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Clinical significance of occult central nervous system disease in adult acute lymphoblastic leukemia: a multicenter report from the Campus ALL Network

In acute lymphoblastic leukemia (ALL), flow cytometry (FCM) detects leukemic cells in patients’ cerebrospinal fluid (CSF) more accurately than conventional cytology (CC). However, the clinical significance of FCM positivity with a negative cytology (i.e., occult central nervous system [CNS] disease)...

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Detalles Bibliográficos
Autores principales: Del Principe, Maria Ilaria, Buzzatti, Elisa, Piciocchi, Alfonso, Forghieri, Fabio, Bonifacio, Massimiliano, Lessi, Federica, Imbergamo, Silvia, Orciuolo, Enrico, Rossi, Giovanni, Fracchiolla, Nicola, Trappolini, Silvia, Neri, Benedetta, Sarlo, Chiara, Zappasodi, Patrizia, Dargenio, Michelina, Cefalo, Mariagiovanna, Irno-Consalvo, Maria Antonietta, Conti, Consuelo, Paterno, Giovangiacinto, De Angelis, Gottardo, Sciumè, Mariarita, Starza, Irene Della, Venditti, Adriano, Foà, Robin, Guarini, Anna Rita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Fondazione Ferrata Storti 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7776237/
https://www.ncbi.nlm.nih.gov/pubmed/31879328
http://dx.doi.org/10.3324/haematol.2019.231704
Descripción
Sumario:In acute lymphoblastic leukemia (ALL), flow cytometry (FCM) detects leukemic cells in patients’ cerebrospinal fluid (CSF) more accurately than conventional cytology (CC). However, the clinical significance of FCM positivity with a negative cytology (i.e., occult central nervous system [CNS] disease) is not clear. In the framework of the national Campus ALL program, we retrospectively evaluated the incidence of occult CNS disease and its impact on outcome in 240 adult patients with newly diagnosed ALL. All CSF samples were investigated by CC and FCM. The presence of ≥10 phenotypically abnormal events, forming a cluster, was considered to be FCM positivity. No CNS involvement was documented in 179 patients, while 18 were positive by modified conventional morphology with CC and 43 were occult CNS disease positive. The relapse rate was significantly lower in CNS disease negative patients and the disease-free and overall survival (OS) were significantly longer in CNS disease negative patients than in those with manifest or occult CNS disease positivity. In multivariate analysis, the status of manifest and occult CNS disease positivity was independently associated with a worse OS. In conclusion, we demonstrate that in adult ALL patients at diagnosis FCM can detect occult CNS disease at high sensitivity and that the status of occult CNS disease positivity is associated with an adverse outcome. (Registered at clinicaltrials.gov identifier: NCT03803670).