Esta página foi traduzida automaticamente e a precisão da tradução não é garantida. Por favor, consulte o versão em inglês para um texto fonte.

Gemcitabine, Bevacizumab, and Abdominal Radiation Therapy in Treating Patients With Localized Pancreatic Cancer

25 de outubro de 2018 atualizado por: Northwestern University

A Phase II Trial of Weekly Gemcitabine Hydrochloride and Bevacizumab in Combination With Abdominal Radiation Therapy in Patients With Localized Pancreatic Cancer

RATIONALE: Drugs used in chemotherapy, such as gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. 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 tumor growth by blocking blood flow to the tumor. Radiation therapy uses high-energy x-rays to kill tumor cells. Gemcitabine and bevacizumab may make tumor cells more sensitive to radiation therapy. Giving gemcitabine together with bevacizumab and radiation therapy may kill more tumor cells.

PURPOSE: This phase II trial is studying how well giving gemcitabine together with bevacizumab and abdominal radiation therapy works in treating patients with localized pancreatic cancer.

Visão geral do estudo

Descrição detalhada

OBJECTIVES:

Primary

  • Determine the objective response rate in patients treated with concurrent bevacizumab, gemcitabine hydrochloride, and abdominal radiotherapy.

Secondary

  • Determine the quantitative toxicity associated with the delivery of this regimen in these patients.
  • Determine the 1-year and median survival of patients treated with this regimen.
  • Determine the time to progression in patients treated with this regimen.
  • Determine the patterns of recurrence in the entire population of patients treated with this regimen and in the subgroup that is resected for cure.
  • Determine the safety of this regimen in these patients.
  • Evaluate the surgical experience of patients who undergo surgical resection after completion of protocol-directed therapy.
  • Evaluate the toxicity associated with surgical resection in these patients.

OUTLINE: Patients receive gemcitabine hydrochloride IV over 30 minutes on days 1 and 8 of courses 1 and 3 and on days 1, 8, and 15 of course 2. Patients also receive bevacizumab IV over 30-90 minutes on days 1 and 15 of course 1, on days 8 and 22 of course 2, and on day 8 of course 3. Treatment repeats every 3-4 weeks for up to 3 courses in the absence of disease progression or unacceptable toxicity. Beginning on day 1 of the second course of chemotherapy, patients undergo concurrent abdominal radiotherapy once daily, five days a week, for 3 weeks.

Patients are evaluated at week 10. Patients whose disease deemed resectable after study treatment undergo standard pancreatic resection at least 6 weeks after completion of bevacizumab. Patients who remain unresectable and have not progressed after completion of chemoradiotherapy may begin maintenance therapy comprising gemcitabine hydrochloride IV over 30 minutes on days 1, 8, and 15 and bevacizumab IV over 30-90 minutes on days 1 and 15. Treatment with gemcitabine hydrochloride and bevacizumab repeats every 4 weeks in the absence of disease progression or unacceptable toxicity.

After completion of study therapy, patients are followed periodically for up to 10 years.

PROJECTED ACCRUAL: A total of 30 patients will be accrued for this study.

Tipo de estudo

Intervencional

Inscrição (Real)

31

Estágio

  • Fase 2

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, 60611-3013
        • Northwestern University

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 a 120 anos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

DISEASE CHARACTERISTICS:

  • Diagnosis of localized pancreatic cancer

    • No metastatic disease
  • Resectable or unresectable tumor based on spiral CT with both oral and intravenous contrast enhancement, defined by the following National Comprehensive Cancer Network (NCCN) criteria for resectability*:

    • Resectable tumors meeting the following criteria:

      • No distant metastases
      • Clear fat plane around celiac and superior mesenteric arteries
      • Patent superior mesenteric vein/portal vein
    • Tumors considered borderline resectable according to NCCN criteria, including any of the following, are considered unresectable for the purpose of this study:

      • Severe unilateral superior mesenteric vein/portal impingement
      • Tumor abutment on the superior mesenteric artery
      • Gastroduodenal artery encasement up to the origin at the hepatic artery
      • Colon invasion NOTE: *Determination of resectability must be made prior to study entry based on NCCN criteria
  • Patients with biliary or gastroduodenal obstruction must have drainage or surgical bypass prior to starting chemoradiotherapy
  • Radiographically assessable disease

    • Malignant disease must be encompassable within a single irradiation field
  • No gross duodenal invasion noted on endoscopy
  • No CNS or brain metastases

PATIENT CHARACTERISTICS:

