EDITORIAL
Anja Mehnert-Theuerkaufa,
, Susanne Oksbjerg Daltonb,c,d
and Christoffer Johansenb,c,e
aDepartment of Medical Psychology and Medical Sociology, Comprehensive Cancer Center Central Germany (CCCG), University Medical Center Leipzig, Leipzig, Germany; bCancer Survivorship, Danish Cancer Institute, Copenhagen, Denmark; cFaculty of Health Sciences, Institute of Clinical Medicine, Copenhagen University, Copenhagen, Denmark; dDepartment of Clinical Oncology and Palliative Care, Zealand University Hospital, Næstved, Denmark; eDepartment of Oncology, CASTLE, Copenhagen University Hospital, Copenhagen, Denmark
Citation: ACTA ONCOLOGICA 2025, VOL. 64, 458–461. https://doi.org/10.2340/1651-226X.2025.43076.
Copyright: © 2025 The Author(s). Published by MJS Publishing on behalf of Acta Oncologica. This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/).
Received: 1 February 2025; Accepted: 1 March 2025; Published: 19 March 2024
CONTACT Anja Mehnert-Theuerkauf anja.mehnert@medizin.uni-leipzig.de Department of Medical Psychology and Medical Sociology, Comprehensive Cancer Center Central Germany (CCCG), University Medical Center Leipzig, Leipzig, Germany
Competing interests and funding: The ECRS 2024 conference was financially supported by an unrestricted educational grant from Acta Oncologica.
Over the past decades, the global burden of disease has shifted from communicable to non-communicable diseases (NCDs) and from premature death to years of life with disability [1]. NCDs, however, are responsible for 41 million deaths per year globally, accounting for 74% of all deaths worldwide. Together with cardiovascular diseases, chronic respiratory diseases and diabetes, cancer is one of the four prevalent diseases responsible for over 80% of all premature NCD deaths [1].
The good news is that numerous studies now show relatively consistently that about 40% of cancers as well as other NCDs could be prevented [2, 3]. However, this number is also disappointing from a public health perspective: Risk modification has played a relatively minor role in recent years, although it has great potential to improve the health of both individuals and society as a whole [4, 5]. As often described, tobacco and harmful alcohol consumption, physical inactivity, unhealthy diet and metabolic risks as well as infections and air pollution increase the risk of dying from cancer – risks, some of which could certainly be modified [6, 7].
These findings are also highly relevant to cancer survivorship. In addition to biological factors, the risk of disease progression, recurrence or second primary cancers is also associated with lifestyle habits [8, 9]. Consequently, adopting a healthy lifestyle is imperative in order to prevent and alleviate the occurrence of serious biopsychosocial late- and long-term consequences [7, 10, 11]. For instance, a cancer-registry based study of depression and anxiety in long-term hematologic cancer survivors demonstrated a significantly elevated relative risk for anxiety and depression, persisting for more than 12 years following diagnosis, in comparison to the age- and gender-matched comparison sample from the general population. Patients in middle age, around 65 years, were particularly affected [12]. The detrimental effects of depression on health [13] are significant, including its considerable impact on quality of life and the development of secondary conditions, such as cardiovascular late effects, in addition to chemo-radio toxicities. These factors emphasise the importance of early detection and treatment of psychosocial distress [14–16], as well as the implementation of healthy lifestyle changes [17, 18].
Nevertheless, evidence shows that despite the potential of a cancer diagnosis to encourage people to adopt a healthier lifestyle, a significant proportion of cancer survivors are physically inactive and overweight. Only a small proportion between 7 and 40% follow the recommendations for a healthy lifestyle [19, 20]. Lower health literacy is one of the main underlying causes associated with lower socioeconomic status, high comorbidities, lack of resources and barriers to timely access to health services and effective treatments [21–24].
The importance of strengthening health literacy and tertiary prevention in the context of cancer survivorship is particularly plausible in view of the fact that we are dealing with an increasingly large and ageing cancer population that not only suffers from cancer, but also from a high level of comorbidity overall [25, 26]. The title chosen by the authors Bluethmann et al. [27] for their paper ‘anticipating the silver tsunami’, published almost 10 years ago, may have been somewhat gimmicky, but it also gets to the heart of the problem. According to the prognoses, the majority of cancer survivors will be over 75 years old in 2040 [27, 28].
