The European Cancer Patient Coalition and its central role in connecting stakeholders to advance patient‐centric solutions in the mission on cancer

There is an urgent need for solutions to the economic and social inequalities in cancer care that still exist in many European countries. Patient preferences, ‘big data’, mobile digital technology and molecular and genomic profiling are among the innovative research topics that connect cancer patients to comprehensive cancer centres, and link translational research to cancer diagnosis, treatment and care. The question is whether Europe can deliver the complex infrastructure needed for universal coverage and equitable access to cancer care. The European Cancer Patient Coalition (ECPC), the leading ‘umbrella’ cancer patient organisation in Europe, has a central role in bringing the unmet needs of patients with cancer to the forefront of cancer policy, care and research. The ECPC is a respected and reliable partner in the oncology community and has effectively collaborated with institutional stakeholders and organisations, as well as with the European Commission, on cancer research projects and in the development of tools to advance health care and cancer policies at the European and national level. The ECPC believes that innovation cannot emerge and grow without patient involvement and is fully committed to increasing patient education and contribution in cancer research through its active participation in various European cancer research programmes and educational resources. The ECPC is expected to play a major role in the mission on cancer, given its previous achievements in policy and research to help overcome the inequalities in cancer prevention, treatment, rehabilitation and survivorship care. The mission on cancer will be facilitated by active collaboration between patient organisations and scientists, clinicians, politicians and industry, with the aim of identifying important research questions regarding quality of life and social issues for cancer patients of all ages.

There is an urgent need for solutions to the economic and social inequalities in cancer care that still exist in many European countries. Patient preferences, 'big data', mobile digital technology and molecular and genomic profiling are among the innovative research topics that connect cancer patients to comprehensive cancer centres, and link translational research to cancer diagnosis, treatment and care. The question is whether Europe can deliver the complex infrastructure needed for universal coverage and equitable access to cancer care. The European Cancer Patient Coalition (ECPC), the leading 'umbrella' cancer patient organisation in Europe, has a central role in bringing the unmet needs of patients with cancer to the forefront of cancer policy, care and research. The ECPC is a respected and reliable partner in the oncology community and has effectively collaborated with institutional stakeholders and organisations, as well as with the European Commission, on cancer research projects and in the development of tools to advance health care and cancer policies at the European and national level. The ECPC believes that innovation cannot emerge and grow without patient involvement and is fully committed to increasing patient education and contribution in cancer research through its active participation in various European cancer research programmes and educational resources. The ECPC is expected to play a major role in the mission on cancer, given its previous achievements in policy and research to help overcome the inequalities in cancer prevention, treatment, rehabilitation and survivorship care. The mission on cancer will be facilitated by active collaboration between patient organisations and scientists, clinicians, politicians and industry, with the aim of identifying important research questions regarding quality of life and social issues for cancer patients of all ages.

