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Management Strategy of 1L Lorlatinib With Hyperlipidemia in Stage IIIB-IV ALK Positive NSCLC

NCT07674524 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 160

Last updated 2026-06-29

No results posted yet for this study

Summary

For Patients and Families

Brief Title: Management of 1L Lorlatinib with Hyperlipidemia in ALK+ Advanced NSCLC

What is this study about?

This study is for people with ALK-positive non-small cell lung cancer (NSCLC) who are taking lorlatinib (Lorbrena®) as their first treatment and have developed high cholesterol (hyperlipidemia) as a side effect.

Why is this study needed?

Lorlatinib is a highly effective targeted therapy, but it frequently causes elevated cholesterol and triglycerides. There is currently no standard guideline on how to best manage this side effect. This study aims to find the best approach to control lipid levels while on lorlatinib treatment.

What will happen in this study?

The study has two parts:

* Part A (Observational) : About 100 participants. Doctors manage hyperlipidemia according to routine clinical practice. Researchers simply observe and record which lipid-lowering treatments are used and how well they work.
* Part B (Randomized Controlled Trial) : 60 participants with high-risk factors are randomly assigned to either:
* Intensive treatment: rosuvastatin + ezetimibe + evolocumab
* Standard treatment: rosuvastatin + ezetimibe

What tests are involved?

* Blood tests for lipid levels at baseline, Weeks 4, 8, 20, and 24
* Routine CT or MRI scans for tumor assessment
* Some participants in Part B may have a non-invasive vascular ultrasound (FMD) test
* Total participation per patient: up to 7 months

Is this study safe?

* ✅ Approved by the Ethics Committee of Sun Yat-sen University Cancer Center
* ✅ All drugs used (lorlatinib, statins, ezetimibe, evolocumab) are already approved and widely used
* ✅ An independent Data Monitoring Committee (DMC) monitors safety throughout the study
* ✅ Participants may withdraw at any time without affecting their regular care

For Healthcare Providers

Study Title: Management strategy of 1L Lorlatinib with Hyperlipidemia in Stage IIIB-IV ALK positive NSCLC: A multi-center prospective study in China

Sponsor / Investigators: Sun Yat-sen University Cancer Center (PI: Prof. Zhang Li)

Study Type:

* Part A: Observational, prospective, real-world cohort study
* Part B: Prospective, randomized controlled trial (RCT)

Estimated Enrollment: 160 participants (Part A: \~100, Part B: 60)

Study Duration: Approximately 4 years (anticipated completion: December 2029)

Key Inclusion Criteria:

* Stage IIIB-IV ALK+ NSCLC (confirmed by IHC, FISH, PCR, NGS, or ctDNA)
* No prior systemic therapy for advanced/metastatic disease
* ECOG PS 0-2
* Age ≥ 18 years
* Hyperlipidemia (ULN ≤ TC \< 12.93 mmol/L, Grade 1-3) while on first-line lorlatinib
* At least one measurable lesion per RECIST v1.1
* Life expectancy ≥ 6 months

Primary Endpoints:

* Part A: Describe real-world treatment patterns for hyperlipidemia management
* Part B: Percentage change in LDL-C from baseline to Week 12

Oversight:

* Independent Data Monitoring Committee (DMC)
* Trial Management Committee
* Ethics Committee of Sun Yat-sen University Cancer Center (Approval No. B2026-159-01)

Participating Centers: 8 sites across China

Conditions

  • Non-Small Cell Lung Cancer (NSCLC)
  • Hyperlipidemia
  • ALK Gene Mutation
  • ALK-positive

Interventions

DRUG

For Part A - Observational Cohort:

No intervention assigned (observational)

DRUG

Part B: Intensive Lipid-Lowering Group

Rosuvastatin + Ezetimibe + Evolocumab

DRUG

For Part B - Intensive Group

Rosuvastatin + Ezetimibe

Sponsors & Collaborators

  • Pfizer

    collaborator INDUSTRY

  • Sun Yat-sen University

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-08-01
Primary Completion
2029-12-31
Completion
2029-12-31

Countries

  • China

Study Locations

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Diseases
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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07674524 on ClinicalTrials.gov