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Vorinostat and Bevacizumab in Treating Patients With Unresectable or Metastatic Kidney Cancer

10 décembre 2015 mis à jour par: National Cancer Institute (NCI)

Phase I/II Study of Suberoylanilide Hydroxamic Acid (SAHA) in Combination With the VEGF Inhibitor Bevacizumab in Patients With Metastatic Renal Cell Carcinoma

This phase I/II trial is studying the side effects and best dose of vorinostat when given together with bevacizumab and to see how well they work in treating patients with unresectable or metastatic kidney cancer. Vorinostat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Bevacizumab may also stop the growth of kidney cancer by blocking blood flow to the tumor. Giving vorinostat together with bevacizumab may kill more tumor cells.

Aperçu de l'étude

Description détaillée

PRIMARY OBJECTIVES:

I. Determine the safety and tolerability of vorinostat (SAHA) in combination with bevacizumab in patients with unresectable or metastatic renal cell carcinoma. (Phase I) II. Determine the recommended dosing in patients treated with this regimen. (Phase I) III. Determine the proportion of patients who are progression-free at 6 months after receiving this regimen. (Phase II) IV. Determine the clinical response rate in patients treated with this regimen. (Phase II)

SECONDARY OBJECTIVES:

I. Determine the toxicity of this regimen in these patients. (Phase II) II. Determine time to progression and duration of progression-free and overall survival in patients treated with this regimen. (Phase II) III. Determine the pharmacodynamic effects in peripheral blood mononuclear cells and tumors before and after treatment with this regimen in these patients. (Phase II) IV. Determine the antiproliferative and apoptotic effects of this regimen in these patients. (Phase II) V. Determine the antiangiogenic effects of this regimen in these patients. (Phase II) VI. Determine the modulation of tumor metabolism and tumor blood flow in patients treated with this regimen. (Phase II)

OUTLINE: This is a phase I, dose-escalation study of vorinostat (SAHA) followed by a phase II study.

PHASE I: Patients receive oral SAHA twice daily on days 1-14 and bevacizumab IV over 30-90 minutes on day 1. Treatment repeats every 21 days in the absence of disease progression or unacceptable toxicity.

Cohorts of 3-6 patients receive escalating doses of SAHA until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity. An additional 6 patients are treated at the MTD.

PHASE II: Patients receive SAHA at the MTD determined in phase I and bevacizumab as in phase I.

After completion of study treatment, patients are followed at 4 weeks and then every 3 months thereafter.

Type d'étude

Interventionnel

Inscription (Réel)

37

Phase

  • Phase 2
  • 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

    • Maryland
      • Baltimore, Maryland, États-Unis, 21287
        • Johns Hopkins University/Sidney Kimmel Cancer Center
      • Salisbury, Maryland, États-Unis, 21801
        • Peninsula Oncology and Hematology PA
    • Wisconsin
      • Madison, Wisconsin, États-Unis, 53792
        • University of Wisconsin Hospital and Clinics

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:

