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临床试验/NCT04550104
NCT04550104招募中1 期

A Platform Study of DNA Damage Response Inhibitors in Combination With Conventional Radiotherapy in Non Small Cell Lung Cancer

University of Leeds14 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2021年3月17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
招募中
入组人数
200
试验地点
14
主要终点
Dose limiting Toxicities

研究概览

简要总结

CONCORDE is a multi-institution, multi-arm, Phase IB study that will determine the recommended phase II dose (RP2D) and safety profiles of different DNA damage repair inhibitors (DDRis) when given in an open label fashion in combination with fixed dose curative intent radiotherapy (RT) in patients with stage IIB/IIIA/IIIB NSCLC, followed by up to 12 months of consolidation durvalumab immunotherapy in selected study arms. The RP2D will be evaluated by incorporating the number of observed dose limiting toxicities (DLTs) into a time to event continuous reassessment method (TiTE- CRM) model within each of the experimental arms. TiTE-CRM is used here to take into account longer-term toxicities up to 13.5 months post start of radiotherapy and use these to inform dose escalation decision making.

详细描述

Radiotherapy is an effective treatment for patients with non-small cell lung cancer (NSCLC) that has not spread beyond the chest area. Radiotherapy is used as a curative treatment but unfortunately for most patients the cancer can return. Radiotherapy kills cells by damaging their DNA. Cells have the ability to repair that damage, especially the cells of normal tissue. If DNA repair can be prevented radiotherapy should be more effective causing the cancer cells to die.

The study will use new drugs that affect how cells repair DNA damage, called DNA damage response inhibitors (DDRi). These will be given together with radiotherapy to hopefully improve the effectiveness of radiotherapy, followed by up to 12 months of durvalumab immunotherapy in selected study arms to develop the trial in line with the standard of care for NSCLC. The study will try to find out the most effective and safe dose of this combination treatment. This will be a clinical trial where patients due to have radiotherapy, with the hope of successful treatment that could lead to cure from their cancer or extension of life, will be offered entry onto the study. All patients will receive their radiotherapy, with 3 out of every 4 people also receiving a single DDRi drug alongside this. Both patients and study doctors will know prior to the start of the actual treatment whether a DDRi will be given, and if so which one; no placebos will be used. The patients will be followed closely to check for side effects and to assess how their cancer is responding to treatment. Blood samples will be taken to monitor treatment progress and to try to predict which patients are most likely to benefit from this type of combined treatment.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
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

AZD1390 + radiotherapy

Experimental

干预措施: AZD1390 (Drug)

Radiotherapy only

Active Comparator

干预措施: Radiotherapy (Radiation)

Olaparib + radiotherapy

Experimental

干预措施: Radiotherapy (Radiation)

Olaparib + radiotherapy

Experimental

干预措施: Olaparib Oral Tablet [Lynparza] (Drug)

AZD1390 + radiotherapy

Experimental

干预措施: Radiotherapy (Radiation)

Ceralasertib (AZD6738) + radiotherapy + Consolidation durvalumab

Experimental

This study arm will include up to 12 months of consolidation durvalumab for eligible participants following the completion of radiotherapy +/- DDRi.

干预措施: Radiotherapy (Radiation)

Ceralasertib (AZD6738) + radiotherapy + Consolidation durvalumab

Experimental

This study arm will include up to 12 months of consolidation durvalumab for eligible participants following the completion of radiotherapy +/- DDRi.

干预措施: Ceralasertib (Drug)

Ceralasertib (AZD6738) + radiotherapy + Consolidation durvalumab

Experimental

This study arm will include up to 12 months of consolidation durvalumab for eligible participants following the completion of radiotherapy +/- DDRi.

干预措施: Durvalumab (Drug)

AZD5305 + radiotherapy + Consolidation durvalumab

Experimental

This study arm will include up to 12 months of consolidation durvalumab for eligible participants following the completion of radiotherapy +/- DDRi.

干预措施: Radiotherapy (Radiation)

AZD5305 + radiotherapy + Consolidation durvalumab

Experimental

This study arm will include up to 12 months of consolidation durvalumab for eligible participants following the completion of radiotherapy +/- DDRi.

干预措施: AZD5305 (Drug)

AZD5305 + radiotherapy + Consolidation durvalumab

Experimental

This study arm will include up to 12 months of consolidation durvalumab for eligible participants following the completion of radiotherapy +/- DDRi.

干预措施: Durvalumab (Drug)

RT + consolidation durvalumab

Active Comparator

干预措施: Radiotherapy (Radiation)

RT + consolidation durvalumab

Active Comparator

干预措施: Durvalumab (Drug)

Arm D - did not proceed

Experimental

Arm D - did not proceed

干预措施: Radiotherapy (Radiation)

结局指标

主要结局

Dose limiting Toxicities

时间窗: 13.5 months after start of radiotherapy

Dose-limiting toxicities (DLTs), within 13.5 months of starting radiotherapy, in order to establish the Recommended Phase II Dose (RP2D) of each DDRi-RT combination.

次要结局

  • Best overall response(2 years after end of RT)
  • Overall survival(2 years post-RT)
  • Changes in Health Related Quality of Life(2 years after end of RT)
  • Objective response rate(2 years after end of RT)
  • Safety and toxicity(2 years after end of RT)
  • Treatment compliance(End of trial treatment (DDRi and RT))
  • Disease control(2 years after end of RT)
  • Progression-free survival(2 years post-RT)
  • Changes in tumour size during and following treatment with DDRi-RT compared to RT alone.(2 years after end of RT)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (14)

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