zakończony

Warunki

Interwencja / Leczenie

Typ studiów

Interwencyjne

Zapisy (Rzeczywisty)

162

Faza

  • Faza 2

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

  • Hiszpania
    • Cantabria
      • Santander, Cantabria, Hiszpania, 39008
        • Pfizer Investigational Site
  • Holandia
      • Amsterdam, Holandia, 1066 CX
        • Pfizer Investigational Site
      • Groningen, Holandia, 9713 GZ
        • Pfizer Investigational Site
  • Kanada
    • Alberta
      • Edmonton, Alberta, Kanada, T6G 1Z2
        • Pfizer Investigational Site
    • Ontario
      • Hamilton, Ontario, Kanada, L8V 5C2
        • Pfizer Investigational Site
  • Polska
      • Bydgoszcz, Polska, 85-796
        • Pfizer Investigational Site
      • Gdansk, Polska, 80-952
        • Pfizer Investigational Site
  • Rumunia
      • Bucuresti, Rumunia, 30171
        • Pfizer Investigational Site
    • Cluj
      • Cluj-Napoca, Cluj, Rumunia, 400015
        • Pfizer Investigational Site
    • Sector 2
      • Bucuresti, Sector 2, Rumunia, 022328
        • Pfizer Investigational Site
  • Stany Zjednoczone
    • Alabama
      • Birmingham, Alabama, Stany Zjednoczone, 35233
        • Pfizer Investigational Site
      • Birmingham, Alabama, Stany Zjednoczone, 35294
        • Pfizer Investigational Site
      • Mobile, Alabama, Stany Zjednoczone, 36604
        • Pfizer Investigational Site
    • California
      • Antioch, California, Stany Zjednoczone, 94531
        • Pfizer Investigational Site
      • Palm Springs, California, Stany Zjednoczone, 92262-4885
        • Pfizer Investigational Site
      • Pleasant Hill, California, Stany Zjednoczone, 94523
        • Pfizer Investigational Site
      • San Leandro, California, Stany Zjednoczone, 94578
        • Pfizer Investigational Site
    • Illinois
      • Chicago, Illinois, Stany Zjednoczone, 60612
        • Pfizer Investigational Site
    • Missouri
      • Creve Coeur, Missouri, Stany Zjednoczone, 63141
        • Pfizer Investigational Site
      • St. Louis, Missouri, Stany Zjednoczone, 63110
        • Pfizer Investigational Site
      • St. Louis, Missouri, Stany Zjednoczone, 63110-1094
        • Pfizer Investigational Site
      • St. Peters, Missouri, Stany Zjednoczone, 63376
        • Pfizer Investigational Site
    • North Carolina
      • Chapel Hill, North Carolina, Stany Zjednoczone, 27599-7600
        • Pfizer Investigational Site
      • Clinton, North Carolina, Stany Zjednoczone, 28328
        • Pfizer Investigational Site
      • Goldsboro, North Carolina, Stany Zjednoczone, 27534
        • Pfizer Investigational Site
      • Wilson, North Carolina, Stany Zjednoczone, 27893
        • Pfizer Investigational Site
    • Ohio
      • Cleveland, Ohio, Stany Zjednoczone, 44106
        • Pfizer Investigational Site
    • Texas
      • Houston, Texas, Stany Zjednoczone, 77030
        • Pfizer Investigational Site
  • Węgry
      • Budapest, Węgry, 1525
        • Pfizer Investigational Site
      • Torokbalint, Węgry, 2045
        • Pfizer Investigational Site
  • Włochy
      • Genova, Włochy, 16132
        • Pfizer Investigational Site
      • Monteforte Irpino, AV, Włochy, 83024
        • Pfizer Investigational Site

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

18 lat i starsze (Dorosły, Starszy dorosły)

Akceptuje zdrowych ochotników

Nie

Płeć kwalifikująca się do nauki

Wszystko

Opis

Inclusion Criteria:

  • Patients with locally advanced/metastatic non-small cell lung cancer
  • Prior treatment with no more than 2 chemotherapy regimens including a platinum-based regimen

Exclusion Criteria:

  • Prior treatment with any receptor tyrosine kinase inhibitors, Vascular endothelial growth factor (VEGF) inhibitors or other angiogenic inhibitors
  • History of or known brain metastases