The European Cancer Survivorship and Rehabilitation Symposium (ECRS) 2024 in Copenhagen demonstrated the extensive nature of the biopsychosocial late- and long-term problems, which are closely interlinked. Thematic areas of focus encompassed novel immunotherapies for haematological malignancies, mental health challenges, lymphoedema, sexual dysfunction, survival after metastatic cancer and enhancing the quality of care for survivors of rare cancers.
A significant theme of the conference was research into the long-term and late effects of cancer therapies, which have been shown to limit the quality of life of patients both with cancer-free survivals and those with metastasised cancer. Larsen et al. [29] emphasise the need for a broader approach to the treatment of lymphoedema in different cancer diagnoses, as lymphoedema symptoms are common among cancer survivors and correlate with more depression and pain disorders as well as lower health-related quality of life (HRQoL). The findings by Pappot et al. [30] demonstrated that increased toxicity across all lines of treatment contributes to an impaired quality of life, thus emphasising the necessity of treating both acute and chronic symptoms in the care of metastatic breast cancer survivors. Clear communication about prognosis is vital for informed decision-making and aligning care with patients’ life goals. New care models should blend survivorship and palliative care, focusing on equitable access to tailored services, considering recent treatment and prognosis changes in patients with advanced or metastatic cancer such as the care model presented by Lai-Kwon et al. [31].
Langballe et al. [32] address the issue of long-term distress and the usefulness of distress screening in the context of breast cancer survivorship. With regard to cancer surveillance in the survivorship phase, Lindahl et al. [33] emphasise a risk-adapted surveillance approach based on identified risk factors for relapse in seminoma survivors. Stegenborg et al. [34] deal with socioeconomic disparities and childhood cancer survival, particularly with regard to children from disadvantaged families.
Thyø et al. [35] and Nahavandipour et al. [36] looked at sexual dysfunction and sexual stress in cancer survivors and showed that almost half of sexually active men with rectal cancer resigned from their sex life within a year due to erection problems [35] and that the prevalence of sexual stress and impairment is high in men with different types of cancer [36]. Both studies underscore the fact that healthcare professionals should pay more attention to sexual health in all men with cancer.
A number of articles examined the effectiveness of interventions for various symptoms and problems in cancer survivors, such as quality of life, work ability or sleep. These interventions included the Guided Self-Determination (GSD) programme in the MyHealth study [37, 38] and the SleepNow intervention [39].
However, despite our growing understanding of the variety of survivorship challenges, it is evident that we are only at the beginning of actually establishing and implementing cancer survivorship care plans that are grounded in empirical evidence and demonstrate tangible effectiveness [40]. In the context of health services and implementation research, the existence of effective interventions and programmes is not the only relevant consideration. Equally important is research into effective ways of implementing these programmes in everyday care, with a view to ensuring optimal target group care.
The demographic shift towards an ageing population combined with a lack of health literacy poses a major challenge for health policy and for us as a society. Achieving good functional health after a cancer diagnosis is therefore an important goal of cancer survivorship research for the coming years. Functional capacity plays a central role in shaping the health of the population as a whole and the well-being of society, emphasising the importance of health both for the individual and for society as a whole [41]. Functional health has recently been posited as a third health indicator alongside morbidity and mortality [41]. In the new model, functional health comprises two aspects: biological health, which refers to the physiological and psychological functions and anatomical structures of the body that represent an individual’s intrinsic ability to perform human activities; and lived health, which refers to the actual performance of activities in interaction with the physical, built and social environment.
In order to achieve better biopsychosocial outcomes and enhanced functional health following a cancer diagnosis, further research is required to address the following dimensions [42, 43]: Firstly, the enhancement of (tertiary) prevention and the implementation of a healthier lifestyle, particularly among high-risk groups, should be prioritised. This encompasses the cessation of tobacco and alcohol consumption, the adoption of a healthy diet and maintenance of optimal body weight, the engagement in regular exercise, the utilisation of sun protection measures, the mitigation of exposure to air pollution, and the completion of human papillomavirus vaccinations. Secondly, the reinforcement of health literacy, the facilitation of early detection and screening measures, and the enhancement of treatment and comprehensive care are imperative. This encompasses the collaborative management of treatment and health goals, and the facilitation of access to supportive services that promote physical and psychosocial wellbeing.
