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A Study of the Hsp90 Inhibitor AUY922 Plus Capecitabine for the Treatment of Patients With Advanced Solid Tumors

2022年2月15日 更新者:SCRI Development Innovations, LLC

A Phase I Study of the Hsp90 Inhibitor AUY922 Plus Capecitabine for the Treatment of Patients With Advanced Solid Tumors

The investigators propose this Phase I trial of the combination of AUY922 and capecitabine to determine the maximum tolerated dose (MTD) in patients with advanced solid tumors. This combination treatment has potential applicability in tumor types where capecitabine or fluorouracil is a treatment option, including colorectal and breast cancer.

研究概览

研究类型

介入性

注册 (实际的)

23

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Florida
      • Fort Myers、Florida、美国、33916
        • Florida Cancer Specialists
    • Oklahoma
      • Oklahoma City、Oklahoma、美国、71304
        • Oklahoma University
    • Tennessee
      • Nashville、Tennessee、美国、37203
        • Tennessee Oncology

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Histologically confirmed metastatic or unresectable solid tumor malignancy that is incurable and for which capecitabine is clinically appropriate.
  2. Patient must be ≥4 weeks from administration of last dose of cancer therapy (including radiation therapy, biologic therapy, hormonal therapy or chemotherapy). Patients who received a small molecule targeted therapy as part of their first line treatment regimen must be ≥4 weeks or ≥5 half lives from administration of last dose whichever is shorter. The patient must have recovered from or come to a new chronic stable baseline from all treatment-related toxicities.
  3. Eastern Collaborative Oncology Group (ECOG) performance status 0 to 1 (see Appendix A).
  4. Life expectancy of ≥3 months.
  5. At least one unidimensional measurable lesion definable by MRI or CT scan. Disease must be measurable per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 criteria (see Section 9).
  6. Normal bone marrow function defined as:

    • Absolute neutrophil count (ANC) ≥1500/μL
    • Hemoglobin (Hgb) ≥9 g/dL
    • Platelets ≥100,000/μL
  7. Adequate hepatic function defined as:

    • AST or ALT and alkaline phosphatase (ALP) must be ≤3 x ULN, or ≤5 x ULN in patients with liver metastases
    • Total bilirubin ≤1.5 x the institutional ULN
  8. Renal function defined as:

    • Serum creatinine ≤1.5 x ULN or 24-hour creatinine clearance ≥40 mL/min

  9. Normal electrolytes defined as:

    • Phosphorous ≥ LLN
    • Magnesium ≥ LLN
  10. Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test performed within 7 days prior to start of treatment. Women of childbearing potential must use effective birth control measures during treatment and during the 6 months following completion of study treatment. If a woman becomes pregnant or suspects she is pregnant while participating in this study, she must agree to inform her treating physician immediately.
  11. Must be ≥18 years of age.
  12. Patients must be accessible for treatment and follow-up.
  13. Patients must be able to understand the investigational nature of this study and give written informed consent prior to study entry.

Exclusion Criteria:

  1. Untreated CNS metastases. Patients with treated CNS metastases may be enrolled, provided the patient is asymptomatic, and the patient does not require antiepileptic drugs or steroids as treatment for the CNS metastases.
  2. Treatment with therapeutic doses of coumarin-type anticoagulants (maximum daily dose of 1 mg allowed for port line patency permitted).
  3. Impaired cardiac function with any one of the following:

