Study of Faecal Bacteria Detection in Early Screening and Diagnosis of GC

Non-invasive and Sensitive Faecal Bacterial Markers for Early Screening and Diagnosis of Gastric Cancer Clinical Trial

Official title:

Faecal Bacteria Detection in Early Screening and Diagnosis of Gastric Cancer: a Large-scale Multi-center Case-control Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04638959
• Other study ID #: KY[2019]130
• Status: Recruiting
• Start date: September 30, 2019
• Est. completion date: September 30, 2021

Study information

• Verified date: November 2020
• Source: Shanghai Jiao Tong University School of Medicine
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

In this clinical trial, we aim to explore the synergistic alteration of specific bacteria both in gastric mucosas and feces of gastric cancer patients for the method of non-invasive and cost-effective faecal marker detection. We aim to select and validate specific microbes as noninvasive, accurate, simple, sensitive and highly-accepted biomarkers that might assist to screen and diagnose gastric cancer, especially early gastric cancer patients.

Description:

We conducted a large-scale multi-centre retrospective case-control study. Approximately a total of 1080 volunteers aging 40-75 in three independent cohorts, discovery cohort, validation cohort 1, validation cohort 2, will be recruited from 10 hospitals throughout China. Among them, 530 subjects in both discovery cohort and validation cohort 1 were from Shanghai Jiao Tong University School of Medicine Renji Hospital from August to December in 2018. Around 550 participants will be enrolled in validation cohort 2 from nine hospitals in China.Each cohort recruits both patients diagnosed with GC (GC group) and gender, age and body mass index (BMI)-matched healthy-control (HC) individuals diagnosed with chronic gastritis by histopathology). Individuals enrolled were either asymptomatic undergoing upper GI endoscopy screening or went to GI clinic with digestive symptoms. Subjects in HC group are conducted colonoscopy within 0.5 year before or after upper endoscopy. We collect gastric tissue biopsies and stool samples from gastric cancer patients and healthy-controls. First in the discovery cohort, which will recruit 20 subjects, 13 pairs of both cancerous & noncancerous gastric tissues and pre-operation feces in GC group will be collected. 7 subjects provide their paired mucosal biopsies and stools in HC group before examination. 16S ribosomal RNA gene sequencing will be used to select the synergistically differential bacteria species as well as find out microbial compositional distinction and diversity from both tissue and stool samples between GC and HC group. Second, the validation cohort 1 recruiting a total of 510 subjects (294 GC patients and 216 HC individuals), 217 pre-operation faecal specimens and 141 fresh tissues (cancerous & noncancerous tissues) from GC group, and 127 faecal samples and 124 gastric biopsies will be collected. Quantitative PCR (qPCR) will be used to validate the high-throughput sequencing results in discovery cohort in a single center. Among them, 35 objects in HC group and 64 patients in GC group will provide their paired tissues and feces. Third, in validation cohort 2, we are going to enroll volunteers from multiple geographic locations to confirm our results. 550 stool samples will be collected to further validate the accuracy, sensitivity and specificity of the cut-off value analyzed from validation cohort 1. All results of laboratory tests including tumor markers CEA, CA199,CA724 were obtained from the electronic query system. The GC stages will be assessed by the TNM system according to AJCC Version 4.2017 based on surgical records, histopathology and radiographic images (eg. PET-CT, abdominal enhanced CT). All subjects will sign up informed consent form before sample collection. The protocol of present study was approved by Ethics Review Committee of all participating hospitals.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 1100
• Est. completion date: September 30, 2021
• Est. primary completion date: March 31, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 40 Years to 75 Years

Eligibility

Inclusion Criteria:

• 1)Age between 40 and 75;

• 2)Subjects in GC group are pathologically diagnosed as gastric cancer prior to any treatment such as surgery, endoscopic resection, chemotherapy, radiotherapy, immunotherapy, traditional Chinese medicine therapy, etc. The results of their preoperative abdominal enhanced CT or PET-CT indicated no obvious bowel abnormalities (inflammation, polyps, ulcers, tumors, erosions, melanosis, etc.);

• 3) Subjects in HC group are diagnosed with chronic gastritis by endoscopy and pathology. without ulcers, polyps, tumors, severe erosions or bile reflux, and no obvious abnormal findings (inflammation, polyps, ulcers, tumors, erosions, melanosis, etc.) by colonoscopy within half a year;

• 4) Subjects are willing to cooperate with this research and provide stool/mucosa samples as required.