Introduction
Europe has played an important role in cancer control. Over the past 30 years, the European Union (EU) has worked alongside its Member States and various stakeholders to control the disease through adequate cancer research and cancer policy. Despite advances in these areas, several unmet needs remain, such as knowledge gaps between patients' outcomes and clinical practice, analysis of the added value of innovation to patients in the real-world setting, timely implementation of innovation in clinical cancer pathways and the overall assessment of the quality of cancer care. Patient involvement in research and treatment decisions is a vital contribution that can influence and impact the advancement of cancer management and care.
The European Cancer Patient Coalition (ECPC), established in 2003, is Europe's largest 'umbrella organisation', consisting of almost 450 cancer patient organisations in 46 countries. The vision of ECPC is to work towards a Europe of equality, where all European cancer patients have timely and affordable access to the best treatment and care available throughout their life. The main priorities of the ECPC are listed in Box 1.
The ECPC plays an essential role in Europe by effectively acting as the voice of cancer patients. The organisation is committed to representing patients' interests and proposing patient-centric solutions to cancer-related problems. As such, the ECPC has been a critical stakeholder in defining cancer policy in Europe. Importantly, the ECPC has been raising awareness of the key issues that lead to disparities in cancer care; it has also been making practical recommendations to bridge the gap between cancer policy and cancer care practice. Supported by the ECPC capacitybuilding strategy, its member patient organisations have the vital role of advocating for cancer policy recommendations at the national level.
The ECPC has worked with the European Commission on the joint actions against cancer, the European Partnership for Action Against Cancer (EPAAC) and the Joint Action on Cancer Control (CanCon), to standardise the approach of reducing the cancer burden in Europe through the development of guidelines for the harmonisation of National Cancer Plans. The CanCon Guide, a comprehensive, patient-centric document and a vital tool for governments and policymakers to improve cancer care, is the main deliverable of CanCon that represents an important example of European collaboration in cancer control. This is because each of the cooperating 17 EU Member States and their respective Ministries of Health were directly involved in developing the final recommendations and policies in collaboration with several other stakeholders. The ECPC was a diligent partner in this enterprise, playing a pivotal role in connecting cancer patients with other stakeholders. The ECPC enabled patients to share their own experiences, and their views were included in the very core of the CanCon methodology, work model and final outcomes. As such, the Joint Action on Cancer Control can be viewed as a milestone in cancer policy for all European patients with cancer.
At the level of the European Parliament, the European Cancer Patient's Bill of Rights was launched on World Cancer Day 2014 by the European Cancer Concord and the ECPC. This Bill was the result of an equal partnership between patients, their advocates and cancer health professionals. It was considered a 'catalyst for change' that recognises the right of each European citizen to optimal and timely access to specialised cancer care, underpinned by research and innovation (Højgaard et al., 2017;Lawler et al., 2014). The ECPC has also collaborated closely with the European Parliament to promote key cancer policies that have been successfully implemented [such as the development of amendments to health technology assessment (HTA) regulations to harmonise HTA at the EU level, a policy recommendation first outlined in the ECPC position paper 'Challenging the Europe of disparities in cancer' in 2015 (European Cancer Patient Coalition, 2015; Fig. 1)], highlighting that patients play a crucial role in advancing policies.
The ECPC has worked with a significant number of oncology and cancer care stakeholders to build a broad consensus on issues important to European cancer patients. These partnerships continue to effectively foster a European community of like-minded cancer experts. The level of cooperation in CanCon and other European Commission cancer-related initiatives (Table 1; Albreht et al., 2017;Grilli et al., 2017;Peir o P erez et al., 2017) should serve as a model on how to involve and interact with patient organisations. The ECPC has also established multiple key alliances between patients and relevant stakeholders/organisations (Table 2; European Cancer Patient Coalition, 2018a). It has further sought to improve the level of collaboration and communication of cancer patients and families with the cancer centres in which they are treated. The active cooperation of patients and families with European cancer centres through open 2-way communication was the objective of the ECPC's collaboration with the Organisation of European Cancer Institutes (OECI), which resulted in joint initiatives of ECPC members with OECI-certified comprehensive cancer centres.
The ECPC is involved in several European research projects (Table 3) and collaborates with the consortium Cancer Core Europe, a patient-centred infrastructure that aims to address the cancer care-cancer research continuum challenge in partnership with major European accredited cancer centres (Eggermont et al., 2014). The role of the ECPC in Cancer Core Europe is to bridge the gap between cancer research and high-quality cancer care, strengthened through quality assurance accreditation, and link both to cancer policy. This role is enhanced through the ECPC's involvement in several important EU-funded cancer research projects. Herein, we further describe the achievements and aims of patient organisations to demonstrate how they can play a major role in the mission on cancer.

Immuno-Oncology Policy Action Framework
The

Expert Group on Cancer Control
The ECPC has representatives in the Expert Group, which was established in 2016 to assist with the preparation of legislative proposals and policy initiatives concerning cancer.

