Discovery of Biomarkers Related to the Efficacy and Adverse Reactions of Immune Checkpoint Inhibitors Based on Metabolism-genomics

Capital Medical University

Status: Enrolling

Conditions: Cancer

Treatments: Other: there is no intervention in our study

Study type: Observational

Funder types: Other

Identifiers

NCT04656119

2020-K-508

Details and patient eligibility

About

Immune checkpoint inhibitors (ICIs) are an important breakthrough in cancer therapy and have been increasingly used.However, ICIs can cause a unique spectrum of side effects termed immune-related adverse events (irAEs),which can affect any organ systems and in some cases are fulminant or even fatal.In clinical practice, irAEs and clinical efficacy maybe various for patients with same standard treatment, and some studies have shown that gene and metabolic differences in cancer patients may be an important factor. In this project, peripheral blood samples from cancer patients will be collected prospectively at baseline, and at regular intervals (2 cycles, about 6 weeks) for about 30 weeks, then these blood samples will be analyzed using the technique of genomics, metabonomics.

The investigators aim to find biomarkers associated with irAE or clinical efficacy. When the sample size and data is big enough, the investigators plan to establish a prediction model using machine learning to access the safety and efficacy of ICIs for cancer patients. Our study have important clinical implications in the prediction and early management of severe, potentially life-threatening immune-related toxicity.

Enrollment: 100 estimated patients

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Histologically confirmed malignant tumor, no relative contraindications for immunotherapy, in line with the standards of immunotherapy
• Receive immune checkpoint inhibitors (ICIs) for the first time or have received ICIs but no immune-related adverse reactions have occurred
• Have provided informed consent, are willing to participate in study and routine follow-up
• At least one measurable lesion according to Guidelines for response criteria for use in trials testing immunotherapeutics (iRECIST)

Exclusion criteria

• Active, known, suspected or a documented history of autoimmune disease
• Eastern Cooperative Oncology Group(ECOG) performance status 3-4
• Long-term hormone therapy，corticosteroids (>10mg/day prednisone curative dose)
• Subjects with human immunodeficiency virus (HIV)
• Subjects with other tumors
• Myocardial infarction, poorly control led arrhythmia, New York Heart Association (NYHA) standard III-IV cardiac insufficiency or left ventricular ejection fraction (LVEF)<50% in the last 6 month
• Active tuberculosis
• Active or a documented history of interstitial pneumonia, pneumoconiosis, radiation pneumonia, drug-related pneumonia, severely impaired lung function
• Common Terminology Criteria for Adverse Events (CTCAE) peripheral neuropathy grade≥2
• History of alcohol abuse

Trial design

100 participants in 2 patient groups

patients without irAEs or patients with good efficacy

Treatment:

Other: there is no intervention in our study

patients with irAEs or patients with poor efficacy

Treatment:

Other: there is no intervention in our study