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临床试验/NCT04127110
NCT04127110进行中(未招募)2 期

Activity of Lorlatinib Based on ALK Resistance Mutations on Blood in ALK Positive NSCLC Patients Previously Treated With 2nd Generation ALK Inhibitor

European Organisation for Research and Treatment of Cancer - EORTC25 个研究点 分布在 7 个国家目标入组 68 人开始时间: 2020年11月17日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
进行中(未招募)
入组人数
68
试验地点
25
主要终点
Progression-free survival (PFS)

研究概览

简要总结

This study includes patients diagnosed with a metastatic non small cell lung cancer (NSCLC) with anaplastic lymphoma kinase (ALK) translocation. The standard treatment for patients with metastatic non small cell lung cancer with ALK translocation is represented by personalized treatment with drugs called ALK inhibitors. During the treatment with an ALK inhibitor, the tumour can start to grow again, because the tumour adapts to the drug and develops escape mechanisms, becoming resistant. At the tumour cells level, the mechanisms underlying resistance can include the development of other alterations, mainly mutations, including in the ALK gene. The alterations that developed depend on the drug the tumour has been exposed to.

The alterations can be identified by analysing tumour tissue obtained through a biopsy, however, repeating a tumour biopsy is difficult and risky and might not be able to provide sufficient tissue for the test. Therefore in the last years, new tests have been developed to identify the mutations in the blood.

Lorlatinib is a drug that inhibits ALK and has already been identified to be able to control the tumour growth when ALK mutations are identified and is already approved as standard treatment after progression to a previous treatment with ALK inhibitors.

The purpose of this study is to identify which patient populations may benefit most from treatment with lorlatinib, based on the alterations found in their genes.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
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

Lorlatinib

Experimental

Lorlatinib is administered orally at the daily dose of 100 mg (four tablets of 25 mg).

Lorlatinib will be taken continuously on a daily basis until disease progression, unacceptable toxicity, occurrence of any withdrawal criterion, whichever comes first.

干预措施: Lorlatinib (Drug)

结局指标

主要结局

Progression-free survival (PFS)

时间窗: 12 months after enrolment of last patient

Progression Free Survival Rate at 12 months (PFSR-12) is defined as the proportion of patients at 12 months who are alive and non-progressing.

次要结局

  • Overall Response Rate (ORR)(12 months after enrolment of last patient)
  • CNS Overall Response Rate (CNS-ORR)(12 months after enrolment of last patient)
  • Overall Survival (OS)(12 months after enrolment of last patient)
  • Duration of Response (DOR)(12 months after enrolment of last patient)
  • Safety profile according to NCI CTCAE v.5(30 days after last dose)

研究者

申办方类型
Network
责任方
Sponsor

研究点 (25)

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