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MK2206 and Paclitaxel in Treating Patients With Locally Advanced or Metastatic Solid Tumors or Metastatic Breast Cancer

24 sierpnia 2017 zaktualizowane przez: National Cancer Institute (NCI)

Phase Ib Dose Escalation and Biomarker Study of MK-2206 in Combination With Standard Doses of Weekly Paclitaxel in Patients With Locally Advanced or Metastatic Solid Tumors With an Expansion in Advanced Breast Cancer

This phase I trial studies the side effects and best dose of Akt inhibitor MK2206 (MK2206) when given together with paclitaxel and to see how well they work in treating patients with solid tumors that have spread to other places in the body and usually cannot be cured or controlled with treatment or breast cancer that has spread to other places in the body. Akt inhibitor MK2206 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving Akt inhibitor MK2206 and paclitaxel may be a better treatment for solid tumors or breast cancer.

Przegląd badań

Szczegółowy opis

PRIMARY OBJECTIVES:

I. To determine the maximum tolerated dose (MTD) of the combination of MK-2206 and weekly paclitaxel. (Dose-escalation phase) II. To determine the safety and anti-tumor activity of the combination in metastatic breast cancer. (Expansion phase)

SECONDARY OBJECTIVES:

I. To determine the pharmacokinetics of MK-2206 and weekly paclitaxel used in combination.

II. To determine the safety of MK-2206 and weekly paclitaxel used in combination.

III. To evaluate the toxicities and tolerability of the combination. IV. To document anti-tumor activity. V. To determine baseline molecular markers that may predict clinical activity. VI. To determine pharmacodynamic markers in blood and tumor tissue that may predict an increase in apoptosis (by cleaved caspase 3) and clinical activity.

VII. To determine concordance of phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha (PIK3CA) and phosphatase and tensin homolog (PTEN) status between primary tumor and distant metastasis.

VIII. To determine concordance of PIK3CA status of circulating tumor cells and distant metastasis.

OUTLINE: This is a dose-escalation study of Akt inhibitor MK2206.

Patients receive paclitaxel intravenously (IV) over 1 hour on days 1, 8, and 15 and Akt inhibitor MK2206 orally (PO) once daily (QD) on days 2, 9, and 16. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up for 3 weeks.

Typ studiów

Interwencyjne

Zapisy (Rzeczywisty)

34

Faza

  • Faza 1

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

    • Massachusetts
      • Boston, Massachusetts, Stany Zjednoczone, 02215
        • Dana-Farber Cancer Institute
    • Tennessee
      • Nashville, Tennessee, Stany Zjednoczone, 37232
        • Vanderbilt University/Ingram Cancer Center
    • Texas
      • Houston, Texas, Stany Zjednoczone, 77030
        • M D Anderson Cancer Center

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

18 lat i starsze (Dorosły, Starszy dorosły)

Akceptuje zdrowych ochotników

Nie

Płeć kwalifikująca się do nauki

Wszystko

Opis

Inclusion Criteria:

  • Patients with histologically or cytologically confirmed locally advanced or metastatic solid tumors who have received at least two lines of therapy; for the expansion phase: female patients with metastatic breast cancer who have received a maximum of three lines of therapy
  • Absolute neutrophil count (ANC) >= 1,000/uL
  • Platelets >= 100,000/uL
  • Hemoglobin (Hgb) >= 9 g/dL
  • Creatinine =< 1.5 x upper limit of normal (ULN)
  • Prothrombin time (PT) within institutional guideline for biopsy procedure
  • Total bilirubin =< 1.5 x ULN
  • Alanine aminotransferase (ALT) =< 2.5 x ULN (=< 3 x ULN for subjects with liver involvement with cancer)
  • A known diabetic patient who is taking insulin or oral anti-diabetic therapy must have a hemoglobin A1C (HBA1C) =< 8% or a fasting serum glucose =< 110% ULN
  • Patient will have a tumor suitable for fine-needle aspirates (FNA) and core biopsy for research purposes (determined by the treating physician)
  • Eastern Cooperative Oncology Group (ECOG) performance status =< 2 (Karnofsky >= 60%)
  • Measurable disease by Response Evaluation Criteria In Solid Tumors (RECIST) or evaluable disease (e.g., bone metastasis or lesions which do not fulfill RECIST criteria for metastatic disease)
  • Patients with central nervous system (CNS) metastasis who have completed a course of therapy (for treatment of CNS metastasis) would be eligible for the study provided they are clinically stable for 1 month prior to entry as defined as:

    • No evidence of new or enlarging CNS metastasis
    • Off steroids and anticonvulsants
  • Corrected QT (QTc) interval =< 450 msec (Bazett's formula)
  • Negative serum pregnancy test beta-human chorionic gonadotropin (hCG) for patients of childbearing age
  • For the dose escalation cohorts, patients must have received front-line, cytotoxic, systemic therapy (combination or single agent, with or without the addition of targeted agents) for advanced cancer
  • For the expansion cohort, patients must have received no more than three lines of cytotoxic systemic therapy (combination or single agent, with or without the addition of targeted agents) for metastatic breast cancer; patients could have received paclitaxel in the adjuvant setting, but not in the metastatic setting
  • The last line of therapy must have been administered > 21 days prior to initiation of treatment on this study
  • Women of childbearing potential and men must use two forms of contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation; should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, the patient should inform the treating physician immediately
  • Ability to understand and the willingness to sign a written informed consent document
  • Both men and women and members of all races and ethnic groups are eligible for this trial

