Publication:
Malignancy and lymphoid proliferation in primary immune deficiencies; hard to define, hard to treat

dc.contributor.coauthorKiykim, Ayca
dc.contributor.coauthorEker, Nursah
dc.contributor.coauthorSurekli, Ozlem
dc.contributor.coauthorNain, Ercan
dc.contributor.coauthorKasap, Nurhan
dc.contributor.coauthorDogru, Omer
dc.contributor.coauthorCanbolat, Aylin
dc.contributor.coauthorSomer, Ayper
dc.contributor.coauthorKoc, Ahmet
dc.contributor.coauthorTokuc, Gulnur
dc.contributor.coauthorBozkurt, Suheyla
dc.contributor.coauthorTurkoz, Kemal
dc.contributor.coauthorKarakoc-Aydiner, Elif
dc.contributor.coauthorOzen, Ahmet
dc.contributor.coauthorBaris, Safa
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorAktürk, Hacer
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-10T00:10:56Z
dc.date.issued2020
dc.description.abstractBackground Regarding the difficulties in recognition and management of the malignancies in primary immune deficiencies (PIDs), we aimed to present the types, risk factors, treatment options, and prognosis of the cancers in this specific group. Methods Seventeen patients with PID who developed malignancies or malignant-like diseases were evaluated for demographics, clinical features, treatment, toxicity, and prognosis. Results The median age of malignancy was 12.2 years (range, 2.2-26). Lymphoma was the most frequent malignancy (n = 7), followed by adenocarcinoma (n = 3), squamous cell carcinoma (n = 2), cholangiocarcinoma (n = 1), Wilms tumor (n = 1), and acute myeloid leukemia (n = 1). Nonneoplastic lymphoproliferation mimicking lymphoma was observed in five patients. The total overall survival (OS) was 62.5% +/- 12.1%. The OS for lymphoma was 62.2% +/- 17.1% and found to be inferior to non-PID patients with lymphoma (P = 0.001). Conclusion In patients with PIDs, malignancy may occur and negatively affect the OS. The diagnosis can be challenging in the presence of nonneoplastic lymphoproliferative disease or bone marrow abnormalities. Awareness of susceptibility to malignant transformation and early diagnosis with multidisciplinary approach can save the patients' lives.
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.issue2
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.volume67
dc.identifier.doi10.1002/pbc.28091
dc.identifier.eissn1545-5017
dc.identifier.issn1545-5009
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85075202621
dc.identifier.urihttps://doi.org/10.1002/pbc.28091
dc.identifier.urihttps://hdl.handle.net/20.500.14288/17381
dc.identifier.wos496750500001
dc.keywordsCancer
dc.keywordsLymphoid proliferation
dc.keywordsLymphoma
dc.keywordsMalignancy
dc.keywordsPrimary immune deficiency
dc.keywordsPrognosis immunodeficiency syndromes
dc.keywordsImmunological phenotype
dc.keywordsCancer
dc.keywordsChildren
dc.keywordsSecondary
dc.keywordsMutation
dc.keywordsPathway
dc.keywordsPatient
dc.keywordsPIK3R1
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofPediatric Blood and Cancer
dc.subjectOncology
dc.subjectHematology
dc.subjectPediatrics
dc.titleMalignancy and lymphoid proliferation in primary immune deficiencies; hard to define, hard to treat
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorAktürk, Hacer
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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