Observational Prospective Study of Immune Checkpoint Inhibitors for Solid Neoplasms
ConditionCancer
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorFudan University
About this trial
This prospective, multicenter observational study included all patients with solid neoplasms who received treatment with immune checkpoint inhibitors (ICIs) in clinical practice, regardless of tumor type, tumor stage, type of immunotherapy, or treatment lines. This study aimed to assess the use, effectiveness, and safety of ICIs for solid neoplasms in real-world populations, which can provide insights into clinical decisions associated with the use of ICIs for the treatment of cancer patients in the real-world setting.
Eligibility criteria
Qualifiers
Age at least 18 years.
Pathologically confirmed diagnosis of a solid tumor cancer.
Patients receiving treatment with immune checkpoint inhibitors.
Ability to understand and willingness to provide the informed consent.
Disqualifiers
Age < 18 years.
Patients with hematological malignancies or solid benign tumors.
Mental disorders, drug abuse, and social condition that may negatively impact compliance in the opinion of the investigator.
Trial design
Treatments tested in this trial
- Not listed
Trial groups
No trial groups listed
Sponsors and collaborators
Source ClinicalTrials.gov