  • No known CNS metastasis
  • ECOG performance status 0-2
  • Life expectancy > 6 months
  • LVEF ≥ 45%
  • Absolute neutrophil count ≥ 1,500/mm3
  • Platelet count ≥ 100,000/mm3
  • Total bilirubin ≤ 1.5 times upper limit of normal (ULN)
  • AST/ALT ≤ 2.5 times ULN
  • Creatinine ≤ 1.5 times ULN OR creatinine clearance ≥ 50 mL/min
  • PT/INR ≤ 1.5
  • Urine protein < 1+ by urinalysis OR < 1 g by 24-hour urine collection
  • Not pregnant
  • No nursing during and for 6 months after completion of study treatment
  • Negative pregnancy test
  • Fertile patients must use effective contraception for 2 weeks prior, during, and for 6 months after completion of study treatment
  • No other currently active malignancy defined as > 30% risk of relapse upon completion of anticancer therapy, except nonmelanoma skin cancer
  • No history of allergic reaction attributed to compounds of similar chemical or biologic composition to vorinostat (SAHA)
  • No hypersensitivity to Chinese hamster ovary cell products or other recombinant human antibodies
  • No evidence of bleeding diathesis or coagulopathy
  • No active bleeding or pathological conditions that carry high risk of bleeding (i.e., tumor involving major vessels or known varices)
  • No ongoing, active infection
  • No New York Heart Association class II-IV congestive heart failure
  • No angina pectoris requiring nitrate therapy
  • No cardiac arrhythmia
  • No myocardial infarction within the past 6 months
  • No history of cerebrovascular accident within the past 6 months
  • No uncontrolled hypertension (defined as systolic blood pressure (BP) > 160 mm Hg and/or diastolic BP > 90 mm Hg on medication)
  • No history of peripheral vascular disease
  • No psychiatric illness or social situation that would preclude study compliance
  • No other uncontrolled illness
  • No serious nonhealing wound, ulcer, or bone fracture
  • No history of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within the past 28 days
  • No significant traumatic injury in the past 28 days
  • At least 4 weeks since prior major surgery or open biopsy
  • More than 4 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin)
  • More than 4 weeks since prior radiotherapy
  • At least 2 weeks since prior tyrosine kinase inhibitor
  • Prior palliative radiotherapy to metastatic lesions allowed provided ≥ 1 measurable and/or evaluable lesion has not been irradiated
  • No more than 2 prior systemic treatments for metastatic disease, including immunotherapy, receptor tyrosine kinase inhibitor therapy, chemotherapy, or investigational therapy
  • No prior therapy with bevacizumab, vascular endothelial growth factor-trap, or histone deacetylase inhibitors, including valproic acid
  • No core biopsy within 1 week prior to day 1 of study treatment
  • No planned major surgery during study treatment
  • No concurrent combination antiretroviral therapy for HIV-positive patients
  • No other concurrent investigational agents
  • Concurrent stable-dose prophylactic anticoagulation (i.e., warfarin or low molecular weight heparin) allowed provided requirements for INR are met
  • Histologically confirmed renal cell carcinoma, clear cell component, unresectable or metastatic disease (patients with a primary tumor in place who are eligible for surgery are strongly encouraged to undergo a nephrectomy prior to study entry to increase potential survival)
  • Measurable disease, defined as ≥ 1 unidimensionally measurable lesion ≥ 20 mm by conventional techniques OR ≥ 10 mm with spiral CT scan
  • The following histologies are not allowed:

    • Papillary, sarcomatoid carcinoma
    • Chromophobe carcinoma
    • Oncocytoma
    • Collecting duct tumor
    • Transitional cell carcinoma
  • WBC ≥ 3,000/mm^3

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: Arm I

Phase I: Patients receive oral SAHA twice daily on days 1-14 and bevacizumab IV over 30-90 minutes on day 1. Treatment repeats every 21 days in the absence of disease progression or unacceptable toxicity.

Cohorts of 3-6 patients receive escalating doses of SAHA until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity. An additional 6 patients are treated at the MTD.

Phase II: Patients receive SAHA at the MTD determined in phase I and bevacizumab as in phase I.

Donné oralement
Autres noms:
  • SAHA
  • Zolinza
  • L-001079038
  • acide subéroylanilide hydroxamique
Étant donné IV
Autres noms:
  • Avastin
  • anticorps monoclonal humanisé anti-VEGF
  • anticorps monoclonal anti-VEGF
  • rhuMAb VEGF

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Progression-free Survival Assessed by Response Evaluation Criteria for Solid Tumors (RECIST) (Phase II)
Délai: At 6 months
Estimated by Kaplan-Meier method
At 6 months

Autres mesures de résultats

Mesure des résultats
Description de la mesure
Délai
Maximum Tolerated Dose
Délai: 18 months from first patient dosing
Determine the maximum tolerated dose of SAHA
18 months from first patient dosing
Clinical Response Rate of SAHA and Bevacizumab
Délai: 7 years
To determine the clinical response rate of SAHA and Bevacizumab in patients with metastatic renal cell carcinoma.
7 years

Collaborateurs et enquêteurs

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

Les enquêteurs

  • Chercheur principal: Michael Carducci, Johns Hopkins University/Sidney Kimmel Cancer Center

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

1 février 2006

Achèvement primaire (Réel)

1 juin 2013

Achèvement de l'étude (Réel)

1 novembre 2013

Dates d'inscription aux études

Première soumission

10 mai 2006

Première soumission répondant aux critères de contrôle qualité

10 mai 2006

Première publication (Estimation)

11 mai 2006

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Estimation)

13 janvier 2016

Dernière mise à jour soumise répondant aux critères de contrôle qualité

10 décembre 2015

Dernière vérification

1 octobre 2013

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • NCI-2009-00093 (Identificateur de registre: CTRP (Clinical Trial Reporting Program))
  • P30CA006973 (Subvention/contrat des NIH des États-Unis)
  • U01CA070095 (Subvention/contrat des NIH des États-Unis)
  • U01CA062491 (Subvention/contrat des NIH des États-Unis)
  • 6884 (CTEP)
  • NA 00001107
  • NCI-6884
  • JHOC-J0570
  • CDR0000467800
  • JHOC-00001107
  • J0570
  • IRB #NA 00001107, SKCCC J0570 (Autre identifiant: Johns Hopkins University/Sidney Kimmel Cancer Center)

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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