Probiotics Enhance the Treatment of PD-1 Inhibitors in Patients With Liver Cancer
Primary Purpose
Liver Cancer
Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
M9
placebo
Sponsored by
About this trial
This is an interventional prevention trial for Liver Cancer
Eligibility Criteria
Inclusion Criteria:
- Karnofsky score ≥90 in patients receiving immunotherapy for liver cancer at our cancer center
Exclusion Criteria:
- any immune system disease under high risk to antimicrobial agents such as Diabetes,infection disease or drug allergy to V9
Sites / Locations
- Chunling JiangRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Placebo Comparator
No Intervention
Arm Label
probiotics group
placebo group
healthy control group
Arm Description
The oral probiotic (Lactobacillus rhamnosus Probio-M9,one times a day during the whole treatment) was isolated from healthy women's breast milk samples in 2017 and was identified as Lactobacillus rhamnosus by physiological and biochemical and 16S rRNA. It is listed as the "List of Probiotics for Health Food" in my country's "List of Bacteria Available for Food", which can be directly applied to food production.
Immunotherapy with placebo alone
healthy control group
Outcomes
Primary Outcome Measures
(objective remission rate)ORR
Proportion of patients whose tumor volume shrinks to a predetermined value and maintains the minimum time limit
Secondary Outcome Measures
PFS
Time from randomness to the first occurrence of disease progression or death from any cause
OS
The time between random onset and the patient's death from any cause
Full Information
NCT ID
NCT05032014
First Posted
June 23, 2021
Last Updated
October 17, 2021
Sponsor
Jiangxi Provincial Cancer Hospital
Collaborators
Inner Mongolia Agricultural University
1. Study Identification
Unique Protocol Identification Number
NCT05032014
Brief Title
Probiotics Enhance the Treatment of PD-1 Inhibitors in Patients With Liver Cancer
Official Title
Probiotics Enhance the Treatment of PD-1 Inhibitors in Patients With Liver Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
October 2021
Overall Recruitment Status
Recruiting
Study Start Date
November 19, 2021 (Anticipated)
Primary Completion Date
December 27, 2022 (Anticipated)
Study Completion Date
December 30, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Jiangxi Provincial Cancer Hospital
Collaborators
Inner Mongolia Agricultural University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Human microbes have been called "the second genome of humanity".On May 13,2016,the White House launched the National Microbiome Initiative (NMI), with an estimated investment of us $521 million, to elevate microbiome research to a national strategic status. The gut is the largest microecological environment in the human body. The research in the field of intestinal microbiome has become one of the most advanced and hot research directions in the scientific field of the world today. At present, more than 50 diseases have been found to be related to intestinal microbiome disorders. Pd-1 (programmed death receptor 1) is an important immunosuppressive molecule.It regulates the immune system and promotes tolerance by down-regulating the immune system's response to human cells and by suppressing T cell inflammatory activity. In the past, the research team and colleagues in related fields have found a strong correlation between Gut Microbiome and the efficacy of anti-PD-1 immunotherapy in cancer patients.This protects against autoimmune diseases, but it also prevents the immune system from killing cancer cells. As more and more scientific evidence shows that intervention of human intestinal flora may improve the efficacy of anti-PD-1 immunotherapy in tumor patients, intestinal flora, as the most effective way to intervene human intestinal flora, has been mentioned by many research institutions and international drug manufacturers in combination with anti-PD-1.Our previous study showed that the abundance of beneficial bacteria such as lactic acid bacteria, bifidobacteria and Akkermansia Muciniphila was significantly correlated with pD-1 inhibitor response, and regulating the intestinal flora content could improve the effect of PD-1 inhibitor on mouse tumors, indicating that microbial flora was involved in regulating cancer immunotherapy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Liver Cancer
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
The random assignment of patients was performed by Nanchang Medical University with a computer-generated random number code. Patients were randomly distributed in a 1:1 ratio to receive probiotics or a placebo (the block size was known only to the statistician). The drug was distributed and packaged in accordance with random numbers, and the documents stating the parameters, such as the blinding codes for the seeds of the random numbers, the block length, and the random numbers, were sealed in envelopes
Allocation
Randomized
Enrollment
46 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
probiotics group
Arm Type
Experimental
Arm Description
The oral probiotic (Lactobacillus rhamnosus Probio-M9,one times a day during the whole treatment) was isolated from healthy women's breast milk samples in 2017 and was identified as Lactobacillus rhamnosus by physiological and biochemical and 16S rRNA. It is listed as the "List of Probiotics for Health Food" in my country's "List of Bacteria Available for Food", which can be directly applied to food production.
Arm Title
placebo group
Arm Type
Placebo Comparator
Arm Description
Immunotherapy with placebo alone
Arm Title
healthy control group
Arm Type
No Intervention
Arm Description
healthy control group
Intervention Type
Other
Intervention Name(s)
M9
Intervention Description
one times a day during the whole treatment
Intervention Type
Other
Intervention Name(s)
placebo
Intervention Description
placebo
Primary Outcome Measure Information:
Title
(objective remission rate)ORR
Description
Proportion of patients whose tumor volume shrinks to a predetermined value and maintains the minimum time limit
Time Frame
6 months
Secondary Outcome Measure Information:
Title
PFS
Description
Time from randomness to the first occurrence of disease progression or death from any cause
Time Frame
6 months
Title
OS
Description
The time between random onset and the patient's death from any cause
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Karnofsky score ≥90 in patients receiving immunotherapy for liver cancer at our cancer center
Exclusion Criteria:
any immune system disease under high risk to antimicrobial agents such as Diabetes,infection disease or drug allergy to V9
Facility Information:
Facility Name
Chunling Jiang
City
NanCHang
State/Province
Jiang XI
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chunling Jiang, doctor
Phone
13979109200
Ext
+086
Email
jclil2002@163.com
12. IPD Sharing Statement
Learn more about this trial
Probiotics Enhance the Treatment of PD-1 Inhibitors in Patients With Liver Cancer
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