Mental illness and non-metastatic colorectal cancer treatment and survival, a nationwide study of almost 70,000 patients
DOI:
https://doi.org/10.2340/1651-226X.2025.42710Keywords:
disparity, Colorectal cancer, cancer survival, Recurrence, cancer-specific survival, survival after recurrenceAbstract
Background and purpose: The impact of mental illness on treatment and outcomes for patients with colorectal cancer (CRC) has not been investigated with potential confounders and mediators accounted for.
Patients and methods: Colorectal Cancer Database (CRCBaSe), a linked national registry database, was used to analyse stage I–III CRC patients diagnosed in Sweden between 2008 and 2021. The exposure of interest was a history of mental illness. Treatment outcomes were analysed with logistic regressions. Flexible parametric models were fitted for survival analysis. Analyses were adjusted for pre-specified confounders.
Results: Patients with a history of severe mental illness presented with more advanced tumours and comorbidities. They were more likely to undergo emergency surgery (OR 1.56, 95% CI 1.32–1.84) and less likely to receive adjuvant treatment (OR 0.65, 95% CI 0.53–0.80) than patients with no history of mental illness. Five-year standardised overall survival (OS) was worse for those with a history of mild and severe mental illness, 64.6% (95%CI 63.9–65.3) and 61.8% (95%CI 59.7–63.8) compared to those without 69.3% (95%CI 68.9–69.7). Although time to recurrence was not significantly impacted, standardised survival after recurrence was worse for patients with a history of severe mental illness, with a 3-year survival after recurrence of 24% compared to 30% in those without a history of mental illness.
Interpretation: Although the differences were smaller compared to previous studies, patients with a history of mental illnesses still do worse. The management of CRC patients with psychiatric comorbidities presents complex challenges necessitating personalised solutions.
Downloads
References
Baillargeon J, Kuo Y-F, Lin Y-L, Raji MA, Singh A, Goodwin JS. Effect of mental disorders on diagnosis, treatment, and survival of older adults with colon cancer: mental disorders and colon cancer. J Am Geriatr Soc. 2011;59:1268–73.
https://doi.org/10.1111/j.1532-5415.2011.03481.x DOI: https://doi.org/10.1111/j.1532-5415.2011.03481.x
Protani MM, Alotiby MKN, Seth R, Lawrence D, Jordan SJ, Logan H, et al. Colorectal cancer treatment in people with severe mental illness: a systematic review and meta-analysis. Epidemiol Psychiatr Sci. 2022;31:e82.
https://doi.org/10.1017/S2045796022000634 DOI: https://doi.org/10.1017/S2045796022000634
Manderbacka K, Arffman M, Lumme S, Suvisaari J, Keskimäki I, Ahlgren-Rimpiläinen A, et al. The effect of history of severe mental illness on mortality in colorectal cancer cases: a register-based cohort study. Acta Oncol. 2018;57:759–64.
https://doi.org/10.1080/0284186X.2018.1429649 DOI: https://doi.org/10.1080/0284186X.2018.1429649
Kaerlev L, Iachina M, Trosko O, Qvist N, Ljungdalh PM, Nørgård BM. Colon cancer patients with a serious psychiatric disorder present with a more advanced cancer stage and receive less adjuvant chemotherapy – a Nationwide Danish Cohort Study. BMC Cancer. 2018;18:1050.
https://doi.org/10.1186/s12885-018-4879-3 DOI: https://doi.org/10.1186/s12885-018-4879-3
Seppänen A-V, Daniel F, Houzard S, Le Bihan C, Coldefy M, Gandré C. The double burden of severe mental illness and cancer: a population-based study on colorectal cancer care pathways from screening to end-of-life care. Epidemiol Psychiatr Sci. 2024;33:e27.
https://doi.org/10.1017/S2045796024000234 DOI: https://doi.org/10.1017/S2045796024000234
Mahar AL, Kurdyak P, Hanna TP, Coburn NG, Groome PA. The effect of a severe psychiatric illness on colorectal cancer treatment and survival: a population-based retrospective cohort study. PLoS One. 2020;15:e0235409.
https://doi.org/10.1371/journal.pone.0235409 DOI: https://doi.org/10.1371/journal.pone.0235409
Hudson CG. Socioeconomic status and mental illness: tests of the social causation and selection hypotheses. Am J Orthopsychiatry. 2005;75:3–18.