Patients' inequalities, priorities, and innovative solutions
Patient-centric approaches in research, medical education, and cancer management and care delivery are critical to an evolving paradigm in cancer care. Currently, various unacceptable inequalities exist across Europe regarding cancer care and rehabilitation and reintegration of people with cancer and cancer survivors in social and professional life. Such inequalities include unequal access to curative cancer treatments; extreme variability and accessibility in cancer screening services; lack of patient-accessible, accurate, and up-to-date information; fragmented or missing cancer rehabilitation services; poor governance; major organisational, structural, and fiscal deficits in health planning; and the lack of a citizenfocused European cancer survivorship plan To establish virtual networks connecting healthcare providers and other stakeholders across Europe with the aim to tackle complex or rare diseases and conditions requiring highly specialised treatment and a wealth of knowledge and resources.
European Liquid Biopsy Academy (ELBA) To educate and provide researchers with skills required to ensure effective development and commercialisation of liquid biopsy approaches.
PREDICT Innovative Training Network To educate researchers in the fields of radiomics and personalised medicine.

Nutrition in cancer care
To analyse the dimension of nutritional alterations among cancer patients and survivors in Europe (Muscaritoli et al., 2017).

Funded by Innovative Medicines Initiative (IMI)
PREFER patient preferences To strengthen patient-centric decision making throughout the life cycle of medicinal products by developing evidence-based recommendations to guide industry, regulatory authorities, health technology assessment (HTA) bodies, reimbursement agencies, academia and healthcare professionals on how and when patient-preference studies should be performed, and the results used to support and inform decision making.

DO-IT Big Data for Better Outcomes
To facilitate the use of 'big data' to promote the development of value-based, outcome-focused healthcare systems in Europe.

PIONEER Big Data for Better Outcomes
To use big data to improve outcomes for prostate cancer.

Funded by Horizon 2020
Transcan-2 European Research Area To contribute to the building of the European Research Area through the coordination of activities of national and regional translational cancer research funding organisations, aiming at the integration of basic, clinical and epidemiologic cancer research and facilitation of transnational cancer funding in Europe with the ultimate aim to streamline EU-wide cancer screening, early diagnosis, prognosis, treatment and care.

DENIM H2020MM04
To demonstrate the efficacy of dendritic cell-based immunotherapy in a randomised phase 2-3 clinical trial in mesothelioma.

IMMUNISA
In a multicentre, randomised phase 2 clinical trial called CervISA-2, IMMUNISA will investigate whether a therapeutic cancer vaccine in combination with chemotherapy can prolong the progression-free survival and overall survival of patients with recurrent or metastatic cervical cancer.  2017), which has been signed by the 17 Member States. In brief, the paper advocates cancer diagnosis and treatment in comprehensive centres of excellence to ensure that patients benefit from high-quality multidisciplinary approaches, surgical expertise, and technological advances, thus increasing their chances of survival. The ECPC also recommends timely access to screening programmes and early diagnosis as preventative strategies.
In line with the CanCon recommendations, EU Member States should establish or update and implement National Cancer Plans, which are currently lacking or are inadequately resourced in many EU countries. Population-based national cancer registries and biobanking are the basic tools for planning and formulating national cancer and national cancer research policies. A multidisciplinary team-based strategy for cancer should be adopted by all Member States, providing a patient-centred approach that addresses all aspects of the cancer journey. Together with the ECPC, all cancer stakeholders should jointly or individually exert pressure on national governments of Member States to ensure implementation of the CanCon policy recommendations.
Access to new treatments remains one of the most significant inequalities across Europe. Currently, patients with cancer face the paradox of life-saving new treatments becoming available but not accessible to them, depending on which Member State they reside in. There are significant variations in pricing and reimbursement decisions made by EU national governments, which twinned with the lack of a harmonised HTA policy (Ades et al., 2014) results in unacceptable delays in access to new treatments. If pricing and/or reimbursement methods remain as they currently are, patient access to innovative treatments such as immunotherapy and biologics and new biomarker testing methodologies and companion diagnostic kits will continue to involve difficulties. This will lead to even greater inequalities than previously experienced.
The ECPC has created momentum on EU cooperation in HTA during the process of amending regulation 726/2004, 'laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency', when the proposed amendments were voted by the European Parliament in March 2016. The ECPC response to the European Commission's 2017 consultation on 'Strengthening of the EU cooperation on Health Technology Assessment' stated that increased EU cooperation will cut costs and duplication of efforts across HTA bodies, decrease the delay in access to innovative health technologies, facilitate participation of patient organisations in the HTA decision-making process and facilitate access to market.

