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Nelfinavir Mesylate and Bortezomib in Treating Patients With Relapsed or Progressive Advanced Hematologic Cancer

14. mai 2019 oppdatert av: Swiss Group for Clinical Cancer Research

Phase I Trial of Nelfinavir and Bortezomib in Advanced Hematologic Malignancies

RATIONALE: Nelfinavir mesylate and bortezomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Bortezomib may also stop the growth of hematologic cancer by blocking blood flow to the cancer. Giving nelfinavir mesylate together with bortezomib may kill more cancer cells.

PURPOSE: This phase I trial is studying the side effects and best dose of nelfinavir mesylate when given together with bortezomib in treating patients with relapsed or progressive advanced hematologic cancer.

Studieoversikt

Detaljert beskrivelse

OBJECTIVES:

  • To assess the safety of nelfinavir mesylate in combination with bortezomib in patients with relapsed or progressive, advanced hematologic malignancies.
  • To establish the phase II recommended dose of nelfinavir mesylate in these patients.

OUTLINE: This is a multicenter, dose-escalation study of nelfinavir mesylate.

Patients receive oral nelfinavir mesylate twice daily on days 1-21 and bortezomib IV on days 8, 11, 15, and 18 in course 1. Course 1 has a duration of 28 days. Beginning in course 2, patients receive oral nelfinavir mesylate twice daily on days 1-14 and bortezomib IV on days 1, 4, 8, and 11. Treatment repeats every 21 days for 2 courses. Patients with responding disease may continue to receive nelfinavir mesylate and bortezomib for up to 4 additional courses.

After completion of study treatment, patients are followed for 30 days.

Studietype

Intervensjonell

Registrering (Faktiske)

18

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

      • Bern, Sveits, CH-3010
        • Inselspital Bern
      • Chur, Sveits, CH-7000
        • Kantonsspital Graubuenden
      • Lausanne, Sveits, CH-1011
        • Centre Hospitalier Universitaire Vaudois
      • St. Gallen, Sveits, CH-9007
        • Kantonsspital - St. Gallen

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

DISEASE CHARACTERISTICS:

  • Diagnosed with advanced hematologic malignancies meeting the following criteria:

    • Multiple myeloma

      • Received ≥ 2 lines of prior chemotherapy (induction chemotherapy followed by high-dose chemotherapy and autologous stem cell transplant with or without maintenance therapy is considered one line of therapy)
    • Acute myeloid leukemia
    • Acute lymphoblastic leukemia
    • Diffuse large B-cell lymphoma
    • Hodgkin lymphoma
    • Mantle cell lymphoma
    • Mature T- and NK-cell neoplasms restricted to the following WHO-defined entities:

      • T-cell prolymphocytic leukemia
      • T-cell large granular lymphocytic leukemia
      • Aggressive NK-cell leukemia
      • Adult T-cell leukemia/lymphoma
      • Extranodal NK/T-cell lymphoma (nasal type)
      • Mycosis fungoides
      • Sézary syndrome
      • Primary CD30-positive T-cell lymphoproliferative disorders
      • Primary cutaneous anaplastic large cell lymphoma
      • Primary cutaneous gamma-delta T-cell lymphoma
      • Peripheral T-cell lymphoma (not otherwise specified)
      • Angioimmunoblastic T-cell lymphoma
      • Anaplastic large cell lymphoma (ALK-positive/ALK-negative)
    • Grade 3B follicular lymphoma
  • Relapsed following or progressed during standard therapy
  • Meeting the following criteria:

    • Standard intensive therapy is not feasible
    • Current disease state for which there is no standard effective therapy
    • Refused standard therapy where no curative option exists
  • Measurable disease, defined as the following:

    • Myeloma: measurable serum monoclonal protein > 1 g/dL for IgG, or > 0.5 g/dL for IgA, IgM or IgD, or difference between involved and uninvolved free light chain levels in serum > 100 mg/L
    • Lymphoma: must have ≥ 1 lesion measurable by CT (longest diameter ≥ 15 mm)
    • Acute leukemia: ≥ 20% blasts in bone marrow or in peripheral blood (≥ 200/mL blasts in peripheral blood)
  • No HIV-associated lymphoma

PATIENT CHARACTERISTICS:

