Impact of Aberrant Antigens in the Outcome of Patients with Acute Leukemia at a Referral Institution in Mexico City
| Autor: | Sergio, Rodríguez-Rodríguez, Alan, Pomerantz, Roberta, Demichelis-Gómez, Georgina, Barrera-Lumbreras, Olga V, Barrales-Benítez, Xavier, Lopez-Karpovitch, Álvaro, Aguayo |
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| Rok vydání: | 2017 |
| Předmět: |
Adult
Aged 80 and over Male Adolescent Middle Aged Precursor Cell Lymphoblastic Leukemia-Lymphoma Disease-Free Survival Leukemia Biphenotypic Acute Leukemia Myeloid Acute Young Adult Antigens CD Antigens Neoplasm Risk Factors Multivariate Analysis Biomarkers Tumor Humans Female Mexico Aged Follow-Up Studies Retrospective Studies |
| Zdroj: | Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion. 68(6) |
| ISSN: | 0034-8376 |
| Popis: | Patients with acute leukemia can express aberrant markers, defined as antigens that are normally restricted to a different lineage. The reported significance and frequency of these markers is inconclusive. We assessed the frequency and impact of aberrant markers in patients with acute leukemia in a referral institution in Mexico City.We included 433 patients, diagnosed and treated between 2005 and 2015 in our institution.Aberrant markers were expressed in 128 patients (29.6%); CD13 and CD33 were the most frequent aberrant markers in patients with acute lymphoblastic leukemia, while CD7 and CD19 were the most frequent in patients with acute myeloid leukemia. In the univariate analysis, the group with aberrant markers had a lower disease-free survival when compared with the aberrant-free group (8 vs. 13 months) (p = 0.03). Aberrant expression of CD10, CD20, and CD33 correlated with a worse outcome in a statistically significant manner. In the multivariate analysis, male gender, lymphoid lineage, secondary leukemia, high risk at diagnosis, and the presence of aberrant markers had a significantly negative impact on disease-free survival.The use of more aggressive treatment strategies could be considered in patients with acute leukemia and an aberrant expression of CD10, CD20, and CD33. |
| Databáze: | OpenAIRE |
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