Variant ALK-fusion positive anaplastic large cell lymphoma (ALCL): A population-based paediatric study of the NHL-BFM study group

. 2024 May ; 204 (5) : 1894-1898. [epub] 20240126

Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid38279625

Grantová podpora
Hamburger Stiftung zur Foerderung der Krebsbekaempfung
Juli Harnack scholarship of the Foerdergemeinschaft Kinderkrebszentrum Hamburg e.V.
KinderkrebsInitiative Buchholz, Holm-Seppensen
Deutsche Kinderkrebsstiftung

Frequency, distribution and prognostic meaning of ALK-partner genes other than NPM1 in ALK-positive anaplastic large-cell lymphoma (ALCL) are unknown. Forty-nine of 316 ALCL diagnosed in the NHL-BFM study group showed no nuclear ALK expression suggestive of a variant ALK-partner; 41 were analysed by genomic capture high-throughput sequencing or specific RT-PCRs. NPM1::ALK was detected in 13 cases. Among the 28 patients with a non-NPM1::ALK-fusion partner, ATIC (n = 8; 29%) and TPM3 (n = 9; 32%) were the most common. Five of eight patients with ATIC::ALK-positive ALCL relapsed, none of nine with TPM3::ALK. Variant ALK-partners are rare and potentially associated with different prognoses.

Bioinformatics Core University Medical Centre Hamburg Eppendorf Hamburg Germany

Department of Paediatric Haematology and Oncology Hannover Medical School and NHL BFM Study Centre Hannover Germany

Department of Paediatric Haematology and Oncology St Anna Children's Hospital Medical University of Vienna Vienna Austria

Department of Paediatrics McMaster Children's Hospital and McMaster University Hamilton Ontario Canada

Department of Pathology 3rd Faculty of Medicine Charles University Prague and University Hospital Kralovske Vinohrady Prague Czech Republic

Department of Pathology and Molecular Medicine 2nd Faculty of Medicine Charles University Prague and University Hospital in Motol Prague Czech Republic

Department of Pathology Haematopathology Section and Lymph Node Registry University Hospital Schleswig Holstein Kiel Germany

Department of Pathology Medical University of Vienna Vienna Austria

Department of Pathology University of Wuerzburg Wuerzburg Germany

Department of Pediatric Hematology and Oncology Charles University Prague and University Hospital Motol Prague Czech Republic

Division of Paediatric Haematology Oncology Children's Hospital of Eastern Switzerland St Gallen Switzerland

Faculty of Health Science and Medicine University of Lucerne Lucerne Switzerland

Institute of Human Genetics Ulm University and Ulm University Medical Centre Ulm Germany

Leibniz Institute of Virology Hamburg Germany

Mildred Scheel Cancer Career Centre HaTriCS4 University Medical Centre Hamburg Eppendorf Hamburg Germany

Paediatric Haematology and Oncology and CoALL Study Centre University Medical Centre Hamburg Eppendorf Hamburg Germany

Paediatric Haematology and Oncology and NHL BFM Study Centre University Medical Centre Hamburg Eppendorf Hamburg Germany

St Anna Children's Cancer Research Institute Vienna Austria

Zobrazit více v PubMed

Alaggio R, Amador C, Anagnostopoulos I, Attygalle AD, Araujo IBO, Berti E, et al. The 5th edition of the World Health Organization classification of haematolymphoid tumours: lymphoid neoplasms. Leukemia. 2022;36(7):1720–1748.

Elenitoba‐Johnson KS, Ott G, Takeuchi K, Klapper W, Lamant‐Rochaix L, d'Amore ESG, et al. ALK‐positive anaplastic large cell lymphoma. WHO classification of tumours editorial board Haematolymphoid tumours. Volume 11. 5th ed. Lyon (France): WHO Classification of Tumours Series, International Agency for Research on Cancer; 2022 [cited 2023 Oct 20]. Available from: https://tumourclassification.iarc.who.int/chapters/63

Falini B, Pulford K, Pucciarini A, Carbone A, De Wolf‐Peeters C, Cordell J, et al. Lymphomas expressing ALK fusion protein(s) other than NPM‐ALK. Blood. 1999;94(10):3509–3515.

Stein H, Foss HD, Durkop H, Marafioti T, Delsol G, Pulford K, et al. CD30(+) anaplastic large cell lymphoma: a review of its histopathologic, genetic, and clinical features. Blood. 2000;96(12):3681–3695.

Benharroch D, Meguerian‐Bedoyan Z, Lamant L, Amin C, Brugieres L, Terrier‐Lacombe MJ, et al. ALK‐positive lymphoma: a single disease with a broad spectrum of morphology. Blood. 1998;91(6):2076–2084.

Falini B, Bigerna B, Fizzotti M, Pulford K, Pileri SA, Delsol G, et al. ALK expression defines a distinct group of T/null lymphomas ("ALK lymphomas") with a wide morphological spectrum. Am J Pathol. 1998;153(3):875–886.

Perkins SL, Pickering D, Lowe EJ, Zwick D, Abromowitch M, Davenport G, et al. Childhood anaplastic large cell lymphoma has a high incidence of ALK gene rearrangement as determined by immunohistochemical staining and fluorescent in situ hybridisation: a genetic and pathological correlation. Br J Haematol. 2005;131(5):624–627.

Damm‐Welk C, Klapper W, Oschlies I, Gesk S, Rottgers S, Bradtke J, et al. Distribution of NPM1‐ALK and X‐ALK fusion transcripts in paediatric anaplastic large cell lymphoma: a molecular‐histological correlation. Br J Haematol. 2009;146(3):306–309.

Lamant L, McCarthy K, D'Amore E, Klapper W, Nakagawa A, Fraga M, et al. Prognostic impact of morphologic and phenotypic features of childhood ALK‐positive anaplastic large‐cell lymphoma: results of the ALCL99 study. J Clin Oncol. 2011;29(35):4669–4676.

Armstrong F, Duplantier MM, Trempat P, Hieblot C, Lamant L, Espinos E, et al. Differential effects of X‐ALK fusion proteins on proliferation, transformation, and invasion properties of NIH3T3 cells. Oncogene. 2004;23(36):6071–6082.

Armstrong F, Lamant L, Hieblot C, Delsol G, Touriol C. TPM3‐ALK expression induces changes in cytoskeleton organisation and confers higher metastatic capacities than other ALK fusion proteins. Eur J Cancer. 2007;43(4):640–646.

van der Krogt JA, Bempt MV, Ferreiro JF, Mentens N, Jacobs K, Pluys U, et al. Anaplastic lymphoma kinase‐positive anaplastic large cell lymphoma with the variant RNF213‐, ATIC‐ and TPM3‐ALK fusions is characterized by copy number gain of the rearranged ALK gene. Haematologica. 2017;102(9):1605–1616.

Ma Z, Hill DA, Collins MH, Morris SW, Sumegi J, Zhou M, et al. Fusion of ALK to the ran‐binding protein 2 (RANBP2) gene in inflammatory myofibroblastic tumor. Genes Chromosomes Cancer. 2003;37(1):98–105.

Pulford K, Lamant L, Espinos E, Jiang Q, Xue L, Turturro F, et al. The emerging normal and disease‐related roles of anaplastic lymphoma kinase. Cell Mol Life Sci. 2004;61(23):2939–2953.

Wehkamp U, Oschlies I, Nagel I, Brasch J, Kneba M, Gunther A, et al. ALK‐positive primary cutaneous T‐cell‐lymphoma (CTCL) with unusual clinical presentation and aggressive course. J Cutan Pathol. 2015;42(11):870–877.

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