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Angiogenesis Inhibitor Plus Anti-PD-1/PD-L1 Antibody in Advanced Esophageal Cancer

Containing Angiogenesis Inhibitor Plus Anti-PD-1/PD-L1 Antibody in Anti-tumor Treatment of Chinese Patients With Unresectable Locally Advanced / Recurrent or Metastatic Esophageal Cancer: a Real World Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05349045
Acronym
AIPAAIAEC
Enrollment
300
Registered
2022-04-27
Start date
2022-05-05
Completion date
2025-05-05
Last updated
2022-04-27

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

Conditions

Esophageal Neoplasms

Brief summary

The combination of an anti-PD-1/PD-L1 antibody with an angiogenesis inhibitor has shown efficacy in many cancers.The purpose of this study is to confirm that the combination of these two drugs can benefit patients with advanced esophageal cancer.

Interventions

DRUGan anti-PD-1/PD-L1 antibody plus an angiogenesis inhibitor

This is an observational study

Sponsors

The First Affiliated Hospital of Zhengzhou University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

1. Esophageal cancer confirmed by histopathology or cytology 2. Unresectable locally advanced/recurrent or metastatic esophageal cancer, or progression after neoadjuvant or adjuvant therapy 3. Esophageal cancer patients who benefit from the use of an anti-PD-1/PD-L1 antibody with an angiogenesis inhibitor evaluated by the researchers 4. Patients who sign informed consent and voluntarily join the study

Exclusion criteria

1. Patients who are recommended not using an anti-PD-1/PD-L1 antibody or an angiogenesis inhibitor in the instructions, or other patients who are judged by the investigators to be unsuitable in the study 2. Patients who are undergoing treatment regimen of blind trial

Design outcomes

Primary

MeasureTime frameDescription
PFSFrom date of admission until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 24 monthsProgression Free Survival

Secondary

MeasureTime frameDescription
OSFrom date of admission until the date of death from any cause, assessed up to 24 monthsOverall Survival

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026