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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://dirros.openscience.si/IzpisGradiva.php?id=28804"><dc:title>Epidemiology and management of malignancies in patients with inborn errors of immunity - an ESID registry study of 19,959 patients</dc:title><dc:creator>Bogaert,	Delfien J. A.	(Avtor)
	</dc:creator><dc:creator>Wolfsberger,	Christina Helene	(Avtor)
	</dc:creator><dc:creator>Attarbaschi,	Andishe	(Avtor)
	</dc:creator><dc:creator>Gathmann,	Jonathan	(Avtor)
	</dc:creator><dc:creator>Warnatz,	Klaus	(Avtor)
	</dc:creator><dc:creator>Mueller,	Gabriele	(Avtor)
	</dc:creator><dc:creator>Mukhina,	Anna	(Avtor)
	</dc:creator><dc:creator>Rusch,	Stephan	(Avtor)
	</dc:creator><dc:creator>Kindle,	Gerhard	(Avtor)
	</dc:creator><dc:creator>van Montfrans,	Joris M.	(Avtor)
	</dc:creator><dc:creator>Seidel,	Markus G.	(Avtor)
	</dc:creator><dc:creator>Avčin,	Tadej	(Sodelavec pri raziskavi)
	</dc:creator><dc:creator>Blazina,	Štefan	(Sodelavec pri raziskavi)
	</dc:creator><dc:creator>Meško Meglič,	Karmen	(Sodelavec pri raziskavi)
	</dc:creator><dc:creator>Kopač,	Peter	(Sodelavec pri raziskavi)
	</dc:creator><dc:creator>Markelj,	Gašper	(Sodelavec pri raziskavi)
	</dc:creator><dc:subject>inborn errors of immunity</dc:subject><dc:subject>IEI</dc:subject><dc:subject>primary immunodeficiency</dc:subject><dc:subject>PID</dc:subject><dc:subject>primary immune disorder</dc:subject><dc:subject>malignancy</dc:subject><dc:subject>cancer predisposition syndromes</dc:subject><dc:subject>tumor predisposition</dc:subject><dc:subject>ESID registry</dc:subject><dc:description>Background Inborn errors of immunity (IEI), or primary immune disorders (PIDs), predispose individuals to infections, autoimmunity, inflammation, allergy, and malignancy. Malignancies are a major cause of morbidity and mortality in patients with IEI/PIDs, with poorer outcomes compared with the general population. Objective We sought to determine the frequency and types of malignancies in patients with IEI/PIDs and to assess clinical management approaches across Europe. Methods Descriptive analyses were performed on malignancy data within each IEI category. In addition, a European Society for Immunodeficiencies Registry survey (05/2022-03/2024) collected data on management strategies and challenges. Results Of 19,959 patients with IEI/PIDs, 1783 (8.9%) developed malignancies, of whom 27.1% presented malignancy as first manifestation of IEI/PIDs. A total of 1210 malignancies were specified; B-cell non-Hodgkin lymphoma was most common (24.2%). Detailed malignancy-IEI/PID association maps are provided. Predominantly antibody deficiencies accounted for 59.1% of malignancy cases, with a higher median age at first malignancy (43.6 years) compared with other IEI/PID categories, for example, combined immunodeficiencies with syndromic or associated features (11.7 years). Survey findings revealed that oncological treatment was modified because of IEI/PIDs in 21.5% of cases, with assumed negative impacts of IEI/PIDs on complications and outcomes (in 27.4% and 30.7%, respectively). IEI/PIDs influenced transplant decisions in 16.5% of cases. Management practices such as interdisciplinary decision finding and guideline availability were recorded. Conclusions This study provides comprehensive epidemiological data on malignancies in IEI/PIDs, highlighting the need for tailored screening and management. Survey results emphasize the real-world challenges and support the development of IEI/PID-specific oncological surveillance guidelines and treatment strategies.</dc:description><dc:date>2026</dc:date><dc:date>2026-04-08 10:24:33</dc:date><dc:type>Neznano</dc:type><dc:identifier>28804</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
