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

2017년 8월 24일 업데이트: 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.

연구 개요

상세 설명

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.

연구 유형

중재적

등록 (실제)

34

단계

  • 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

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

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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.
상관 연구
상관 연구
주어진 IV
주어진 PO

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
Antitumor activity of the combination in metastatic breast cancer (Expansion phase)
기간: 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)
기간: 21 days
21 days

2차 결과 측정

결과 측정
측정값 설명
기간
Change in average number of circulating tumor cells (CTCs)
기간: 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
기간: Baseline to up to day 17
Baseline to up to day 17
Change in percentage of biomarkers assessed using immunohistochemistry
기간: 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
기간: 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)
기간: 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
기간: 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
기간: 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

기타 결과 측정

결과 측정
측정값 설명
기간
Change in expression of plasma markers
기간: 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
기간: 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
기간: Up to day 17
Descriptive analysis will be performed.
Up to day 17

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2011년 1월 5일

기본 완료 (실제)

2012년 10월 19일

연구 완료 (실제)

2012년 10월 19일

연구 등록 날짜

최초 제출

2010년 12월 17일

QC 기준을 충족하는 최초 제출

2010년 12월 17일

처음 게시됨 (추정)

2010년 12월 20일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2017년 8월 25일

QC 기준을 충족하는 마지막 업데이트 제출

2017년 8월 24일

마지막으로 확인됨

2017년 8월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • NCI-2011-02562 (레지스트리 식별자: CTRP (Clinical Trial Reporting Program))
  • P30CA016672 (미국 NIH 보조금/계약)
  • U01CA062490 (미국 NIH 보조금/계약)
  • U01CA062461 (미국 NIH 보조금/계약)
  • 8739 (기타 식별자: CTEP)
  • 2010-0245 (기타 식별자: M D Anderson Cancer Center)
  • CDR0000690723

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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