Clinical Trials Directory

Trials / Completed

CompletedNCT05688046

Efficacy and Safety Analysis of ICIs Plus Angiogenesis Inhibitors for Treatment of Advanced NSCLC in Elderly Patients

Efficacy and Safety Analysis of Immune Checkpoint Inhibitors Plus Angiogenesis Inhibitors for Treatment of Advanced Driver-negative NSCLC in Elderly Patients:A Retrospective Study

Status
Completed
Phase
Study type
Observational
Enrollment
79 (actual)
Sponsor
Suzhou Municipal Hospital · Academic / Other
Sex
All
Age
65 Years
Healthy volunteers
Not accepted

Summary

Immune checkpoint inhibitors(ICIs) combined with angiogenesis inhibitors may is synergistic in elderly patients with advanced non-small cell lung cancer(NSCLC), however its true efficacy is still unclear. The investigators retrospectively compared clinical efficacy and safety of driver-negative elderly patients with advanced NSCLC treated with ICIs with(or without)angiogenesis inhibitors in the Cancer Center of the Affiliated Suzhou Hospital of Nanjing Medical University.

Detailed description

The investigators reviewed the medical records of all lung cancer patients in the Cancer Diagnosis and Treatment Center of Suzhou Hospital Affiliated to Nanjing Medical University from January 1, 2019 to December 31, 2021, and a total of 79 patients were enrolled. The subjects were divided into two groups: the group treated with immune checkpoint inhibitors plus antiangiogenic drugs(IA group) and the group treated with immune checkpoint inhibitors without antiangiogenic drugs(NIA group). The data of PFS, OS, ORR, covariates, and Immune-related adverse events (irAEs) were collected through electronic medical records and follow-up. The primary endpoint of the study was PFS, and the secondary endpoints were OS, ORR and irAEs.All enrolled patients were followed up until August 1, 2022.

Conditions

Interventions

TypeNameDescription
DRUGImmune checkpoint inhibitors plus angiogenesis inhibitorsPD-(L)1-based therapy plus Bevacizumab or Anlotinib
DRUGImmune checkpoint inhibitors without angiogenesis inhibitorsPD-(L)1-based therapy

Timeline

Start date
2019-01-01
Primary completion
2022-08-01
Completion
2022-12-31
First posted
2023-01-18
Last updated
2023-01-19

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05688046. Inclusion in this directory is not an endorsement.