The DOI matches its Crossref record; 130 of the 130 references it cites were found in a registry or an index.
Understanding and Supporting Informal Cancer Caregivers
Open accessAbstract
Opinion statement Informal caregivers invest a significant amount of time and effort to provide cancer patients with physical, psychological, information, and social support. These challenging tasks can harm their own health and well-being, while a series of social-ecological factors may also influence the outcomes of cancer caregiving. Several instruments have been developed to help clinicians and researchers understand the multi-dimensional needs and concerns of caregivers. A growing body of evidence indicates that supportive interventions including psychoeducation, skills training, and therapeutic counseling can help improve the burden, information needs, coping strategies, physical functioning, psychological well-being, and quality of life of caregivers. However, there is difficulty in translating research evidence into practice. For instance, some supportive interventions tested in clinical trial settings are regarded as inconsistent with the actual needs of caregivers. Other significant considerations are the lack of well-trained interdisciplinary teams for supportive care provision and insufficient funding. Future research should include indicators that can attract decision-makers and funders, such as improving the efficient utilization of health care services and satisfaction of caregivers. It is also important for researchers to work closely with key stakeholders, to facilitate evidence dissemination and implementation, to benefit caregivers and the patient.
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“When compared to previous literature on caregivers of other oncology patients, the prevalence of caregiver burden, anxiety, depression, and distress found in this review appears clinically significant and, in some ways, might be comparable to or higher than estimates reported in mixed cancer caregivers.32, 33”
From Caregiver burden, quality of life, and psychosocial outcomes among informal caregivers of patients with glioma: A systematic review and meta-analysis (2026) · cites this paper as [33]
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“Caregivers of patients with advanced forms of cancer are known to have impaired QoL and higher psychological morbidities.”
From Caregiver burden, quality of life, and psychosocial outcomes among informal caregivers of patients with glioma: A systematic review and meta-analysis (2026) · cites this paper as [33]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
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“Prior studies in cancer caregiving consistently show that informal caregivers experience higher rates of anxiety, depressive symptoms, and reduced QoL compared with population norms, with burden influenced by caregiving intensity, financial toxicity, and perceived lack of support.33”
From Caregiver burden, quality of life, and psychosocial outcomes among informal caregivers of patients with glioma: A systematic review and meta-analysis (2026) · cites this paper as [33]
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In the citing paper
“This is because symptom burden, treatment intensity, and end-of-life care needs for the patients are high.32,33”
From Caregiver burden, quality of life, and psychosocial outcomes among informal caregivers of patients with glioma: A systematic review and meta-analysis (2026) · cites this paper as [33]
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Metadata
- Authors
- Molassiotis, A., & Wang, M.
- Affiliations
- Hong Kong Polytechnic University (HK)
- Corresponding author
- Molassiotis, Alex
- Venue
- Current Treatment Options in Oncology
- Published
- 2022-03-14
- Volume
- 23
- Issue
- 4
- Pages
- 494-513
- ISSN
- 1527-2729 (ISSN-L)
- 1534-6277
- PMC
- PMC8918600
- OpenAlex
- W4220745051
- Cited by
- 138
- References
- 130
- Citations by year
- 2026: 38 · 2025: 43 · 2024: 41 · 2023: 13 · 2022: 3
- FWCI
- 5.69
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Current Treatment Options in Oncology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Nursing › Research and Theory › Nursing care and research
- Health Sciences › Medicine › Oncology › Cancer survivorship and care
- Social Sciences › Psychology › Clinical Psychology › Family Caregiving in Mental Illness
- Keywords
- informal caregivers, cancer caregiving, caregiver burden, caregiver well-being, support measures, psychoeducation, skills training, therapeutic counseling, caregiver needs assessment, implementation of evidence-based interventions, interdisciplinary care teams, caregiver quality of life, caregiver coping
- MeSH terms
- Adaptation, Psychological, Humans, Neoplasms, Quality of Life, Social Support, Caregivers
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