Patient-centred research
The primary missions of the ECPC are to educate patients, increase their involvement in research and to disseminate information about cancer and cancer research results to the general public. This active engagement of patients is vital to improving the quality of health care in Europe and to understanding patient preferences about their treatment and care, and they are crucial elements of patient-centred care.
Research projects allow the ECPC to be at the forefront of scientific developments, and the organisation is actively involved in the design and implementation of various EU-funded projects (summarised in Table 3). Within these projects, the ECPC emphasises the importance of involving patients as coresearchers and strongly advocates for patients' early participation in defining research priorities and patient-centric treatment decisions. The ECPC encourages a strong partnership between researchers, cancer centres and patients that allows the latter to share their unique experiences, with the aim of achieving a more patient-centric approach to cancer research and care. The ECPC offers several resources as part of its capacity-building strategy to guide its member organisations on the crucial role of patients in clinical trials and research programmes. An important project to highlight the advancement of patients' involvement in research is the Innovative Medicines Initiative (IMI) Project Patient Preferences in Benefit-Risk Assessments during the Drug Life Cycle (PREFER). The initiative aims to provide evidencebased recommendations to support guidelines development on how patient preferences should be assessed to inform decision making (de Bekker-Grob et al., 2017).

Sustainability
To ensure the sustainability and access to innovative cancer care and treatment in European healthcare systems, resources must be secured through budget increases and/or reallocation of resources to interventions and treatments meaningful to patients. To achieve this, current medical and healthcare practices should be continuously re-evaluated to identify which practices are delivering sufficient value to patients in the most cost-effective way for health systems. This approach is outlined in the CanCon Policy Paper 'Enhancing the value of cancer care through a more appropriate use of healthcare interventions', which the ECPC co-authored. The paper includes recommendations on improving access to medicines, surgery, and radiotherapy by reducing waste and improving efficiency (Grilli et al., 2017), as well as making use of technology to improve cancer care. The ECPC's contribution helped to define the methodology used to identify healthcare interventions that do not provide sufficient value to patients with cancer and healthcare systems.

