Resistance Mechanisms and Sequential Treatment Strategies Following First-Line Lorlatinib in ALK-Positive NSCLC

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorShanghai Chest Hospital

About this trial

This is a prospective, multicenter, non-interventional, single-arm, real-world study planned to be conducted in China, aimed at exploring the resistance mechanisms of first-line lorlatinib treatment in patients with ALK-positive locally advanced or metastatic NSCLC, as well as the efficacy and safety of sequential treatments following lorlatinib resistance in the real-world setting.

Eligibility criteria

Qualifiers

Age: Patients aged 18 years or older;

Histologically or cytologically confirmed locally advanced or metastatic NSCLC

Documened ALK resrrangemen by approved test (eg.. FisH,IHC. .r NGS).

first-line loelaninab treatment fom Apr2023-Apr-2027.

Disqualifiers

Previous treatment with other ALK-TKIs: Patients who have previously received any ALK TKI other than lorlatinib;

Concomitant medications: Patients who have received any systemic anti-tumor treatment other than lorlatinib before enrollment.

Trial design

Treatments tested in this trial

  • No intervention administered
  • Non Interventional Study

Treatment groups

No treatment groups listed

Locations

This trial has no locations

Sponsors and collaborators