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Podwójnie

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Aktywny komparator: B
Lek: erlotinib
erlotinib 150 mg daily by tablets in a continuous regimen, until progression or unacceptable toxicity
Lek: placebo
Placebo daily by oral capsule in a continuous regimen plus erlotinib 150 mg daily by tablets in a continuous regimen, until progression or unacceptable toxicity
Eksperymentalny: A
Lek: erlotinib
erlotinib 150 mg daily by tablets in a continuous regimen, until progression or unacceptable toxicity
Lek: sunitinib
Sunitinib 37.5 mg daily by oral capsule in a continuous regimen plus erlotinib 150 mg daily by tablets in a continuous regimen, until progression or unacceptable toxicity
Inne nazwy:
  • Sutent

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Progression-Free Survival (PFS)
Ramy czasowe: From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
PFS=time from randomization date to date of first documentation of progressive disease (PD; defined as greater than or equal to [≥]20% increase in sum of longest dimensions of target lesions taking as a reference smallest sum of longest dimensions recorded since first dose or appearance of ≥1 new lesions) or death on-study due to any cause, whichever occurred first based on third party independent imaging review laboratory assessment. PFS calculated as (first event date minus randomization date plus 1) divided by 7.02. Used 7.02 days as it equals 365 days per year divided by 52 weeks per year.
From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Percentage of Participants With Objective Response
Ramy czasowe: From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
Objective Response Rate (ORR)=participants with confirmed complete response (CR) or partial response (PR) according to Response Evaluation Criteria in Solid Tumors (RECIST,Version 1.0) based on third party independent imaging review laboratory assessment. A CR was defined as the disappearance of all target lesions that persisted on repeat imaging study at least 4 weeks after initial documentation of response. A PR was defined as a ≥30% decrease in sum of longest dimensions of target lesions taking as a reference the baseline sum longest dimensions.
From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
Time to Tumor Progression (TTP)
Ramy czasowe: From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
TTP was defined as the time from date of randomization to first documentation of PD based on third party independent imaging review laboratory assessment. TTP was calculated as (first event date minus randomization date plus 1) divided by 7.02.
From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
Duration of Response (DR)
Ramy czasowe: From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
DR was defined as time from first documentation of objective tumor response (CR or PR) that was subsequently confirmed to the first documentation of PD or death on-study due to any cause, whichever occurred first. DR was calculated as (first date of PD or death minus first date of CR or PR that was subsequently confirmed plus 1) divided by 7.02.
From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
Overall Survival (OS)
Ramy czasowe: From randomization until death (up to Month 17)
OS was defined as time from date of randomization to date of death due to any cause. OS was calculated as (date of death minus date of randomization plus 1) divided by 30.4. For participants still alive at the time of analysis, OS time was censored on last date that participants were known to be alive.
From randomization until death (up to Month 17)
Percentage of Participants Surviving at 1 Year
Ramy czasowe: From randomization until death (up until Month 17)
Percentage of participants alive at 1 year after date of first administration of study medication.
From randomization until death (up until Month 17)
Area Under the Curve From Time Zero to 24 Hours [AUC(0-24)] of Erlotinib
Ramy czasowe: Days 1 and 22 (Cycle 1) at 0, 1, 2, 4, 6, 8, and 24 hours postdose
AUC0-24=Area under the plasma concentration versus time curve from time zero (pre-dose) to 24 hours (0-24) of erlotinib
Days 1 and 22 (Cycle 1) at 0, 1, 2, 4, 6, 8, and 24 hours postdose
AUC(0-24) of Sunitinib
Ramy czasowe: Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, and 24 hours postdose
AUC0-24=Area under the plasma concentration versus time curve from time zero (pre-dose) to 24 hours (0-24) of sunitinib
Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, and 24 hours postdose
AUC(0-24) of SU-012662 (Metabolite of Sunitinib)
Ramy czasowe: Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, and 24 hours postdose
AUC0-24=Area under the plasma concentration versus time curve from time zero (pre-dose) to 24 hours (0-24) of SU-012662 (metabolite of sunitinib)
Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, and 24 hours postdose
AUC(0-24) of Total Drug (Sunitinib + SU-012662)
