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A Phase I/II Trial of VELCADE & Gemcitabine for Patients With Relapsed or Refractory Aggressive B- and T-cell Non-Hodgkin's Lymphoma

24 de maio de 2019 atualizado por: Northwestern University

A Phase I/II Trial of Combination Bortezomib (VELCADE) and Gemcitabine Therapy for Patients With Relapsed or Refractory Aggressive B- and T-cell Non-Hodgkin's Lymphoma

RATIONALE: Drugs used in chemotherapy, such as gemcitabine, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Bortezomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Giving gemcitabine together with bortezomib may kill more cancer cells.

PURPOSE: This phase I/II trial is studying the side effects and best dose of bortezomib when given together with gemcitabine and to see how well they work in treating patients with relapsed or refractory B-cell or T-cell non-Hodgkin's lymphoma.

Visão geral do estudo

Status

Rescindido

Condições

Descrição detalhada

OBJECTIVES:

Primary

  • Determine the response rate (complete and partial remission) in patients with relapsed or refractory aggressive B- or T-cell non-Hodgkin's lymphoma treated with gemcitabine hydrochloride and bortezomib.
  • Determine the maximum tolerated dose of bortezomib when administered with gemcitabine hydrochloride in these patients.

Secondary

  • Determine the time to treatment failure, duration of response, and overall survival of patients treated with this regimen.
  • Determine the safety and tolerability of this regimen in these patients.

OUTLINE: This is a phase I, dose-escalation study of bortezomib followed by a phase II, open-label study.

  • Phase I: Patients receive gemcitabine hydrochloride IV over 30 minutes and bortezomib IV over 3-5 seconds on days 1 and 8. Treatment repeats every 21 days for up to 9 courses in the absence of disease progression or unacceptable toxicity.

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

  • Phase II: Patients receive gemcitabine hydrochloride and bortezomib as in phase I at the MTD.

After completion of study therapy, patients are followed periodically for 3 years.

PROJECTED ACCRUAL: A total of 37 patients will be accrued for this study.

Tipo de estudo

Intervencional

Inscrição (Real)

32

Estágio

  • Fase 2
  • Fase 1

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • Illinois
      • Chicago, Illinois, Estados Unidos, 60611
        • Northwestern University
      • Chicago, Illinois, Estados Unidos, 60637
        • University of Chicago Cancer Research Center
      • Chicago, Illinois, Estados Unidos, 60611
        • Veterans Affairs Medical Center - Lakeside Chicago

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

18 anos e mais velhos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

DISEASE CHARACTERISTICS:

  • Diagnosis of B- or T-cell non-Hodgkin's lymphoma (NHL)

    • Intermediate histology B-cell NHL, including any of the following:

      • Diffuse large B-cell lymphoma
      • Transformed large cell lymphoma
    • Any T-cell NHL histology
    • Cutaneous T-cell lymphoma (CTCL) or mycosis fungoides (MF) allowed
  • Relapsed or refractory disease, defined as disease progressed after prior complete remission (CR), partial remission (PR), or stable disease (SD) to last therapy OR failure to achieve CR, PR, or SD after completion of last therapy
  • Must have received 1-3 prior therapeutic regimens

    • Cyclophosphamide, doxorubicin hydrochloride, vincristine, and prednisone (CHOP) AND cyclophosphamide, vincristine, and prednisone (CVP) OR CHOP with rituximab (CHOP-R) AND CVP with rituximab (CVP-R) is considered 1 regimen
    • Monoclonal antibody (e.g., rituximab) given as maintenance therapy is considered 1 regimen
    • Salvage chemotherapy followed by an autologous stem cell transplant is considered 1 regimen
    • No more than 7 prior therapeutic regimens for patients with CTCL or MF
  • No mantle cell lymphoma

PATIENT CHARACTERISTICS:

  • ECOG performance status 0-2
  • Life expectancy > 3 months
  • Absolute neutrophil count ≥ 1,500/mm^3
  • Platelet count ≥ 100,000/mm^3

    • At least 50,000/mm^3 if documented bone marrow involvement
  • Hemoglobin ≥ 8.0 g/dL
  • AST and ALT ≤ 3 times upper limit of normal (ULN)
  • Alkaline phosphatase ≤ 3 times ULN
  • Bilirubin ≤ 2 times ULN
  • Creatinine ≤ 2.0 mg/dL
  • No known history of HIV infection
  • No other active infection
  • No uncontrolled hypertension
  • No peripheral neuropathy ≥ grade 2 within the past 2 weeks
  • No myocardial infarction within the past 6 months
  • No New York Heart Association class III or IV heart failure
  • No uncontrolled angina
  • No severe uncontrolled ventricular arrhythmias
  • No acute ischemia or active conduction system abnormalities by ECG
  • No hypersensitivity to bortezomib, boron, or mannitol
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective barrier-method contraception
  • No serious medical or psychiatric illness that would preclude study participation

