FMOD expression in whole blood aids in distinguishing between chronic lymphocytic leukemia and other leukemic lymphoproliferative disorders. A pilot study

Autor: Sílvia Beà, Diana Marcela Ruíz Domínguez, Sara Vergara, Esther Plensa, Silvia-Zdenka Mostacedo, Andrea Espasa, Marc Sorigue, Christelle Ferra, Laia Pinyol, Rocio Ruiz, Joan Buch, Jessica Aranda, Lurdes Zamora, Gustavo Tapia, Marta Cabezón, Silvia Marcé, Neus Ruiz-Xivillé, Isabel Granada, Laia Lopez-Viaplana, José-Tomás Navarro, Jordi Juncà, Minerva Raya
Rok vydání: 2020
Předmět:
Zdroj: Cytometry Part B: Clinical Cytometry. 98:421-428
ISSN: 1552-4957
1552-4949
Popis: BACKGROUND Within the hematopoietic compartment, fibromodulin (FMOD) is almost exclusively expressed in chronic lymphocytic leukemia (CLL) lymphocytes. We set out to determine whether FMOD could be of help in diagnosing borderline lymphoproliferative disorders (LPD). METHODS We established 3 flow cytometry-defined groups (CLL [n = 65], borderline LPD [n = 28], broadly defined as those with CLLflow score between 35 and -20 or discordant CD43 and CLLflow, and non-CLL LPD [n = 40]). FMOD expression levels were determined by standard RT-PCR in whole-blood samples. Patients were included regardless of lymphocyte count but with tumor burden ≥40%. RESULTS FMOD expression levels distinguished between CLL (median 98.5, interquartile range [IQR] 37.8-195.1) and non-CLL LPD (median 0.012, IQR 0.003-0.033) with a sensitivity and specificity of 1. Most borderline LPDs were CD5/CD23/CD200-positive with no loss of B-cell antigens and negative or partial expression of CD43. 16/22 patients with available cytogenetic analysis showed trisomy 12. In 25/28 (89%) of these patients, FMOD expression levels fell between CLL and non-CLL (median 3.58, IQR 1.06-6.21). DISCUSSION This study could suggest that borderline LPDs may constitute a distinct group laying in the biological spectrum of chronic leukemic LPDs. Future studies will have to confirm these results with other biological data. Quantification of FMOD can potentially be of help in the diagnosis of phenotypically complex LPDs.
Databáze: OpenAIRE