About this trial

Patients with leukemia and concomitant neutropenia are at high risk of developing invasive fungal infections (IFI) that are associated with high morbidity and mortality. As these patients typically have severe thrombocytopenia, direct diagnostic sampling with invasive procedures is often not possible due to the high peri-interventional risk. Therefore, the presumptive diagnosis of IFI is primarily based on compatible lung findings on computed tomography and serologic detection of fungal cell wall components, which, however, have limited sensitivity and specificity.

With the present study, the investigators aim to determine a set of specific volatile biomarkers in leukemia patients with proven or probable IFI using secondary electrospray ionization high-resolution mass spectrometry (SESI-HRMS).

Eligibility criteria

Qualifiers

Diagnosis of acute leukemia

Planned chemotherapy with a duration of hospitalisation of 2 weeks or longer

Neutropenia (<500/µl) present at inclusion or planned chemotherapy with expected neutropenia (<500/µl) for more than 7 days

Disqualifiers

Unable to follow instructions for breath analysis

Anatomic abnormalities precluding the use of a mouthpiece for breath analysis

Trial design

Treatments tested in this trial

  • Secondary electrospray ionization high-resolution mass spectrometry (SESI-HRMS)

Treatment groups

130 Participants
are divided into 4 treatment groups

Locations

1
University Hospital of Zurich8091, ZurichCanton of Zurich, Switzerland

Sponsors and collaborators

University of Zurich

Lead sponsor