Survivorship and rehabilitation
Cancer survivorship can often be a lifelong struggle. In Europe, more than 3 million people are diagnosed with cancer every year, and nearly 2% of Europeans have been diagnosed with cancer within the previous 6 years (Ferlay et al., 2013). Approximately one-quarter of people who are living after a cancer diagnosis have already reached the same life expectancy as the general population (AIRTUM Working Group, 2014), and the proportion of people who will survive following a diagnosis of cancer is increasing by 3% each year (Guzzinati et al., 2018). For example, in Italy, cancer is now the most common noncommunicable disease responsible for disability pensions, with an even higher incidence than cardiovascular disease (Li Ranzi et al., 2013).
Despite these increasing numbers, almost all EU countries lack adequate policies to ensure rehabilitation and smooth reintegration of cancer survivors into social and professional life. At least one-quarter of cancer survivors face long-term poor health and disability. The increasing number of cancer survivors who require a disability pension impacts the health and social support systems of national governments.
Healthcare providers need to be made more aware of the importance of strategies to improve patient rehabilitation processes, as these are a crucial factor of successful survivorship (Baili et al., 2013;De Lorenzo et al., 2018). Cancer survivorship often focuses on the distinct phase of cancer care that takes place after the end of the acute phase of cancer treatment and may encompass the physical, mental and/or social aspects of living with, and after, a life-threatening cancer diagnosis. Consequently, although substantial progress has been made in survivorship research, especially in the area of immediate, persistent and late-term effects of cancer treatments, more research is needed into the early or late effects of cancer and its treatment, which may cause physical and psychosocial morbidity as well as premature death.
Following the adoption of new treatments in clinical guidelines and current clinical practice, long-term follow-up of patients receiving such treatments is required to study patient-reported outcomes (PROs) and their impact on the quality of life (QOL) of patients. The ECPC has contributed to the recommendations on survivorship, psychosocial support and rehabilitation already developed by the EPAAC and to those generated by CanCon in a chapter in the Can-Con guide titled 'Survivorship and rehabilitation: policy recommendations for quality improvement in cancer survivorship and rehabilitation in EU Member States' , which has been endorsed by all 17 participating EU Member States. These recommendations are provided for the development of quality national Survivorship Care Plan . This guidance offers actionable solutions for the rising number of patients surviving cancer and should serve as a valuable resource for all EU countries. While acknowledging that survivorship care should be an integral part of National Cancer Plans, the recommendations also underscore that more research on survivorship is required to generate data on late effects, as well as on the impact and cost-effectiveness of supportive care, rehabilitation, and palliative and psychosocial care interventions.
Following the release of the CanCon recommendations, and through its existing collaboration with the European Society for Medical Oncology (ESMO; Table 2; European Cancer Patient Coalition, 2018a), the ECPC proposed that a survivorship care follow-up plan should be put in place for all European patients with cancer. This resulted in the adoption and publication of the Survivorship Guide (ESMO Patient Guide Series. European Society for Medical Oncology, 2017) and was the first time that ESMO recognised the need for such a resource. The purpose of the Survivorship Care Plan, which has its roots in the CanCon Survivorship Work Package and the sustained ECPC advocacy efforts throughout the years, is to offer physicians and patients a concise but comprehensive summary of patient diagnosis and treatment in addition to follow-up care. The guide bridges the gap between the oncologist and the family doctor and empowers the person with cancer to ask the right questions to their healthcare team. It includes a section on the management of tumour-related symptoms and rehabilitation, as well as a survivorship checklist, to facilitate continuous care and return to a normal life. The intention is that vital information about a patient's cancer history is readily available to any oncologist or physician the patient may need to consult in the future. The ultimate objective is that the Survivorship Cancer Treatment Summary should become an integral part of the discharge instructions of cancer patients throughout Europe. The Survivorship Guide is a prime example of how the ECPC effectively links cancer policy to clinical practice.

Supportive care
Nutritional and metabolic disorders are prevalent among cancer patients. As oncologists focus on treating cancer, other important aspects of the disease and effects of cancer treatment are often neglected. Many patients with cancer face challenges related to nutrition, physical activity and health issues that are associated with their treatment and not adequately addressed by their healthcare team.
Cancer-related nutritional issues, such as malnutrition and cachexia, can substantially impact a patient's QOL, and awareness surrounding these issues is suboptimal. The ECPC has been bringing nutrition in cancer to the attention of patients, health professionals and politicians and is advocating for the right to nutritional support for cancer patients (Caccialanza et al., 2017).
Indeed, the ECPC pan-European nutrition survey aimed to analyse the dimension of nutritional alterations among patients with cancer and survivors by using a structured questionnaire encompassing the perspectives of patients and their physicians on nutritional issues. A total of 92% of patients with cancer did not receive information about cachexia, and 65% stated that their doctors rarely or never checked their weight (Muscaritoli et al., 2017).
Rehabilitation care including plastic surgery, logotherapy, swallowing and breathing training, artificial limbs, and cancer ulcers and ostomy care is not considered part of cancer care in many EU Member States. After the acute phase of treatment, patients are often left on their own to recover basic life skills. Rehabilitation should start immediately upon interventional cancer care (e.g. surgery, radiotherapy, highly toxic systemic treatments) so that the patient can start their recovery without delay. The ECPC believes that integrative cancer care that offers rehabilitation services should be part of the cancer care continuum.
In Europe, long-term follow-up data on the effect of treatment on physical and psychosocial functioning or health-related QOL are still lacking or are fragmented for most cancer diagnoses. These long-term data are important for providing a comprehensive understanding of the outcome of innovations in diagnostics and treatments, as well as of the quality of cancer care. Knowledge and understanding of these long-term outcomes are important to clinicians, to healthcare policymakers, to patients who are either cured or have no evidence of active disease and to those living with cancer as a chronic condition. Also, many patients want to know what more they can do on their own to improve their health and well-being after diagnosis. As a result, more research is required on the factors that help cancer survivors return to normal life, to prevent a secondary tumour and relapses and to prevent the appearance of late effects deriving from cancer treatment, to ensure a smooth process of rehabilitation.

