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

2017年8月24日 更新者: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.

調査の概要

詳細な説明

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.

研究の種類

介入

入学 (実際)

34

段階

  • フェーズ 1

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Massachusetts
      • Boston、Massachusetts、アメリカ、02215
        • Dana-Farber Cancer Institute
    • Tennessee
      • Nashville、Tennessee、アメリカ、37232
        • Vanderbilt University/Ingram Cancer Center
    • Texas
      • Houston、Texas、アメリカ、77030
        • M D Anderson Cancer Center

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的: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.
相関研究
相関研究
与えられた IV
与えられたPO

この研究は何を測定していますか?

主要な結果の測定

結果測定
時間枠
Antitumor activity of the combination in metastatic breast cancer (Expansion phase)
時間枠: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)
時間枠:21 days
21 days

二次結果の測定

結果測定
メジャーの説明
時間枠
Change in average number of circulating tumor cells (CTCs)
時間枠: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
時間枠:Baseline to up to day 17
Baseline to up to day 17
Change in percentage of biomarkers assessed using immunohistochemistry
時間枠: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
時間枠: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)
時間枠: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
時間枠: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
時間枠: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

その他の成果指標

結果測定
メジャーの説明
時間枠
Change in expression of plasma markers
時間枠: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
時間枠: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
時間枠:Up to day 17
Descriptive analysis will be performed.
Up to day 17

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2011年1月5日

一次修了 (実際)

2012年10月19日

研究の完了 (実際)

2012年10月19日

試験登録日

最初に提出

2010年12月17日

QC基準を満たした最初の提出物

2010年12月17日

最初の投稿 (見積もり)

2010年12月20日

学習記録の更新

投稿された最後の更新 (実際)

2017年8月25日

QC基準を満たした最後の更新が送信されました

2017年8月24日

最終確認日

2017年8月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • NCI-2011-02562 (レジストリ識別子:CTRP (Clinical Trial Reporting Program))
  • P30CA016672 (米国 NIH グラント/契約)
  • U01CA062490 (米国 NIH グラント/契約)
  • U01CA062461 (米国 NIH グラント/契約)
  • 8739 (その他の識別子:CTEP)
  • 2010-0245 (その他の識別子:M D Anderson Cancer Center)
  • CDR0000690723

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

IV期乳がんの臨床試験

  • University of Tartu
    Tartu University Hospital; Estonian Science Foundation
    募集
    下肢動脈疾患 (Fontaine Stage IIb-IV)
    エストニア
  • Assiut University
    わからない
    CKD Stage(III,IV,V)および血液透析患者
  • Mayo Clinic
    National Cancer Institute (NCI)
    積極的、募集していない
    子宮頸部腺扁平上皮がん | 特に明記されていない子宮頸部扁平上皮癌 | 再発子宮頸がん | ステージ IB3 子宮頸がん FIGO 2018 | ステージ II 子宮頸がん FIGO 2018 | ステージ IIA 子宮頸がん FIGO 2018 | Stage IIA1 子宮頸がん FIGO 2018 | Stage IIA2 子宮頸がん FIGO 2018 | ステージ IIB 子宮頸がん FIGO 2018 | ステージ III 子宮頸がん FIGO 2018 | ステージ IIIA 子宮頸がん FIGO 2018 | Stage IIIB 子宮頸がん FIGO 2018 | ステージ IIIC 子宮頸がん FIGO 2018 | Stage... およびその他の条件
    アメリカ

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