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Nivolumab and Bevacizumab in Patients With Advanced and or Metastatic Hepatocellular Carcinoma (NUANCE)

9. desember 2019 oppdatert av: University of Utah

A Phase I Open Label Trial of a Combination of Nivolumab and Bevacizumab in Patients With Advanced and or Metastatic Hepatocellular Carcinoma

This is an open label, phase I study to test for maximum tolerated dose (MTD) or recommended phase II dose (RP2D) of the combination of nivolumab and bevacizumab. The study will use a 3+3 phase I study design using a fixed dose of nivolumab (240mg) and escalating doses of bevacizumab (1-10mg).

Studieoversikt

Status

Avsluttet

Studietype

Intervensjonell

Registrering (Faktiske)

1

Fase

  • Fase 1

Kontakter og plasseringer

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

Studiesteder

    • Utah
      • Salt Lake City, Utah, Forente stater, 84112
        • Huntsman Cancer Institute

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:

  • Confirmed unresectable or metastatic hepatocellular carcinoma. Confirmation either by histologic confirmation or accepted radiographic criteria.
  • Received at least one line of therapy with a TKI (including, but not limited to sorafenib, lenvatinib, and/or regorafenib) with evidence of disease progression clinically or radiographically as deemed by investigator, or refused therapy with a TKI. No more than two lines of prior therapy are allowed.
  • Measurable disease per RECIST1.1.
  • Age ≥18 years.
  • ECOG performance status of 0 to 1.
  • Life expectancy ≥ 12 weeks.
  • Childs Pugh A (5-6 points). Demonstrate adequate organ function as defined in the table below

Hematologic:

Absolute neutrophil count (ANC) ≥ 1.5 k/µL. Platelets ≥ 100 k/µL Hemoglobin ≥ 9 g/dL

Renal:

Creatinine < 2 × ULN OR

- Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines.

Exclusion Criteria:

  • Prior treatment with anti-PD1 or anti-PD-L1 antibody therapy.
  • Subjects with a prior history of DVT/PE, who have not been on stable doses of anticoagulation with low molecular weight heparin or oral anticoagulant for at least two weeks.
  • History of arterial thromboembolic event in past 6 months (including CVA, MI).
  • Systemic anti-cancer treatment within 2 weeks, all ongoing adverse events related to previous systemic anti-cancer therapy resolved to grade ≤1.
  • Radiotherapy within 2 weeks of first dose of study medications.
  • Major surgery within 6 weeks of first dose of study medications. Minor procedures (e.g. port placement, endoscopy with intervention) within 4 weeks of first dose of study medications.
  • Presence of ≥ CTCAE grade 2 toxicity due to prior cancer therapy (except alopecia, peripheral neuropathy which are excluded if ≥ CTCAE grade 3).
  • Medical condition that requires chronic systemic steroid therapy, or any other form of immunosuppressive medication.
  • Active ongoing infection requiring therapy.
  • Active HIV infection.
  • History of severe hypersensitivity reaction to another monoclonal antibody.
  • Active central nervous system metastases and/or carcinomatous meningitis (stable treated brain metastases not requiring steroids >4 weeks allowed).
  • Cardiac conditions: class 3-4 New York Heart Association congestive heart failure, known baseline LVEF < 50%, transmural myocardial infarction, uncontrolled hypertension, angina pectoris requiring medication, clinically significant valvular disease, high-risk arrhythmia in the past 12 months.
  • Any history of autoimmune disease requiring treatment in the past 5 years or felt to be at risk to reactivate autoimmune disease. Patients who are felt to no longer be at risk of activating a known autoimmune disease (e.g. type 1 diabetes, ulcerative colitis s/p complete colectomy, autoimmune thyroiditis s/p thyroidectomy or medical ablation, etc.) may be allowed to participate after discussion with the PI
  • Pregnant, breast feeding, or planning to become pregnant.
  • Women of childbearing potential (WOCBP) must agree to follow instructions for method(s) of contraception for the duration of study treatment with nivolumab and 5 months after the last dose of study treatment i.e., 30 days (duration of ovulatory cycle) plus the time required for the investigational drug to undergo approximately five half-lives. Contraception as described in section 7.3
  • Males who are sexually active with WOCBP must agree to follow instructions for method(s) of contraception for the duration of study treatment with nivolumab and 7 months after the last dose of study treatment i.e., 90 days (duration of sperm turnover) plus the time required for the investigational drug to undergo approximately five half-lives. Contraception as described in section 7.3
  • Received any live vaccine within the last 30 days.
  • Other malignancy requiring treatment in the prior 2 years with the exception of locally treated squamous or basal cell carcinoma.

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: Nivolumab and bevacizumab, all patients

Nivolumab will be administered as a 240mg IV infusion given once every two weeks (+/- 3 days).

Subjects will remain on study treatment for up to two years or until progression or excessive toxicity

Andre navn:
  • OPDIVO

Bevacizumab will be administered as an IV infusion from 1-10mg/kg in accordance with the appropriate subject cohort being examined as described below:

Dose level 1: 5 mg/kg intravenously once every two weeks Dose level 2: 10 mg/kg intravenously once every two weeks Dose level -1: 1 mg/kg intravenously once every two weeks

Dosing is based on actual body weight. There is no dose adjustment for obese or frail individuals. Dosing is recalculated if patient weight changes by more than 10% as reviewed by the principal investigator.

Subjects will remain on study treatment for up to two years or until progression or excessive toxicity

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Adverse Events that occur
Tidsramme: Every 14 day cycle for up to 2 years - Patients are expected to be on treatment for an average of 6 months

Investigate the safety and tolerability of 14-day cycles of nivolumab plus bevacizumab.

Adverse events will be collected for each subject that received the study treatment combination.

Every 14 day cycle for up to 2 years - Patients are expected to be on treatment for an average of 6 months
Determine the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D)
Tidsramme: The DLT period will begin at Cycle 1 Day 1 and continue through Cycle 1 Day 28 for each patient

Determine the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D).

Dose Limiting Toxicities (DLT) will define subsequent subject accrual and dose escalation

The DLT period will begin at Cycle 1 Day 1 and continue through Cycle 1 Day 28 for each patient

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Progression Free Survival (PFS)
Tidsramme: 3 years after treatment stops

To examine the effect of the study treatment combination on the rate of progression-free survival (PFS).

Subjects will have regular imaging scans to measure disease status and response will be defined by RECIST1.1.

3 years after treatment stops
Overall Survival
Tidsramme: 3 years after treatment stops
To examine the effect of the study treatment combination on the rate of overall survival.
3 years after treatment stops

Samarbeidspartnere og etterforskere

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

Samarbeidspartnere

Etterforskere

  • Hovedetterforsker: Glynn W Gilcrease, MD, University of Utah

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 (Faktiske)

11. april 2018

Primær fullføring (Faktiske)

26. juli 2018

Studiet fullført (Faktiske)

2. juli 2019

Datoer for studieregistrering

Først innsendt

19. desember 2017

Først innsendt som oppfylte QC-kriteriene

19. desember 2017

Først lagt ut (Faktiske)

26. desember 2017

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

12. desember 2019

Siste oppdatering sendt inn som oppfylte QC-kriteriene

9. desember 2019

Sist bekreftet

1. desember 2019

Mer informasjon

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. .

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