Work-life balance for cancer carers
The multifaceted burden experienced by carers of patients with cancer has a significant effect on the well-being of carers, although support for the related financial and psychosocial effects remains inadequate in the EU. Carers often must acquire technical caring skills rapidly with no educational support to learn these skills. In the EU, the cost of unpaid care provided by relatives or friends is approximately €23 billion per year (Luengo-Fernandez et al., 2013). The EU Work-Life Balance Directive for Parents and Carers proposed by the European Commission clearly outlines the provisions to recognise and protect carers' right to flexible working conditions and paid caring leave.
The critical role of carers within social and healthcare systems, as well as communities, is recognised by the ECPC and advocates for formal recognition of carers, for implementation of policies that facilitate flexible work arrangements and for training and psychological support to be provided. The ECPC, in collaboration with Members of the European Parliament, proposed amendments to the Work-Life Balance Directive, which have now been included in the Directive and include formal recognition of the carer. This action highlights a major achievement for the rights of informal caregivers for people with cancer in Europe.

Digital health
Digital health, which is the combination of digital technologies with health care, aims to improve health and healthcare systems by enhancing accessibility, effectiveness, efficiency and personalisation of care. Mobile technologies are extensively used in hospital systems and should improve supportive care processes. Electronic processes supporting healthcare processes (eHealth) and mobile digital technologies (mHealth) are information and communication technologies that are applied to care pathways to collect patient data (Nasi et al., 2015). These technologies can help advance patient-centric healthcare systems by providing innovative ways for patients to monitor their health and well-being and by providing patients with increased access to information. This information can be shared with their healthcare providers.
The ECPC is very involved in the mHealth EU-funded, Seventh Framework Programme (FP7) project electronic Symptom Management using the Advanced Symptom Management System (ASyMS) Remote Technology (eSMART; Table 3). This is a clinical trial that aims to evaluate the impact of a mobile phone-based, remote-monitoring, symptommanagement intervention (ASyMS) on PROs and the delivery of care. Patients have a prominent coresearcher role in eSMART and have been participating in all project activities from project conception to implementation, including the writing of the trial protocol (Maguire et al., 2017).
Digital health is becoming increasingly integrated into the healthcare systems, and it should be recognised that cancer centres participating in Cancer Core Europe have incorporated several aspects of digital health in a wide spectrum of their services. The Internet and digital mobile technologies have brought tremendous changes in how data are transferred, stored, processed and communicated to patients and how patients communicate among themselves and with their physicians. Moreover, the Internet has empowered patients to learn about their disease and ask their healthcare providers questions.

