Characterization and Clinical Impact of the Gut Microbiota in Diffuse Large B-cell Lymphoma Patients
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 200
- 试验地点
- 1
- 主要终点
- Intestinal microbiota baseline characterization
研究概览
简要总结
The study is a prospective observational single-center cohort study which compare the gut microbiome of newly diagnosed Diffuse Large B-cell Lymphoma patients with the gut microbiome of healthy controls. Furthermore the impact of lymphoma treatment, immune phenotypes, cytokine profiles, metabolomics, inflammation, driver mutations, comorbidity, body composition and lifestyle on the microbiome is also investigated
详细描述
Microbiota refers to an ecological community of commensal, symbiotic and pathogenic microorganisms that colonize the various compartments within the human body including the gastrointestinal tract. The composition has been shown to play an important role in the pathophysiology of many diseases as well as influence host homeostatic processes such as regulation of metabolic processes, defense against pathogens, immune system development, regulation of the immune response and inflammation. However, the connection between the gut microbiota and lymphoma remain poorly understood.
The purpose of this study is to evaluate the composition and diversity of the gut microbiome in a large homogeneous group of patients with newly diagnosed and treatment-naive Diffuse Large B-cell Lymphoma (DLBCL). The investigators aim to identify the relationship between the intestinal microbiota, clinical and molecular subtypes of DLBCL and outcome of the disease. The association between nutrition, physical activity, body composition, toxicity to the antineoplastic therapy, infections, use of antibiotics, comorbidity and tumor genetics versus gut microbiota composition and diversity is also explored.
The project is carried out in collaboration between clinical departments, institutes and laboratories with expertise in microbiology, hematology, pathology, nutrition, molecular biology, immunology and bioinformatics.
Hypothesis of the study are:
- Patients with DLBCL have distinct baseline microbiota signatures that differ from healthy subjects.
- Significant changes in the microbiota composition and diversity can be identified during and after treatment (immunochemotherapy) of DLBCL.
- Lymphoma response and outcome is affected by the composition and diversity of the DLBCL microbiota.
- The intestinal microbiota changes towards a microbiota more like the microbiota of healthy controls in patients who remain in lymphoma remission one year after completion of therapy.
- Distinct DLBCL microbiota profiles are associated with treatment-related toxicity.
- The intestinal microbiota affects the risk of infections (clinically and/or microbiologically documented).
- The intestinal microbiota is affected using antibiotics both as prophylaxis and treatment of infections.
- The DLBCL microbiota depends on the dietary intake, smoking, physical activity and the body composition.
- Distinct intestinal microbiota signatures can be associated with molecular subtypes of DLBCL (or vice versa)
- The JAK2V617F, TET2, DNMT3A and ASXL1 mutations affect the intestinal microbiota signature and are associated with comorbidity and outcome in DLBCL
- There is a vicious circle between intestinal dysbiosis and lymphoma with the crosstalk between the gut microbiota and the cancer being expressed as alterations in the profile of cytokines, chemokines and growth factors; an immune response reflected by immunophenotypic profiles of peripheral blood mononuclear cells; and characteristic metabolite signatures in the blood.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- 未提供
排除标准
- 未提供
结局指标
主要结局
Intestinal microbiota baseline characterization
时间窗: 1.5 years
Assessment using amplicon-based sequencing of ribosomal (r)RNA genes
次要结局
- Intestinal microbiota characterization at mid-, post-treatment and at follow up(2.5 years)
- Alcohol intake(2.5 years)
- Infections(1.5 years)
- Lymphoma response(1.5 years)
- Mutations(1.5 years)
- Peripheral blood mononuclear cell (PBMC) profiles(1.5 years)
- Assessment of energy and macronutrient intake(2.5 years)
- Treatment-related toxicity(1.5 years)
- Statins(1.5 years)
- Assessment of habitual diet(2.5 years)
- Body composition(2.5 years)
- Antibiotics(1.5 years)
- Molecular signatures(1.5 years)
- Cytokine profiles(1.5 years)
- Assessment of physical activity(2.5 years)
- Smoking(2.5 years)
- Chromosome abnormalities(1.5 years)
- Medication(1.5 years)
- Metabolite signatures(1.5 years)
研究者
Lars Møller Pedersen
MD, PhD
Herlev Hospital