Trajectories of health-related quality of life and psychological distress in patients with colorectal cancer: A population-based study. (November 2021)

• Record Type: Journal Article
• Authors: Qaderi, Seyed M.; van der Heijden, Joost A.G.; Verhoeven, Rob H.A.; de Wilt, Johannes H.W.; Custers, Jose A.E.; Beets, Geerard L.; Belt, Eric J.Th.; Berbée, Maaike; Beverdam, Frederique H.; Blankenburgh, Ruud; Coene, Peter Paul L.O.; de Groot, Jan Willem B.; de Hingh, Ignace H.J.T.; de Vos, Aad I.; de Wilt, Johannes H.W.; Dekker, Jan Willem T.; Erdkamp, Frans L.G.; Haringhuizen, Annebeth W.; Helgason, Helgi H.; Hendriks, Mathijs P.; Hoekstra, Ronald; Ijzermans, Jan N.M.; Jansen, Jan; Kloppenberg, Frank W.H.; Los, Maartje; Meijerink, Martijn R.; Mekenkamp, Leonie J.M.; Nieboer, Peter; Peeters, Koen C.M.J.; Peters, Natascha A.J.B.; Polée, Marco B.; Pruijt, Johannes F.M.; van Ufford-Mannesse, Patricia Quarles; Rietbroek, Ron C.; Schiphorst, Anandi H.W.; van der Velden, Arjan Schouten; Schrauwen, Ruud W.M.; Sie, Mark P.S.; Simkens, Lieke; Sommeijer, Dirkje W.; Sonneveld, Dirk J.A.; Spierings, Leontine E.A.; Stockmann, Hein B.A.C.; Talsma, Koen; ten Tije, Albert J.; Terheggen, Frederiek; Tjin-A-Ton, Manuel L.R.; Valkenburg-van Iersel, Liselot B.J.; van Cruijsen, Hester; Velden, Ankie M.T. van der; van Dodewaard-de Jong, Joyce M.; van Lent, Anja U.G.; van Voorthuizen, Theo; Vermaas, Maarten; Vles, Wouter J.; Vogelaar, Jeroen F.J.; Zimmerman, David D.E.;
• Is Part Of: European journal of cancer. Volume 158(2021)
• Page Start: 144
• Page End: 155
• Publication Date: 2021-11
• Subjects: Colorectal cancer -- Quality of life -- Psychological distress -- Symptom burden -- Follow-up -- Surveillance -- Cancer; Cancer -- Periodicals; Neoplasms -- Periodicals; Cancer -- Périodiques; Cancer; Tumors; Electronic journals; Periodicals; Electronic journals; 616.994
• DOI: 10.1016/j.ejca.2021.08.050
• Languages: English
• ISSNs: 0959-8049

Abstract

Abstract: Background: The aim of this nationwide cohort study was to examine the course of symptoms and trajectories of health-related quality of life (HR-QoL) and psychological distress during follow-up and to identify vulnerable patients. Methods: Patients with pathological stage I–III colorectal cancer (CRC) between 2013 and 2018 were included. Baseline characteristics were collected from the Netherlands Cancer Registry, and patients completed the European Organisation for Research and Treatment of Cancer QLQ-C30/CR29, Hospital Anxiety and Depression Scale and low anterior resection syndrome (LARS) questionnaires at the baseline and subsequently at 3, 6, 12, 18 and 24 months. Latent class growth and multinomial logistic regression analyses were performed to outline 24-month trajectories in HR-QoL and distress and to identify predictive factors. Results: : A total of 1535 patients with colon cancer or rectal cancer were included. Trajectory analysis of HR-QoL identified three patient classes: high HR-QoL (62.7%), improving HR-QoL (29.0%) and low HR-QoL (8.3%). The following patient groups were identified with having low distress (64.0%), moderate distress (26.9%) and high distress (9.1%). Around 13% of the total cohort had either persistent low HR-QoL or high psychological distress throughout follow-up. Patients belonging to this vulnerable group were significantly more likely to be female, to be younger aged, to have lower education, to have disease stage II–III or to have major LARS. Conclusions: Although most patients treated for stage I–III CRC fared well, a small but significant proportion of around 13% did not recover during follow-up and reported low HR-QoL and/or high psychological distress levels throughout. This study's findings should be taken into account when organising and selecting patients for tailored follow-up. Highlights: The number of patients with colorectal cancer (CRC) requiring follow-up increased. Quality of life (QoL) and distress among recently diagnosed patients with CRC are unclear. Most patients with stage I–III CRC did well and reported high QoL and low distress. Trajectory analysis revealed vulnerable patient groups and identified predictive factors. Patient-reported outcome measures should be used when personalising CRC follow-up.