Ramy czasowe: Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, and 24 hours postdose
AUC0-24=Area under the plasma concentration versus time curve from time zero (pre-dose) to 24 hours (0-24) of total drug (sunitinib + SU-012662)
Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, and 24 hours postdose
Maximum Observed Plasma Concentration (Cmax) of Erlotinib
Ramy czasowe: Days 1 and 22 (Cycle 1) at 0, 1, 2, 4, 6, 8, and 24 hours postdose
Days 1 and 22 (Cycle 1) at 0, 1, 2, 4, 6, 8, and 24 hours postdose
Cmax of Sunitinib
Ramy czasowe: Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose
Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose
Cmax of SU-012662 (Metabolite of Sunitinib)
Ramy czasowe: Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose
Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose
Cmax of Total Drug (Sunitinib + SU-012662)
Ramy czasowe: Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose
Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose
Area Under the Curve From Time Zero to Extrapolated Infinite Time (AUC0-inf) for Erlotinib
Ramy czasowe: Days 1 and 22 (Cycle 1) at 0, 1, 2, 4, 6, 8, and 24 hours postdose; predose on Days 22 and 23 (Cycle 1)
AUC (0-inf) = Area under the plasma concentration versus time curve (AUC) from time zero (pre-dose) to extrapolated infinite time (0-inf) for erlotinib. It is obtained from AUC from time zero (pre-dose) to last quantifiable concentration(AUC[0-t]) plus AUC from time last quantifiable concentration extrapolated infinite time (AUC[t-inf])
Days 1 and 22 (Cycle 1) at 0, 1, 2, 4, 6, 8, and 24 hours postdose; predose on Days 22 and 23 (Cycle 1)
AUC(0-inf) for Sunitinib
Ramy czasowe: Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose; predose on Days 15, 16, and 17 (Cycle 1)
AUC (0 - inf) = Area under the plasma concentration versus time curve (AUC) from time zero (pre-dose) to extrapolated infinite time (0-inf) for sunitinib. It is obtained from AUC(0-t) plus AUC(t-inf)
Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose; predose on Days 15, 16, and 17 (Cycle 1)
AUC(0-inf) for SU-012662 (Metabolite of Sunitinib)
Ramy czasowe: Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose; predose on Days 15, 16, and 17 (Cycle 1)
AUC(0-inf) = Area under the plasma concentration versus time curve (AUC) from time zero (pre-dose) to extrapolated infinite time (0-inf) for SU-012662 (metabolite of sunitinib). It is obtained from AUC(0-t) plus AUC(t-inf)
Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose; predose on Days 15, 16, and 17 (Cycle 1)
AUC(0-inf) for Total Drug (Sunitinib + SU-012662)
Ramy czasowe: Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose; predose on Days 15, 16, and 17 (Cycle 1)
AUC(0-inf) = Area under the plasma concentration versus time curve (AUC) from time zero (pre-dose) to extrapolated infinite time (0-inf) for total drug (sunitinib + SU-012662). It is obtained from AUC(0-t) plus AUC(t-inf)
Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose; predose on Days 15, 16, and 17 (Cycle 1)
Plasma Decay Half-life (t1/2) of Erlotinib
Ramy czasowe: Days 1 and 22 (Cycle 1) at 0, 1, 2, 4, 6, 8, and 24 hours postdose
Plasma decay half-life is the time measured for the plasma concentration to decrease by one half.
Days 1 and 22 (Cycle 1) at 0, 1, 2, 4, 6, 8, and 24 hours postdose
Plasma Decay Half-life (t1/2) of Sunitinib
Ramy czasowe: Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose
Plasma decay half-life is the time measured for the plasma concentration to decrease by one half.
Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose
Erlotinib Clearance at Steady State After Oral Administration (CL/F)
Ramy czasowe: Day 15 (Cycle 1) at 0, 1, 2, 4, 6, 8, and 24 hours postdose
Day 15 (Cycle 1) at 0, 1, 2, 4, 6, 8, and 24 hours postdose
Sunitinib Clearance at Steady State After Oral Administration (CL/F)
Ramy czasowe: Day 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose
Day 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose
Time to Reach Maximum Observed Plasma Concentration (Tmax) for Erlotinib
Ramy czasowe: Days 1 and 22 (Cycle 1) at 0, 1, 2, 4, 6, 8, and 24 hours postdose
Days 1 and 22 (Cycle 1) at 0, 1, 2, 4, 6, 8, and 24 hours postdose
Tmax for Sunitinib
Ramy czasowe: Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose
Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose
Tmax for SU-012662 (Metabolite of Sunitinib)
Ramy czasowe: Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose
Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose
Tmax for Total Drug (Sunitinib + SU-012662)
Ramy czasowe: Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose
Days 1 and 15 of Cycle 1 at 0, 1, 2, 4, 6, 8, 24 and 48 hours postdose
Dose-Corrected Observed Plasma Trough Concentrations (Ctrough) for Erlotinib on Day 1 of Cycles 3-13 (Original and Amended, Arms A and B), and Day 1 of Cycles 1-18 (Randomized)
