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European cancer rehabilitation and survivorship, 2018: one of a kind

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In a world of digital solutions to almost every problem and a change in communication from a hand-written letter traveling for weeks over long distances to short messages reaching you… Click to show full abstract

In a world of digital solutions to almost every problem and a change in communication from a hand-written letter traveling for weeks over long distances to short messages reaching you within milliseconds – no matter where in the world, the question of whether we should continue to organize scientific meetings to present, discuss and reflect upon science and practice arises. Why not just organize a videoconference and transmit presentations to the remote audiences? When we initiated the European Cancer Rehabilitation and Survivorship meetings almost 10 years ago, we could not foresee the success in terms of participation, eagerness to present and the bibliometric success of the publications emerging from these bi-annual symposia generously sponsored by Acta Oncologica. In short, during these 10 years, we organized five ECRS symposia and produced 140 papers of which many are among the most downloaded and cited papers published in Acta Oncologica [1–4]. We have had attendees from all over the world, many returning enjoying the spirit and fellowship of the ECRS. This is a remarkable achievement as the field of survivorship in broad terms is quite new. Although the term cancer survivor was introduced back in the 1980s [5], it has not been many years since the term survivorship was launched by clinical societies like IOM and ASCO [6,7] on the background of a population of cancer survivors which today is growing almost exponentially. Many of these cancer survivors are living complex everyday lives as about 50% of them have one or more additional chronic condition at the time of diagnosis and close to 30% use five or more prescribed medications on a daily basis— data coming from a nationwide and population-based study in Denmark (unpublished data). Not only the cancer disease and the aftermath of treatment require attention and followup but also other health problems and conditions. Looking at the population of survivors, they have a higher risk of hospitalization for a broad range of incident somatic diseases after the cancer diagnosis than cancer-free people in comparison, most pronounced in the first years after the cancer diagnosis [8]. In combination, this information points to the need for an ampler model of follow-up considering all diseases affecting an individual, not only the cancer, and thereby moving the care from disease specific to a comprehensive personalized intervention in line with the general idea of personalized genotyped treatment of disease. The course and risk of late effects in childhood cancer survivors are well described and risk factors identified are all closely related to the specific treatment provided for the cancer disease. In adults, we need more knowledge in order to prevent, detect early and treat late effects, which may have a more systemic character such as depression, fatigue, or pain. Some late effects and symptoms may be a result of surgery like lymphedema, ostomies, and speech problems or an effect of radiation therapy such as chronic diarrhea, cardiovascular effects, or pulmonary changes or chemotherapy like peripheral neuropathies [9]. Numerous late effects may be listed associated with the specific treatment. Probably, these symptoms and diseases require symptomatic treatment. This implies, that we in principle define the post-treatment symptoms as normal symptoms and not specific for cancer patients or cancer treatment. Cancer and its treatment cause other chronic diseases and these diseases must be addressed just as we treat these diseases when they occur in persons not characterized by being cancer patients. This fifth ECRS symposium had a strong track of late effect researchers presenting data and perspectives in this field of research. The newly establishment of three Danish late effect research units covering separate research themes; general late effects as well as late effects after breast cancer and after pelvic cancer diseases. In a collaboration between these national units, research results may inform the development of guidelines for clinical practice in most common late effects (www.cancer.dk/bedrevidenomsenfoelger [In Danish]). Likewise, the papers selected for publication from the symposium cover diverse aspects of survivorship research. Research on prehabilitation and optimization of patients to provide better foundations for better survivorship among patients is a fast growing area and is represented by papers on prehabilitation before surgery [10–12]. Also papers address Patient Reported Outcomes (PRO) use and readiness

Keywords: european cancer; treatment; survivorship; late effects; cancer; research

Journal Title: Acta Oncologica
Year Published: 2019

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