Evidence map›Paper›PMID 36374643›Full record

ArticleEuropean journal of public health2022

Is rare cancer care organized at national health system level? Multiple case study in six EU countries.

Joan Prades, Annalisa Trama, Paolo G Casali, Jean-Francois Emile, Nathalie Gaspar, Ramunas Janavicius, Rasa Jančiauskienė, Sakari Karjalainen, Katerina Kopeckova, Liisa Pylkkänen and 2 more

Abstract read
In one paragraph

Article in European journal of public health, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Joan PradesCatalonian Cancer Strategy, Department of Health, Barcelona, Spain.ORCID 0000-0003-0416-323X
Annalisa TramaEvaluative Epidemiology Unit, Fondazione IRCCS, Istituto Nazionale dei Tumori, Milan, Italy.ORCID 0000-0001-8220-9833
Paolo G CasaliMedical Oncology Unit 2, Fondazione IRCCS, Istituto Nazionale Tumori, Milan, Italy.ORCID 0000-0003-4056-8023
Jean-Francois EmileResearch Unit EA4340, Versailles University, Paris-Saclay University, Boulogne, France.ORCID 0000-0002-6073-4466
Nathalie GasparDépartement de cancérologie de l'enfant et l'adolescent, Gustave-Roussy cancer campus, 114, rue Edouard Vaillant, 94800 Villejuif, France.ORCID 0000-0002-1827-8903
Ramunas JanaviciusDepartment of Human and Medical Genetics, Vilnius University Faculty of Medicine, Vilnius, Lithuania.
Rasa JančiauskienėDepartment of Oncology and Hematology, Medical Academy, Lithuanian University of Health Sciences, Kaunas, Lithuania.
Sakari KarjalainenCancer Society of Finland, Helsinki, Finland.ORCID 0000-0002-5756-0178
Katerina KopeckovaDepartment of Oncology, 2nd Faculty of Medicine, Charles University, Prague, Czech Republic.ORCID 0000-0002-1907-163X
Liisa PylkkänenFinnish Medicines Agency Fimea, Helsinki, Uusimaa, Finland.ORCID 0000-0002-8375-6035
Marek SvobodaDepartment of Comprehensive Cancer Care, Masaryk Memorial Cancer Institute, Brno, Czech Republic.
Josep M BorrasCatalonian Cancer Strategy, Department of Health, Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs a system of European Reference Networks (ERNs) emerges, the differences in quality of care for patients with rare cancers may increase at national level. We aimed to elucidate the processes and healthcare planning principles through which the reference centres (RCs) for rare cancers are embedded in national health systems.

methodsWe used a multiple case-study design based on the experiences of Czechia, Finland, France, Italy, Lithuania and Spain. Using sarcoma as an example of rare cancer, 52 semi-structured interviews were conducted during on-site visits, including a multidisciplinary group of professionals, Ministry of Health professionals, patient representatives and European policymakers.

resultsThe comparative analysis showed substantial heterogeneity in the processes for formalizing RCs' status and in their levels of integration in the different health systems, but two models (centre-based and the network-based) can be envisaged at national level. RCs for rare cancers were legally established only in France and Spain. Expert clinicians cooperate in a structured way, using network mechanisms, in France and Italy, and these countries, plus Finland and Lithuania, had a referral system to facilitate patients' access from non-expert centres to RCs. Seven key healthcare planning principles in instituting RCs at the national level were identified.

conclusionsThe conditions governing patient access to treatment centres-whether RCs or not-are decided at the national level. It is advisable to progressively align the European and national levels so that the RCs that participate in the ERNs also play a significant role at the national level.

Indexed as

NeoplasmsFranceHumansItalyReferral and ConsultationSpain

Identifiers

PMID36374643
PMCPMC9713415

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.