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PROGNOSTIC IMPACT OF P53 EXPRESSION IN BONE MARROW BIOPSY OF PATIENTS WITH ACUTE MYELOID LEUKEMIA
Author(s): ,
Heloíza Souza
Affiliations:
University of Campinas,Campinas,Brazil
,
Sara Saad
Affiliations:
University of Campinas,Campinas,Brazil
,
Irene Lorand-Metze
Affiliations:
University of Campinas,Campinas,Brazil
,
Bruno Duarte
Affiliations:
University of Campinas,Campinas,Brazil
,
Gabriela Hayakawa
Affiliations:
University of Campinas,Campinas,Brazil
,
Paula Campos
Affiliations:
University of Campinas,Campinas,Brazil
,
Márcia Delamain
Affiliations:
University of Campinas,Campinas,Brazil
,
Gislaine Duarte
Affiliations:
University of Campinas,Campinas,Brazil
,
José Vassallo
Affiliations:
University of Campinas,Campinas,Brazil
Kátia Pagnano
Affiliations:
University of Campinas,Campinas,Brazil
(Abstract release date: 05/18/17) EHA Library. Souza H. 05/18/17; 182388; PB1674
Heloíza Souza
Heloíza Souza
Contributions
Abstract

Abstract: PB1674

Type: Publication Only

Background

Several studies have shown that the presence of the TP53 mutation is related to an unfavorable prognosis in patients with acute myeloid leukemia (AML). However there are few reports on the evaluation of its expression by immunohistochemistry in bone marrow (BM) biopsy.

Aims

To evaluate the expression of p53 in BM biopsy of AML patients at diagnosis and its impact on survival.

Methods
This retrospective analysis included 85 patients with de novo AML diagnosed from January 2005 to December 2015 submitted to BM biopsy at diagnosis. p53 expression was detected by immunohistochemistry, and staining was evaluated using the H-score (range 0-300). The t-test and Mann-Whitney U test were used to detect differences in the distribution of continuous parametric and nonparametric variables, respectively. Overall survival (OS), disease-free survival (DFS) and event-free survival (EFS) were calculated using the Kaplan-Meier method. The log-rank test was used for comparison of survival curves. The interaction between the examined prognostic variables was tested with univariate and multivariate Cox regression analysis.

Results
Median age was 60 years (17-81). There was a predominance of patients >60 years (54.1%) and males (56.5%). The median H-score for p53 was 11.8 (0.4-161.1), with no significant correlation with age or cytogenetic risk. p53 expression was significantly higher in patients with a complex karyotype (p = 0.0031) and high risk by European Leukemia Net (ELN) criteria (p = 0.047). There was a positive correlation with complex karyotype and prognostic risk by ELN. Excluding early deaths (<30 days from induction), patients younger than 60 years with H-score > 60 showed worse overall survival when compared with patients with H-score <60 (0% vs 14.6%, respectively) (p = 0.048). There was no statistical difference in disease-free survival and event-free survival. In the Cox univariate analysis including all cases, peripheral leukocyte counts at diagnosis (p = 0.014), cytogenetic risk groups (p = 0.07), ELN risk categories (p = 0.023) and H-score (p = 0.025) were significant. In a multivariate model including leukocytes, ELN risk and p53, all variables remained in the model.

Conclusion

Expression of p53 assessed by immunohistochemistry is a fast, objective and promptly available tool for prognostic evaluation of AML. A high expression of p53 (H-score > 60) was related to a lower overall survival in de novo AML.

Session topic: 4. Acute myeloid leukemia - Clinical

Keyword(s): Immunohistochemistry, Acute Myeloid Leukemia, Survival, P53

Abstract: PB1674

Type: Publication Only

Background

Several studies have shown that the presence of the TP53 mutation is related to an unfavorable prognosis in patients with acute myeloid leukemia (AML). However there are few reports on the evaluation of its expression by immunohistochemistry in bone marrow (BM) biopsy.

Aims

To evaluate the expression of p53 in BM biopsy of AML patients at diagnosis and its impact on survival.

Methods
This retrospective analysis included 85 patients with de novo AML diagnosed from January 2005 to December 2015 submitted to BM biopsy at diagnosis. p53 expression was detected by immunohistochemistry, and staining was evaluated using the H-score (range 0-300). The t-test and Mann-Whitney U test were used to detect differences in the distribution of continuous parametric and nonparametric variables, respectively. Overall survival (OS), disease-free survival (DFS) and event-free survival (EFS) were calculated using the Kaplan-Meier method. The log-rank test was used for comparison of survival curves. The interaction between the examined prognostic variables was tested with univariate and multivariate Cox regression analysis.

Results
Median age was 60 years (17-81). There was a predominance of patients >60 years (54.1%) and males (56.5%). The median H-score for p53 was 11.8 (0.4-161.1), with no significant correlation with age or cytogenetic risk. p53 expression was significantly higher in patients with a complex karyotype (p = 0.0031) and high risk by European Leukemia Net (ELN) criteria (p = 0.047). There was a positive correlation with complex karyotype and prognostic risk by ELN. Excluding early deaths (<30 days from induction), patients younger than 60 years with H-score > 60 showed worse overall survival when compared with patients with H-score <60 (0% vs 14.6%, respectively) (p = 0.048). There was no statistical difference in disease-free survival and event-free survival. In the Cox univariate analysis including all cases, peripheral leukocyte counts at diagnosis (p = 0.014), cytogenetic risk groups (p = 0.07), ELN risk categories (p = 0.023) and H-score (p = 0.025) were significant. In a multivariate model including leukocytes, ELN risk and p53, all variables remained in the model.

Conclusion

Expression of p53 assessed by immunohistochemistry is a fast, objective and promptly available tool for prognostic evaluation of AML. A high expression of p53 (H-score > 60) was related to a lower overall survival in de novo AML.

Session topic: 4. Acute myeloid leukemia - Clinical

Keyword(s): Immunohistochemistry, Acute Myeloid Leukemia, Survival, P53

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