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Recruiting NCT06276088

Plasma and Tissue SAA1 Levels in Cancer Patients to Predict Hyperprogression of Immunotherapy

Observational Immunotherapy Hyperprogression Biomarker

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Immunotherapy, Hyperprogression, Biomarker. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

A Prospective Cohort Study of Plasma and Tissue SAA1 Levels in Cancer Patients to Predict Hyperprogression of Immunotherapy

Overview

Immune checkpoint inhibitors have ushered in a new era of cancer treatment, bringing significant survival benefits to patients. However, some patients have accelerated tumor growth in the early stage of immunotherapy, called hyperprogression. The quality of life of patients with hyperprogression is seriously reduced, and there is no effective treatment at present, and the prognosis is extremely poor. Therefore, early identification of high-risk groups of hyperprogression is the key to prevent hyperprogression. However, there are no effective biomarkers to predict hyperprogression. By sequencing, proteomics and metabolomics analysis of clinical tissue and blood samples, we found that the level of SAA1 was significantly increased in patients with hyperprogression, and SAA1 was an effective marker for predicting hyperprogression in pan-cancer. We planned to conduct a multicenter, prospective cohort study to verify the reliability of SAA1 as a marker for predicting hyperprogression of immunotherapy in pan-cancer patients.

Primary outcome measures

  • Incidence of hyperprogression [Time frame: 2 years]
Secondary outcome measures (3)
  • Event-free survival [Time frame: 3 years]
  • Progression-free survival [Time frame: 3 years]
  • Overall survival [Time frame: 3 years]

Eligibility criteria

Inclusion criteria

  • Over 18 years of age
  • Voluntarily sign informed consent
  • The pathological diagnosis was nasopharyngeal carcinoma, head and neck tumor, lung cancer, breast cancer, stomach cancer, colorectal cancer, glioma, esophageal cancer, liver cancer, bile duct cancer, cervical cancer, prostate cancer, bladder cancer and other malignant tumors
  • Need to be treated with immune checkpoint inhibitors
  • ECOG PS Score: 0/1.

Exclusion criteria

  • There are contraindications to immunotherapy
  • Combined with other tumors (basal cell or squamous cell skin cancer that has been cured, and cervical cancer in situ removed) External)
  • Patients had any serious coexisting medical conditions that could pose an unacceptable risk or negatively affect trial adherence. For example, unstable heart disease requiring treatment, chronic hepatitis, kidney disease, poor disease status, uncontrolled diabetes (fasting blood glucose > 1.5 × ULN), and mental illness.
  • At the investigator's discretion, those who was not considered to be suitable for participation in the study.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

China · 5 centers
  • Nanfang hospital, Southern medical university — Guangzhou
  • Fujian Provinical Hospital — Fuzhou
  • Huizhou Central People's Hospital — Huizhou
  • Jieyang people's hospital — Jieyang
  • Meizhou People's Hospital, Meizhou Academy of Medical Sciences Meizhou — Meizhou

Identifiers

NCT: NCT06276088 · NFEC-2024-067

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