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Investigating COVID-19 infection in patients with acute myeloid leukaemia (AML) undergoing chemotherapy

Not Applicable
Completed
Conditions
Acute myeloid leukaemia, COVID-19 (SARS-CoV-2 infection)
Cancer
Registration Number
ISRCTN16865769
Lead Sponsor
niversity of Birmingham
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
321
Inclusion Criteria

1. Acute myeloid leukaemia (AML) including known AML presenting with relapse or Myelodysplastic Syndrome With Excess Blasts (MDS-EB2)
2. Currently receiving (at any treatment stage), or planned for, intensive (i.e. curative intent) or non-intensive chemotherapy. Intensive treatment includes regimens including Daunorubicin/Cytarabine, Fludarabine/Cytarabine/Idarubicin, intermediate/high dose Cytarabine, CPX-351, Gemtuzumab Ozogamacin, Midostaurin. Non-intensive treatments include Azacitidine, low dose Cytarabine, and Venetoclax based regimens.
3. Written informed consent to participate

Exclusion Criteria

1. Aged <16 years
2. Undergoing allogeneic stem cell transplant at trial entry
3. Supportive care only (including hydroxycarbamide alone)
4. Acute promyelocytic leukaemia (APML)

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Incidence of COVID-19 infection developing during AML treatment measured using SAR-CoV-2 PCR test and from hospital records from baseline until 4 weeks subsequent to the last cycle of treatment
Secondary Outcome Measures
NameTimeMethod
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