Esophageal Cancer, Neoantigen
Conditions
Brief summary
This study is to develop computational pipelines and experimental validation assays for improving the identification of neoantigens from patients with esophageal cancer.
Detailed description
Esophageal cancer (EC) is the common malignant tumor with poor survival. The long-term surival rate of patients with advanced EC stages has not been improved with multidisciplinary treatments including surgery and chemotherapy and radiation. Recently, immunotherapy approaches using checkpoint inhibitors (CPI), cancer vaccine, and adoptive T cell therapy have improved survival outcomes of EC patients. The clinical outcomes are associated with expression levels as well as the immunogenicity of neoantigens which arise from soma mutations. Therefore, the identification of immunogenic neoantigens is essential for achieving effective therapies. Recent data published by the Tumor Neoantigen Selection Alliance (TESLA) show that the majority (98%) of predicted neoantigens are lack of immunogenicity and ineffective in activating antitumor immune responses. In our study, we aim to develop a pipeline with both computational prediction tools and experimental validation assays to enhance the accuracy of neoantigen identification.
Interventions
10 ml of whole blood is collected from each patient prior surgery Fresh tumor tissue samples (\ 1cm3 ) are collected during surgery
Sponsors
University Medical Center Ho Chi Minh City (UMC)
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
15 Years to 90 Years
Healthy volunteers
Yes
Inclusion criteria
1. Male or Female patients aged 18 years and older 2. Diagnosed with advanced esophageal cancer 3. Treatment-Naive 4. Not known for other concomitant cancers 5. Provide written informed consent
Exclusion criteria
1. Insufficient tumor tissues (less than 1 cm3 ) 2. Unable to sign informed consent 3. Underwent treatment
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The neoantigen landscape of patients with esophageal cancer | 3 months from the begining of study | The analysis of tumor DNA and RNA sequencing data will provide the mutational distribution of patients with esophageal cancer, which could give rise to neoantigens. Of those, neoantigens derived from hotspot mutations in Vietnamese esophageal cancer patients will be identified. |
| The ratio of predicted neoantigens being presented by HLA-I | 6 months from the begining of study | Computational pipelines will be employed to predict the pairing of neoantigens and HLA molecules. Subsequently, the ratio of those predicted neoantigens will be validated by co-immunoprecipitation with anti-HLA antibodies and mass spectrometry analysis for their binding to corresponding HLA molecules. |
| The ratio of predicted neoantigens being immunogenic | 12 months from the begining of study | Immunoassays will be employed to identify neoantigens that could activate CD4 and CD8 T cells to kill tumor cells and serve as putative candidates for immunotherapy. |
Countries
Vietnam
Contacts
Primary ContactLong Vo Duy, PhD
Backup ContactThong Dang Quang
Outcome results
None listed