https://doi.org/10.1037/0002-9432.75.1.3 DOI: https://doi.org/10.1037/0002-9432.75.1.3
Chan JKN, Correll CU, Wong CSM, Chu RST, Fung VSC, Wong GHS, et al. Life expectancy and years of potential life lost in people with mental disorders: a systematic review and meta-analysis. eClinicalMedicine. 2023;65:102294.
https://doi.org/10.1016/j.eclinm.2023.102294 DOI: https://doi.org/10.1016/j.eclinm.2023.102294
Osterman E, Syriopoulou E, Martling A, Andersson TM-L, Nordenvall C. Despite multi-disciplinary team discussions the socioeconomic disparities persist in the oncological treatment of non-metastasized colorectal cancer. Eur J Cancer. 2024;199:113572.
https://doi.org/10.1016/j.ejca.2024.113572 DOI: https://doi.org/10.1016/j.ejca.2024.113572
Hussain SK, Lenner P, Sundquist J, Hemminki K. Influence of education level on cancer survival in Sweden. Ann Oncol. 2008;19:156–62.
https://doi.org/10.1093/annonc/mdm413 DOI: https://doi.org/10.1093/annonc/mdm413
Cunningham R, Sarfati D, Stanley J, Peterson D, Collings S. Cancer survival in the context of mental illness: a national cohort study. Gen Hosp Psychiatry. 2015;37:501–6.
https://doi.org/10.1016/j.genhosppsych.2015.06.003 DOI: https://doi.org/10.1016/j.genhosppsych.2015.06.003
Liang X, Hendryx M, Qi L, Lane D, Luo J. Association between prediagnosis depression and mortality among postmenopausal women with colorectal cancer. PLoS One. 2020;15:e0244728.
https://doi.org/10.1371/journal.pone.0244728 DOI: https://doi.org/10.1371/journal.pone.0244728
Kurashige J, Iwatsuki M, Mima K, Nomoto D, Shigaki H, Yamashita K, et al. Analysis of the survival and clinical characteristics of colorectal cancer patients with mental disorders. Ann Gastroenterol Surg. 2021;5:314–20.
https://doi.org/10.1002/ags3.12421 DOI: https://doi.org/10.1002/ags3.12421
Weibull CE, Boman SE, Glimelius B, Syk I, Matthiessen P, Smedby KE, et al. CRCBaSe: a Swedish register-based resource for colorectal adenocarcinoma research. Acta Oncol. 2023;62(4):342–9.
https://doi.org/10.1080/0284186X.2023.2197121 DOI: https://doi.org/10.1080/0284186X.2023.2197121
Charlson ME, Pompei P, Ales KL, MacKenzie CR. A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis. 1987;40:373–83.
https://doi.org/10.1016/0021-9681(87)90171-8 DOI: https://doi.org/10.1016/0021-9681(87)90171-8
Ludvigsson JF, Appelros P, Askling J, Byberg L, Carrero J-J, Ekström AM, et al. Adaptation of the Charlson Comorbidity Index for Register-Based Research in Sweden. Clin Epidemiol. 2021;13:21–41.
https://doi.org/10.2147/CLEP.S282475 DOI: https://doi.org/10.2147/CLEP.S282475
Fitz-Henry J. The ASA classification and peri-operative risk. Ann R Coll Surg Engl. 2011;93:185–7.
https://doi.org/10.1308/rcsann.2011.93.3.185a DOI: https://doi.org/10.1308/rcsann.2011.93.3.185a
Bower H, Crowther MJ, Rutherford MJ, Andersson TM-L, Clements M, Liu X-R, et al. Capturing simple and complex time-dependent effects using flexible parametric survival models: a simulation study. Commun Stat – Simul Comput. 2021;50:3777–93.
https://doi.org/10.1080/03610918.2019.1634201 DOI: https://doi.org/10.1080/03610918.2019.1634201
Syriopoulou E, Mozumder SI, Rutherford MJ, Lambert PC. Robustness of individual and marginal model-based estimates: a sensitivity analysis of flexible parametric models. Cancer Epidemiol. 2019;58:17–24.
https://doi.org/10.1016/j.canep.2018.10.017 DOI: https://doi.org/10.1016/j.canep.2018.10.017
Liu X-R, Pawitan Y, Clements M. Parametric and penalized generalized survival models. Stat Methods Med Res. 2018;27:1531–46.
