- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT00434226
A Study of Sunitinib in Combination With Bevacizumab, Carboplatin, and Paclitaxel in Patients With Advanced Non-Small Cell Lung Cancer (SABRE-L)
9. juli 2009 oppdatert av: Genentech, Inc.
A Randomized, Controlled, Open-Label, Multicenter, Phase II Study of the Safety and Efficacy of Sunitinib in Combination With Bevacizumab, Carboplatin, and Paclitaxel in Previously Untreated Patients With Advanced Non-Small Cell Lung Cancer
This is a Phase II, randomized, controlled, open-label, multicenter trial designed to provide a preliminary assessment of the safety and efficacy of sunitinib when combined with carboplatin and paclitaxel chemotherapy and bevacizumab in patients with locally advanced, recurrent or metastatic NSCLC who have not received prior systemic therapy for NSCLC.
All patients will have advanced, histologically or cytologically confirmed NSCLC (Stage IIIb with pleural effusions, Stage IV, or recurrent).
Studieoversikt
Status
Avsluttet
Forhold
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Faktiske)
56
Fase
- Fase 2
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år og eldre (Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria:
- Signed Informed Consent Form
- Age ≥ 18 years
- Advanced histologically or cytologically confirmed NSCLC (Stage IIIb with malignant pleural or pericardial effusion, Stage IV, or recurrent)
- Measurable or non-measurable disease
- Patients with treated brain metastases are eligible if there is no evidence of progression or hemorrhage after treatment, as ascertained by clinical examination and brain imaging (MRI or CT) during the screening period (brain imaging to be competed Day -7 to Day 1).
- Prior treatment for CNS disease as deemed appropriate by the treating physician
- ECOG performance status 0 or 1
- Ability and willingness to comply with study and follow-up procedures
Exclusion Criteria:
- Prior systemic chemotherapy for metastatic disease
- Active malignancy other than lung cancer
- Current, recent, or planned participation in another experimental drug study
- Prior treatment with anti-VEGF agent or agents targeting similar pathways as sunitinib
- Adjuvant chemotherapy or prior combined modality neoadjuvant therapy (chemotherapy plus radiotherapy with or without surgery) within 6 months prior to Day 1 of Cycle 1
- Life expectancy of < 12 weeks
- Current, recent, or planned participation in an experimental drug study
- Inability to take oral medication or requirement of IV alimentation or total parenteral nutrition, or prior surgical procedures affecting absorption
- Inadequate organ function
- Known evidence of disseminated intravascular coagulopathy
- Active infection or fever > 38.5°C within 3 days prior to Day 1 of Cycle 1
- Untreated abnormal thyroid function tests as defined by institutional standards (patients with controlled hypothyroidism are eligible for study participation)
- Any other medical condition(s) (including mental illness or substance abuse) deemed by the clinician to be likely to interfere with a patient's ability to provide informed consent, cooperate, or participate in the study, or to interfere with the interpretation of the results
- Intrathoracic lung carcinoma of squamous cell histology
- Known CNS disease except for treated brain metastases
- Inadequately controlled hypertension
- Prior history of hypertensive crisis or hypertensive encephalopathy
- New York Heart Association (NYHA) Class II or greater CHF
- History of myocardial infarction or unstable angina within 12 months prior to Day 1 of Cycle 1
- History of stroke or transient ischemic attack within 12 months prior to Day 1 of Cycle 1
- Significant vascular disease (e.g., aortic aneurysm, aortic dissection) or recent peripheral arterial thrombosis within 6 months prior to Day 1 of Cycle 1
- History of hemoptysis within 1 month prior to Day 1 of Cycle 1
- Evidence of bleeding diathesis or significant coagulopathy (in the absence of therapeutic anticoagulation)
- Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to Day 1 of Cycle 1 or anticipation of need for major surgical procedure during the course of the study
- Core biopsy or other minor surgical procedure, excluding placement of a vascular access device, within 7 days prior to Day 1 of Cycle 1
- History of abdominal fistula or gastrointestinal perforation within 6 months prior to Day 1 of Cycle 1
- Serious, non-healing wound, active ulcer, or untreated bone fracture
- Proteinuria at screening, as demonstrated by a urine protein/creatinine ratio of ≥ 1.0 at screening
- Known hypersensitivity to any component of bevacizumab or sunitinib
- Pregnancy (positive pregnancy test) or lactation
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Bevacizumab + Carboplatin/Paclitaxel + Sunitinib
|
Intravenously at a dose of 15mg/kg on the first day of each 21-day cycle
25 mg/day for 2 weeks, followed by 1 week of rest
On the first day of each cycle for 4 cycles
On the first day of each cycle for 4 cycles
|
|
Placebo komparator: Bevacizumab + Carboplatin/Paclitaxel
|
Intravenously at a dose of 15mg/kg on the first day of each 21-day cycle
On the first day of each cycle for 4 cycles
On the first day of each cycle for 4 cycles
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Best Response
Tidsramme: From randomization until disease progression/recurrence
|
The best overall response is the best response, per RECIST criteria, recorded from randomization until disease progression/recurrence (includes both confirmed and unconfirmed responses).
Although the original primary outcome was progression-free survival, there was insufficient data available to report on that outcome.
|
From randomization until disease progression/recurrence
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Serious Adverse Events
Tidsramme: 60 days following the last administration of study treatment
|
All grades according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE), v3.0
|
60 days following the last administration of study treatment
|
|
Incidence of Grade ≥ 3 Adverse Events
Tidsramme: 60 days following the last administration of study treatment
|
All grades according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE), v3.0
|
60 days following the last administration of study treatment
|
|
Incidence of Adverse Events Leading to Sunitinib Discontinuation, Dose Interruption, or Dose Reduction
Tidsramme: 60 days following the last administration of study treatment
|
All grades according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE), v3.0
|
60 days following the last administration of study treatment
|
|
Incidence of Adverse Events Leading to Bevacizumab Discontinuation or Dose Interruption
Tidsramme: 60 days following the last administration of study treatment
|
All grades according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE), v3.0
|
60 days following the last administration of study treatment
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Etterforskere
- Studieleder: Julie Hambleton, M.D., Genentech, Inc.
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. mars 2007
Primær fullføring (Faktiske)
1. april 2008
Datoer for studieregistrering
Først innsendt
11. februar 2007
Først innsendt som oppfylte QC-kriteriene
11. februar 2007
Først lagt ut (Anslag)
13. februar 2007
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
21. august 2009
Siste oppdatering sendt inn som oppfylte QC-kriteriene
9. juli 2009
Sist bekreftet
1. juli 2009
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Sykdommer i luftveiene
- Neoplasmer
- Lungesykdommer
- Neoplasmer etter nettsted
- Neoplasmer i luftveiene
- Thoracale neoplasmer
- Karsinom, bronkogent
- Bronkiale neoplasmer
- Lungeneoplasmer
- Karsinom, ikke-småcellet lunge
- Fysiologiske effekter av legemidler
- Molekylære mekanismer for farmakologisk virkning
- Enzymhemmere
- Antineoplastiske midler
- Tubulin modulatorer
- Antimitotiske midler
- Mitosemodulatorer
- Antineoplastiske midler, fytogene
- Antineoplastiske midler, immunologiske
- Angiogenese-hemmere
- Angiogenesemodulerende midler
- Vekststoffer
- Veksthemmere
- Proteinkinasehemmere
- Karboplatin
- Paklitaksel
- Sunitinib
- Bevacizumab
Andre studie-ID-numre
- AVF3996g
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .