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Trial in Metastatic Colorectal Cancer With FOLFIRI Plus Aflibercept as First Line Treatment (MINOAS)

20 de fevereiro de 2019 atualizado por: Hellenic Oncology Research Group

A Open Label, Non Randomized, Phase Two Trial in Metastatic Colorectal Cancer (mCRC) With the Combination of m FOLFIRI Plus Aflibercept as First Line Treatment: MINOAS Trial

Investigators propose to study the combination of m FOLFIRI plus Aflibercept in a Phase II trial of patients with metastatic colorectal cancer. The promising results of aflibercept derived from preclinical studies and from clinical trials conducted in patients with refractory of recurrent to oxaliplatin-based 1st line treatment in patients with mCRC open the field to explore such therapeutic approaches in the 1st line setting in combination with the FOLFIRI regimen.

Visão geral do estudo

Descrição detalhada

Colorectal cancer accounts for 8% of all malignant tumors in adults and is considered as a major cause of cancer morbidity and mortality worldwide. Although curative surgical resection is possible in 70-80% of patients at diagnosis, almost half of them will develop local or/and metastatic recurrence and will die of the disease with the liver been the most common site of metastatic spread from CRC.

Combinations of infusional administrated 5-fluorouracil/Leucovorin with irinotecan or oxaliplatin are accepted as the mainstay of first-line treatment and have increase the median overall survival of patients with advanced CRC from 12 months to about 21-22 months. In addition, resection for colorectal metastases (mainly in the liver), has become the standard of care, for patients with limited metastatic disease confounded to the liver and currently remains the only potentially curative therapy Aflibercept, also known as vascular endothelial growth factor (VEGF) Trap, is an angiogenesis inhibitor with a unique mechanism of action. Aflibercept is a recombinant fusion protein that consists of portions of human VEGFR1 and VEGFR2 extracellular domains fused to the Fc portion of human immunoglobulin G1. This fusion protein binds all forms of Vascular Endothelial Growth Factor-A, as well as VEGF-B and placental growth factor, additional angiogenic growth factors that appear to play a role in tumor angiogenesis and inflammation. Aflibercept has been shown to bind VEGF-A, VEGF-B, and placental growth factor (PlGF) with higher affinity than their native receptors. In vitro and in vivo studies have shown that aflibercept can inhibit new vessel growth and tumor vascularization in tumor models.

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

      • Athens, Grécia
        • 251 Air Forces Military Hospital of Athens
      • Athens, Grécia
        • Anicancer Hospital of Athens "Agios Savvas"
      • Athens, Grécia
        • Anticanscer Hospital of Athens "Agios Savvas"
      • Athens, Grécia
        • Athens Hospital "Mitera" Hygia Polis
      • Athens, Grécia
        • General Hospital of Athens "Aretaieio"
      • Athens, Grécia
        • General Hospital of Athens "Sotiria"
      • Athens, Grécia
        • IASO general hospital
      • Río, Grécia
        • University Hospital of Patras-Rio
      • Thessaloniki, Grécia
        • Thessaloniki Bioclinic
    • Crete
      • Heraklion, Crete, Grécia, 71110
        • University Hospital of Heraklion Crete

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

Inclusion Criteria:

  • Patients with histologically documented adenocarcinomas of colon or rectum with unresectable metastatic disease.
  • No prior treatment for metastatic disease
  • Metastatic liver disease assessable with diffusion-weighted Magnetic Resonance Imaging (MRI)
  • No previous treatment with bevacizumab or Cetuximab or Panitumumab.
  • Patients may have receive fluoropyrimidines with or without oxaliplatin as adjuvant treatment, if they have progressed > 12 months after the end of the last cycle of the adjuvant treatment
  • Performance Status (ECOG) 0-2
  • Life expectancy ≥ 3 months.
  • Effective contraception for both male and female subjects if the risk of conception exists.
  • Adequate laboratory parameters: Absolute neutrophils count ≥ 1.5 x 109 /L, Platelets ≥ 100 x 109 /L, Leucocytes > 3,000/mm; Hemoglobin> 10.5g/dl, creatinine clearance ≥ 60 ml/min, Proteinuria <2+ (dipstick urinalysis) or ≤1g/24hour, Magnesium ≥ lower limit of normal, Calcium ≥ lower limit of normal, total Bilirubin ≤ 1.5 times the upper limit of normal; aspartate and alanine aminotransferase ≤ 3 times of the upper normal limit in absence of liver metastases, or ≤5x Upper Normal Limits (UNL) in presence of liver metastases, alkaline phosphatases < 5x UNL
  • All patients will have to sign written informed consent in order to participate in the study.
  • Female patients must commit to using reliable and appropriate methods of contraception until at least three months after the end of study treatment (when applicable). Male patients with a partner of childbearing potential must agree to use contraception in addition to having their partner use another contraceptive method during the trial