    • History (or family history) of long QT syndrome
    • Mean QTc ≥450 msec on baseline ECG
    • History of clinically manifested ischemic heart disease (i.e. myocardial infarction and/or unstable angina) ≤6 months prior to study start
    • History of heart failure or left ventricular (LV) dysfunction (LVEF ≤45%) by MUGA or ECHO
    • Clinically significant ECG abnormalities including 1 or more of the following: left bundle branch block (LBBB), right bundle branch block (RBBB) with left anterior hemiblock (LAHB). ST segment elevation or depression > 1mm, or 2nd (Mobitz II), or 3rd degree AV block.
    • History or presence of atrial fibrillation, atrial flutter or ventricular arrhythmias including ventricular tachycardia or Torsades de Pointes
    • Other clinically significant heart disease (e.g. congestive heart failure, uncontrolled hypertension, history of labile hypertension, or history of poor compliance with an antihypertensive regimen)
    • Clinically significant resting bradycardia (< 50 beats per minute)
    • Patients who are currently receiving treatment with any medication which has a relative risk of prolonging the QTcF interval or inducing Torsades de Pointes and cannot be switched to an alternative drug or discontinued prior to commencing AUY922 (see Appendix D).
    • Obligate use of a cardiac pacemaker
  4. Impairment of gastrointestinal function or gastrointestinal disease that in the opinion of the Investigator may significantly alter the absorption of study drugs (e.g., Crohn's disease, ulcerative disease, uncontrolled vomiting, diarrhea, or malabsorption syndrome).
  5. Patients with known diagnosis of human immunodeficiency virus (HIV), hepatitis C virus, or acute or chronic hepatitis B infection.
  6. Concurrent severe, intercurrent illness including, but not limited to, ongoing or active infection, or psychiatric illness/social situations that would limit compliance with study requirements.
  7. Women who are pregnant (positive pregnancy test) or lactating.
  8. Any condition that would prevent patient comprehension of the nature of, and risk associated with, the study, and the inability to comply with study and/or follow-up procedures.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:非随机化
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Dose Level 1
Hsp90 Inhibitor AUY922: 22mg/m2 IV days 1, 8, and 15 of 21-day cycles Capecitabine: 1000mg/m2 PO BID d 1-14 of 21-day cycles
Taken orally twice daily on Days 1 through 14 of 21 day cycle.
其他名称:
  • 希罗达
IV infusion over 60 minutes on Days 1, 8, and 15 of each 21 day cycle
实验性的:Dose Level 2
Hsp90 Inhibitor AUY922: 28mg/m2 IV days 1, 8, and 15 of 21-day cycles Capecitabine: 1000mg/m2 PO BID d 1-14 of 21-day cycles
Taken orally twice daily on Days 1 through 14 of 21 day cycle.
其他名称:
  • 希罗达
IV infusion over 60 minutes on Days 1, 8, and 15 of each 21 day cycle
实验性的:Dose Level 3
Hsp90 Inhibitor AUY922: 40mg/m2 IV days 1, 8, and 15 of 21-day cycles Capecitabine: 1000mg/m2 PO BID d 1-14 of 21-day cycles
Taken orally twice daily on Days 1 through 14 of 21 day cycle.
其他名称:
  • 希罗达
IV infusion over 60 minutes on Days 1, 8, and 15 of each 21 day cycle
实验性的:Dose Level 4
Hsp90 Inhibitor AUY922: 55mg/m2 IV days 1, 8, and 15 of 21-day cycles Capecitabine: 1000mg/m2 PO BID d 1-14 of 21-day cycles
Taken orally twice daily on Days 1 through 14 of 21 day cycle.
其他名称:
  • 希罗达
IV infusion over 60 minutes on Days 1, 8, and 15 of each 21 day cycle
实验性的:Dose Level 5
Hsp90 Inhibitor AUY922: 70mg/m2 IV days 1, 8, and 15 of 21-day cycles Capecitabine: 1000mg/m2 PO BID d 1-14 of 21-day cycles
Taken orally twice daily on Days 1 through 14 of 21 day cycle.
其他名称:
  • 希罗达
IV infusion over 60 minutes on Days 1, 8, and 15 of each 21 day cycle
实验性的:Dose Level 6
Hsp90 Inhibitor AUY922: 70mg/m2 IV days 1, 8, and 15 of 21-day cycles Capecitabine: 1250mg/m2 PO BID d 1-14 of 21-day cycles
Taken orally twice daily on Days 1 through 14 of 21 day cycle.
其他名称:
  • 希罗达
IV infusion over 60 minutes on Days 1, 8, and 15 of each 21 day cycle

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Dose Determination
大体时间:18 months
To determine the maximum tolerated dose (MTD) of AUY922 plus capecitabine in patients with advanced solid tumors.
18 months

次要结果测量

结果测量
措施说明
大体时间
Drug Related Toxicities
大体时间:18 months
To evaluate the drug related toxicities associated with different doses of the drugs used in this regimen.
18 months
Preliminary Efficacy Assessment: Response Rate (RR)
大体时间:18 months
Response Rate (RR) is defined as the total number of patients with Complete Response (CR) or Partial Response (PR) as defined in RECIST v2. CR is defined as the dissappearance of all target lesions, disappearance of all non-target lesions and normalization of tumor markers. PR is defined as at least a 30% decrease in the sum of the longest diameter (LD) of target lesions, taking as reference the baseline sum LD.
18 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 学习椅:Johanna C Bendell, MD、SCRI Development Innovations, LLC

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2010年11月1日

初级完成 (实际的)

2013年7月1日

研究完成 (实际的)

2014年6月1日

研究注册日期

首次提交

2010年10月18日

首先提交符合 QC 标准的

2010年10月20日

首次发布 (估计)

2010年10月22日

研究记录更新

最后更新发布 (实际的)

2022年3月8日

上次提交的符合 QC 标准的更新

2022年2月15日

最后验证

2022年2月1日

更多信息

与本研究相关的术语

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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