Skip to content

Efficacy and safety analysis of Endostar in cross-line therapy in patients with advanced non-small cell lung cancer

Efficacy and safety analysis of recombinant human endostatin in cross-line therapy in patients with advanced non-small cell lung cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500100417
Enrollment
Unknown
Registered
2025-04-09
Start date
2025-04-09
Completion date
Unknown
Last updated
2025-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-small cell lung cancer

Interventions

Cross-line group:None. Continue Endostar antiangiogenic therapy after the first progression
Non-cross-line group:None. Endostar antiangiogenic therapy is no longer used after the first progression

Sponsors

The first affiliated hostipal of nanchang university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.IIIB-IV non-small cell lung cancer (NSCLC) patients with histopathologically confirmed TNM stage; 2.Between the ages of 18 and 75, with an Eastern Cooperative Oncology Group (ECOG) performance status (PS) score of 0-2; 3.The presence of one or more measurable double-diameter tumor foci was assessed according to the Solid Tumor Response Evaluation Criteria (RECIST, 1.1) ; 4.Endostar combined with platinum-containing double-drug chemotherapy was initially accepted as first-line treatment, during which programmed cell death protein-1 (PD-1) inhibitors were allowed, and the efficacy was evaluated as disease progression (PD); 5. Have not received any prior anti-tumor therapy and have an expected survival time of more than 3 months

Exclusion criteria

Exclusion criteria: 1.Combined with primary tumors of other sites; 2.Genetic testing indicated the presence of a positive gene mutation; 3.Pregnant or lactating women; 4.Incomplete medical records or failed follow-up; 5.Poor compliance or abandonment of treatment for personal reasons; 6.The treatment course was less than 2 cycles, and the efficacy could not be evaluated;

Design outcomes

Primary

MeasureTime frame
Progression-free survival;Overall survival;

Secondary

MeasureTime frame
Objective response rate;Disease control rate;Adverse reactions;

Countries

China

Contacts

Public ContactZhihui Lu

The first affiliated hostipal of nanchang university

904645759@qq.com+86 13576950992

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026