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

9 décembre 2019 mis à jour par: 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).

Aperçu de l'étude

Statut

Résilié

Type d'étude

Interventionnel

Inscription (Réel)

1

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Utah
      • Salt Lake City, Utah, États-Unis, 84112
        • Huntsman Cancer Institute

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans et plus (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

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.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: N / A
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: 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

Autres noms:
  • 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

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Adverse Events that occur
Délai: 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)
Délai: 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

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Progression Free Survival (PFS)
Délai: 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
Délai: 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

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Collaborateurs

Les enquêteurs

  • Chercheur principal: Glynn W Gilcrease, MD, University of Utah

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

11 avril 2018

Achèvement primaire (Réel)

26 juillet 2018

Achèvement de l'étude (Réel)

2 juillet 2019

Dates d'inscription aux études

Première soumission

19 décembre 2017

Première soumission répondant aux critères de contrôle qualité

19 décembre 2017

Première publication (Réel)

26 décembre 2017

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

12 décembre 2019

Dernière mise à jour soumise répondant aux critères de contrôle qualité

9 décembre 2019

Dernière vérification

1 décembre 2019

Plus d'information

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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