Variant ALK-fusion positive anaplastic large cell lymphoma (ALCL): A population-based paediatric study of the NHL-BFM study group.
Jette LuedersenUdo Zur StadtJulia RichterIlske OschliesWolfram KlapperAndreas RosenwaldMarketa KalinovaIngrid Simonitsch-KluppReiner SiebertMartin ZimmermannMinyue QiJacqueline NakelKatrin ScheinemannFabian KnörrAndishe AttarbaschiEdita KabickovaWilhelm WoessmannChristine Damm-WelkPublished in: British journal of haematology (2024)
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.
Keyphrases
- advanced non small cell lung cancer
- acute myeloid leukemia
- diffuse large b cell lymphoma
- single cell
- stem cells
- epidermal growth factor receptor
- poor prognosis
- cell therapy
- dna methylation
- acute lymphoblastic leukemia
- hiv testing
- hepatitis c virus
- mesenchymal stem cells
- men who have sex with men
- tyrosine kinase
- advanced cancer