Literature DB >> 24411984

Aberrant expression of CD13 identifies a subgroup of standard-risk adult acute lymphoblastic leukemia with inferior survival.

Bakul I Dalal1, Areej Al Mugairi2, Steven Pi2, Soo Yeon Lee2, Nikisha S Khare2, Jason Pal2, Adam Bryant3, Alok P Vakil2, Sally Lau3, Yasser R Abou Mourad3.   

Abstract

BACKGROUND: The standard-risk (SR) subgroup of acute lymphoblastic leukemia in adults (aALL) is a heterogeneous category, with a 20% to 40% relapse rate and a wide range of relapse-free survival (RFS) and overall survival (OS). There is a need to identify at the outset those patients with SR-aALL who are likely to have shorter RFS and OS, so they can be treated more aggressively. PATIENTS AND METHODS: Flow cytometric data of 81 patients with SR-aALL treated with a standardized protocol were retrospectively analyzed. Thirty-two patients (40%) relapsed; the median RFS and OS were 12.5 months (range, 1-136 months) and 30 months (range, 3-235 months), respectively. Twenty-six patients survived ≥ 48 months.
RESULTS: Expression of myeloid antigen CD13, using the conventional ≥ 20% threshold and a lower ≥ 5% threshold, was seen in 17 (29%) of 59 and 29 (49%) of 59 patients, respectively, whereas dual expression of CD13 and CD33 was seen in 8 patients. CD13 positivity at ≥ 20% and ≥ 5% threshold was associated with a shorter RFS (P = .0158 and P < .0001, respectively) and OS (P = .0072 and P < .0001, respectively). Dual expression of CD13 (at ≥ 5% or ≥ 20% threshold) and CD33 was associated with inferior OS (P = .0038 and P = .0032, respectively) and RFS (P = .0705 and P = .2516, respectively). For ≥ 20% and ≥ 5% threshold of positivity, 16 of 42 and 28 of 42 who survived < 48 months were positive, compared with 1 of 17 and 1 of 17 who survived ≥ 48 months (P = .0133 and P < .0001, respectively).
CONCLUSION: Aberrant expression of CD13 in ≥ 5% of blasts of patients with SR-aALL is an adverse prognostic factor, delineating a subgroup of patients with SR-aALL that should be considered for more aggressive treatment.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Flow cytometry; Immunophenotyping; Prognosis; Risk-stratification

Mesh:

Substances:

Year:  2013        PMID: 24411984     DOI: 10.1016/j.clml.2013.10.003

Source DB:  PubMed          Journal:  Clin Lymphoma Myeloma Leuk        ISSN: 2152-2669


  4 in total

1.  Identification of alanyl aminopeptidase (CD13) as a surface marker for isolation of mature gastric zymogenic chief cells.

Authors:  Benjamin D Moore; Ramon U Jin; Luciana Osaki; Judith Romero-Gallo; Jennifer Noto; Richard M Peek; Jason C Mills
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2015-10-29       Impact factor: 4.052

2.  Aminopeptidase Expression in Multiple Myeloma Associates with Disease Progression and Sensitivity to Melflufen.

Authors:  Juho J Miettinen; Romika Kumari; Gunnhildur Asta Traustadottir; Maiju-Emilia Huppunen; Philipp Sergeev; Muntasir M Majumder; Alexander Schepsky; Thorarinn Gudjonsson; Juha Lievonen; Despina Bazou; Paul Dowling; Peter O Gorman; Ana Slipicevic; Pekka Anttila; Raija Silvennoinen; Nina N Nupponen; Fredrik Lehmann; Caroline A Heckman
Journal:  Cancers (Basel)       Date:  2021-03-26       Impact factor: 6.639

3.  CD13 and ROR2 Permit Isolation of Highly Enriched Cardiac Mesoderm from Differentiating Human Embryonic Stem Cells.

Authors:  Rhys J P Skelton; Bevin Brady; Suhail Khoja; Debashis Sahoo; James Engel; Deevina Arasaratnam; Kholoud K Saleh; Oscar J Abilez; Peng Zhao; Edouard G Stanley; Andrew G Elefanty; Murray Kwon; David A Elliott; Reza Ardehali
Journal:  Stem Cell Reports       Date:  2016-01-12       Impact factor: 7.765

4.  Prognostic relevance of HER2/neu in acute lymphoblastic leukemia and induction of NK cell reactivity against primary ALL blasts by trastuzumab.

Authors:  Sebastian P Haen; Benjamin J Schmiedel; Kathrin Rothfelder; Bastian J Schmied; Truong-Minh Dang; Nora Mirza; Robert Möhle; Lothar Kanz; Wichard Vogel; Helmut R Salih
Journal:  Oncotarget       Date:  2016-03-15
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.