Exclusion Criteria:

  • Patients may not be receiving any other investigational agents
  • Patients taking a potent cytochrome P450, family 3, subfamily A, polypeptide 4 (CYP3A4) inhibitor or inducer will be excluded; patients who have discontinued any of these medications must have a wash-out period of at least 5 days or at least 5 half-lives of the drug (whichever is longer) prior to the first dose MK-2206
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to MK-2206 or other agents used in the study
  • Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, bradycardia, related to cardiac disease, bundle branch block, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
  • Pregnant women are excluded from this study; breastfeeding should be discontinued

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Nie dotyczy
  • Model interwencyjny: Zadanie dla jednej grupy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Treatment (Akt inhibitor MK2206 and paclitaxel)
Patients receive paclitaxel IV over 1 hour on days 1, 8, and 15 and Akt inhibitor MK2206 PO QD on days 2, 9, and 16. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.
Badania korelacyjne
Badania korelacyjne
Biorąc pod uwagę IV
Biorąc pod uwagę PO

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Ramy czasowe
Antitumor activity of the combination in metastatic breast cancer (Expansion phase)
Ramy czasowe: Up to 3 weeks after completion of study treatment
Up to 3 weeks after completion of study treatment
MTD of the combination of MK-2206 and paclitaxel defined as the dose level in which less than or equal to 1 out of 6 patients develop dose limiting toxicity assessed using Common Terminology Criteria for Adverse Events version 4 (Phase I)
Ramy czasowe: 21 days
21 days

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Change in average number of circulating tumor cells (CTCs)
Ramy czasowe: Baseline to up to 2 weeks
Will be determined by chi-square analysis or Fisher's Exact test and compared by Student t-test.
Baseline to up to 2 weeks
Change in multiplex proteomics
Ramy czasowe: Baseline to up to day 17
Baseline to up to day 17
Change in percentage of biomarkers assessed using immunohistochemistry
Ramy czasowe: Baseline to up to 2 weeks
Baseline to up to 2 weeks
Change in percentage of marker of proliferation Ki-67 (Ki-67) positive cells
Ramy czasowe: Baseline to up to 2 weeks
Will be calculated using a two-sided one-sample t-test, at a significance level of 0.05.
Baseline to up to 2 weeks
Change in reverse phase proteomic arrays (RPPA)
Ramy czasowe: Baseline to up to day 8
Will be analyzed using the Wilcoxon rank test.
Baseline to up to day 8
Pharmacokinetic parameters of Akt inhibitor MK2206
Ramy czasowe: On days 1-3, 5, 8, 16, 17, and 19 of course 1 and then on day 1 of all subsequent courses
Standard analyses for the pharmacokinetic endpoints will be conducted, including summary of descriptive measures, e.g., tabulation of frequencies for categorical variables, numerical (mean, range, standard deviation, 95% confidence intervals) and graphical (box plots, histograms) summary of the distribution for continuous endpoints, correlation analyses (Pearson and Spearman), and linear and nonlinear regression analyses, etc.
On days 1-3, 5, 8, 16, 17, and 19 of course 1 and then on day 1 of all subsequent courses
Pharmacokinetic parameters of paclitaxel
Ramy czasowe: On days 1, 2, 15, and 16 of course 1
Standard analyses for the pharmacokinetic endpoints will be conducted, including summary of descriptive measures, e.g., tabulation of frequencies for categorical variables, numerical (mean, range, standard deviation, 95% confidence intervals) and graphical (box plots, histograms) summary of the distribution for continuous endpoints, correlation analyses (Pearson and Spearman), and linear and nonlinear regression analyses, etc.
On days 1, 2, 15, and 16 of course 1

Inne miary wyników

Miara wyniku
Opis środka
Ramy czasowe
Change in expression of plasma markers
Ramy czasowe: Baseline to up to day 17
The marker expression will be compared by Student t-test.
Baseline to up to day 17
PIK3CA mutation status
Ramy czasowe: Up to day 17
Chi-square or Fisher's exact status will be used to calculate associations between PIK3CA status and clinical parameters.
Up to day 17
Prevalence of single nucleotide polymorphisms (SNPs) in PI3K pathway genes
Ramy czasowe: Up to day 17
Descriptive analysis will be performed.
Up to day 17

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

5 stycznia 2011

Zakończenie podstawowe (Rzeczywisty)

19 października 2012

Ukończenie studiów (Rzeczywisty)

19 października 2012

Daty rejestracji na studia

Pierwszy przesłany

17 grudnia 2010

Pierwszy przesłany, który spełnia kryteria kontroli jakości

17 grudnia 2010

Pierwszy wysłany (Oszacować)

20 grudnia 2010

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

25 sierpnia 2017

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

24 sierpnia 2017

Ostatnia weryfikacja

1 sierpnia 2017

Więcej informacji

Terminy związane z tym badaniem

Inne numery identyfikacyjne badania

  • NCI-2011-02562 (Identyfikator rejestru: CTRP (Clinical Trial Reporting Program))
  • P30CA016672 (Grant/umowa NIH USA)
  • U01CA062490 (Grant/umowa NIH USA)
  • U01CA062461 (Grant/umowa NIH USA)
  • 8739 (Inny identyfikator: CTEP)
  • 2010-0245 (Inny identyfikator: M D Anderson Cancer Center)
  • CDR0000690723

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