Clinical trial · Interventional
Investigating the Microbiome and Volatile Organic Compound Profile of Children With Neuroblastoma
Investigating the Microbiome and Volatile Organic Compound Profile of Children With Neuroblastoma - a Pilot Study
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Background: Malignant tumors may lead to a catabolic state with loss of muscle and adipose tissue. The full picture of catabolism is termed cachexia and is associated with significant morbidity and mortality of cancer patients. Although the full picture is rarely observed up to 50% of children with cancer suffer from significant malnourishment. Additionally to tumor-induced catabolism, side-effects of chemotherapy may be problematic for the patients. In this regard up to 60% of children suffer from gastrointestinal mucositis presenting with nausea, vomiting, diarrhea or constipation and abdominal pain. In the worst case, mucositis may lead to bacterial translocation with life-threatening inflammatory response. Clinically this may require a reduction of the dosage or the number of chemotherapy cycles resulting in reduced effectivity. Up to now the therapy of mucositis is only symptomatic. Recent research of the applicant has shown a significant reduction of Lactobacilli in mice with neuroblastoma (a malignant childhood tumor). The dysbiosis was associated with catabolism, increased gut permeability and inflammation. Astonishingly, chemotherapy alone also leads to a significant reduction of Lactobacilli compared to sham mice, which may be linked to the development of mucositis clinically. Overall, the intestinal microbiome seems to play an essential role in the development of tumor-associated catabolism and chemotherapy-induced mucositis. Aim: The aim of this project is to determine if the changes in the intestinal microbiome observed in mice can also be seen in children with neuroblastoma. Methods: One part of the study will include 10 children with neuroblastoma (inclusion after verification of the diagnosis) and 10 healthy controls. The fecal microbiome will be determined by 16S-ribosomal deoxyribonucleic acid (rDNA) pyrosequencing. Volatile organic compounds in the breath will be sampled and measured by Gas Chromatography/Mass Spectroscopy. A basic science human work package will address the question if there are differences. In the second part serial investigations in children with neuroblastoma will assess whether or not these patients show alterations of the intestinal microbiome under chemotherapy.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Children, Only | — | UNRESOLVED | — |
| Microbial Colonization | — | UNRESOLVED | — |
| Neuroblastoma | Neuroblastoma | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (9)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Breath volatile organic compounds under chemotherapy | Diagnostic Test | — | UNRESOLVED |
| Fecal volatile organic compounds under chemotherapy | Diagnostic Test | — | UNRESOLVED |
| Final breath volatile organic compounds | Diagnostic Test | — | UNRESOLVED |
| Final fecal volatile organic compounds | Diagnostic Test | — | UNRESOLVED |
| Final microbiome | Diagnostic Test | — | UNRESOLVED |
| Initial breath volatile organic compounds | Diagnostic Test | — | UNRESOLVED |
| Initial fecal microbiome | Diagnostic Test | — | UNRESOLVED |
| Initial fecal volatile organic compounds |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Neuroblastoma group
- description
- 10 children with neuroblastoma. Inclusion after verification of diagnosis and informed consent. Sampling of fecal microbiome (Initial microbiome, microbiome under chemotherapy, final microbiome), fecal volatile organic compounds (initial fecal volatile organic compounds, fecal volatile organic compounds under chemotherapy and final fecal volatile organic compounds) and breath organic volatile compounds (initial breath organic compounds, breath volatile organic compounds under chemotherapy and final breath volatile organic compounds). Samples will be taken after verifying diagnosis before initiation of chemotherapy, 1 week after completion of each cycle and 3 weeks after the end of chemotherapy.
- interventionNames
- Diagnostic Test: Initial fecal microbiome
- Diagnostic Test: Initial fecal volatile organic compounds
- Diagnostic Test: Initial breath volatile organic compounds
- Diagnostic Test: Microbiome under chemotherapy
- Diagnostic Test: Fecal volatile organic compounds under chemotherapy
- Diagnostic Test: Breath volatile organic compounds under chemotherapy
- Diagnostic Test: Final microbiome
- Diagnostic Test: Final fecal volatile organic compounds
- Diagnostic Test: Final breath volatile organic compounds
- type
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 1 Month
- Maximum age
- 8 Years
Show eligibility criteria text
Inclusion Criteria: * Age 2-8 years * Neuroblastoma group: verified neuroblastoma * Control group: absence of pulmonary or gastro-intestinal disease * Written parental informed consent obtained Exclusion Criteria: * Active gastro-intestinal or pulmonary disease * Antibiotic or probiotic treatment within 3 weeks before sampling * Negative parental informed consent
References
Publications (0)
Data not yet available