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Hidden in plain sight - Survival consequences of baseline symptom burden in women with recurrent ovarian cancer
Univ Sydney, Australia; Western Sydney Univ, Australia; Campbelltown Hosp, Australia.
Univ Sydney, Australia.
Univ Sydney, Australia.
Univ Sydney, Australia; UNSW, Australia; Prince Wales & Royal Hosp Women, Australia.
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2024 (English)In: Gynecologic Oncology, ISSN 0090-8258, E-ISSN 1095-6859, Vol. 185, p. 128-137Article in journal (Refereed) Published
Abstract [en]

Objective. To describe the baseline symptom burden(SB) experienced by patients(pts) with recurrent ovarian cancer(ROC) prior and associations with progression free survival (PFS) and overall survival (OS). Methods. We analysed baseline SB reported by pts. with platinum resistant/refractory ROC (PRR-ROC) or potentially-platinum sensitive ROC receiving their third or greater line of chemotherapy (PPS-ROC >= 3) enrolled in the Gynecologic Cancer InterGroup - Symptom Benefit Study (GCIG-SBS) using the Measure of Ovarian Symptoms and Treatment concerns (MOST). The severity of baseline symptoms was correlated with PFS and OS. Results. The 948 pts. reported substantial baseline SB. Almost 80% reported mild to severe pain, and 75% abdominal symptoms. Shortness of breath was reported by 60% and 90% reported fatigue. About 50% reported moderate to severe anxiety, and 35% moderate to severe depression. Most (89%) reported 1 or more symptoms as moderate or severe, 59% scored 6 or more symptoms moderate or severe, and 46% scored 9 or more symptoms as moderate or severe. Higher SB was associated with significantly shortened PFS and OS; five symptoms had OS hazard ratios larger than 2 for both moderate and severe symptom cut-offs (trouble eating, vomiting, indigestion, loss of appetite, and nausea; p < 0.001). Conclusion. Pts with ROC reported high SB prior to starting palliative chemotherapy, similar among PRR-ROC and PPS-ROC >= 3. High SB was strongly associated with early progression and death. SB should be actively managed and used to stratify patients in clinical trials. Clinical trials should measure and report symptom burden and the impact of treatment on symptom control. (c) 2024 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license (http://

Place, publisher, year, edition, pages
ACADEMIC PRESS INC ELSEVIER SCIENCE , 2024. Vol. 185, p. 128-137
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Cancer and Oncology
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URN: urn:nbn:se:liu:diva-203128DOI: 10.1016/j.ygyno.2024.02.025ISI: 001206203200001PubMedID: 38412736OAI: oai:DiVA.org:liu-203128DiVA, id: diva2:1855252
Note

Funding Agencies|NHMRC [1063012, 570893]; Target Ovarian Cancer [UCL-P001AL]; Cancer Research UK and UCL Cancer Trials Centre [C444/A15953]; Australian Government through Cancer Australia; Department of Health

Available from: 2024-04-30 Created: 2024-04-30 Last updated: 2024-04-30

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Åvall Lundqvist, Elisabeth
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Division of Surgery, Orthopedics and OncologyFaculty of Medicine and Health SciencesDepartment of Oncology
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