Exclusion Criteria:

• 1) with severe systemic infection, nasopharyngeal/oral cavity inflammation (periodontitis, gingivitis, tonsillitis, etc.), respiratory tract infection, soft tissue or skin infection, abscess or endocarditis within 3 months prior to recruitment;

• 2)prior medication history of the following medicine within 3 months: nonsteroidal anti-inflammatory drugs (NSAIDs), immunosuppressor, antibiotics, probiotics, hormones or immune-suppressants at least 1 week;

• 3)prior medication history of proton-pump inhibitors or H2 receptor inhibitors for over 2 months within 1 year;

• 4) with a history of H.pylori eradication therapy within 1 year;

• 5) with severe constipation, diarrhea or defecation habits changes within 3 months;

• 6) personal history of cancer, organ transplantation, parasites infection or other severe digestive system diseases (inflammatory bowel disease, liver cirrhosis, etc.);

• 7) with uncontrolled digestive bleeding, obstruction, perforation and any trauma or surgery within 3 months;

• 8) with uncontrolled chronic metabolic or endocrine disorders, e.g. hypertension, diabetes, hyperlipidemia, hyperuricemia, etc.

• 9) on a vegetarian diet or with great changes of eating habits within 3 months;

• 10) refusal of participate in this study.

Related Conditions & MeSH terms

• Non-invasive and Sensitive Faecal Bacterial Markers for Early Screening and Diagnosis of Gastric Cancer
• Stomach Neoplasms

Intervention

Other:
• collect gastric tissue and stool samples
collect gastric tissue and stool samples

Locations

Country	Name	City	State
China	Department of Gastroenterology, the Seventh Medical Center of PLA General Hospital	Beijing	Beijing
China	Department of Gastroenterology, Nanfang Hospital, Southern Medical Univerisity	Guangdong	Guangzhou
China	Division of Gastroenterology and Hepatology, The Affiliated DrumTower of Nanjing University Medical School	Nanjing	Jiangsu
China	Division of Gastroenterology and Hepatology, Ren-Ji Hospital, Shanghai Jiao-Tong University School of Medicine, Shanghai Institute of Digestive Disease; Key Laboratory of Gastroenterology & Hepatology, Ministry of Health	Shanghai	Shanghai
China	Jing'an District Central Hospital of Shanghai	Shanghai
China	Shanghai Changzheng Hospital	Shanghai
China	Shanghai Ninth People's Hospital	Shanghai
China	Shanghai Ruijin Hospital	Shanghai
China	Department of Gastroenterology and Hepatology, General Hospital, Tianjin Medical University	Tianjin	Tianjin
China	Department of Gastroenterology, Zhongshan Hospital, Xiamen University	Xiamen	Fujian

Sponsors (10)

Lead Sponsor

Collaborator

Shanghai Jiao Tong University School of Medicine

Jing'an District Central Hospital of Shanghai, Nanfang Hospital of Southern Medical University, Ruijin Hospital, Shanghai Changzheng Hospital, Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University, The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School, the Seventh Medical Center of PLA General Hospital, Tianjin Medical University General Hospital, Zhongshan Hospital Xiamen University

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Basic information of patients with different clinical outcomes	Basic information of patients with different clinical outcomes by a questionnaire	1 year
Primary	differences in abundance of gut microbiota	differences in abundance of gut microbiota for participants with different clinical outcomes confirmed by qPCR(quantitive polymerase chain reaction)	1 year
Secondary	evidence of gastric carcinoma	Different outcomes for gastric carcinoma confirmed by endoscopy and pathology	1 year