[1] GBD 2019 Cancer Risk Factors Collaborators. The global burden of cancer attributable to risk factors, 2010–19: a systematic analysis for the Global Burden of Disease Study 2019. Lancet. 2022;400(10352):563–91. https://doi.org/10.1016/S0140-6736(22)01438-6
[2] Mons U, Gredner T, Behrens G, Stock C, Brenner H. Cancers due to smoking and high alcohol consumption. Dtsch Arztebl Int. 2018;115(35–36):571–7. https://doi.org/10.3238/arztebl.2018.0571
[3] Magnussen C, Ojeda FM, Leong DP, Alegre-Diaz J, Amouyel P, Aviles-Santa L, et al. Global effect of modifiable risk factors on cardiovascular disease and mortality. N Engl J Med. 2023;389(14):1273–85. https://doi.org/10.1056/NEJMoa2206916
[4] Kvaavik E, Weemes Grøtting M, Halkjelsvik T, van Helvoirt R, Kirkhorn IH, Bjaanes MM, et al. The effect of a smoking cessation program for patients in cancer treatment: a quasi-experimental intervention study. Acta Oncol. 2023;62(12):1890–7. https://doi.org/10.1080/0284186X.2023.2277883
[5] Lauridsen SV, Jensen BT, Tønnesen H, Dalton SO, Rasmussen M. The gold standard program (GSP) for smoking cessation: a cohort study of its effectiveness among smokers with and without cancer. Acta Oncol. 2023;62(7):774–81. https://doi.org/10.1080/0284186X.2023.2228445
[6] Sipilä LJ, Tanskanen T, Heikkinen S, Seppä K, Aavikko M, Ravantti J, et al. Cancer incidence following non-neoplastic medical conditions: a prospective population-based cohort study. Acta Oncol. 2024;63:841–9. https://doi.org/10.2340/1651-226X.2024.40757
[7] Andersen R, Rostgaard K, Pedersen O, Jemec GBE, Hjalgrim H. Increased cancer incidence among patients with hidradenitis suppurativa – a Danish nationwide register study 1977–2017. Acta Oncol. 2024;63:220–8. https://doi.org/10.2340/1651-226X.2024.26182
[8] Jahreiß MC, Incrocci L, Aben KKH, De Vries KC, Hoogeman M, Hooning MJ, et al. The impact of baseline health factors on second primary cancer risk after radiotherapy for prostate cancer. Acta Oncol. 2024;63:511–17. https://doi.org/10.2340/1651-226X.2024.24334
[9] Nikkilä R, Hirvonen E, Haapaniemi A, Tapiovaara L, Pitkäniemi J, Malila N, et al. Significant risk of second primary cancer among laryngeal squamous cell carcinoma patients even after 20 years. Acta Oncol. 2023;62(10):1322–30. https://doi.org/10.1080/0284186X.2023.2254482
[10] Koivisto HAM, Nevala AO, Miettinen JM, Pitkäniemi JM, Malila NK, Heikkinen SMM. Relative risk of second malignant neoplasms highest among young adult cancer patients – a population-based registry study in Finland. Acta Oncol. 2024;63:418–425. https://doi.org/10.2340/1651-226X.2024.34138
[11] Ataei A, Deng J, Muhammad W. Liver cancer risk quantification through an artificial neural network based on personal health data. Acta Oncol 2023;62(5):495–502. https://doi.org/10.1080/0284186X.2023.2213445
[12] Kuba K, Esser P, Mehnert A, Hinz A, Johansen C, Lordick F, et al. Risk for depression and anxiety in long-term survivors of hematologic cancer. Health Psychol. 2019;38(3):187–95. https://doi.org/10.1037/hea0000713
[13] Gold SM, Köhler-Forsberg O, Moss-Morris R, Mehnert A, Miranda JJ, Bullinger M, et al. Comorbid depression in medical diseases. Nat Rev Dis Primers. 2020;6(1):69. https://doi.org/10.1038/s41572-020-0200-2
[14] Dahl AA, Smeland KB, Eikeland S, Fagerli UM, Bersvendsen HS, Fosså A, et al. Distressed personality is associated with late adverse effects in long-term survivors of Hodgkin lymphoma. Acta Oncol. 2024;63:600–6. https://doi.org/10.2340/1651-226X.2024.40312
[15] Romare Strandh M, Enebrink P, Stålberg K, Sörensdotter R, Ljungman L, Wikman A. Parenting under pressure: a cross-sectional questionnaire study of psychological distress, parenting concerns, self-efficacy, and emotion regulation in parents with cancer. Acta Oncol. 2024;63:468–76. https://doi.org/10.2340/1651-226X.2024.40404
