Please use this identifier to cite or link to this item: https://swslhd.intersearch.com.au/swslhdjspui/handle/1/12772
Title: Hidden in plain sight ? Survival consequences of baseline symptom burden in women with recurrent ovarian cancer
Authors: Roncolato, F.
King, M. T.
O'Connell, R. L.
Lee, Y. C.
Joly, F.
Hilpert, F.
Lanceley, A.
Yoshida, Y.
Bryce, J.
Donnellan, P.
Oza, A.
Avall-Lundqvist, E.
Berek, J. S.
Ledermann, J. A.
Berton, D.
Sehouli, J.
Kaminsky, M. C.
Stockler, M. R.
Friedlander, M.
SWSLHD Author: Roncolato, Felica T.
Affiliates: The University of Sydney, NHMRC Clinical Trials Centre, School of Medicine, Australia Western Sydney University, Australia Department of Medical Oncology, Macarthur Cancer Therapy Centre, Campbelltown Hospital, Campbelltown, NSW, Australia The University of Sydney, School of Psychology, Sydney, NSW, Australia School of Clinical Medicine, UNSW, Sydney, Australia Department of Medical Oncology, Prince of Wales and Royal Hospital for Women, Randwick, NSW, Australia Group d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens (GINECO), Paris, France Centre Francois Baclesse, Caen, France Arbeitsgesmeinschaft Gynakologische Onkologie Studiengruppe (AGO) und North-Eastern German Society of Gynecological Oncology (NOGGO), Kiel, Germany Onkologisches Therapiezentrum, Krankenhaus, Jerusalem, Hamburg, Germany Department of Women's Cancer, UCL Elizabeth Garrett Anderson Institute for Women's Health, Faculty of Population Health Sciences, University College London, United Kingdom Department of Obstetrics and Gynecology, University of Fukui, Japan Multicenter Italian Trials in Ovarian cancer and gynecologic malignancies (MITO), Napoli, Italy Ascension St. John Clinical Research Institute, Tulsa, OK, United States Istituto Nazionale Tumori IRCCS Fondazione Pascale, Campania, Napoli, Italy Cancer Trials Ireland, Galway University Hospital, Galway, Ireland Princess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada Nordic Society of Gynaecological Oncology (NSGO), Copenhagen, Denmark Department of Oncology and Department of Clinical and Experimental Medicine, Linkoping University, Linkoping, Sweden Department of Oncology-Pathology, Karolinksa Institutet, Stockholm, Sweden Cooperative Gynecologic Oncology Investigators (COGI), Stanford, CA, United States Stanford Women's Cancer Centre, Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA, United States The Cancer Research UK and UCL Cancer Trials Centre, NCRI UK, London, United Kingdom Institut de Cancerologie de l'Ouest, Centre Rene, Gauducheau, Saint Herblain, France Arbeitsgesmeinschaft Gynakologische Onkologie Studiengruppe (AGO) und North-Eastern German Society of Gynecological Oncology (NOGGO), Berlin, Germany Department of Gynecology and Oncological Surgery, Charite Universitatsmedizin Berlin, Berlin, Germany Institut de Cancerologie de Lorraine, Vandoeuvre Les Nancy, France
Department: Campbelltown Hospital, Macarthur Cancer Therapy Centre
Issue Date: 2024
Journal: Gynecologic Oncology
Publisher: Academic Press Inc.
Abstract: 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. � 2024 The Authors
URI: https://swslhd.intersearch.com.au/swslhdjspui/handle/1/12772
ISSN: 00908258 (ISSN)
Digital object identifier: 10.1016/j.ygyno.2024.02.025
Appears in Collections:Camden and Campbelltown Hospitals

Files in This Item:
There are no files associated with this item.


Items in Prosentient are protected by copyright, with all rights reserved, unless otherwise indicated.

Google Media

Google ScholarTM

Who's citing