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The role of baseline and persistent depression in adjuvant cancer therapy: impact on toxicity and quality of life

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dc.contributor.author Obispo, Berta; Calderon, Caterina; Carmona-Bayonas, Alberto; Ghanem, Ismael; Cano-Cano, Juana Maria; Jimenez-Fonseca, Paula
dc.date.accessioned 2026-03-10T11:55:45Z
dc.date.available 2026-03-10T11:55:45Z
dc.date.issued 2025-10
dc.identifier.citation Obispo B, Calderon C, Carmona-Bayonas A, Ghanem I, Cano-Cano JM, Jiménez-Fonseca P. The role of baseline and persistent depression in adjuvant cancer therapy: impact on toxicity and quality of life. International Journal of Clinical and Health Psychology. octubre de 2025;25(4):100640. doi:10.1016/j.ijchp.2025.100640
dc.identifier.issn 1697-2600
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/25358
dc.description.abstract INTRODUCTION: Depression is common among cancer patients, adversely affecting treatment adherence, toxicity, and quality of life (QoL). However, its course during adjuvant therapy and its impact on outcomes in resected cancer remain poorly understood. This study evaluated changes in depression from treatment initiation (T1) to six months later (T2) and examined associations with demographic, clinical, and psychological factors, treatment-related toxicities, and QoL. METHODS: In this multicenter, prospective observational study, 927 patients with resected, non-metastatic cancer receiving adjuvant treatment were enrolled. Depressive symptoms were measured using the Brief Symptom Inventory-18 (BSI-18) at T1 and T2. Patients were classified as "never" (no symptoms at T1 or T2), "new-onset" (absent at T1, present at T2), "remission" (present at T1, absent at T2), or "persistent" (present at both time points). Treatment-related toxicities were evaluated according to CTCAE v4.0, and QoL was assessed with the EORTC QLQ-C30. RESULTS: At T2, 50.8% of patients remained asymptomatic, 12.3% experienced remission, 23.4% exhibited persistent depression, and 13.5% developed new-onset depression. Persistent depression was more common among women, younger patients, those without a partner, and breast cancer patients. Patients with persistent symptoms showed significantly higher toxicities-including hematologic, digestive, and neuropathic events, as well as increased asthenia (p < .001)-and poorer functioning with greater symptom burden, resulting in markedly reduced overall QoL. In multivariate analyses, baseline depression and ECOG performance status were the main predictors of depressive symptoms at six months, while age predicted changes over time; other sociodemographic or clinical factors were not significant. Logistic regression confirmed that younger age, female sex, breast cancer, and poorer ECOG were associated with higher odds of persistent depression compared with never-depressed patients. CONCLUSION: Both baseline depression and functional impairment (ECOG) are independent predictors of depressive symptoms during adjuvant therapy. Persistent depression is significantly associated with increased treatment toxicity and poorer QoL in patients with early-stage resected cancer, highlighting the need for routine screening and early psychological intervention during adjuvant treatment.
dc.language.iso eng
dc.publisher ELSEVIER SCIENCE INC
dc.rights Atribución/Reconocimiento-NoComercial-SinDerivados 4.0 Internacional
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.title The role of baseline and persistent depression in adjuvant cancer therapy: impact on toxicity and quality of life
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 41146968
dc.relation.publisherversion https://linkinghub.elsevier.com/retrieve/pii/S1697260025000973
dc.type.version info:eu-repo/semantics/publishedVersion
dc.identifier.doi 10.1016/j.ijchp.2025.100640
dc.journal.title International Journal of Clinical and Health Psychology
dc.identifier.essn 2174-0852


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