[16] Springer F, Kuba K, Ernst J, Friedrich M, Glaesmer H, Platzbecker U, et al. Symptoms of posttraumatic stress disorder and adjustment disorder in hematological cancer patients with different treatment regimes. Acta Oncol. 2023;62(9):1110–17. https://doi.org/10.1080/0284186X.2023.2239477
[17] Kreiberg M, Bandak M, Lauritsen J, Wagner T, Rosenvilde J, Agerbaek M, et al. Adverse health behaviours in long-term testicular cancer survivors: a Danish nationwide study. Acta Oncol. 2021;60(3):361–9. https://doi.org/10.1080/0284186X.2020.1851765
[18] Scherer-Trame S, Jansen L, Arndt V, Chang-Claude J, Hoffmeister M, Brenner H. Inpatient rehabilitation therapy among colorectal cancer patients – utilization and association with prognosis: a cohort study. Acta Oncol. 2021;60(8):1000–10. https://doi.org/10.1080/0284186X.2021.1940274
[19] Bøhn SH, Lie HC, Reinertsen KV, Fosså SD, Haugnes HS, Kiserud CE, et al. Lifestyle among long-term survivors of cancers in young adulthood. Support Care Cancer. 2021;29(1):289–300. https://doi.org/10.1007/s00520-020-05445-6
[20] Tollosa DN, Tavener M, Hure A, James EL. Adherence to multiple health behaviours in cancer survivors: a systematic review and meta-analysis. J Cancer Surviv. 2019;13(3):327–43. https://doi.org/10.1007/s11764-019-00754-0
[21] Halgren Olsen M, Maltesen T, Lassen P, Kjaer TK, Johansen J, Primdahl H, et al. Socioeconomic position and the pre-diagnostic interval among patients diagnosed with head and neck squamous cell carcinoma – a population-based study from DAHANCA. Acta Oncol. 2023;62(11):1394–402. https://doi.org/10.1080/0284186X.2023.2254478
[22] Fuhrmann J, Heinävaara S, Sarkeala T, Lehtinen M, Pankakoski M. Coverage of mammography imaging in and outside an organized breast cancer screening program – variation by age and sociodemographic groups. Acta Oncol. 2024;63:833–40. https://doi.org/10.2340/1651-226X.2024.40830
[23] Paakkola NM, Jekunen A, Sihvo E, Johansson M, Andersén H. Area-based disparities in non-small-cell lung cancer survival. Acta Oncol. 2024;63:146–53. https://doi.org/10.2340/1651-226X.2024.27507
[24] Ibfelt EH, Jensen H, Vrou Offersen B, Bang Hansen M, Møller H, Christiansen P, et al. Diagnosis and treatment of breast cancer in Denmark during the COVID-19 pandemic: a nationwide population-based study. Acta Oncol. 2023;62(12):1749–56. https://doi.org/10.1080/0284186X.2023.2259598
[25] Thomsen MK, Løppenthin KB, Bidstrup PE, Andersen EW, Dalton S, Petersen LN, et al. Impact of multimorbidity and polypharmacy on mortality after cancer: a nationwide registry-based cohort study in Denmark 2005–2017. Acta Oncol. 2023;62(12):1653–60. https://doi.org/10.1080/0284186X.2023.2270145
[26] Spampinato S, Rancati T, Waskiewicz JM, Avuzzi B, Garibaldi E, Faiella A, et al. Patient-reported persistent symptoms after radiotherapy and association with quality of life for prostate cancer survivors. Acta Oncol. 2023;62(11):1440–50. https://doi.org/10.1080/0284186X.2023.2259597
[27] Bluethmann SM, Mariotto AB, Rowland JH. Anticipating the ‘Silver Tsunami’: prevalence trajectories and comorbidity burden among older cancer survivors in the United States. Cancer Epidemiol Biomarkers Prev. 2016;25(7):1029–36. https://doi.org/10.1158/1055-9965.EPI-16-0133
[28] Miller KD, Nogueira L, Devasia T, Mariotto AB, Yabroff KR, Jemal A, et al. Cancer treatment and survivorship statistics, 2022. CA Cancer J Clin. 2022;72(5):409–36. https://doi.org/10.3322/caac.21731
[29] Larsen GS, Johansen C, Von Heymann A, Rafn BS. Prevalence of lymphedema symptoms across cancer diagnoses and association with depression, pain interference and health-related quality of life. Acta Oncol. 2025;64:87–95. https://doi.org/10.2340/1651-226X.2025.42203