  • WHO performance status 0-2
  • Absolute neutrophil count ≥ 1,500/mm³
  • Platelet count ≥ 75,000/mm³ (if bone marrow impairment, ≥ 20,000/mm^3)
  • Hemoglobin > 80 g/L (if considered to be caused by the underlying hematologic malignancy or bone marrow impairment, > 80 g/L after transfusion)
  • Bilirubin ≤ 1.5 times upper limit of normal (ULN) (if suspected hemolysis, direct bilirubin ≤ 1.5 times ULN)
  • ALT ≤ 2.5 times ULN
  • Calculated creatinine clearance > 30 mL/min
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception during and for 12 months after completion of study treatment
  • Willing and capable to comply with an oral regimen
  • Capable of understanding information given by the investigator on the trial
  • Able to adhere and remain in geographic proximity to allow proper staging, treatment, and followup
  • No other non-hematologic malignancy within the past 5 years, except adequately treated cervical carcinoma in situ or localized nonmelanoma skin cancer
  • No known chronic hepatitis B or C infection or known HIV infection
  • No serious underlying medical condition (at the judgment of the investigator) which would impair the ability of the patient to participate in the trial, including any of the following:

    • Active autoimmune disease
    • Uncontrolled diabetes
    • Ongoing or active infection
    • Symptomatic congestive heart failure
    • Unstable angina pectoris
    • Cardiac arrhythmia
    • Psychiatric disorder
  • No myocardial infarction within the past 6 months
  • No polyneuropathy > grade 1 significantly interfering with activities of daily living or painful polyneuropathy
  • No known hypersensitivity to trial drugs or hypersensitivity to any other component of the trial drugs

PRIOR CONCURRENT THERAPY:

  • See Disease Characteristics
  • No more than 4 prior lines of chemotherapeutic regimens (induction chemotherapy followed by high-dose chemotherapy and autologous stem cell transplant with or without maintenance therapy is considered one line of therapy)
  • More than 30 days since prior treatment in a clinical trial
  • More than 30 days since prior and no concurrent chemotherapy or biologic agents

    • For patients with acute leukemia, hydroxyurea may be given up to 48 hours before first administration of the trial treatment, and low dose cytarabine (up to 20 mg/m^2) and mitoxantrone up to 20 mg up to 14 days before first dosing
  • At least 1 week since prior and no concurrent CYP3A4 modulators
  • No concurrent other experimental drugs
  • No concurrent radiotherapy
  • No concurrent antineoplastic therapy with chemotherapeutic or biologic agents

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: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: bortezomib + nelfinavir
escalation 3 by 3 cohorts
Bortezomib i.v., day 8, 11, 15, 18; 1.3 mg/m2
Andre navn:
  • Velcade
p.o., days 1 to 21; dose level: (625), 1250, 1875, or 2500 mg, 2x/d
Andre navn:
  • Viracept

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Dose limiting toxicity
Tidsramme: during first cycle
during first cycle

Sekundære resultatmål

Resultatmål
Tidsramme
Objective response
Tidsramme: during treatment
during treatment
Adverse events according to NCI CTCAE v.4.0
Tidsramme: during treatment + 30 days
during treatment + 30 days

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Studiestol: Christoph Driessen, MD, Cantonal Hospital of St. Gallen
  • Hovedetterforsker: Dagmar Hess, MD, Cantonal Hospital of St. Gallen
  • Hovedetterforsker: Roger von Moos, MD, Kantonsspital Graubuenden
  • Hovedetterforsker: Thomas Pabst, MD, University Hospital Inselspital, Berne

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

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. juli 2010

Primær fullføring (Faktiske)

1. juli 2012

Studiet fullført (Faktiske)

1. november 2013

Datoer for studieregistrering

Først innsendt

16. juli 2010

Først innsendt som oppfylte QC-kriteriene

16. juli 2010

Først lagt ut (Anslag)

19. juli 2010

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

15. mai 2019

Siste oppdatering sendt inn som oppfylte QC-kriteriene

14. mai 2019

Sist bekreftet

1. mai 2019

Mer informasjon

Begreper knyttet til denne studien

Nøkkelord

Andre studie-ID-numre

  • SAKK 65/08
  • SWS-SAKK-65/08
  • EU-21051
  • SWS-SAKK-JC26866138LYM1005
  • CDR0000681442 (Registeridentifikator: CDR0000681442)

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. .

Kliniske studier på bortezomib

3
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