Rare Cancer Perspective in the EUCERD

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EURORDIS' activities on EU and National Policies Rare Cancer Perspective in the EUCERD Jan Geissler Alternate Member, EU Committee of Experts for Rare Diseases (EUCERD) Director, European Patients Academy on Therapeutic Innovation (EUPATI) Co-founder, Leukemia Patient Advocates Foundation Chair, LeukaNET Secretary, European Forum For Good Clinical Practice (EFGCP)

Hype or hope: success stories only for small number of cancers Main attention is on common cancers Only small number of rare cancers have effective treatments Source: RareCare (2012)

Patients with rare cancers share common problems with rare diseases 1. Prevention/screening mostly not relevant 2. Late or incorrect diagnosis 3. Experienced doctor not available locally 4. Lack of access and referral 5. Few centres of expertise, few networks of excellence 6. Slowness of research, lack of funding 7. Stigma and inequity 8. Lack of harmonisation in health policy 9. Limited data on the burden of RC/RD

~200 RARE CANCERS Rare diseases and rare cancers: Unite, not divide Rare Cancers are often lost between common cancers and rare diseases Contradictions in RD/Onc health policy, in RD plans and national cancer plans might not beneficial for any side 230 Cancers 6000-8000 Rare Diseases

On the Commission level, there are two Joint Actions Reduce cancer incidence by 15% by 2020 Make better use of limited resources, avoid duplication Integrated cancer plans in MS Cancer registries, health promotion, NoE/CoE, research coordination 126 partners Facilitate implementation of national rare disease plans standardization of RD nomenclature mapping the provision of specialised social services for RD integration of RD initiatives and mapping of national initiatives 51 members (incl 27 MS, POs,...)

Suggested: Joining forces between EUCERD and EPAAC! On initiative by the EURORDIS team in EUCERD + the Istituto Nazinale Dei Tumori Milan to consider: Mapping of national cancer plans (EPAAC WP10) and national rare disease plans (in Europlan) Harmonisation of stakeholder views on rare disease/cancer policy Alignment of criteria for accreditation of centres of excellence, and criteria for ERN Harmonization of framework for Clinical Guidelines Bridging EU pre-marketing authorization and MS-level post-market authorization Alignment on methodologies for disease registries Evaluate ongoing EU initiatives on cancer/rd on health equity impact +

Thank you! Jan Geißler jan@patientsacademy.eu Twitter @jangeissler http://www.patientsacademy.eu http://www.cmladvocates.net

WP1: Coordination & Management WP 10 National Cancer Plans WP5: Health Promotion and Prevention WP6: Screening and early diagnosis WP7: Healthcare WP8: Research WP9: Information & data WP2: Dissemination, Virtual partnership WP3: Evaluation

National Cancer Plan - NCP A public health programme designed to: reduce the number of cancer cases and deaths and improve quality of life of cancer patients, through the systematic and equitable implementation of evidence-based strategies for: prevention, early detection, diagnosis and treatment, rehabilitation, palliation and research to search for innovative solutions and evaluate outcomes. EPAAC Steering Committee Meeting, Brussels, 8 December 2010

Work Organisation Work on NCPs will be organised on 3 levels First level: Partners from WP 10 (Belgium, Ireland, Italy, Malta, Slovenia) Preparation of the background documents, questionnaires, analyses.. Second level: Working Group on the NCPs Review of the work done on first level Third level: SC of the Partnership Review of the work done on second level and adoption of decisions EPAAC Steering Committee Meeting, Brussels, 8 December 2010

New Working Bodies Working Group (WG) for NCPs Representatives of all MSs WHO Europe EUREGHA EOHSP Steering Commitee (SC) of the Partnership Members of the WG Members of the SC of the JA EPAAC Representatives of IARC, the EOHSP, ECPC, ECCO Representative of an industry association Individual renowned experts Workpackage leaders EPAAC Steering Committee Meeting, Brussels, 8 December 2010

Specific Objectives To obtain an overview of the current state regarding NCPs in MSs, Norway and Iceland To obtain a review of the content of NCPs from all MSs, Norway and Iceland To identify benefits of every existing NCP To define areas to be respected in NCPs To finally evaluate the effectivenness of WP 10 regarding the outcome indicators To prepare guidelines for a high level standard NCP which includes the listed areas To define specific indicators for each area listed in the high level standard NCP EPAAC Steering Committee Meeting, Brussels, 8 December 2010