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RO4929097 and Letrozole in Treating Post-Menopausal Women With Hormone Receptor-Positive Stage II or Stage III Breast Cancer

27 de septiembre de 2013 actualizado por: National Cancer Institute (NCI)

A Phase Ib Neoadjuvant Study of the Gamma Secretase Inhibitor (RO4929097) in Combination With the Aromatase Inhibitor Letrozole in Post-Menopausal Women With Stage II/III Hormone Receptor-Positive Breast Cancer

This phase I trial is studying the side effects and best dose of RO4929097 when given together with letrozole in treating post-menopausal women with stage II or stage III breast cancer. RO4929097 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Estrogen can cause the growth of breast cancer cells. Hormone therapy using letrozole may fight breast cancer by blocking the use of estrogen by the tumor cells. Giving RO4929097 together with letrozole may be an effective treatment for breast cancer.

Descripción general del estudio

Descripción detallada

PRIMARY OBJECTIVES:

I. To establish the maximum-tolerated dose and the recommended phase II dose of gamma-secretase inhibitor RO4929097 (RO4929097) in combination with letrozole in post-menopausal women with hormone receptor-positive stage II or III breast cancer.

II. To assess the safety of this regimen in these patients.

SECONDARY OBJECTIVES:

I. To evaluate the pharmacokinetics of this regimen, taking into consideration the induction of CYP3A4, in these patients.

II. To characterize the pharmacodynamic effects of letrozole prior to and during administration of RO4929097 with attention to suppression of estradiol and estrone levels.

III. To describe the pharmacodynamic effects of letrozole with or without RO4929097 on the NOTCH pathway, proliferation, angiogenesis, stromal cell infiltration/pathways, and comprehensive genomic analysis in tumor tissue of these patients.

IV. To describe the response, including clinical complete or partial objective response, pathological complete response, and attainment of pathologic stage 0 or I status in these patients.

OUTLINE: This is a multicenter, dose-escalation study of gamma-secretase inhibitor RO4929097(RO4929097).

Patients receive oral letrozole once daily on days 1-21. Beginning in course 2, patients also receive oral RO4929097 on days 1-3, 8-10, and 15-18. Treatment repeats every 21 days for 6 courses in the absence of disease progression or unacceptable toxicity.

Beginning 1 week after completion of neoadjuvant therapy, patients undergo surgery or tumor biopsy. Patients continue to receive oral letrozole once daily during surgery and for an additional 4 weeks.

Blood and tumor tissue samples are collected at baseline and periodically during study for pharmacokinetics, pharmacodynamics, and correlative studies.

After completion of study therapy, patients are followed up for 1 month and then every 6 months for 5 years.

Tipo de estudio

Intervencionista

Inscripción (Actual)

28

Fase

  • Fase 1

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Alabama
      • Birmingham, Alabama, Estados Unidos, 35294
        • University of Alabama at Birmingham
    • Pennsylvania
      • Pittsburgh, Pennsylvania, Estados Unidos, 15213
        • Magee-Womens Hospital of UPMC
      • Pittsburgh, Pennsylvania, Estados Unidos, 15232
        • University of Pittsburgh Cancer Institute

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Femenino

Descripción

Inclusion Criteria:

  • Pathologically confirmed invasive breast cancer

    • Stage II or III disease (T2-T3, N0-2)

      • No N3, T4 disease
    • Estrogen receptor-positive (ER+) and/or progesterone receptor-positive (PR+)

      • H score ≥ 10 or positivity ≥ 10%
    • HER2 negative as determined by IHC (1 or 2+) or FISH (< 2.0+)
  • Bilateral disease allowed as long as all tumors are ER+ and ≥ 1 is T2-T3
  • Patient must have disease that is palpable on physical exam and able to be imaged via breast ultrasound

    • Defined as ≥ 1 T2 tumor > 2 cm
    • Multifocal disease allowed provided that ≥ 1 of the tumors is > 2 cm
  • No metastatic disease by CT scans of the chest, abdomen, and pelvis, a PET/CT bone scan, or nuclear medicine bone scan
  • No inflammatory breast cancer or presence of breast tumor cells in the dermal lymphatics of the breast
  • Post-menopausal meeting 1 of the following criteria:

