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Quality of life and late effects in leukemia survivors

Conditions
eukemia+
C92.0
C92.5
C92.6
C92.3
C93.0
C94.0
C94.2
Acute myeloblastic leukaemia [AML]
Acute myelomonocytic leukaemia
Registration Number
DRKS00023991
Lead Sponsor
Medizinische Klinik IUniversitätsklinikum Leipzig
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
427
Inclusion Criteria

Patients suffering from acute myeloid leukemia (AML) who were enrolled into the patient registry of the German AML Cooperative Group (AML-CG, DRKS00020816) and/or one of the following interventional trials: AMLCG-1999 (clinicaltrials.gov NCT00266136), AMLCG-2004 (European Leukemia Trial Registry Nr. LN_AMLINT_2004_230), AMLCG-2008 (clinicaltrials.gov NCT01382147).
- Study participants have survived =5 years from initial diagnosis off AML.

Exclusion Criteria

- Current leukemia relapse
- Age <18 years
- Inability to give valid informed consent
- Insufficient german language proficiency which makes the participant unable to answer the study questionnaires

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Primary endpoint of this study is a comparison of quality of life (QoL) and general and health-related life satisfaction (LS) in AML survivors, compared to an age- and sex-matched healthy control cohort. QoL and LS will be measured using the FACT-G and FLZ-A/G questionnaires, respectively. We will use a graph-based sequential testing procedure to control for multiple testing of the co-primary endpoints (Bretz F et al., Stat Med 2009; 28:586).
Secondary Outcome Measures
NameTimeMethod
- Frequency of clonal hematopoiesis in AML long-term survivors<br>- Medical, psycho-social and demographic factors associated with an increased risk of somatic or psychological health problems in AML survivors<br>- Associations between clonal hematopoiesis and somatic morbidity in AML survivors
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