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临床试验/NCT02768337
NCT02768337终止1 期

Cambridge Brain Mets Trial 1: A Proof-of-principle Phase 1b/Randomised Phase 2 Study of Afatinib Penetration Into Cerebral Metastases for Patients Undergoing Neurosurgical Resection, Both With and Without Prior Low-dose, Targeted Radiotherapy

Cambridge University Hospitals NHS Foundation Trust6 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2015年3月10日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
终止
入组人数
26
试验地点
6
主要终点
Ratio of afatinib concentration in: [resected brain metastases] / [plasma] - each measured in (ng/mL) on day 12

研究概览

简要总结

Proof of principle phase 1b / randomised phase 2 study of afatinib penetration into cerebral metastases for patients undergoing neurosurgical resection, both with and without prior low-dose, targeted radiotherapy.

详细描述

Brain metastases occur in 20-40% of all patients with cancer, with an incidence 10 times higher than that of primary malignant brain tumours. patients with brain metastases are an underserved population. Overall they have a poor prognosis with a median survival of 1-2 months with corticosteroids and only 5-7 months after whole brain radiotherapy. An important factor in the poor prognosis of patients with brain metastases is the inability of many drugs to penetrate the blood-brain-barrier into tumour tissue.Combination therapy with surgical excision, radiotherapy and novel drugs could potentially improve the prognosis for some patients.

CamBMT1 is an open label, 3 Arm randomised Phase 2 trial investigating whether administration of a low dose of targeted radiotherapy during afatinib treatment could increase the concentration of drug penetration into brain metastases.

Eligible patients in Phase 2 will be randomised to 1 of 3 Arms:

Arm 1: no radiotherapy Arm 2: 2Gy radiotherapy Arm 3: 4Gy radiotherapy All patients will also receive 11 days of afatinib treatment at the recommended Phase 2 dose, previously determined in a Phase 1b safety run-in phase.

On Day 10, of afatinib treatment patients randomised to Arms 2 or 3 will receive their allocated dose of radiotherapy On Day 12, patients will undergo neurosurgical resection of their brain metastasis/ses.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Arm 1: Afatinib only at Recommended Phase 2 dose (RP2D)

Other

No targeted radiotherapy. Afatinib at Recommended Phase 2 Dose for 11 days.

干预措施: Afatinib (Drug)

Arm 2: Afatinib RP2D + 2 Gy targeted radiotherapy

Experimental

Patient will receive the RP2D of afatinib for 11 days and will receive targeted radiotherapy at a dose level of 2 Gy on Day 10 of treatment.

干预措施: Afatinib (Drug)

Arm 2: Afatinib RP2D + 2 Gy targeted radiotherapy

Experimental

Patient will receive the RP2D of afatinib for 11 days and will receive targeted radiotherapy at a dose level of 2 Gy on Day 10 of treatment.

干预措施: 2 Gy targeted radiotherapy (Radiation)

Arm 3: Afatinib RP2D + 4 Gy targeted radiotherapy

Experimental

Patient will receive the RP2D of afatinib for 11 days and will receive targeted radiotherapy at a dose level of 4 Gy on Day 10 of treatment.

干预措施: Afatinib (Drug)

Arm 3: Afatinib RP2D + 4 Gy targeted radiotherapy

Experimental

Patient will receive the RP2D of afatinib for 11 days and will receive targeted radiotherapy at a dose level of 4 Gy on Day 10 of treatment.

干预措施: 4 Gy targeted radiotherapy (Radiation)

结局指标

主要结局

Ratio of afatinib concentration in: [resected brain metastases] / [plasma] - each measured in (ng/mL) on day 12

时间窗: Day 12 of treatment

次要结局

  • Safety of afatinib alone and combined with targeted low-dose radiotherapy - assessed by number of participants with treatment- related adverse events as assessed by CTCAE v4.0(From consent to Day 41+/-7 days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Richard D. Baird MD PhD

Dr Richard Baird

Cambridge University Hospitals NHS Foundation Trust

研究点 (6)

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