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PEG-Interferon Alfa-2b and Sorafenib in Treating Patients With Unresectable or Metastatic Kidney Cancer

4 juni 2015 uppdaterad av: Thomas Olencki

A Phase I Study Of Peginterferon Alfa-2b (PEG-INTRON) With Sorafenib (Nexavar) In Patients With Unresectable Or Metastatic Clear Cell Renal Carcinoma (RCC).

RATIONALE: PEG-interferon alfa-2b may interfere with the growth of tumor cells. Sorafenib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. It may also stop the growth of kidney cancer by blocking blood flow to the tumor. Giving PEG-interferon alfa-2b together with sorafenib may kill more tumor cells.

PURPOSE: This phase I trial is studying the side effects and best dose of PEG-interferon alfa-2b and sorafenib in treating patients with unresectable or metastatic kidney cancer.

Studieöversikt

Detaljerad beskrivning

OBJECTIVES:

Primary

  • To determine the maximum tolerated dose and toxicity of PEG-interferon alfa-2b and sorafenib tosylate in patients with unresectable or metastatic clear cell renal cell carcinoma.

Secondary

  • To determine the progression-free survival of patients treated with this regimen.
  • To evaluate, in a preliminary manner, the response rate and overall survival of patients treated with this regimen.
  • To evaluate the activation of interferon-induced transcription factors in immune cell subsets (including regulatory T cells [T regs]) using a novel flow cytometric assay and correlate this information with clinical outcome.
  • To measure circulating levels of IFN-γ and IL-5 for determination of Th1/Th2 status and CD4+, CD25+, and FoxP3 cell number (T regs) in peripheral blood.

OUTLINE: Patients receive PEG-interferon alfa-2b subcutaneously on days 1, 8, 15, 22, 29, 36, 43, and 50. Patients also receive oral sorafenib tosylate 2-3 times daily on days 15-56 of course 1 and on days 1-56 of all subsequent courses. Courses repeat every 56 days for up to 1 year in the absence of disease progression or unacceptable toxicity.

Blood samples are collected at baseline and periodically during study for correlative laboratory studies. Peripheral blood mononuclear cells are analyzed for STAT proteins (STAT1, STAT2, STAT3, STAT4, STAT5) and CD4+, CD25+, and FoxP3 regulatory T cells by flow cytometric assays. Samples are also analyzed for the presence of VEGF, VEGFR, IFN-γ, and IL-5 by ELISA assays; baseline expression of Jak-STAT signaling intermediates (Jak1, Tyk2, IFNAR, and IRF9) by immunoblot analysis; and interferon-stimulated gene expression by real time PCR and RT-PCR analysis.

After completion of study therapy, patients are followed every 3 months for 1 year, every 4 months for 1 year, every 6 months for 2 years, and then annually thereafter.

Studietyp

Interventionell

Inskrivning (Faktisk)

1

Fas

  • Fas 1

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • Ohio
      • Columbus, Ohio, Förenta staterna, 43210
        • Ohio State University Comprehensive Cancer Center

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  • Must have histologically or cytologically confirmed clear cell renal cell carcinoma (RCC)
  • Measurable disease, defined as ≥ 1 lesion that can be accurately measured in ≥ 1 dimension and is ≥ 1.0 cm by spiral CT scan
  • No prior treatment except

PATIENT CHARACTERISTICS:

  • ECOG performance status 0-1
  • Life expectancy > 6 months
  • Good/intermediate Motzer prognostic status
  • ANC ≥ 1,000/mm³
  • Platelet count ≥ 100,000/mm³
  • Hemoglobin ≥ 10.0 g/dL
  • Total bilirubin ≤ 2.0 mg/dL
  • AST and ALT < 2.5 times normal
  • Creatinine ≤ 1.8 mg/dL OR creatinine clearance > 50 mL/min
  • Calcium < 12 mg/dL (when corrected for serum albumin)
  • INR < 1.5 times upper limit of normal
  • Adequate cardiac function, defined as left ventricular ejection fraction ≥ 40% by 2D echo
  • Pulse oximetry ≥ 90% at rest on room air
  • Not pregnant
  • Negative pregnancy test
  • Fertile patients must use effective contraception
  • No evidence of bleeding diathesis
  • No uncontrolled coagulation disorders
  • No active infections requiring IV antibiotics
  • No known HIV, hepatitis C, or hepatitis B
  • No autoimmune disease requiring ongoing therapy
  • No requirement for adrenal replacement
  • No angina (controlled or uncontrolled)
  • No uncontrolled hypertension
  • No history of other major medical illnesses including, but not limited to, any of the following:

    • Cardiac ischemia
    • Myocardial infarction
    • Major cardiac arrhythmias
    • Inflammatory bowel disorders
  • No other prior malignancy except for previously treated basal cell or squamous cell skin cancer, in situ cervical cancer, or other cancer for which the patient has been disease-free for 3 years
  • No significant psychiatric disease that, in the opinion of the principal investigator, would preclude giving adequate informed consent or render immunotherapy unsafe

PRIOR CONCURRENT THERAPY:

  • No prior treatment for RCC except sunitinib malate

    • Patients may have progressed or have been intolerant to sunitinib malate
  • No prior systemic treatment for metastatic disease (other than sunitinib malate)
  • No prior organ allografts
  • At least 2 weeks since prior laparoscopic/robotic surgery
  • At least 4 weeks since prior open nephrectomy
  • More than 4 weeks since prior and no concurrent radiotherapy or other surgery
  • More than 4 weeks since prior systemic steroids
  • More than 2 weeks since prior topical, injected, or inhaled steroids
  • No concurrent steroid therapy
  • No concurrent Hypericum perforatum (St. John's wort)

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: N/A
  • Interventionsmodell: Enskild gruppuppgift
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Peginterferon alfa-2b
Peginterferon alfa-2b will be administered SC on day 1 of each week of therapy. This will most likely be a Monday or a Tuesday. Sorafenib will be initiated on day 15 (start of week 3) of the first course and continued daily without breaks.
Andra namn:
  • Nexavar
  • BAY 54-9085 är tosylatsaltet av BAY 43-9006
administered SC on day 1 of each week of therapy. This will most likely be a Monday or a Tuesday. Sorafenib will be initiated on day 15 (start of week 3) of the first course and continued daily without breaks.
Andra namn:
  • peginterferon alfa-2b

Vad mäter studien?

Primära resultatmått

Resultatmått
Tidsram
Maximum Tolerated Dose of PEG-interferon Alfa-2b and Sorafenib Tosylate
Tidsram: up to 2 months
up to 2 months
Characterize the Toxicity of Peginterferon Alfa-2b and Sorafenib in Patients With Metastatic or Unresectable Clear Cell Renal Cell Carcinoma.
Tidsram: up to 2 months
up to 2 months

Sekundära resultatmått

Resultatmått
Tidsram
Progression-free Survival of Patients Receiving Peginterferon Alfa-2b and Sorafenib.
Tidsram: up to 1 year
up to 1 year
Response Rate of Patients Receiving Peginterferon Alfa-2b and Sorafenib.
Tidsram: up to 1 year
up to 1 year
Overall Survival
Tidsram: up to 1 year
up to 1 year
Activation of Interferon-induced Transcription Factors in Immune Cell Subsets by Flow Cytometry and Correlation of This Information With Clinical Outcome
Tidsram: up to 1 year
up to 1 year
Circulating Levels of IFN-γ and IL-5 for Determination of Th1/Th2 Status and CD4+, CD25+, and FoxP3 Cell Number (T Regs) in Peripheral Blood
Tidsram: Up to 1 year
Up to 1 year

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Sponsor

Samarbetspartners

Utredare

  • Studiestol: Thomas E. Olencki, DO, Ohio State University Comprehensive Cancer Center

Publikationer och användbara länkar

Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.

Användbara länkar

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 februari 2008

Primärt slutförande (Faktisk)

1 januari 2009

Avslutad studie (Faktisk)

1 januari 2009

Studieregistreringsdatum

Först inskickad

5 januari 2008

Först inskickad som uppfyllde QC-kriterierna

5 januari 2008

Första postat (Uppskatta)

9 januari 2008

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

8 juni 2015

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

4 juni 2015

Senast verifierad

1 juni 2015

Mer information

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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