Molecular testing and personalised medicine
Molecular diagnostics, involving genomic testing and immunotyping, are prerequisites for personalised medicine and are becoming a reality throughout Europe. However, it remains to be seen whether the EU Member States are able to build the complex infrastructure required to support personalised medicine. There is a need for DNA-sequencing facilities, biobanks for storing samples, 'big data' and interoperability solutions, as well as the integration of electronic patient records. Furthermore, health professionals need to be trained to ensure that they can interpret the results of the new tests and data and communicate them effectively to their patients.
The age of personalised medicine is well underway, and further advancement is needed from one-off assessments to real-time oncology, where liquid biopsies, artificial intelligence and new companion diagnostics are fully deployed. Multiple targets in each tumour require multiplexed testing, but despite promising results, there are many obstacles facing patients' access to new biomarker testing and treatments. New companion diagnostics are not available in all EU Member States, and if they are available, they may not be reimbursed, as EU national markets are highly fragmented and lack a consistent approach to HTA both in medicines and companion diagnostics.
Personalised medicine is essential not only for cancer treatment, but also for cancer prevention. Healthcare professionals are increasingly able to identify whether a person is at higher risk for developing cancer via knowledge of mutations commonly linked to cancer and access to more cost-effective genetic testing.
The concept of molecular and genomic testing is still largely unknown to most patients, and they are often unaware that these newer options are available. Also, healthcare professionals often hesitate to inform patients about new diagnostic and therapeutic options because they are not available or reimbursed, or due to lack of confidence and knowledge regarding genomic and molecular testing. The need for continuing education for healthcare professionals of all oncology specialties is necessary as an increasing number of new biomarker tests and treatments become available. Similarly, information suitable for cancer patients and the general public is needed, to keep pace with the latest scientific and technological developments. The role of the comprehensive cancer centres in Cancer Core Europe and the OECI and of patient organisations in the ECPC will be important in disseminating such information about the new and more complex approaches to cancer diagnosis and treatment (see also other articles in this issue).
The ECPC continuously and diligently aims to offer to its member organisations and the general public information validated by renowned cancer experts about cancer and cancer treatments. To raise patient awareness for molecular testing, the ECPC collaborated with a team of European experts in immunooncology to deliver basic facts in a user-friendly format to patients, the public and physicians via its immunooncology portal (http://iop.ecpc.org/; European Cancer Patient Coalition). Moreover, in an effort to make HTA more easily accessible to cancer patients, health professionals and the general public, the ECPC is currently developing an online educational module that aims to equip users with the knowledge to participate in the HTA of cancer treatments. The ECPC has also launched several awareness campaigns to raise the profile of several cancers by sharing facts, statistics, risk factors and symptoms on social media.

