Real-Time Breath Analysis in Acute Myeloid Leukaemia for a Rapid Characterisation of Biological Subtypes and to Predict Therapy Responses

ConditionAML
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorJeremy Deuel

About this trial

Patients with acute myeloid leukaemia (AML) respond to treatment to differing degrees, owing to the biological diversity of the disease. The diagnostic tests currently available for identifying genetic alterations and selecting the best possible treatment usually take several days before a result is obtained. In our study, the investigators aim to determine whether breath analysis can detect metabolic products of the leukaemia that allow the disease to be classified rapidly.

Participants will undergo additional blood tests and a breath analysis during their routine appointments. This will take place only during the 1st and 2nd treatment cycles. They will also be asked to complete a questionnaire about their state of health. In addition, the study team will collect further information on their state of health (type of leukaemia, type of treatment, other medications, vital signs) from their medical records.

In total, participants will complete 4 such measurements before and during their treatment. The measurements will be coordinated with their outpatient appointments. No assessments will be carried out unless the participants are at the hospital in any case, and they will not have to attend the hospital more often because of their participation in this study.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosis of an acute myeloid leukaemia and undergoing treatment

OR undergoing autoHSCT for lymphoid/myeloma disease in remission

Disqualifiers

inability to perform brath analysis

anatomical barriers preventing use of the mouthpiece.

Trial population

100 AML patients and 20 autologous-transplant controls

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

120 Participants
are grouped into 2 trial groups
Group A: AML
Group B: Negative Controls

Trial outcomes

Primary outcomes

1

A breath metabolite signature representing AML disease burden

A breath metabolite signature representing AML disease burden, and might represent novel AML subtypes or describe cancer metabolic status.

Time frame
8 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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Jeremy Deuel

Lead sponsor

University of Zurich

Sponsor institution

University Hospital, Zürich

Collaborator

ETH Zurich

Collaborator

This trial is not recruiting at the moment. You can still explore other options: