Evidence map›Paper›PMID 41647706›Full record

ArticleESMO real world data and digital oncology2025

Prevalence of functional iron deficiency in patients with malignancies and its impact on fatigue-specific quality of life.

S Zimmermann, S Aebi, O Gautschi, M Gregor, B Müller, H Nilius, E Pardo, D Weiler, S S Zeerleder, A Rüfer

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Article in ESMO real world data and digital oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

S ZimmermannDepartment of Haematology, Luzerner Kantonsspital Luzern, Luzern, Switzerland.
S AebiCancer Centre Luzerner Kantonsspital Luzern, Luzern, Switzerland.
O GautschiCancer Centre Luzerner Kantonsspital Luzern, Luzern, Switzerland.
M GregorDepartment of Haematology, Luzerner Kantonsspital Luzern, Luzern, Switzerland.
B MüllerCancer Centre Luzerner Kantonsspital Luzern, Luzern, Switzerland.
H NiliusDepartment of Clinical Chemistry, University Hospital Bern, Bern, Switzerland.
E PardoCancer Centre Luzerner Kantonsspital Luzern, Luzern, Switzerland.
D WeilerCancer Centre Luzerner Kantonsspital Luzern, Luzern, Switzerland.
S S ZeerlederDepartment of Haematology, Luzerner Kantonsspital Luzern, Luzern, Switzerland.
A RüferDepartment of Haematology, Luzerner Kantonsspital Luzern, Luzern, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Functional iron deficiency (FID) as defined by the European Society for Medical Oncology (ESMO) occurs in patients with malignant neoplasms and might be a target to improve fatigue-specific quality of life (QoL). The prevalence of FID in that population, especially in patients with a haemoglobin (Hb) of 10-11 g/dl and Hb > 11 g/dl, is unclear. The aim of this study was to obtain data on the prevalence of FID in patients with solid tumours and haematological malignancies independent of Hb and age, and to investigate the potential of FID as a target to improve fatigue-specific QoL. Patients and methods: This was a prospective, observational single-centre study assessing adult patients with malignancies 4 weeks before disease-directed therapy. Patients without known iron deficiency (ID), iron supplementation, therapy with erythropoiesis-stimulating agents, or red blood cell transfusions 8 weeks before inclusion were eligible. Fatigue-specific QoL data were assessed by the Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F) questionnaire. Results: FID was found in 30% of 146 assessed patients, of which 77% had a Hb > 11 g/dl. FID was documented in 63% of patients with a Hb of 10-11 g/dl and in 26% of patients with Hb > 11 g/dl. The total scores for FACIT-F were not significantly different between patients with FID, absolute ID, and no ID. Conclusion: FID is highly prevalent also in patients with a Hb of 10-11 g/dl and Hb > 11 g/dl and should be distinguished from absolute ID. Fatigue-specific QoL was not influenced by iron status, and improvement of QoL by treating FID without anaemia in patients with malignancies is therefore unlikely.

Indexed as

fatiguefunctional iron deficiency (FID)ironiron deficiencymalignancyquality of life

Identifiers

PMID41647706
PMCPMC12836532

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