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Br J Haematol ; 204(5): 1894-1898, 2024 May.
Artículo en Inglés | MEDLINE | ID: mdl-38279625

RESUMEN

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.


Asunto(s)
Quinasa de Linfoma Anaplásico , Linfoma Anaplásico de Células Grandes , Nucleofosmina , Humanos , Linfoma Anaplásico de Células Grandes/genética , Linfoma Anaplásico de Células Grandes/patología , Niño , Masculino , Femenino , Quinasa de Linfoma Anaplásico/genética , Quinasa de Linfoma Anaplásico/análisis , Adolescente , Preescolar , Proteínas de Fusión Oncogénica/genética , Pronóstico , Proteínas Nucleares/genética , Proteínas Nucleares/metabolismo , Lactante , Tropomiosina
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