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Study of High-dose, Intermittent Sunitinib in Patients With Solid Tumors.

2019年7月12日 更新者:H.M.W. Verheul、Amsterdam UMC, location VUmc

A Phase I Study of High-dose, Intermittent Sunitinib in Patients With Solid Tumors.

The primary objective of this study is:

  • To determine the maximum tolerated dose (MTD) of sunitinib when administered once weekly or once every two weeks.
  • To assess the safety and tolerability of sunitinib in a once weekly or once every two weeks dose schedule.

研究概览

地位

完全的

条件

详细说明

Our hypothesis is that sunitinib, when given in a high-dose, intermittent schedule may exhibit improved efficacy with an acceptable toxicity profile. In the present phase I trial, we aim to determine the maximum tolerated dose of sunitinib when administered high-dose, once weekly or once every two weeks. Furthermore, by acquiring skin and tumor biopsies, we will assess intratumoral concentrations of sunitinib, correlate these to skin and plasma concentrations and gain more insight into the biological effects of the drug. Additionally, we aim to preliminary assess the efficacy of sunitinib administered at the MTD level in both schedules. Known serum angiogenesis markers will be correlated to efficacy endpoints.

研究类型

介入性

注册 (实际的)

101

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

      • Amsterdam、荷兰、1081HV
        • VU University Medical Center

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

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Signed (by the patient or legally acceptable representative) and dated Informed Consent Form
  • Histological or cytological documentation of incurable locally advanced or metastatic solid malignancy for which no standard therapy exists.
  • Primary tumor or metastatic site must be accessible for biopsy. Patients eligible for the expansion cohort must be willing to undergo tumor biopsies, while tumor biopsy remains optional for patients enrolled in the escalation cohort. Bone metastases are excluded as a biopsy site.
  • Evaluable disease by RECIST version 1.1 criteria (see appendix III; at least 1 target or non-target lesion for dose escalation cohorts; at least 1 target lesion for dose expansion cohort).
  • Patients must have documented radiographic or clinical progressive disease.
  • Age ≥ 18 years.
  • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1.
  • Normal 12-lead ECG (clinically insignificant abnormalities permitted), and Left Ventricular Ejection Fraction (LVEF) > 50% by multigated acquisition (MUGA) scan or echocardiogram.
  • Normal regulated thyroid function- suppletion or blocking drugs permitted.
  • Urinalysis: no clinically significant abnormalities.
  • Adequate bone marrow, liver and renal function as assessed by the following laboratory requirements to be conducted within 14 days prior to screening:

    1. Hemoglobin >= 5.6 mmol/l
    2. Absolute neutrophil count (ANC) >=1,5 x 10*9/l
    3. Platelet count >= 100 x 10*9/l
    4. Total bilirubin <=1.5 times the upper limit of normal (ULN)
    5. ALT and AST 2.5 x ULN (In case of liver metastases: < 5 x ULN)
    6. Alkaline phosphatase < 4 x ULN
    7. Serum creatinine <= 1.5 x ULN or Creatinine clearance >= 50 ml/min (based on MDRD)
    8. PT-INR/PTT < 1.5 x ULN, unless coumarin derivatives are used
    9. Activated partial thromboplastin time < 1.25 x ULN (therapeutic anticoagulation therapy is allowed, if this treatment can be interrupted for a biopsy as judged by the treating physician)
  • Patients with known Gilbert's disease who have serum bilirubin <= 3x ULN may be enrolled.
  • Pregnant or breast-feeding subjects: Women of childbearing potential must have a negative pregnancy test performed within 7 days of the start of treatment. For fertile men or women of childbearing potential: documented willingness to use a highly effective means of contraception (e.g., hormonal methods [implants, injectables, or combined oral contraceptives], intrauterine devices, sexual abstinence, or vasectomized or surgically sterilized partner). Contraception is necessary for at least 6 months after receiving the study kinase inhibitor.

