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A Trial of Cediranib in the Treatment of Patients With Alveolar Soft Part Sarcoma (CASPS) (CASPS)

A Phase II Trial of Cediranib in the Treatment of Patients With Alveolar Soft Part Sarcoma (CASPS)

The study is a two-arm, randomised, double-blind, international, multi-centre phase II trial of cediranib in Alveolar Soft Part Sarcoma (ASPS).

The study aims to confirm the ability of cediranib to halt disease progression in patients with metastatic ASPS, as measured by the change in tumour size at 24 weeks after randomisation, and to produce objective response according to RECIST criteria.

研究概览

详细说明

Patients aged 16 years and older with a histologically confirmed diagnosis of ASPS will be recruited. Eligible patients will be randomised to receive cediranib (30 mg daily po) or placebo (30 mg daily po) in a 2:1 ratio. At 24 weeks post randomisation, treatment will be unblinded after which time all patients on placebo and those who have not progressed on active treatment will be given cediranib. Treatment will then continue until objective disease progression or death.

研究类型

介入性

注册 (预期的)

36

阶段

  • 阶段2

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

      • Brisbane、澳大利亚
        • Princess Alexandra Hospital
      • Sydney、澳大利亚
        • Royal Prince Alfred Hospital
      • Bristol、英国
        • Bristol Haematology and Oncology Centre
      • London、英国
        • University College London Hospital
      • London、英国
        • Royal Marsden Hospital
      • Manchester、英国
        • Christie Hospital
      • Newcastle-Upon-Tyne、英国
        • Royal Victoria Infirmary/Freeman Hospital
      • Nottingham、英国
        • Nottingham University Hospitals
      • Barcelona、西班牙
        • Hospital Santa Cruz i Sant Pau
      • Madrid、西班牙
        • Hospital Puerta de Hierro
      • Zaragoza、西班牙
        • Hospital Miguel Servet

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

16年 及以上 (孩子、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 diagnosis of ASPS (central confirmation not required at study entry)
  2. Age 16 years and older
  3. Availability of archived tissue blocks or unstained slides to enable confirmation of t(X;17) translocation
  4. ECOG Performance Status of 0-1
  5. Life expectancy of >12 weeks
  6. Progressive disease as defined by RECIST v1.1 within 6 months prior to randomisation
  7. Measurable metastatic disease using RECISTv1.1, i.e. at least one lesion 10 mm in diameter (15 mm in short axis for nodal lesions) assessable by CT (or MRI for brain metastases).
  8. Patients with brain metastases are permitted provided disease is controlled with a stable dose of corticosteroid and/or non-enzyme inducing anticonvulsant
  9. The capacity to understand the patient information sheet and ability to provide written informed consent
  10. Willingness and ability to comply with scheduled visits, treatment plans, laboratory tests and other study procedures
  11. Able to swallow and retain oral medication

Exclusion Criteria:

  1. Inadequate bone marrow reserve as demonstrated by an absolute neutrophil count ≤1.5 x 109/L or platelet count ≤100 x 109/L
  2. Serum bilirubin ≥ 1.5 x ULN (unless Gilbert's syndrome)
  3. ALT or AST ≥ 2.5 x ULN. If liver metastases are present, ALT or AST > 5 x ULN
  4. Serum creatinine > 1.5 x ULN or a creatinine clearance (calculated or measured) of ≤ 50mL/min
  5. Greater than +1 proteinuria unless urinary protein < 1.5g in a 24 hr period or protein/creatinine ratio < 1.5.
  6. History of significant gastrointestinal impairment, as judged by the Investigator, that would significantly affect the absorption of cediranib.
  7. Patients with a history of poorly controlled hypertension with resting blood pressure >150/100 mmHg in the presence or absence of a stable regimen of anti-hypertensive therapy.
  8. Any evidence of severe or uncontrolled co-morbidities e.g. unstable or uncompensated respiratory, cardiac, hepatic or renal disease, or active and uncontrolled infection.
  9. Evidence of prolonged QTc >480 msec (using Bazetts correction, for which the formula is: QTc = QT/√RR) or history of familial long QT syndrome.
  10. Significant recent haemorrhage (>30mL bleeding/episode in previous 3 months) or haemoptysis (>5mL fresh blood in previous 4 weeks).
  11. Major thoracic or abdominal surgery in the 14 days prior to entry into the study, or a surgical incision that is not fully healed.
  12. Pregnant or breast-feeding women; women of childbearing potential with a positive pregnancy test prior to receiving study medication; women the intention of pregnancy during study treatment; women of child bearing potential unwilling to have a urine or serum pregnancy test prior to study entry (even if surgically sterilised).
  13. Men and women of childbearing potential unwilling to use adequate birth control measures (e.g. abstinence, oral contraceptives, intrauterine device, barrier method with spermicide, implantable or injectable contraceptives or surgical sterilisation) for the duration of the study and should continue such precautions for 2 weeks after receiving the last study treatment.
  14. History of anticancer (including investigational, non-registered) treatment in the four weeks prior to first dose of cediranib, with the exception of palliative radiotherapy for symptom control.
  15. Previous treatment with cediranib.
  16. Known hypersensitivity to any excipient of cediranib.
  17. History of other malignancies (except for adequately treated basal or squamous cell carcinoma or carcinoma in situ) within 5 years, unless the patient has been disease free for 2 years and there is a tissue diagnosis of the primary cancer of interest from a target lesion.
  18. Other concomitant anti-cancer therapy (including LHRH agonists) except steroids
  19. Recent history of thrombosis
  20. Patients with brain metastases if they are symptomatic requiring increasing steroids in the previous six weeks to study entry or those with evidence of recent and/or active bleeding, or those causing uncontrolled seizures.

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:随机化
  • 介入模型:并行分配
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
实验性的:Blinded Cediranib
30mg once daily, oral until disease progression
安慰剂比较:Blinded Placebo
30mg, once daily, oral until 24 weeks or disease progression if sooner

研究衡量的是什么?

主要结果指标

结果测量
大体时间
To evaluate the efficacy of cediranib in the treatment of ASPS by measuring the percentage change in the sum of target marker lesion diameters from randomisation to week 24 (or progression if sooner) compared to treatment with placebo.
大体时间:24 Weeks of treatment
24 Weeks of treatment

次要结果测量

结果测量
大体时间
Response rate at week 24, best response using RECISTv1.1 and best reduction (%) in tumour size
大体时间:24 Weeks of treatment
24 Weeks of treatment
Progression-free survival and percentage alive and progression-free at 12 months (APF12)
大体时间:12 months of treatment
12 months of treatment
Length of Overall survival
大体时间:Patients will be followed up every 12 weeks
Patients will be followed up every 12 weeks
The safety and tolerability profile of cediranib in patients with ASPS
大体时间:Assessments will be made at every study visit (8-12 weekly)
Assessments will be made at every study visit (8-12 weekly)

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 (实际的)

2011年7月1日

初级完成 (预期的)

2019年7月1日

研究完成 (预期的)

2020年1月1日

研究注册日期

首次提交

2011年4月11日

首先提交符合 QC 标准的

2011年4月15日

首次发布 (估计)

2011年4月18日

研究记录更新

最后更新发布 (实际的)

2019年1月24日

上次提交的符合 QC 标准的更新

2019年1月22日

最后验证

2019年1月1日

更多信息

与本研究相关的术语

其他研究编号

  • ICR-CTSU/2010/10027
  • 2010-021163-33 (EudraCT编号)
  • CRUK/10/021 (其他赠款/资助编号:Cancer Research UK)
  • ISRCTN63733470 (注册表标识符:Randomised controlled Trials)
  • ISSRECE0036 (其他赠款/资助编号:AstraZeneca)

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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