    • Bilateral oophorectomy
    • Age ≥ 50 years and amenorrheic for > 12 months in the absence of chemotherapy, tamoxifen, toremifene, or ovarian suppression (spontaneous amenorrhea)
  • ECOG performance status (PS) 0-2 (Karnofsky PS 60-100%)
  • Life expectancy > 3 months
  • ANC ≥ 1,000/mm³
  • Platelet count ≥ 100,000/mm³
  • Hemoglobin ≥ 9 g/dL
  • Total bilirubin normal
  • AST and ALT ≤ 2.5 times upper limit of normal
  • Creatinine normal OR creatinine clearance ≥ 60 mL/min
  • Baseline QTcF ≤ 470 msec
  • No history of allergic reactions attributed to compounds of similar chemical or biologic composition to gamma secretase inhibitor RO4929097 or other agents used in the study
  • No malabsorption syndrome or other condition that would interfere with intestinal absorption
  • Able to swallow tablets
  • Not serologically positive for hepatitis A, B, or C, or have a history of liver disease, other forms of hepatitis, or cirrhosis
  • No uncontrolled electrolyte abnormalities including hypocalcemia, hypomagnesemia, hyponatremia, hypophosphatemia, or hypokalemia despite adequate electrolyte supplementation
  • No uncontrolled intercurrent illness including, but not limited to, any of the following:

    • Ongoing or active infection
    • Symptomatic congestive heart failure
    • Unstable angina pectoris
    • History of torsades de pointes or other significant cardiac arrhythmia other than chronic, stable atrial fibrillation
    • Psychiatric illness and/or social situations that would limit compliance with study requirements
  • Recovered to < grade 2 CTCAE toxicities related to prior therapy
  • No prior chemotherapy, hormonal therapy, radiotherapy, or biological therapy for breast cancer

    • Prior treatment for non-melanoma skin cancer or carcinoma in situ of the cervix allowed
    • No prior hormone therapy for ductal carcinoma in situ (DCIS)
  • No other concurrent investigational agents
  • No concurrent medications with narrow therapeutic indices that are metabolized by cytochrome P450 (CYP450), including warfarin sodium (Coumadin®)
  • No concurrent medications that are strong inducers and/or inhibitors or substrates of CYP3A4

    • Switching to alternative medications allowed
  • No concurrent combination antiretroviral therapy for HIV-positive patients
  • No concurrent antiarrhythmics or other medications known to prolong QTc
  • No other concurrent anticancer agents or therapies
  • No concurrent grapefruit juice

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Arm I

Patients receive oral letrozole once daily on days 1-21. Beginning in course 2, patients also receive oral RO4929097 on days 1-3, 8-10, and 15-18. Treatment repeats every 21 days for 6 courses in the absence of disease progression or unacceptable toxicity.

Beginning 1 week after completion of neoadjuvant therapy, patients undergo surgery or tumor biopsy. Patients continue to receive oral letrozole once daily during surgery and for an additional 4 weeks.

Otros nombres:
  • estudios farmacológicos
Otros nombres:
  • CGS 20267
  • Fémara
  • LTZ
Otros nombres:
  • biopsia de mama
Otros nombres:
  • RO4929097
  • R4733

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
MTD defined as the dose level at which no more than 1 of 6 patients experience a DLT, and the dose below that at which at least 2/6 patients have DLT according to NCI CTCAE version 4.0
Periodo de tiempo: 21 days
21 days