Ramy czasowe: predose Day 1 (Cycles 3-13); predose Day 1 (Cycles 1-18)
Ctrough = plasma concentration of erlotinib prior to study drug administration. Dose correction was made to the initial intended dose in Cycle 1. Assessed in the Original and Amended Lead-In (Arms A and B) Cohorts predose on Day 1 (Cycles 3-13) and in the Randomized Cohort (Sunitinib + Erlotinib treatment group only) predose on Day 1 of Cycles 1-18.
predose Day 1 (Cycles 3-13); predose Day 1 (Cycles 1-18)
Dose-Corrected Ctrough for Erlotinib on Day 15 Cycle 1 (Original), Day 1 of Cycle 3 (Original and Amended, Arms A and B), and Day 1 of Cycles 1-18 (Randomized)
Ramy czasowe: predose Day 15 (Cycle1); predose Day 1 (Cycle 3); predose Day 1 (Cycles 1-18)
Ctrough = plasma concentration of erlotinib prior to study drug administration. Dose correction was made to the initial intended dose in Cycle 1. Assessed in the Original Cohort predose on Day 15 (Cycle 1, Time Zero) and Day 1 (Cycle 3), in the Amended Lead-In Cohort (Arms A and B) predose on Day 1 (Cycle 3) and in the Randomized Cohort (Sunitinib + Erlotinib treatment group only) predose on Day 1 of Cycles 1-18.
predose Day 15 (Cycle1); predose Day 1 (Cycle 3); predose Day 1 (Cycles 1-18)
Dose-Corrected Ctrough for Sunitinib on Day 1 of Cycles 3-13 (Original and Amended, Arms A and B), and Day 1 of Cycles 1-18 (Randomized)
Ramy czasowe: predose Day 1 (Cycles 3-13); predose Day 1 (Cycles 1-18)
Ctrough = plasma concentration of sunitinib prior to study drug administration. Dose correction was made to the initial intended dose in Cycle 1. Assessed in the Original and Amended Lead-In (Arms A and B) Cohorts predose on Day 1 (Cycles 3-13) and in the Randomized Cohort (Sunitinib + Erlotinib treatment group only) predose on Day 1 of Cycles 1-18.
predose Day 1 (Cycles 3-13); predose Day 1 (Cycles 1-18)
Dose-Corrected Ctrough for Sunitinib on Day 15 Cycle 1 (Original), Day 1 of Cycle 3 (Original and Amended, Arms A and B), and Day 1 of Cycles 1-18 (Randomized)
Ramy czasowe: predose Day 15 (Cycle 1) and Day 1 (Cycle 3); predose Day 1 (Cycle 3); predose Day 1 (Cycles 1-18)
Ctrough = plasma concentration of sunitinib prior to study drug administration. Dose correction was made to the initial intended dose in Cycle 1. Assessed in the Original Cohort predose on Day 15 (Cycle 1, Time Zero) and Day 1 (Cycle 3), in the Amended Lead-In Cohort (Arms A and B) predose on Day 1 (Cycle 3) and in the Randomized Cohort (Sunitinib + Erlotinib treatment group only) predose on Day 1 of Cycles 1-18.
predose Day 15 (Cycle 1) and Day 1 (Cycle 3); predose Day 1 (Cycle 3); predose Day 1 (Cycles 1-18)
Dose-Corrected Ctrough for SU-012662 (Metabolite of Sunitinib) on Day 1 of Cycles 3-13 (Original and Amended, Arms A and B), and Day 1 of Cycles 1-18 (Randomized)
Ramy czasowe: predose Day 1 (Cycles 3-13); predose Day 1 (Cycles 1-18)
Ctrough = plasma concentration of SU-012662 prior to study drug administration. Dose correction was made to the initial intended dose in Cycle 1. Assessed in the Original and Amended Lead-In (Arms A and B) Cohorts predose on Day 1 (Cycles 3-13) and in the Randomized Cohort (Sunitinib + Erlotinib treatment group only) predose on Day 1 of Cycles 1-18.
predose Day 1 (Cycles 3-13); predose Day 1 (Cycles 1-18)
Dose-Corrected Ctrough for SU-012662 (Metabolite of Sunitinib) on Day 15 Cycle 1 (Original), Day 1 of Cycle 3 (Original and Amended, Arms A and B), and Day 1 of Cycles 1-18 (Randomized)
Ramy czasowe: predose Day 15 (Cycle 1) and Day 1 (Cycle 3); predose Day 1 (Cycle 3); predose Day 1 (Cycles 1-18)
Ctrough = plasma concentration of SU-012662 prior to study drug administration. Dose correction was made to the initial intended dose in Cycle 1. Assessed in the Original Cohort predose on Day 15 (Cycle 1, Time Zero) and Day 1 (Cycle 3), in the Amended Lead-In Cohort (Arms A and B) predose on Day 1 (Cycle 3) and in the Randomized Cohort (Sunitinib + Erlotinib treatment group only) predose on Day 1 of Cycles 1-18.
predose Day 15 (Cycle 1) and Day 1 (Cycle 3); predose Day 1 (Cycle 3); predose Day 1 (Cycles 1-18)
Percentage of Participants With Epidermal Growth Factor Receptor (EGFR) Expression by Immunohistochemistry (IHC) Using 0 Percent [%] Cutoff
Ramy czasowe: Baseline
Percentage of participants with EGFR expression by IHC using a 0% cutoff; Reported as positive, negative, or unmeasured (where positive was greater than 0% of cells demonstrating membranous staining for EGFR). Correlative analysis of EGFR expression was conducted using tumor biopsy samples collected at the time of initial diagnosis (preferred) or at the time of most recent recurrence/progression, although any time was acceptable.
Baseline
PFS in Subgroups That Were Defined by EGFR Expression (Using 0% Cutoff)
Ramy czasowe: From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