Exclusion Criteria:

  • Evidence of a significant uncontrolled concomitant disease, such as cardiovascular disease (including stroke, New York Heart Association Class III or IV cardiac disease or myocardial infarction within 6 months prior to screening, unstable arrhythmia, clinically significant valvular heart disease and unstable angina); nervous system, pulmonary (including obstructive pulmonary disease and history of symptomatic bronchospasm), renal, hepatic, endocrine, or gastrointestinal disorders; or a serious non-healing wound or fracture.
  • Poorly controlled hypertension despite adequate blood pressure medication. Blood pressure must be ≤160/95 mmHg at the time of screening on a stable antihypertensive regimen. Blood pressure must be stable on at least 2 separate measurements.
  • Seizure disorders requiring anticonvulsant therapy.
  • jor surgery, other than diagnostic surgery, within 4 weeks prior to Day 1, without complete recovery.
  • Known active bacterial, viral, fungal, mycobacterial, or other infection (including HIV and atypical mycobacterial disease, but excluding fungal infection of the nail beds.)
  • Known hypersensitivity to sunitinib or to its excipients.
  • Presence of any significant central nervous system or psychiatric disorder(s) that would interfere with the patient's compliance.
  • Drug or alcohol abuse.
  • Females who are pregnant or breast-feeding.
  • Any evidence of a disease or condition that might affect compliance with the protocol or interpretation of the study results or render the patient at high risk from treatment complications.
  • Unwillingness or inability to comply with study and follow-up procedures.
  • No chemotherapy, radiotherapy, or biologic therapy within the previous 4 weeks; no nitrosoureas or mitomycin C within the previous 6 weeks; no investigational agents within the previous 4 weeks.
  • Clinically significant history of liver disease, including viral or other hepatitis, current alcohol abuse, or cirrhosis.
  • Untreated or active central nervous system (CNS) metastases (progressing or requiring anticonvulsants or corticosteroids for symptomatic control);
  • Patients with a history of treated CNS metastases are eligible, provided that all of the following criteria are met:

    1. Presence of evaluable or measurable disease outside the CNS
    2. Radiographic demonstration of improvement upon completion of CNS-directed therapy and no evidence of interim progression between completion of CNS-directed therapy and the screening radiographic study
    3. Completion of radiotherapy ≥ 8 weeks prior to the screening radiographic study
    4. Discontinuation of corticosteroids and anticonvulsants ≥ 4 weeks prior to the screening radiographic study.

Note: Prior sunitinib therapy does not constitute an exclusion criterion.

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:阶乘赋值
  • 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:Sunitinib high dose, weekly schedule
Initial dose of sunitinib is set at 200 mg once weekly. Three patients are treated at the current dose level. If at least 2 patients are observed to have Dose Limiting Toxicity (DLT), the prior dose level is defined as the Maximum Tolerated Dose (MTD) (unless only 3 patients have been treated at that level, in which case it is the tentative MTD). If 0 of the 3 patients are observed to have DLT, the dose level is escalated one step for the next cohort of 3 patients. If exactly 1 of the 3 patients treated show DLT, 3 additional patients are treated at the current dose level. If none of these show DLT, the dose level is escalated for the next cohort of 3 patients; otherwise, the prior dose level is defined as the MTD (unless only 3 patients have been treated at that level, in which case it is the tentative MTD). A tentative MTD becomes final when a total of 6 patients are treated with less than 2 showing DLT
实验性的:Sunitinib high dose, biweekly schedule
When the final MTD is reached for the cohort of patients treated once weekly and depending on the toxicities developed and defining MTD, enrollment of patients in the once every 2 weeks escalation cohort will begin, with the initial dose set at the MTD dose of the once weekly schedule, escalating again at 100 mg increments per dose level.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
maximum tolerated dose (MTD) of sunitinib
大体时间:6 weeks
6 weeks
Number of participants with serious and non-serious adverse events
大体时间:6 weeks
6 weeks

次要结果测量

结果测量
大体时间
Calculation of maximum plasma drug concentration, sunitinib half life, Area Under the Concentration-Time Curve (AUC 0-48h), clearance and volume of distribution
大体时间:Prior to the initial dose on day 1 and 2, 4, 6, 8, 10, 24, and 48 hours post-dose
Prior to the initial dose on day 1 and 2, 4, 6, 8, 10, 24, and 48 hours post-dose
Time to Disease Progression
大体时间:end of study
end of study
Recommended phase II dose (RP2D) and the optimal dose schedule
大体时间:End of study
End of study
Measurement of intratumoral and skin concentration of sunitinib
大体时间:2 weeks
2 weeks

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。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

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

2013年7月1日

初级完成 (实际的)

2019年6月1日

研究完成 (实际的)

2019年6月1日

研究注册日期

首次提交

2013年9月30日

首先提交符合 QC 标准的

2014年2月7日

首次发布 (估计)

2014年2月10日

研究记录更新

最后更新发布 (实际的)

2019年7月17日

上次提交的符合 QC 标准的更新

2019年7月12日

最后验证

2019年7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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