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Measurement of NOTCH 1 and 4, activated NOTCH (ICN), Hey 1 and NOTCH ligands (DLL4 and Jagged 1)
Periodo de tiempo: Baseline
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
Baseline
Measurement of NOTCH 1 and 4, activated NOTCH (ICN), Hey 1 and NOTCH ligands (DLL4 and Jagged 1)
Periodo de tiempo: 21 days
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
21 days
Measurement of NOTCH 1 and 4, activated NOTCH (ICN), Hey 1 and NOTCH ligands (DLL4 and Jagged 1)
Periodo de tiempo: 42 days
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
42 days
Measurement of NOTCH 1 and 4, activated NOTCH (ICN), Hey 1 and NOTCH ligands (DLL4 and Jagged 1)
Periodo de tiempo: At time of surgery
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
At time of surgery
Genomic analysis of RNA transcriptome, mirco-RNA transcriptome, and DNA methylation
Periodo de tiempo: Baseline
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value. For the analysis of the gene expression data, the overall false discovery rate (FDR), which is defined as the expected portion of false positives, will be controlled at 20% to generate a list of genes for further investigation.
Baseline
Genomic analysis of RNA transcriptome, mirco-RNA transcriptome, and DNA methylation
Periodo de tiempo: 21 days
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value. For the analysis of the gene expression data, the overall FDR, which is defined as the expected portion of false positives, will be controlled at 20% to generate a list of genes for further investigation.
21 days
Genomic analysis of RNA transcriptome, mirco-RNA transcriptome, and DNA methylation
Periodo de tiempo: 42 days
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value. For the analysis of the gene expression data, the overall FDR, which is defined as the expected portion of false positives, will be controlled at 20% to generate a list of genes for further investigation.
42 days
Genomic analysis of RNA transcriptome, mirco-RNA transcriptome, and DNA methylation
Periodo de tiempo: At time of surgery
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value. For the analysis of the gene expression data, the overall FDR, which is defined as the expected portion of false positives, will be controlled at 20% to generate a list of genes for further investigation.
At time of surgery
Measurement of cell proliferation (Ki-67)
Periodo de tiempo: Baseline
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
Baseline
Measurement of cell proliferation (Ki-67)
Periodo de tiempo: 21 days
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
21 days
Measurement of cell proliferation (Ki-67)
Periodo de tiempo: 42 days
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
42 days
Measurement of cell proliferation (Ki-67)
Periodo de tiempo: At time of surgery
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
At time of surgery
Measurement of appoptosis (TUNEL and activated caspase)
Periodo de tiempo: Baseline
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
Baseline
Measurement of appoptosis (TUNEL and activated caspase)
Periodo de tiempo: 21 days
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
21 days
Measurement of appoptosis (TUNEL and activated caspase)
Periodo de tiempo: 42 days
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
42 days
Measurement of appoptosis (TUNEL and activated caspase)
Periodo de tiempo: At time of surgery
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
At time of surgery
Measurement of angiogenesis (VEGF and CD31)
Periodo de tiempo: Baseline
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
Baseline
Measurement of angiogenesis (VEGF and CD31)
Periodo de tiempo: 21 days
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
21 days
Measurement of angiogenesis (VEGF and CD31)
Periodo de tiempo: 42 days
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
42 days
Measurement of angiogenesis (VEGF and CD31)
Periodo de tiempo: At time of surgery
All measurements are continuous. Descriptive statistics will be calculated to summarize change of each measurement from the baseline value. A two-sided Wilcoxon signed rank test will be used to compare each measurement at a specific time to the baseline value.
At time of surgery

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Investigador principal: Shannon Puhalla, University of Pittsburgh

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio

1 de noviembre de 2010

Finalización primaria (Actual)

1 de diciembre de 2011

Fechas de registro del estudio

Enviado por primera vez

23 de septiembre de 2010

Primero enviado que cumplió con los criterios de control de calidad

23 de septiembre de 2010

Publicado por primera vez (Estimar)

24 de septiembre de 2010

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

30 de septiembre de 2013

Última actualización enviada que cumplió con los criterios de control de calidad

27 de septiembre de 2013

Última verificación

1 de septiembre de 2013

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • NCI-2011-02487 (Identificador de registro: CTRP (Clinical Trial Reporting Program))
  • U01CA099168 (Subvención/contrato del NIH de EE. UU.)
  • UPCI-09-080
  • CDR0000683397
  • UPCI 09-080 (Otro identificador: University of Pittsburgh Cancer Institute)
  • 8554 (Otro identificador: CTEP)

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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