PRIOR CONCURRENT THERAPY:

  • Prior autologous and/or allogeneic stem cell transplantation allowed
  • More than 3 weeks since prior chemotherapy, radiotherapy, or immunotherapy
  • More than 3 weeks since prior systemic biologic anticancer therapy
  • More than 3 weeks since prior systemic corticosteroids (e.g., oral prednisone > 10 mg per day)
  • More than 2 weeks since prior investigational drug
  • No prior bortezomib or gemcitabine hydrochloride
  • No other concurrent systemic cytotoxic chemotherapy or investigational agents

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: N / D
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Gemcitabine 800 mg/m2 + Bortezomib IVP over 3-5 seconds
Gemcitabine dose of 800 mg/m2 over 30 minutes followed by Bortezomib IVP given over 3-5 seconds on day 1 and day 15 of each cycle every 28 days for up to 8 cycles.
Bortezomib 1.6mg/m2 on days 1 and 15 of each cycle, given over 3-5 seconds on day 1 and day 15 of each cycle every 28 days for up to 8 cycles.
Outros nomes:
  • PS-341
  • Velcade®
Gemcitabine dose of 800 mg/m2 over 30 minutes on day 1 and day 15 of each cycle every 28 days for up to 8 cycles.
Outros nomes:
  • Gemzar®

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Response Rate in Patients With Relapsed or Refractory B- and T-cell NHL With Gemcitabine and Bortezomib Combination Treatment.
Prazo: At screening and after completing cycle 3, cycle 6 and 30 days after Cycle 8

Response rate in patients with relapsed or refractory B- and T-cell NHL with Gemcitabine and Bortezomib combination treatment will be defined as the number of patients with Complete Remission [CR] and Partial Remission [PR]. CT scans at screening and after completing cycle 3, cycle 6 and 30 days after Cycle 8 assessed by the Response Criteria for Non-hodgkins Lymphoma will be used to determine response where:

CR=Complete disappearance of all detectable clinical and radiographic evidence of disease PR=> 50% decrease in SPD of the six largest dominant nodes or nodal masses

At screening and after completing cycle 3, cycle 6 and 30 days after Cycle 8

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Time to Treatment Failure and Duration of Response
Prazo: At screening and after completing cycle 3, cycle 6 and 30 days after cycle 8, then every 6 months for 3 years
Time to treatment failure and duration of response will be measured by CT Scan at screening and after completing cycle 3, cycle 6 and 30 days after cycle 8, then every 6 months for 3 years
At screening and after completing cycle 3, cycle 6 and 30 days after cycle 8, then every 6 months for 3 years
Overall Survival
Prazo: Every 6 months while on treatment and then every 6 months while off of treatment for up to 3 years
Overall survival will be evaluated every 6 months while on treatment and then every 6 months while off of treatment for up to 3 years
Every 6 months while on treatment and then every 6 months while off of treatment for up to 3 years
Evaluate Safety and Tolerability of Bortezomib and Gemcitabine Therapy
Prazo: During treatment through a maximum of 8 Cycles (1 Cycle = 28 Days) and 30 days post last treatment

Safety and tolerability of the study drugs will be assessed on Day 1 and on either Day 8 or Day 15 of each treatment cycle (1 Cycle - 28 days) while on active treatment; and 30 days post last treatment. Adverse Events that are experienced by patients, determined to be either grade 3 or grade 4 and at least possibly related to at least one of the study drugs as assessed according to the National Cancer Institute's Common Toxicity Criteria for adverse events version 3.0 (CTCAE v3.0) will be collected. In general adverse events (AEs) will be graded according to the following:

Grade 1 Mild AE Grade 2 Moderate AE Grade 3 Severe AE Grade 4 Life-threatening or disabling AE Grade 5 Death related to AE

During treatment through a maximum of 8 Cycles (1 Cycle = 28 Days) and 30 days post last treatment

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Investigador principal: Leo Gordon, MD, Northwestern University

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

7 de abril de 2006

Conclusão Primária (Real)

11 de fevereiro de 2011

Conclusão do estudo (Real)

5 de setembro de 2012

Datas de inscrição no estudo

Enviado pela primeira vez

9 de fevereiro de 2006

Enviado pela primeira vez que atendeu aos critérios de CQ

9 de fevereiro de 2006

Primeira postagem (Estimativa)

13 de fevereiro de 2006

Atualizações de registro de estudo

Última Atualização Postada (Real)

28 de maio de 2019

Última atualização enviada que atendeu aos critérios de controle de qualidade

24 de maio de 2019

Última verificação

1 de maio de 2019

Mais Informações

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

Ensaios clínicos em bortezomib

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