PFS defined as time in weeks from date of randomization to date of first documentation of PD or death on-study due to any cause, whichever occurred first, in the following subgroups: positive, negative, or unmeasured EGFR expression. EGFR expression was analyzed using a 0% cutoff where positive was greater than 0% of cells demonstrating membranous staining for EGFR. PFS calculated as (first event date minus randomization date plus 1) divided by 7.02.
From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
Percentage of Participants With EGFR Expression by IHC (Using 10% Cutoff)
Ramy czasowe: Baseline
Percentage of participants with EGFR Expression by IHC using a 10% cutoff; Reported as positive (positive values were defined as being greater than 10% of cells demonstrating membranous staining for EGFR), negative, or unmeasured. Correlative analysis of EGFR expression was conducted using tumor biopsy samples collected at the time of initial diagnosis (preferred) or at the time of most recent recurrence/progression, although any time was acceptable.
Baseline
PFS in Subgroups That Were Defined by EGFR Expression (Using 10% Cutoff)
Ramy czasowe: From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
PFS defined as time in weeks from date of randomization to date of first documentation of PD or death on-study due to any cause, whichever occurred first, in the following subgroups: positive, negative, or unmeasured EGFR expression. EGFR expression was analyzed using a 10% cutoff where positive was greater than 10% of cells demonstrating membranous staining for EGFR. PFS calculated as (first event date minus randomization date plus 1) divided by 7.02.
From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
Percentage of Participants With EGFR Gene Copy Number Increase
Ramy czasowe: Baseline
The number of copies corresponding to exon 19 of the EGFR gene was determined by real-time quantitative polymerase chain reaction (PCR). The percentage of participants with EGFR Gene Copy Number Increase (defined as greater than 4 copies) was determined using deoxyribonucleic acid (DNA) from tumor biopsy samples collected at the time of initial diagnosis (preferred) or at the time of most recent recurrence/progression, although any time was acceptable. Reported as yes, no or unmeasured.
Baseline
PFS in Subgroups That Were Defined by EGFR Gene Copy Number Increase
Ramy czasowe: From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
PFS, defined as time from date of randomization to the date of the first documentation of PD or death on-study due to any cause, whichever occurred first, in subgroups that were defined by EGFR gene copy number increase (reported as yes, no, or unmeasured). The number of copies corresponding to exon 19 of the EGFR gene was determined and an increase was defined as greater than 4 copies. PFS was calculated as (first event date minus randomization date plus 1)/7.02.
From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
Percentage of Participants With EGFR Gene Amplification
Ramy czasowe: Baseline
The percentage of participants with EGFR gene amplification (defined as greater than 15) was determined and reported as yes, no, or unmeasured. Correlative analysis of EGFR gene amplification was conducted using tumor biopsy samples collected at the time of initial diagnosis (preferred) or at the time of most recent recurrence/progression, although any time was acceptable.
Baseline
PFS in Subgroups That Were Defined by EGFR Gene Amplification
Ramy czasowe: From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
PFS, defined as time from date of randomization to date of first documentation of PD or death on-study due to any cause, whichever occurred first, in subgroups that were defined by EGFR gene amplification (defined as greater than 15) and reported as no or unmeasured. PFS was calculated as (first event date minus randomization date plus 1) divided by 7.02.
From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
Percentage of Participants With EGFR Gene Mutation
Ramy czasowe: Baseline
Mutations in exons 18 through 21 of the EGFR gene were analyzed by high-performance liquid chromatography using DNA from tumor biopsy samples collected at the time of initial diagnosis (preferred) or at the time of most recent recurrence/progression, although any time was acceptable. The percentage of participants with EGFR mutations categorized as mutated, wild type or indeterminate was reported.
Baseline
PFS in Subgroups That Were Defined by EGFR Gene Mutation
Ramy czasowe: From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
PFS, defined as time from date of randomization to date of first documentation of PD or to death on-study due to any cause, whichever occurred first, in subgroups that were defined by EGFR gene mutation (reported as mutated, wild type, or indeterminate). PFS was calculated as (first event date minus randomization date plus 1) divided by 7.02.
From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
Percentage of Participants With KRAS (V-Ki-ras2 Kirsten Rat Sarcoma Viral Oncogene Homolog) Gene Mutations
Ramy czasowe: Baseline