Conclusions and future perspectives
Cancer patients have a growing role in bridging the gap between cancer research, cancer care centres and survivorship and will play an important role moving forward in patients' and society's ultimate goals: cure and care for cancer patients. Despite successes such as the increasing role of patients in research (e.g. in the IMI-PREFER and the FP7 eSMART research projects) and the crucial role the ECPC has had in integrating disparities in cancer care, survivorship care and research in the deliverables of the Joint Action CanCon, there is still work to be done before true patient centricity will be achieved in Europe. Central to achieving this goal is ensuring that patients and patient organisations are genuinely involved in the decision-making processes, which can be achieved by formalising their participation in professional bodies that develop cancer policy recommendations at national and European levels. The key future challenge for the ECPC is to ensure that these recommendations are recognised, adopted and implemented.
A truly patient-centric healthcare system requires a multidisciplinary approach that is based on scientific guidance readily available to clinicians. With the complexity of cancer biology and the fast-paced advances in oncology, up-to-date guidelines are increasingly important to oncologists to help them improve the quality of their daily practice. As the multidisciplinary approach to cancer diagnosis and care is considered the gold standard, state-of-the-art clinical guidelines describing the essentials of multidisciplinary treatment, and how these can be evidencebased to ensure adoption of innovative strategies in cancer care, are necessary; these guidelines are currently lacking and it is expected that Cancer Core Europe in collaboration with the other cancer care stakeholders will undertake to develop them. Defining cancer clinical pathways that encompass the continuum of care is even more important and should be developed with input from patients and cancer care providers. European comprehensive cancer centres in collaboration with relevant learned societies, such as the ESMO, the European Society of Surgical Oncology (ESSO) and the European Society for Radiotherapy and Oncology (ESTRO), are the logical key players in coordinating the development and updating of these guidelines. This collaborative effort should facilitate the adoption of multidisciplinary oncology care pathways by the healthcare organisations, thereby improving the standard of care for every patient, encouraging the uptake of innovative research and ensuring the continuum of research from bench to bedside.
Comprehensive cancer centres now offer many of the latest cancer diagnostics and treatments via clinical trials or in the clinical setting. However, access to these centres can be daunting for patients and there is a drive for collaboration between hospitals and comprehensive cancer centres to facilitate the sharing of expertise and resources and increase dissemination of information and best clinical practices. Moreover, partnerships between cancer centres and smaller hospitals should be encouraged to promote knowledge transfer and enable patients to obtain access to specialised services near their home.
It is expected that the Innovative Partnership for Action Against Cancer (iPAAC), the third joint action following on from CanCon that has policy and science at its core, will build upon the deliverables of the Joint Action CanCon and implement innovative approaches to cancer control. A Roadmap on Implementation and Sustainability of Cancer Control Actions will be the main deliverable of this Joint Action and the ECPC will participate in the work packages relating to genomics, cancer information and registries, and challenges in cancer care. In particular, the aim of the genomics work package is to develop practical guidance for EU Member States on important aspects of successful integration of genomics in the healthcare system.
The ECPC's alliances with scientific societies promote a close and patient-centric collaboration among all stakeholders. The ECPC advocates the use of the CanCon Guide as a roadmap to implement national cancer care plans and to translate policy into practice. The important contribution of the ECPC to cancer research has been recognised by having ECPC representatives appointed to the Scientific Committee of the European Academy of Cancer Sciences (EACS), Cancer Core Europe, board of the Cancer Drug Development Forum (CDDF) and, to the General Assembly of the Worldwide Innovative Networking (WIN) Consortium. Moving forward, it is hoped that the European Commission will continue to sustain and increase its engagement in the fight against cancer and to collaborate with the Member States for the recognition and adoption of the CanCon recommendations.
While cancer research has revolutionised cancer care, it has also created problems, particularly with regards to affordability as many patients in the EU still cannot access innovative life-saving treatments and diagnostic tests. Currently, the oncology community is somewhat fragmented, a fact that has impacted on its ability to cooperate and effectively counteract the increasing global burden of cancer. The missionoriented approach to cancer recently proposed by Celis and Pavalkis (Celis and Pavalkis, 2017), which has been endorsed by members of the oncology community in Europe, has provided a novel strategy to overcome the burden. A primary aim of the mission on cancer is to achieve the long-term survival of 75% of patients with cancer by 2030 through combining innovative prevention and treatment strategies, as well as rehabilitation and multidisciplinary follow-up, in a sustainable, contemporary, virtual European cancer infrastructure that has tremendous social and economic implications. The establishment of both Cancer Core Europe (Eggermont et al., 2014) and Cancer Prevention Europe (Forman et al., 2018) has been key to this endeavour (see also other articles in this issue), and the active participation of the ECPC in the infrastructure should act as a bridge between research and care, strengthening the social impact of translational research and integrating patients' views into research and cancer care.
Member States and the general public should be involved in the mission on cancer in a coherent and systemic way, encompassing quality assurance and accreditation. The ECPC strongly supports the deployment of quality assurance schemes and the accreditation of cancer centres and to this purpose closely collaborates with the OECI. Dissemination of information to the general public on the genomics revolution in cancer diagnosis and treatment by comprehensive cancer centres and patient organisations will facilitate this process. Patient organisations will collaborate with scientists, clinicians, politicians and industry to overcome the unacceptable disparities in cancer treatment and care, and the associated stigma by identifying important research questions concerning QOL and social issues for all cancer patients, regardless of age. The ECPC can and does facilitate these collaborations and consequently plays a central role in the mission on cancer.