[30] Pappot H, Jørgensen A, Bjørum AH, Jakobsen CB, Jørgensen CU, Høeg BL, et al. Understanding quality of life in Danish women with metastatic breast cancer undergoing multiple treatments. Acta Oncol. 2025;64:292–302. https://doi.org/10.2340/1651-226X.2025.42446
[31] Lai-Kwon J, Heynemann S, Hart N, Chan RJ, Smith T, Smith AL, et al. Delivering improved survivorship care for people affected by advanced or metastatic cancer. Acta Oncol. 2024;63:939–42. https://doi.org/10.2340/1651-226X.2024.42197
[32] Langballe R, Mertz B, Kroman N, Maltesen T, Rosthøj S, Envold Bidstrup P. Are breast cancer patients with low distress at diagnosis at risk of psychological symptoms later in their disease trajectory? Considerations for when to screen for distress. Acta Oncol. 2025;64:105–13. https://doi.org/10.2340/1651-226X.2025.42367
[33] Lindahl NB, Lauritsen J, Wagner T, Daugaard G, Bandak M. Relapse detection in the Danish surveillance program of patients with clinical stage I seminoma: a nationwide study. Acta Oncol. 2025;64:191–9. https://doi.org/10.2340/1651-226X.2025.42281
[34] Stegenborg F, Bek M, Nilsson C, Pedersen LH, Scheike T, Hjalgrim L, et al. Socioeconomic characteristics and relapse-free and overall survival from childhood cancer – a nationwide study based on data from the Danish Childhood Cancer Registry. Acta Oncol. 2025;64:179–87. https://doi.org/10.2340/1651-226X.2025.42131
[35] Thyø A, Christensen P, Gögenur I, Krogsgaard M, Lauritzen MB, Laursen BS, et al. The decline of male sexual activity and function after surgical treatment for rectal cancer. Acta Oncol. 2025;64:47–55. https://doi.org/10.2340/1651-226X.2025.42015
[36] Nahavandipour J, Johansen C, Giraldi A, Rafn BS, Von Heymann A. Sexual distress among men with cancer – a cross-sectional study. Acta Oncol. 2025;64:214–21. https://doi.org/10.2340/1651-226X.2025.42525
[37] Biener SN, Høeg BL, Saltbæk L, Dalton SO, Johansen C, Karlsen RV, et al. Fidelity of the guided self-determination program in the MyHealth study during breast cancer follow-up. Acta Oncol. 2025;64:284–91. https://doi.org/10.2340/1651-226X.2025.42253
[38] Horsbøl TA, Saltbæk L, Urhammer C, Karlsen RV, Johansen C, Bidstrup PE, et al. Work ability following breast cancer – the MyHealth randomized controlled trial. Acta Oncol. 2025;64:34–9. https://doi.org/10.2340/1651-226X.2025.42221
[39] Høeg BL, Løppenthin KB, Savard J, Johansen C, Christensen JF, Svendsen MN, et al. SleepNow – a combined cognitive behavioral therapy for insomnia and physical exercise intervention in men with metastatic prostate cancer: results from a feasibility randomized controlled trial. Acta Oncol. 2025;64:222–8. https://doi.org/10.2340/1651-226X.2025.42246
[40] van de Poll-Franse LV, Nicolaije KA, Ezendam NP. The impact of cancer survivorship care plans on patient and health care provider outcomes: a current perspective. Acta Oncol. 2017;56(2):134–8. https://doi.org/10.1080/0284186X.2016.1266080
[41] Bickenbach J, Rubinelli S, Baffone C, Stucki G. The human functioning revolution: implications for health systems and sciences. Front Sci. 2023;1:1118512. https://doi.org/10.3389/fsci.2023.1118512
[42] Liu ZY, Wang C, Zhang YJ, Zhu HL. Combined lifestyle, mental health, and mortality in US cancer survivors: a national cohort study. J Transl Med. 2022;20(1):376. https://doi.org/10.1186/s12967-022-03584-4
[43] Arnold M, Rutherford MJ, Bardot A, Ferlay J, Andersson TM, Myklebust TÅ, et al. Progress in cancer survival, mortality, and incidence in seven high-income countries 1995–2014 (ICBP SURVMARK-2): a population-based study. Lancet Oncol. 2019;20(11):1493–505. https://doi.org/10.1016/S1470-2045(19)30456-5