Mutations in exons 2-3 of the KRAS gene (including codons 12, 13, and 61) were analyzed by high-performance liquid chromatography using DNA from tumor biopsy samples collected at the time of initial diagnosis (preferred) or at the time of most recent recurrence/progression, although any time was acceptable. The percentage of participants with KRAS mutations categorized as mutated, wild type or indeterminate was reported.
Baseline
PFS in Subgroups That Were Defined by KRAS Gene Mutation
Ramy czasowe: From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
PFS, defined as time from date of randomization to date of first documentation of PD or death on-study due to any cause, whichever occurred first, in subgroups that were defined by KRAS gene mutation (reported as mutated, wild type, or indeterminate). PFS was calculated as (first event date minus randomization date plus 1) divided by 7.02.
From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
Percentage of Participants With Germline Vascular Endothelial Growth Factor Receptor 2 (VEGFR2) Polymorphisms
Ramy czasowe: Baseline
Blood samples were collected at baseline for multiplex reverse transcription (RT) analysis of genes expressing proteins that are targets of sunitinib or involved in angiogenesis or tumor growth to determine expression levels. Percentage of participants with germline VEGFR2 single nucleotide polymorphisms (SNPs) was reported for the following genotype frequencies: homozygous C alleles (C/C), T alleles (T/T), G alleles (G/G), or A alleles (A/A), and the following heterozygous genotypes C/T, G/T, T/A, and G/A.
Baseline
PFS in Subgroups That Were Defined by Germline VEGFR2 Polymorphisms
Ramy czasowe: From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
PFS, defined as time from date of randomization to date of first documentation of PD or death on-study due to any cause, whichever occurred first, in subgroups that were defined by VEGFR2 polymorphisms. PFS was calculated as (first event date minus randomization date plus 1) divided by 7.02.
From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
Overall Survival (OS) in Subgroups That Were Defined by Germline VEGFR2 Polymorphisms
Ramy czasowe: From randomization until death (up to Month 17)
OS, defined as time from date of randomization to date of death due to any cause, in subgroups that were defined by VEGFR2 polymorphisms. OS was calculated as (date of death minus date of randomization plus 1) divided by 30.4.
From randomization until death (up to Month 17)
Percentage of Participants With Germline Platelet-derived Growth Factor Receptor Beta (PDGFRB) Polymorphisms
Ramy czasowe: Baseline
Blood samples were collected at baseline for multiplex RT analysis of genes expressing proteins that are targets of sunitinib or involved in angiogenesis or tumor growth to determine expression levels. Percentage of participants with germline PDGFRB SNPs was reported for the following genotype frequencies: homozygous C alleles (C/C), T alleles (T/T), G alleles (G/G), or A alleles (A/A), and the following heterozygous genotypes C/T, A/T, A/G, T/C, T/G, G/C, C/A and G/A.
Baseline
PFS in Subgroups That Were Defined by Germline PDGFRB Polymorphisms
Ramy czasowe: From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
PFS, defined as time from date of randomization to date of first documentation of PD or death on-study due to any cause, whichever occurred first, in subgroups that were defined by PDGFRB polymorphisms. PFS was calculated as (first event date minus randomization date plus 1) divided by 7.02.
From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
OS in Subgroups That Were Defined by Germline PDGFRB Polymorphisms
Ramy czasowe: From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
OS, defined as time from date of randomization to date of death due to any cause, in subgroups that were defined by PDGFRB polymorphisms. OS was calculated as (date of death minus date of randomization plus 1) divided by 30.4.
From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
Percentage of Participants by Tumor VEGFR Mutation
Ramy czasowe: Baseline
Percentage of participants with VEGFR mutations in DNA from tumor samples collected at the time of initial diagnosis (preferred) or at the time of most recent recurrence/progression, although any time was acceptable.
Baseline
Correlation of Polymorphisms in Stem Cell Factor Receptor (c-Kit), FMS-like Tyrosine Kinase 3 Receptor (FLT-3), and c-FMS With Blood Counts
Ramy czasowe: Baseline (Day 1, Cycle 1)
A blood sample (6 mL) was collected before on-study treatment and was used to isolate DNA. These samples were not anonymized. Correlation was investigated by the percentage of participants with anemia (based on hemoglobin count), neutropenia (based on neutrophil count) and thrombocytopenia (based on platelet count) endpoints and genetic variation as measured by c-KIT, FLT-3, and c-FMS was to be analyzed.
Baseline (Day 1, Cycle 1)