https://doi.org/10.1177/0962280216664760 DOI: https://doi.org/10.1177/0962280216664760
Liu X, Pawitan Y, Clements MS. Generalized survival models for correlated time‐to‐event data. Stat Med. 2017;36:4743–62.
https://doi.org/10.1002/sim.7451 DOI: https://doi.org/10.1002/sim.7451
Jestin P, Nilsson J, Heurgren M, Påhlman L, Glimelius B, Gunnarsson U. Emergency surgery for colonic cancer in a defined population. Br J Surg. 2005;92:94–100.
https://doi.org/10.1002/bjs.4780 DOI: https://doi.org/10.1002/bjs.4780
Sargent DJ, Wieand HS, Haller DG, Gray R, Benedetti JK, Buyse M, et al. Disease-free survival versus overall survival as a primary end point for adjuvant colon cancer studies: individual patient data from 20,898 patients on 18 randomized trials. J Clin Oncol. 2005;23:
8664–70.
https://doi.org/10.1200/JCO.2005.01.6071 DOI: https://doi.org/10.1200/JCO.2005.01.6071
Ljunggren M, Weibull CE, Palmer G, Osterlund E, Glimelius B, Martling A, et al. Sex differences in metastatic surgery following diagnosis of synchronous metastatic colorectal cancer. Int J Cancer. 2022;152(3):363–372.
https://doi.org/10.1002/ijc.34255 DOI: https://doi.org/10.1002/ijc.34255
Ljunggren M, Weibull CE, Rosander E, Palmer G, Glimelius B, Martling A, et al. Hospital factors and metastatic surgery in colorectal cancer patients, a population-based cohort study. BMC Cancer. 2022;22:907.
https://doi.org/10.1186/s12885-022-10005-8 DOI: https://doi.org/10.1186/s12885-022-10005-8
Moberger P, Sköldberg F, Birgisson H. Evaluation of the Swedish Colorectal Cancer Registry: an overview of completeness, timeliness, comparability and validity. Acta Oncol. 2018;57:1611–21.
https://doi.org/10.1080/0284186X.2018.1529425 DOI: https://doi.org/10.1080/0284186X.2018.1529425
Osterman E, Hammarström K, Imam I, Osterlund E, Sjöblom T, Glimelius B. Completeness and accuracy of the registration of recurrences in the Swedish Colorectal Cancer Registry (SCRCR) and an update of recurrence risk in colon cancer. Acta Oncol. 2021;60:842–9.
https://doi.org/10.1080/0284186X.2021.1896033 DOI: https://doi.org/10.1080/0284186X.2021.1896033
Eklöv K, Nygren J, Bringman S, Löfgren J, Sjövall A, Nordenvall C, et al. Colon cancer treatment in Sweden during the COVID‐19 pandemic: a nationwide register‐based study. Colorectal Dis. 2022;24:925–32.
https://doi.org/10.1111/codi.16129 DOI: https://doi.org/10.1111/codi.16129
Eklöv K, Nygren J, Bringman S, Löfgren J, Sjövall A, Nordenvall C, et al. Trends in treatment of colorectal cancer and short-term outcomes during the first wave of the COVID-19 pandemic in Sweden. JAMA Netw Open. 2022;5:e2211065.
https://doi.org/10.1001/jamanetworkopen.2022.11065 DOI: https://doi.org/10.1001/jamanetworkopen.2022.11065
Howard LM, Barley EA, Davies E, Rigg A, Lempp H, Rose D, et al. Cancer diagnosis in people with severe mental illness: practical and ethical issues. Lancet Oncol. 2010;11:797–804.
https://doi.org/10.1016/S1470-2045(10)70085-1 DOI: https://doi.org/10.1016/S1470-2045(10)70085-1
Miovic M, Block S. Psychiatric disorders in advanced cancer. Cancer. 2007;110:1665–76.
https://doi.org/10.1002/cncr.22980 DOI: https://doi.org/10.1002/cncr.22980
Additional Files
Published
How to Cite
License
Copyright (c) 2025 Erik Osterman, Elisavet Syriopoulou, Anna Martling, Therese M-L Andersson, Caroline Nordenvall

This work is licensed under a Creative Commons Attribution 4.0 International License.