Exclusion Criteria:

  • Known hypersensitivity reaction to the component of the treatment.
  • Inability to underwent a diffusion-weighted MR Imaging at baseline and in predefined time points
  • Subject pregnant or breast feeding, or planning to become pregnant within 6 months after the end of treatment.
  • History or evidence upon physical examination of Central Nervous System (CNS) metastasis unless adequately treated (e.g. non irradiated CNS metastasis, seizure not controlled with standard medical therapy),
  • Concomitant protocol unplanned antitumor therapy (e.g. chemotherapy, molecular targeted therapy, immunotherapy),
  • Treatment with any other investigational medicinal product within 28 days prior to study entry.
  • Other serious and uncontrolled non-malignant disease
  • Uncontrolled hypertension (defined as systolic blood pressure >150 mmHg and/or diastolic blood pressure >100 mmHg), or history of hypertensive crisis, or hypertensive encephalopathy.
  • Gilbert's syndrome
  • Intolerance to atropine sulfate or loperamide
  • Known dihydropyrimidine dehydrogenase deficiency
  • Treatment with CYP3A4 inducers unless discontinued > 7 days prior to randomization
  • Any of the following in 3 months prior to inclusion: grade 3-4 gastrointestinal bleeding (unless due to resected tumor), treatment resistant peptic ulcer disease, erosive esophagitis or gastritis, infectious or inflammatory bowel disease, or diverticulitis
  • Any other serious and uncontrolled non-malignant disease, major surgery or traumatic injury within the last 28 days
  • INR in absence of anticoagulation therapy > 1.25 or poorly controlled anti-coagulation therapy on coumadin or heparin compounds (INR >3.0)
  • History of myocardial infarction and/or stroke within 6 months prior to randomization, New York Heart Association (NYHA) class III and IV congestive heart failure
  • History of life threatening (grade 4) venous thromboembolic events (including pulmonary embolism) within 6 months prior to registration,
  • Bowel obstruction
  • Legal incapacity or limited legal capacity.
  • Medical or psychological condition which in the opinion of the investigator would not permit the subject to complete the study or sign meaningful informed consent.
  • A second primary tumour other than non-melanoma skin cancer or in situ cervical cancer.
  • History of interstitial lung disease e.g. pneumonitis or pulmonary fibrosis or evidence of interstitial lung disease on chest CT scan.

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: FOLFIRI/Aflibercept
5 Fluorouracil/Leucovorin/Irinotecan/Aflibercept
5 Fluorouracil: 400mg/m2, bolus infusion in <5min followed by 5 Fluorouracil: 2400mg/m2, i.v in 46 hours continuous infusion (cycle repeated every two weeks)
Outros nomes:
  • 5 Fluorouracil (5-FU)
Leucovorin: 400mg/m2, i.v in 2 hours infusion (cycle repeated every two weeks)
Outros nomes:
  • Leucovorina (LV)
Irinotecan: 180mg/m2, i.v in 90min infusion (cycle repeated every two weeks)
Outros nomes:
  • Irinotecan (CPT-11)
Aflibercept: 4mg/kg i.v in 1 hour infusion (cycle repeated every two weeks)
Outros nomes:
  • Zaltrap

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Prazo
Taxa de resposta geral
Prazo: Avaliação da doença na semana 8
Avaliação da doença na semana 8

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Sobrevivência geral
Prazo: 1 ano
1 ano
Sobrevivência Livre de Progressão
Prazo: 1 ano
1 ano
Toxicity profile (CTCAE v4.0)
Prazo: Every 2 weeks up to 100 weeks
From date of randomization until the date of last follow up or death from any cause, assessed up to 100 weeks
Every 2 weeks up to 100 weeks

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: John Souglakos, MD, Hellenic Oncology Research Group
  • Investigador principal: Athanasios Kotsakis, MD, Hellenic Oncology Research Group

Publicações e links úteis

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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

1 de janeiro de 2016

Conclusão Primária (Real)

1 de outubro de 2018

Conclusão do estudo (Antecipado)

1 de março de 2019

Datas de inscrição no estudo

Enviado pela primeira vez

24 de novembro de 2015

Enviado pela primeira vez que atendeu aos critérios de CQ

4 de dezembro de 2015

Primeira postagem (Estimativa)

8 de dezembro de 2015

Atualizações de registro de estudo

Última Atualização Postada (Real)

22 de fevereiro de 2019

Última atualização enviada que atendeu aos critérios de controle de qualidade

20 de fevereiro de 2019

Última verificação

1 de janeiro 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 .

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