  • ECOG performance status 0-1
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception during and for up to 3 months after completion of study therapy
  • Bilirubin ≤ 2.0 mg/dL
  • AST or ALT ≤ 2.5 times upper limit of normal
  • Urine protein:creatinine ratio < 1.0
  • Proteinuria < 2+ by dipstick urinalysis OR baseline protein ≤ 1 g/24-hour urine collection
  • Absolute neutrophil count ≥ 1,500/mm³
  • Platelet count ≥ 100,000/mm³
  • Hemoglobin ≥ 9.0 g/dL (transfusion or epoetin alfa support allowed)
  • INR ≤ 1.5
  • No other malignancy within the past 5 years except nonmelanomatous skin cancer or carcinoma in situ of the cervix, uterus, or bladder
  • No concurrent significant infection or other medical condition that would preclude protocol treatment
  • No history of other disease, metabolic dysfunction, physical examination finding, or clinical laboratory finding that would contraindicate use of an investigational drug, affect the interpretation of the results of the study, or render the patient at high risk for treatment complications
  • No clinically significant cardiac disease, including any of the following:

    • Uncontrolled hypertension (i.e., blood pressure > 150/100 mm Hg despite antihypertensive medication)
    • Myocardial infarction within the past year
    • Unstable angina
    • New York Heart Association class II-IV congestive heart failure
    • Unstable symptomatic arrhythmia requiring medication

      • Chronic atrial arrhythmia (i.e., atrial fibrillation or paroxysmal supraventricular tachycardia) allowed
  • No clinically significant peripheral vascular disease
  • No evidence of bleeding diathesis or coagulopathy
  • No significant traumatic injury within the past 28 days
  • No serious, nonhealing wound or ulcer, or concurrent healing fracture
  • No history of aneurysm, stroke, transient ischemic attack, or arteriovenous malformation
  • No abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within the past 6 months

PRIOR CONCURRENT THERAPY:

  • See Disease Characteristics
  • No prior treatment for pancreatic cancer
  • More than 5 years since prior chemotherapy for malignancies other than pancreatic cancer
  • No prior radiotherapy to the target volume
  • More than 28 days since prior major surgical procedure or open biopsy
  • At least 28 days since prior surgical bypass
  • More than 7 days since prior fine-needle aspiration or core biopsy
  • No prior organ transplant
  • At least 4 weeks since prior sorivudine or brivudine
  • At least 30 days since prior cimetidine
  • No concurrent major surgical procedure

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: Treatment Arm
Concurrent gemcitabine, bevacizumab, and radiation therapy
10 mg/kg every 2 weeks as an intravenous infusion after gemcitabine and before radiation
Outros nomes:
  • AvastinName
1000 mg/m2, 30 minute intravenous infusion, cycle 1 (weeks 1, 2), cycle 2 (weeks 4, 5, 6) and cycle 3 (weeks 8 and 9). During cycle 2, gemcitabine will be delivered prior to radiation therapy
Outros nomes:
  • cloridrato de gencitabina
If resectable, patients will undergo surgery no less than 6 weeks following last dose of bevacizumab. Unresectable patients will not undergo surgery.
2.4 Gy fractions, 5 fractions/week during cycle 2 only (weeks 4, 5, 6). Total dose 36 Gy.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Response rate
Prazo: After 10 weeks of concurrent therapy
Response will be measured by CT scans using Recist and defined as Complete Response, Partial Response, Stable disease/no response, Progressive Disease.
After 10 weeks of concurrent therapy

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Toxicity profile of bevacizumab and gemcitabine with radiation therapy
Prazo: After every cycle of therapy (cycle = 3-4 weeks), then every 3 months for 2 years, then every 6 months for 3 years, then yearly up to 10 years or until disease progression.

Toxicities will be measured using National Cancer Institute's Common Toxicity Criteria for adverse events version 3.0 (CTCAE v3.0). Adverse events (AE)are graded:

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

After every cycle of therapy (cycle = 3-4 weeks), then every 3 months for 2 years, then every 6 months for 3 years, then yearly up to 10 years or until disease progression.

Colaboradores e Investigadores

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

Publicações e links úteis

A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.

Publicações Gerais

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)

10 de outubro de 2005

Conclusão Primária (Real)

17 de dezembro de 2007

Conclusão do estudo (Real)

16 de julho de 2010

Datas de inscrição no estudo

Enviado pela primeira vez

11 de abril de 2007

Enviado pela primeira vez que atendeu aos critérios de CQ

11 de abril de 2007

Primeira postagem (Estimativa)

13 de abril de 2007

Atualizações de registro de estudo

Última Atualização Postada (Real)

29 de outubro de 2018

Última atualização enviada que atendeu aos critérios de controle de qualidade

25 de outubro de 2018

Última verificação

1 de outubro de 2018

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 .

Se inscrever