Host RNA Signature in Children With Cancer and Infection

Sponsor
Rigshospitalet, Denmark (Other)
Overall Status
Recruiting
CT.gov ID
NCT04669418
Collaborator
Børnecancerfonden (Other), Lundbeck Foundation (Other), Danish Cancer Society (Other)
300
5
38
60
1.6

Study Details

Study Description

Brief Summary

The aim is to investigate if RNA expression signature can discriminate bacterial from viral infection or non-infectious inflammation in children with cancer.

Earlier studies in immunocompetent children have shown promising results, but studies in immunocompromised children are lacking.

We aim to include 300 febrile episodes in children with cancer. The samples will be analysed by RNA sequencing. If succesfull, this method can help prevent unnecessary antibiotic treatment, reduce hospital admissions, side effects and antimicrobial resistance and improve quality of life for children during cancer treatment.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: RNA expression signature

Detailed Description

Children with cancer are at high risk of invasive bacterial infections particularly during neutropenia. Febrile neutropenia is an early sign of a potentially fatal infection requiring broad-spectrum empiric antibiotics. However, the majority of children do not have a bacterial infection, but still receive antibiotics, since current tests cannot distinguish causes of fever. A number of transcriptomic studies of immunocompetent patients show that host leukocyte patterns of activated RNA can discriminate bacterial infection from non-infectious inflammation with high accuracy, but studies in immunocomprised patients are few.

Methods

A prospective non-interventional observational multicentre study including febrile childhood cancer patients during 24 months at all Danish Pediatric Oncology Departments (Rigshospitalet, Aarhus, Odense and Aalborg University Hospitals). Leukocyte RNA expression will be analysed in whole blood samples by RNA sequencing adjusted for low RNA input. 300 febrile episodes will be included, and predictive host RNA signatures will be identified in a discovery cohort and assessed in a validation cohort. Further, to explore the transcriptome in non-febrile children with neutropenia, we include a control group of 15 children with cancer and no fever.

Time frame Inclusion of children: 1st of June 2019 to 31st of May 2021 Analysis of samples (RNA sequencing): 1st of June 2021 - 1st of December 2021

Perspective

The study will create a base for a randomised trial regarding implementation of RNA signature versus normal procedure in handling febrile children with cancer. This can lead to the development of a targeted RNA-expression analytical platform that can prevent unnecessary antibiotic treatment in the majority of children with febrile neutropenia. This will reduce hospital admissions, side effects, antimicrobial resistance and improve quality of life during cancer treatment. The results can be extrapolated to the adult patients with cancer, who are often treated with prophylactic antibiotics, which complicate finding the infectious agent. Additionally, the test may be applied in other immunosuppressed children with infections.

Study Design

Study Type:
Observational
Anticipated Enrollment :
300 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Host RNA Signature to Discriminate Bacterial From Viral Infection and Non-specific Inflammation in Children With Cancer
Actual Study Start Date :
Jun 1, 2019
Anticipated Primary Completion Date :
May 31, 2021
Anticipated Study Completion Date :
Jul 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Group 1

70 children with cancer and a positive blood culture.

Diagnostic Test: RNA expression signature
Whole transcriptome profiling using RNA sequencing

Group 2

50 children with cancer and no positive blood culture.

Diagnostic Test: RNA expression signature
Whole transcriptome profiling using RNA sequencing

Outcome Measures

Primary Outcome Measures

  1. RNA signature [1.5 years]

    To detect specific RNA signatures in whole blood in children with febrile neutropenia

Secondary Outcome Measures

  1. Time study [1,5 years]

    An investigation of the change in RNA expression over time during an infection period

  2. Application of known RNA signatures [1,5 years]

    To test RNA signatures from genes published in other studies eg. the genes IFI44L and FAM89A

  3. Differences in RNA signature according to pathogen [1,5 years]

    To investigate potential differences in RNA signatures in patients with gram positive versus gram negative bacteria

  4. Comparishment of RNA signatures in neutropenic and non-neutropenic children [1,5 years]

    To compare RNA signatures in febrile neutropenic and non-neutropenic children with a positive blood culture

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A to 17 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Children with cancer and fever. Fever defined as temperature above 38.5 °C measured once, or 38.0-38.5 °C for ≥ 1 hour.

Exclusion Criteria:

The children can be excluded if they turn out to have a different diagnosis than expected or if it is not possible to draw the blood tests.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Pediatrics, Aalborg University Hospital Aalborg Denmark 9000
2 Department of Pediatric Oncology, Aarhus University Hospital Aarhus Denmark 8200
3 Center for Genomic Medicine Copenhagen Denmark 2100
4 Department of pediatric and adolescent medicine, Rigshospitalet (Copenhagen University Hospital) Copenhagen Denmark 2100
5 Department of Pediatrics, The H.C. Andersen's Children's hospital Odense Denmark 5000

Sponsors and Collaborators

  • Rigshospitalet, Denmark
  • Børnecancerfonden
  • Lundbeck Foundation
  • Danish Cancer Society

Investigators

  • Principal Investigator: Lotte M. Smedegaard, M.D., ph.d.-student

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Lotte Møller Smedegaard, M.D., Rigshospitalet, Denmark
ClinicalTrials.gov Identifier:
NCT04669418
Other Study ID Numbers:
  • H-2-2010-002_1
First Posted:
Dec 16, 2020
Last Update Posted:
Dec 16, 2020
Last Verified:
Dec 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 16, 2020