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A Study of the Hsp90 Inhibitor AUY922 Plus Capecitabine for the Treatment of Patients With Advanced Solid Tumors

15 de fevereiro de 2022 atualizado por: SCRI Development Innovations, LLC

A Phase I Study of the Hsp90 Inhibitor AUY922 Plus Capecitabine for the Treatment of Patients With Advanced Solid Tumors

The investigators propose this Phase I trial of the combination of AUY922 and capecitabine to determine the maximum tolerated dose (MTD) in patients with advanced solid tumors. This combination treatment has potential applicability in tumor types where capecitabine or fluorouracil is a treatment option, including colorectal and breast cancer.

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Real)

23

Estágio

  • 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

    • Florida
      • Fort Myers, Florida, Estados Unidos, 33916
        • Florida Cancer Specialists
    • Oklahoma
      • Oklahoma City, Oklahoma, Estados Unidos, 71304
        • Oklahoma University
    • Tennessee
      • Nashville, Tennessee, Estados Unidos, 37203
        • Tennessee Oncology

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:

  1. Histologically confirmed metastatic or unresectable solid tumor malignancy that is incurable and for which capecitabine is clinically appropriate.
  2. Patient must be ≥4 weeks from administration of last dose of cancer therapy (including radiation therapy, biologic therapy, hormonal therapy or chemotherapy). Patients who received a small molecule targeted therapy as part of their first line treatment regimen must be ≥4 weeks or ≥5 half lives from administration of last dose whichever is shorter. The patient must have recovered from or come to a new chronic stable baseline from all treatment-related toxicities.
  3. Eastern Collaborative Oncology Group (ECOG) performance status 0 to 1 (see Appendix A).
  4. Life expectancy of ≥3 months.
  5. At least one unidimensional measurable lesion definable by MRI or CT scan. Disease must be measurable per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 criteria (see Section 9).
  6. Normal bone marrow function defined as:

    • Absolute neutrophil count (ANC) ≥1500/μL
    • Hemoglobin (Hgb) ≥9 g/dL
    • Platelets ≥100,000/μL
  7. Adequate hepatic function defined as:

    • AST or ALT and alkaline phosphatase (ALP) must be ≤3 x ULN, or ≤5 x ULN in patients with liver metastases
    • Total bilirubin ≤1.5 x the institutional ULN
  8. Renal function defined as:

    • Serum creatinine ≤1.5 x ULN or 24-hour creatinine clearance ≥40 mL/min

  9. Normal electrolytes defined as:

    • Phosphorous ≥ LLN
    • Magnesium ≥ LLN
  10. Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test performed within 7 days prior to start of treatment. Women of childbearing potential must use effective birth control measures during treatment and during the 6 months following completion of study treatment. If a woman becomes pregnant or suspects she is pregnant while participating in this study, she must agree to inform her treating physician immediately.
  11. Must be ≥18 years of age.
  12. Patients must be accessible for treatment and follow-up.
  13. Patients must be able to understand the investigational nature of this study and give written informed consent prior to study entry.

Exclusion Criteria:

  1. Untreated CNS metastases. Patients with treated CNS metastases may be enrolled, provided the patient is asymptomatic, and the patient does not require antiepileptic drugs or steroids as treatment for the CNS metastases.
  2. Treatment with therapeutic doses of coumarin-type anticoagulants (maximum daily dose of 1 mg allowed for port line patency permitted).
  3. Impaired cardiac function with any one of the following:

    • History (or family history) of long QT syndrome
    • Mean QTc ≥450 msec on baseline ECG
    • History of clinically manifested ischemic heart disease (i.e. myocardial infarction and/or unstable angina) ≤6 months prior to study start
    • History of heart failure or left ventricular (LV) dysfunction (LVEF ≤45%) by MUGA or ECHO
    • Clinically significant ECG abnormalities including 1 or more of the following: left bundle branch block (LBBB), right bundle branch block (RBBB) with left anterior hemiblock (LAHB). ST segment elevation or depression > 1mm, or 2nd (Mobitz II), or 3rd degree AV block.
    • History or presence of atrial fibrillation, atrial flutter or ventricular arrhythmias including ventricular tachycardia or Torsades de Pointes
    • Other clinically significant heart disease (e.g. congestive heart failure, uncontrolled hypertension, history of labile hypertension, or history of poor compliance with an antihypertensive regimen)
    • Clinically significant resting bradycardia (< 50 beats per minute)
    • Patients who are currently receiving treatment with any medication which has a relative risk of prolonging the QTcF interval or inducing Torsades de Pointes and cannot be switched to an alternative drug or discontinued prior to commencing AUY922 (see Appendix D).
    • Obligate use of a cardiac pacemaker
  4. Impairment of gastrointestinal function or gastrointestinal disease that in the opinion of the Investigator may significantly alter the absorption of study drugs (e.g., Crohn's disease, ulcerative disease, uncontrolled vomiting, diarrhea, or malabsorption syndrome).
  5. Patients with known diagnosis of human immunodeficiency virus (HIV), hepatitis C virus, or acute or chronic hepatitis B infection.
  6. Concurrent severe, intercurrent illness including, but not limited to, ongoing or active infection, or psychiatric illness/social situations that would limit compliance with study requirements.
  7. Women who are pregnant (positive pregnancy test) or lactating.
  8. Any condition that would prevent patient comprehension of the nature of, and risk associated with, the study, and the inability to comply with study and/or follow-up procedures.

