RO4929097 and Letrozole in Treating Post-Menopausal Women With Hormone Receptor-Positive Stage II or Stage III Breast Cancer
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
Panoramica dello studio
Stato
Stato
Condizioni
Condizioni
Intervento / Trattamento
Intervento / Trattamento
Descrizione dettagliata
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 di studio
Tipo di studio
Iscrizione (Effettivo)
Iscrizione
Fase
Fase
- Fase 1
Contatti e Sedi
Luoghi di studio
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Alabama
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Birmingham, Alabama, Stati Uniti, 35294
- University of Alabama at Birmingham
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Pennsylvania
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Pittsburgh, Pennsylvania, Stati Uniti, 15213
- Magee-Womens Hospital of UPMC
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Pittsburgh, Pennsylvania, Stati Uniti, 15232
- University of Pittsburgh Cancer Institute
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-
Criteri di partecipazione
Criteri di ammissibilità
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
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
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Numero di armi
Armi e interventi
Gruppo di partecipanti / ArmGruppo di partecipanti / Arm |
Intervento / TrattamentoIntervento / Trattamento |
|---|---|
|
Sperimentale: 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. |
Altri nomi:
Altri nomi:
Altri nomi:
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
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
Lasso di tempo: 21 days
|
21 days
|
Misure di risultato secondarie
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Measurement of NOTCH 1 and 4, activated NOTCH (ICN), Hey 1 and NOTCH ligands (DLL4 and Jagged 1)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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
|
Collaboratori e investigatori
Sponsor
Sponsor
Investigatori
Investigatori
- Investigatore principale: Shannon Puhalla, University of Pittsburgh
Studiare le date dei record
Studia le date principali
Inizio studio
Inizio studio
Completamento primario (Effettivo)
Completamento primario
Date di iscrizione allo studio
Primo inviato
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Primo Inserito
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento pubblicato
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Malattie della pelle
- Neoplasie
- Neoplasie per sede
- Malattie del seno
- Neoplasie mammarie
- Effetti fisiologici delle droghe
- Meccanismi molecolari dell'azione farmacologica
- Inibitori enzimatici
- Agenti antineoplastici
- Ormoni, sostituti ormonali e antagonisti ormonali
- Antagonisti ormonali
- Inibitori dell'aromatasi
- Inibitori della sintesi di steroidi
- Antagonisti degli estrogeni
- Letrozolo
- R04929097
Altri numeri di identificazione dello studio
Altri numeri di identificazione dello studio
- NCI-2011-02487 (Identificatore di registro: CTRP (Clinical Trial Reporting Program))
- U01CA099168 (Sovvenzione/contratto NIH degli Stati Uniti)
- UPCI-09-080
- CDR0000683397
- UPCI 09-080 (Altro identificatore: University of Pittsburgh Cancer Institute)
- 8554 (Altro identificatore: CTEP)
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