Predicting Treatment Response to Immunotherapy Combined with Chemotherapy in Advanced Gastric/gastroesophageal Junction Cancer Based on the Multi-omics Information During Tumor Evolution.

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

In this project, based on the information of advanced gastric/gastroesophageal junction cancer in evolution under immunotherapy combined with chemotherapy treatment, we will integrate multi-omics dynamic data to identify essential features that correlate to therapeutic effects of immunotherapy therapy, screen potential molecular markers/dominant microbiota for predicting the efficacy of immunotherapy and establish a multimodal predictive model for patients that benefit from immunotherapy. Our project could provide evidence to predict response to immunotherapy for patients with advanced gastric/gastroesophageal junction cancer and potentially optimize the clinical decision-making about therapy for advanced gastric/gastroesophageal junction cancer.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Patients with gastric or gastroesophageal junction adenocarcinoma confirmed by pathology and with advanced or metastatic disease that cannot be resected

• HER2 negative

• Not received any anti-tumor treatment before.

• After evaluation, the treatment plan is chemotherapy combined with immunotherapy.

• Aged 18 to 75 years old, gender is not limited.

Locations
Other Locations
China
Cancer Hospital of the University of Chinese Academy of Sciences (Zhejiang Cancer Hospital)
RECRUITING
Hangzhou
Contact Information
Primary
Xiangdong Cheng Cheng, PhD
Chengxd516@126.com
+0086-0571-88128041
Time Frame
Start Date: 2024-03-25
Estimated Completion Date: 2026-02-01
Participants
Target number of participants: 150
Treatments
Patients with advanced gastric cancer
Advanced gastric cancer patients receiving chemotherapy combined with immunotherapy
Sponsors
Leads: Xiangdong Cheng

This content was sourced from clinicaltrials.gov

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