Associations with the quality of life of adult family members or partners (informal carers) of people with leukaemia: results from a cross-sectional online global survey - Report - MDSpire

Associations with the quality of life of adult family members or partners (informal carers) of people with leukaemia: results from a cross-sectional online global survey

  • By

  • Alan J. Poots

  • Samantha Nier

  • Sarah Gunn

  • Sam Salek

  • June 22, 2026

  • 0 min

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Impact of Leukaemia on the Quality of Life of Adult Informal Caregivers

Overview

This study investigates the quality of life (QoL) of informal caregivers of individuals with leukaemia. Findings indicate that a proportion of caregivers experience poor QoL, particularly those supporting patients with acute leukaemia.

Background

Leukaemia affects not only patients but also their informal caregivers, who provide essential support during treatment. Understanding the QoL of these caregivers is crucial, as their wellbeing can influence healthcare utilization. The challenges faced by informal caregivers of leukaemia patients have been underexplored.

Data Highlights

GroupMedian FROM-16 ScorePercentage Above Critical Threshold
Acute Leukaemia1638%
Chronic Leukaemia8Not specified

Key Findings

  • Median FROM-16 score for all respondents was 14.
  • 38% of caregivers scored above the critical threshold of 17.
  • Caregivers of patients with acute leukaemia had a higher median FROM-16 score (16) compared to those with chronic leukaemia (8).
  • Increased caregiving hours correlated with lower QoL.
  • Providing medication was associated with moderate effect sizes for both groups, while personal care showed small to moderate effects.

Clinical Implications

The findings suggest that informal caregivers, particularly those supporting patients with acute leukaemia, experience significant QoL challenges. Healthcare providers should consider integrating support for informal caregivers into leukaemia care strategies to address their unique needs.

Conclusion

The study highlights the substantial burden faced by informal caregivers of leukaemia patients, emphasizing the need for tailored support strategies to improve their quality of life.

Related Resources & Content

  1. The ASCO Post, 2017 -- Attrition High but Positive Trends Observed in Web-Based Intervention Addressing Caregiver Burden
  2. Journal of Neuro-Oncology, 2011 -- Assessing the Needs of Patients with Brain Tumors and Their Caregivers
  3. The ASCO Post, 2025 -- New Application May Help Caregivers of Patients Undergoing Bone Marrow Transplant
  4. Journal of Neuro-Oncology, 2025 -- Psychological Well-being and Contributing Factors Among Caregivers of Individuals with Malignant Brain Tumors
  5. Patient-Clinician Communication: ASCO Guideline Update | Journal of Clinical Oncology, 2026
  6. Family caregiver quality of life and symptom burden in patients with hematological cancer: A Danish nationwide cross-sectional study - ScienceDirect, 2024
  7. Patient-Clinician Communication: ASCO Guideline Update | Journal of Clinical Oncology
  8. Family caregiver quality of life and symptom burden in patients with hematological cancer: A Danish nationwide cross-sectional study - ScienceDirect

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