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

2013. szeptember 27. frissítette: 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.

A tanulmány áttekintése

Részletes leírás

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.

Tanulmány típusa

Beavatkozó

Beiratkozás (Tényleges)

28

Fázis

  • 1. fázis

Kapcsolatok és helyek

Ez a rész a vizsgálatot végzők elérhetőségeit, valamint a vizsgálat lefolytatásának helyére vonatkozó információkat tartalmazza.

Tanulmányi helyek

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

Részvételi kritériumok

A kutatók olyan embereket keresnek, akik megfelelnek egy bizonyos leírásnak, az úgynevezett jogosultsági kritériumoknak. Néhány példa ezekre a kritériumokra a személy általános egészségi állapota vagy a korábbi kezelések.

Jogosultsági kritériumok

Tanulmányozható életkorok

18 év és régebbi (Felnőtt, Idősebb felnőtt)

Egészséges önkénteseket fogad

Nem

Tanulmányozható nemek

Női

Leírás

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

Tanulási terv

Ez a rész a vizsgálati terv részleteit tartalmazza, beleértve a vizsgálat megtervezését és a vizsgálat mérését.

Hogyan készül a tanulmány?

Tervezési részletek

  • Elsődleges cél: Kezelés
  • Kiosztás: N/A
  • Beavatkozó modell: Egyetlen csoportos hozzárendelés
  • Maszkolás: Nincs (Open Label)

Fegyverek és beavatkozások

Résztvevő csoport / kar
Beavatkozás / kezelés
Kísérleti: 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.

Más nevek:
  • farmakológiai vizsgálatok
Más nevek:
  • CGS 20267
  • Femara
  • LTZ
Más nevek:
  • mell biopsziája
Más nevek:
  • RO4929097
  • R4733

Mit mér a tanulmány?

Elsődleges eredményintézkedések

Eredménymérő
Időkeret
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
Időkeret: 21 days
21 days

Másodlagos eredményintézkedések

Eredménymérő
Intézkedés leírása
Időkeret
Measurement of NOTCH 1 and 4, activated NOTCH (ICN), Hey 1 and NOTCH ligands (DLL4 and Jagged 1)
Időkeret: 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)
Időkeret: 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)
Időkeret: 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)
Időkeret: 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
Időkeret: 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
Időkeret: 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
Időkeret: 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
Időkeret: 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)
Időkeret: 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)
Időkeret: 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)
Időkeret: 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)
Időkeret: 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)
Időkeret: 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)
Időkeret: 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)
Időkeret: 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)
Időkeret: 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)
Időkeret: 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)
Időkeret: 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)
Időkeret: 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)
Időkeret: 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

Együttműködők és nyomozók

Itt találhatja meg a tanulmányban érintett személyeket és szervezeteket.

Nyomozók

  • Kutatásvezető: Shannon Puhalla, University of Pittsburgh

Tanulmányi rekorddátumok

Ezek a dátumok nyomon követik a ClinicalTrials.gov webhelyre benyújtott vizsgálati rekordok és összefoglaló eredmények benyújtásának folyamatát. A vizsgálati feljegyzéseket és a jelentett eredményeket a Nemzeti Orvostudományi Könyvtár (NLM) felülvizsgálja, hogy megbizonyosodjon arról, hogy megfelelnek-e az adott minőség-ellenőrzési szabványoknak, mielőtt közzéteszik őket a nyilvános weboldalon.

Tanulmány főbb dátumok

Tanulmány kezdete

2010. november 1.

Elsődleges befejezés (Tényleges)

2011. december 1.

Tanulmányi regisztráció dátumai

Először benyújtva

2010. szeptember 23.

Először nyújtották be, amely megfelel a minőségbiztosítási kritériumoknak

2010. szeptember 23.

Első közzététel (Becslés)

2010. szeptember 24.

Tanulmányi rekordok frissítései

Utolsó frissítés közzétéve (Becslés)

2013. szeptember 30.

Az utolsó frissítés elküldve, amely megfelel a minőségbiztosítási kritériumoknak

2013. szeptember 27.

Utolsó ellenőrzés

2013. szeptember 1.

Több információ

A tanulmányhoz kapcsolódó kifejezések

Egyéb vizsgálati azonosító számok

  • NCI-2011-02487 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
  • U01CA099168 (Az Egyesült Államok NIH támogatása/szerződése)
  • UPCI-09-080
  • CDR0000683397
  • UPCI 09-080 (Egyéb azonosító: University of Pittsburgh Cancer Institute)
  • 8554 (Egyéb azonosító: CTEP)

Ezt az információt közvetlenül a clinicaltrials.gov webhelyről szereztük be, változtatás nélkül. Ha bármilyen kérése van vizsgálati adatainak módosítására, eltávolítására vagy frissítésére, kérjük, írjon a következő címre: register@clinicaltrials.gov. Amint a változás bevezetésre kerül a clinicaltrials.gov oldalon, ez a webhelyünkön is automatikusan frissül. .

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