Evidence map›Paper›PMID 41948508›Full record

ArticleFrontiers in oncology2026

Symptom severity clusters in myeloproliferative neoplasms are unrelated to disease phenotype: results from a multicenter survey of the East German study group for hematology and oncology (OSHO #97).

Sabine Felser, Maximilian Koeppel, Rea Kuehl, Philipp le Coutre, Haifa K Al-Ali, Susann Schulze, Lars-Olof Muegge, Julia Bormann, Jan Geissler, Armin Dadgar and 2 more

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Article in Frontiers in oncology, 2026. 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

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Sabine FelserDepartment of Internal Medicine, Clinic for Hematology, Hemostaseology, Oncology, Stem Cell Therapy and Palliative Care, Rostock University Medical Center, Rostock, Germany.
Maximilian KoeppelWorking Group Exercise Oncology, Department of Medical Oncology, Heidelberg University Hospital, Medical Faculty Heidelberg, Heidelberg University, National Center for Tumor Diseases Heidelberg, a partnership between DKFZ and Heidelberg University Hospital, Heidelberg, Germany.
Rea KuehlWorking Group Exercise Oncology, Department of Medical Oncology, Heidelberg University Hospital, Medical Faculty Heidelberg, Heidelberg University, National Center for Tumor Diseases Heidelberg, a partnership between DKFZ and Heidelberg University Hospital, Heidelberg, Germany.
Philipp le CoutreCharité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, and Berlin Institute of Health, Department of Hematology, Oncology, and Cancer Immunology, Berlin, Germany.
Haifa K Al-AliKrukenberg Cancer Center Halle (Saale), University Hospital Halle, Halle (Saale), Germany.
Susann SchulzeKrukenberg Cancer Center Halle (Saale), University Hospital Halle, Halle (Saale), Germany.
Lars-Olof MueggeDepartment of Internal Medicine III, Heinrich Braun Klinikum Zwickau, Zwickau, Germany.
Julia BormannDepartment of Internal Medicine, Clinic for Hematology, Hemostaseology, Oncology, Stem Cell Therapy and Palliative Care, Rostock University Medical Center, Rostock, Germany.
Jan GeisslerLeukaemie-Online/LeukaNET e.V, Riemering, Germany.
Armin Dadgarmpn-netzwerk e. V., Bonn, Germany.
Christian Junghanss *Department of Internal Medicine, Clinic for Hematology, Hemostaseology, Oncology, Stem Cell Therapy and Palliative Care, Rostock University Medical Center, Rostock, Germany.
Sabina Ulbricht *Institut for Community Medicine, Department SHIP-KEF, University Medicine Greifswald, Greifswald, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Myeloproliferative neoplasms (MPNs) comprise a heterogeneous group of clonal hematopoietic stem cell disorders with distinct molecular pathogenesis and treatment strategies. Across all MPN subtypes, patients experience a substantial and persistent symptom burden that impairs health-related quality of life (HrQoL). Because MPNs are typically chronic diseases, lifelong symptom management and supportive therapies play a central role in patient care. Supportive care primarily targets disease- and treatment-related symptoms rather than the underlying malignancy itself. However, it remains unclear whether symptom profiles are comparable across MPN subtypes independent of disease phenotype. Therefore, this analysis aimed to identify symptom severity clusters (SSCs) in a cohort of patients with MPN. Methods: A multicenter cross-sectional survey was conducted. Patients with MPN aged ≥18 years completed questionnaires assessing sociodemographic and disease-specific variables (e.g., sex, age, diagnosis, and current therapies) as well as the severity of 14 symptoms (e.g., fatigue, musculoskeletal pain, and itching), rated on continuous scales ranging from 0 (absent) to 100 (worst imaginable). Hierarchical and K-means cluster analysis as well as multinomial logistic regression were used to identify SSCs and their associations with patient characteristics. Results: The sample comprised 644 patients (63% female; mean age 56.8 ± 13.4 years), including 187 patients with chronic myeloid leukemia, 174 with polycythemia vera, 154 with essential thrombocythemia, and 129 with myelofibrosis. Four SSCs were identified: very high, high, middle, and low symptom severity. Compared with the low SSC, membership in the very high SSC was associated with younger age (95% CI: -0.04 to 0.00) and lower educational level (95% CI: -1.17 to -0.04). Membership in the high SSC was associated with female sex (95% CI: 1.26 to 2.60), higher body mass index (95% CI: 0.00 to 0.11), and lower educational level (95% CI: -1.20 to -0.19). Membership in the very high, high, or middle SSCs, compared with the low SSC, was not associated with diagnostic group. Conclusion: Symptom severity in patients with MPN appears to be comparable across disease subtypes. These findings support a shift toward symptom-focused, multimodal supportive care approaches (e.g., exercise and psychological support) in patients with MPN.

Indexed as

chronic myeloid leukemia (CML)exercise therapyfatiguehealth-related quality of life (HRQoL)myeloproliferative neoplasms (MPN)supportive care

Identifiers

PMID41948508
PMCPMC13050751

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.