Percentage of Participants by Ribonucleic Acid (RNA) Expression Profile
Ramy czasowe: Baseline
Includes colony-stimulating factor 1 receptor (CSF-1R), PDGFRalpha, PDGFRbeta, vascular endothelial growth factor (VEGF), VEGF C (VEGF-C), VEGF receptor 1 (VEGFR1), VEGF receptor 2 (VEGFR2), VEGF receptor 3 (VEGFR3), fibroblast growth factor (FGF), FLT-3, KIT (stem cell factor receptor), and RET (rearranged during transfection). Correlative analysis was conducted using tumor biopsy samples collected at the time of initial diagnosis (preferred) or at the time of most recent recurrence/progression, although any time was acceptable.
Baseline
PFS in Subgroups That Were Defined by RNA Expression Profile
Ramy czasowe: From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
PFS, defined as time from date of randomization to date of first documentation of PD or death on-study due to any cause, whichever occurred first, in subgroups that were defined by RNA Gene expression (CSF-1R, PDGFRalpha, PDGFRbeta, VEGF, VEGF-C, VEGFR1, VEGFR2, VEGFR3, FGF, FLT-3, KIT, and RET). PFS was calculated as (first event date minus randomization date plus 1) divided by 7.02.
From randomization to Weeks 8 and 12, then every 8 weeks until disease progression or death (up to Month 17)
Health Related Quality of Life (HRQoL) and Lung Cancer Related Symptoms as Assessed With European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC-QLQ-C30) Score
Ramy czasowe: Baseline (Cycle [C] 1, Day [D] 1) to Cycle 18, Day 1
EORTC QLQ-C30: self-administered questionnaire assessing global health status/quality of life (QoL), functional domains (physical, role, cognitive, emotional, and social), symptom scales/items (fatigue, pain, nausea and vomiting, dyspnea, insomnia, loss of appetite, constipation, and diarrhea), and financial difficulties. Recall period: past week; response range: not at all (1) to very much (4); global/QoL range: very poor (1) to excellent (7). Scale score range: 0 to 100. Higher functional/global QoL score = better functioning and higher symptom score = greater degree of symptoms.
Baseline (Cycle [C] 1, Day [D] 1) to Cycle 18, Day 1
EORTC-QLQ-C30 Lung Cancer Module (LC13) Score
Ramy czasowe: Baseline (Cycle 1 [Day 1]) to Cycle 18 (Day 1)
The EORTC-QLQ-C30 LC13 is a self-administered questionnaire assessing specific lung cancer disease related symptoms (dyspnea, coughing, hemoptysis, sore mouth, dysphagia, peripheral neuropathy, alopecia, pain in the chest, arm/shoulder or other parts of the body). Recall period: past week; response range: not at all (1) to very much (4). Scale score range: 0 to 100. Higher symptom score = greater degree of symptoms.
Baseline (Cycle 1 [Day 1]) to Cycle 18 (Day 1)
Number of Participants With Blood Pressure (BP) Greater Than 150/100 Millimeters of Mercury (mmHg)
Ramy czasowe: Randomization up until Month 17
Systolic/diastolic BP measured in triplicate (separated by approximately 2 minutes [min]) using validated electronic device (same device for all measurements), recorded to nearest mmHg. Dominant arm used (same one each time) with appropriate cuff size encircling at least 80% of arm. BP measured after 5 min rest and before invasive procedures, while seated in a chair with back supported, arms bared, supported at heart level. No smoking or caffeine use allowed during 30 min before measurement. Number of participants with systolic BP >150 mmHg/diastolic BP >100 mmHg at any timepoint postbaseline.
Randomization up until Month 17
Number of Participants With BP Greater Than 200/110 mmHg
Ramy czasowe: Randomization up until Month 17
Systolic/diastolic BP measured in triplicate (separated by approximately 2 minutes [min]) using validated electronic device (same device for all measurements), recorded to nearest mmHg. Dominant arm used (same one each time) with appropriate cuff size encircling at least 80% of arm. BP measured after 5 min rest and before invasive procedures, while seated in a chair with back supported, arms bared, supported at heart level. No smoking or caffeine use allowed during 30 min before measurement. Number of participants with systolic BP >150 mmHg/diastolic BP >100 mmHg at any timepoint postbaseline.
Randomization up until Month 17
Number of Participants on Anti-hypertensive Medications
Ramy czasowe: Randomization to Day 28 of Cycle 18
Number of participants with BP greater than 150/100 mmHg or 200/110 mmHg who were treated with anti-hypertensive medications.
Randomization to Day 28 of Cycle 18
Plasma Concentration of VEGF-C at Baseline
Ramy czasowe: Baseline (Cycle 1, Day 1)
Baseline (Cycle 1, Day 1)
Plasma Concentration of Soluble VEGFR-2 at Baseline
Ramy czasowe: Baseline (Cycle 1, Day 1)
Baseline (Cycle 1, Day 1)
Plasma Concentration of Soluble VEGFR-3 at Baseline
Ramy czasowe: Baseline (Cycle 1, Day 1)
Baseline (Cycle 1, Day 1)
Plasma Concentration of Soluble KIT (sKIT) at Baseline
Ramy czasowe: Baseline (Cycle 1, Day 1)
Baseline (Cycle 1, Day 1)