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: Não randomizado
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Dose Level 1
Hsp90 Inhibitor AUY922: 22mg/m2 IV days 1, 8, and 15 of 21-day cycles Capecitabine: 1000mg/m2 PO BID d 1-14 of 21-day cycles
Taken orally twice daily on Days 1 through 14 of 21 day cycle.
Outros nomes:
  • Xeloda
IV infusion over 60 minutes on Days 1, 8, and 15 of each 21 day cycle
Experimental: Dose Level 2
Hsp90 Inhibitor AUY922: 28mg/m2 IV days 1, 8, and 15 of 21-day cycles Capecitabine: 1000mg/m2 PO BID d 1-14 of 21-day cycles
Taken orally twice daily on Days 1 through 14 of 21 day cycle.
Outros nomes:
  • Xeloda
IV infusion over 60 minutes on Days 1, 8, and 15 of each 21 day cycle
Experimental: Dose Level 3
Hsp90 Inhibitor AUY922: 40mg/m2 IV days 1, 8, and 15 of 21-day cycles Capecitabine: 1000mg/m2 PO BID d 1-14 of 21-day cycles
Taken orally twice daily on Days 1 through 14 of 21 day cycle.
Outros nomes:
  • Xeloda
IV infusion over 60 minutes on Days 1, 8, and 15 of each 21 day cycle
Experimental: Dose Level 4
Hsp90 Inhibitor AUY922: 55mg/m2 IV days 1, 8, and 15 of 21-day cycles Capecitabine: 1000mg/m2 PO BID d 1-14 of 21-day cycles
Taken orally twice daily on Days 1 through 14 of 21 day cycle.
Outros nomes:
  • Xeloda
IV infusion over 60 minutes on Days 1, 8, and 15 of each 21 day cycle
Experimental: Dose Level 5
Hsp90 Inhibitor AUY922: 70mg/m2 IV days 1, 8, and 15 of 21-day cycles Capecitabine: 1000mg/m2 PO BID d 1-14 of 21-day cycles
Taken orally twice daily on Days 1 through 14 of 21 day cycle.
Outros nomes:
  • Xeloda
IV infusion over 60 minutes on Days 1, 8, and 15 of each 21 day cycle
Experimental: Dose Level 6
Hsp90 Inhibitor AUY922: 70mg/m2 IV days 1, 8, and 15 of 21-day cycles Capecitabine: 1250mg/m2 PO BID d 1-14 of 21-day cycles
Taken orally twice daily on Days 1 through 14 of 21 day cycle.
Outros nomes:
  • Xeloda
IV infusion over 60 minutes on Days 1, 8, and 15 of each 21 day cycle

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Dose Determination
Prazo: 18 months
To determine the maximum tolerated dose (MTD) of AUY922 plus capecitabine in patients with advanced solid tumors.
18 months

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Drug Related Toxicities
Prazo: 18 months
To evaluate the drug related toxicities associated with different doses of the drugs used in this regimen.
18 months
Preliminary Efficacy Assessment: Response Rate (RR)
Prazo: 18 months
Response Rate (RR) is defined as the total number of patients with Complete Response (CR) or Partial Response (PR) as defined in RECIST v2. CR is defined as the dissappearance of all target lesions, disappearance of all non-target lesions and normalization of tumor markers. PR is defined as at least a 30% decrease in the sum of the longest diameter (LD) of target lesions, taking as reference the baseline sum LD.
18 months

Colaboradores e Investigadores

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

Colaboradores

Investigadores

  • Cadeira de estudo: Johanna C Bendell, MD, SCRI Development Innovations, LLC

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 novembro de 2010

Conclusão Primária (Real)

1 de julho de 2013

Conclusão do estudo (Real)

1 de junho de 2014

Datas de inscrição no estudo

Enviado pela primeira vez

18 de outubro de 2010

Enviado pela primeira vez que atendeu aos critérios de CQ

20 de outubro de 2010

Primeira postagem (Estimativa)

22 de outubro de 2010

Atualizações de registro de estudo

Última Atualização Postada (Real)

8 de março de 2022

Última atualização enviada que atendeu aos critérios de controle de qualidade

15 de fevereiro de 2022

Última verificação

1 de fevereiro de 2022

Mais Informações

Termos relacionados a este estudo

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