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Clinical Trials in China / NCT06962449
Enrolling by invitation Observational

Real-World Assessment of Therapeutic Strategies and Survival Outcomes Following First-Line Tislelizumab Therapy in Advanced Non-Small Cell Lung Cancer

NCT06962449 · tracked via the Priya Life Science China tracker
Sponsor
Shanghai Chest Hospital
Phase
Observational
Started
2024-08-16
Last updated
2025-05-08

Condition(s) studied

Non-Small-Cell Lung CancerNon-Small-Cell Lung Cancer Stage IV

Study summary

This study is an observational study evaluating the treatment patterns and clinical outcomes after progression on first-line Tislelizumab treatment in advanced NSCLC. Based on the inclusion and exclusion criteria, patients with advanced NSCLC who received first-line Tislelizumab treatment and progressed will be retrospectively screened and collected from January 1, 2020, to the study initiation date, and followed up for observation.

Eligibility

Sex
ALL
Min age
Max age
Healthy volunteers
No
Inclusion Criteria: * Histologically or cytologically confirmed unresectable locally advanced or metastatic NSCLC based on the 8th edition of the AJCC staging system. * Previously received first-line treatment with Tislelizumab for advanced NSCLC. * Medical records of disease progression after first-line treatment. Exclusion Criteria: * Patients with incomplete key baseline and treatment information,including clinical stage, pathological type, treatment regimen, tumor assessment record after treatment ect. * Patients included in anti-tumor drug intervention or unblinded clinical trials, in which the treatment being administered is unknown.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Shanghai Chest Hospital Shanghai Shanghai Municipality

More Shanghai Chest Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06962449 on ClinicalTrials.gov ↗ ← All trials in China