Inne miary wyników

Miara wyniku
Opis środka
Ramy czasowe
VEGF-C Ratio to Baseline at Each Timepoint
Ramy czasowe: Baseline to Cycle 2 (Day 1) and Cycle 3 (Day 1)
Plasma VEGF-C concentration at each time point divided by VEGF-C concentration at baseline (ratio to baseline)
Baseline to Cycle 2 (Day 1) and Cycle 3 (Day 1)
VEGFR-2 Ratio to Baseline at Each Timepoint
Ramy czasowe: Baseline to Cycle 2 (Day 1) and Cycle 3 (Day 1)
Plasma VEGFR-2 concentration at each time point divided by VEGFR-2 concentration at baseline (ratio to baseline)
Baseline to Cycle 2 (Day 1) and Cycle 3 (Day 1)
VEGFR-3 Ratio to Baseline at Each Timepoint
Ramy czasowe: Baseline to Cycle 2 (Day 1) and Cycle 3 (Day 1)
Plasma VEGFR-3 concentration at each time point divided by VEGFR-3 concentration at baseline (ratio to baseline)
Baseline to Cycle 2 (Day 1) and Cycle 3 (Day 1)
sKIT Ratio to Baseline at Each Timepoint
Ramy czasowe: Baseline to Cycle 2 (Day 1) and Cycle 3 (Day 1)
Plasma sKIT concentration at each time point divided by sKIT concentration at baseline (ratio to baseline)
Baseline to Cycle 2 (Day 1) and Cycle 3 (Day 1)

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Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów

1 czerwca 2006

Zakończenie podstawowe (Rzeczywisty)

1 stycznia 2010

Ukończenie studiów (Rzeczywisty)

1 stycznia 2012

Daty rejestracji na studia

Pierwszy przesłany

12 grudnia 2005

Pierwszy przesłany, który spełnia kryteria kontroli jakości

12 grudnia 2005

Pierwszy wysłany (Oszacować)

14 grudnia 2005

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Oszacować)

6 lutego 2013

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

31 stycznia 2013

Ostatnia weryfikacja

1 stycznia 2013

Więcej informacji

Terminy związane z tym badaniem

Słowa kluczowe

Dodatkowe istotne warunki MeSH

Inne numery identyfikacyjne badania

  • A6181058

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