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CEBPA mutations in patients with de novo acute myeloid leukemia: data analysis in a Chinese population

Authors Su L , Gao S, Liu X, Tan Y, Wang L, Li W

Received 28 January 2016

Accepted for publication 24 April 2016

Published 3 June 2016 Volume 2016:9 Pages 3399—3403

DOI https://doi.org/10.2147/OTT.S94975

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 3

Editor who approved publication: Dr William C. Cho



Long Su, SuJun Gao, XiaoLiang Liu, YeHui Tan, Lu Wang, Wei Li

Cancer Center, The First Hospital, Jilin University, Changchun, People’s Republic of China

Background: This study was aimed to explore the clinical characteristics and prognoses of acute myeloid leukemia (AML) patients with CEBPA mutations.
Patients and methods: Three hundred and forty-five patients with de novo AML were retrospectively analyzed with regard to CEBPA mutations, clinical characteristics, therapeutic responses, and long-term outcomes.
Results: CEBPA mutations were detected in 59 patients (17.10%), with 47 cases harboring double mutations and 12 cases harboring single mutations. In those with a normal karyotype (NK), 44 cases (25.29%) were detected with CEBPA mutations. The following characteristics were observed in CEBPA-mutated patients: most (66.10%) of them were M1 or M2; they presented with higher peripheral white blood cell counts (23.71 [12.6, 60.02] ×109/L versus 7.34 [2.38, 26.63] ×109/L; u=4.944, P<0.001) and higher hemoglobin levels (89.64±23.05 g/L versus 75.65±23.65 g/L; t=4.156, P<0.001) than those observed in patients without the mutation; and the expression of CD7 and HLA-DR was higher, whereas that of CD34 and CD56 was lower in patients with the mutation than in those without the mutation. Compared with those without the mutation, patients with CEBPA mutations had a superior complete remission rate (75.0% versus 56.54%; χ2=6.185, P=0.013) and superior overall survival (P=0.034).
Conclusion: The frequency of CEBPA mutations may be higher in Chinese patients with AML than has been reported in populations of western countries, and the presence of CEBPA mutations is an indication of favorable prognoses for these patients.

Keywords: acute myeloid leukemia, CEBPA mutations, immunophenotype, complete remission, long-term prognoses

Introduction

Genetic mutations can provide important information for the prognoses of patients with acute myeloid leukemia (AML). CEBPA is a leucine zipper transcription factor with a pivotal role in myeloid differentiation. Mutations in CEBPA have been described in ~5%–14% of patients with AML.18 They can occur across the whole gene, but cluster in two main hotspots: N-terminal out-of-frame insertions/deletions cause translation of a 30 kDa protein, from an internal ATG start site, that lacks transactivation domain 1 and has a dominant negative effect over the full-length p42 protein, and C-terminal mutations are generally in-frame insertions/deletions, in the DNA-binding or leucine zipper domains, that disrupt binding to DNA or dimerization.2 Patients who have AML with CEBPA mutations can be separated into two subgroups, namely, those with a single mutation CEBPA (CEBPAsm) and those with a double mutation CEBPA (CEBPAdm).8 AML patients with mutated CEBPA have better overall survival (OS) and relapse-free survival (RFS) and tend to possess a higher complete remission (CR) rate than those without CEBPA mutations.18 However, recent data have suggested that the good prognoses may be limited to patients with CEBPAdm and may not extend to those with CEBPAsm.2,46,8 CEBPA mutations were adopted as important indicators for AML, in both the National Comprehensive Cancer Network guideline and the European Leukemia Net classification. AML with mutated CEBPA has been designated as a provisional disease entity in the category “AML with recurrent genetic abnormalities” in the current World Health Organization classification of AML.

Although CEBPA mutations have been studied for many years in AML, there were limited data about its prevalence and prognostic significance in Chinese patients with AML. In this study, we retrospectively analyzed CEBPA mutations in 345 patients with de novo AML in our clinical center.

Patients and methods

Patients and treatment

From August 1, 2011, to May 30, 2015, 345 patients with de novo AML (including 183 males and 162 females), aged 3–80 years (median age: 44 years), and who were residents of the northeast region of the People’s Republic of China, including the Jilin, Heilongjiang, and Liaoning provinces, were enrolled in this study. The patients were categorized into French–American–British (FAB) subtypes based on morphological diagnoses. Acute promyelocytic leukemia (APL) patients were treated with arsenic trioxide and all-trans retinoic acid for induction therapy. Darubicin + cytarabine and mitoxantrone + cytarabine regimens were consolidated for the subsequent therapy. Non-APL patients were treated with the standard “3+7” regimen for initial induction therapy (darubicin/idarubicin + cytarabine). In some elderly patients, a cytarabine + aclarubicin + granulocyte-colony stimulating factor (G-CSF) regimen was administered. Response was assessed by bone marrow aspiration performed on days 14 and 28. The first consolidation therapy was generally the same as that used to achieve CR. Four courses of high-dose cytarabine at 2–3 g/m2 (for some patients >60 years, cytarabine at 1–1.5 g/m2) were administered for consolidation therapy. High-risk patients, and those with a matched sibling, were treated with hematopoietic stem cell transplantation (HSCT). All the participating patients gave written informed consent prior to enrollment in the study, and this study was approved by the ethics committee of the First Hospital of Jilin University and conducted in accordance with the Declaration of Helsinki.

Cytogenetic, molecular mutation, and surface marker analyses

Standard culturing and banding techniques were used to analyze the chromosome karyotype, and the clonal abnormalities were defined and described according to the International System for Human Cytogenetic Nomenclature.9 Mutational statuses of NPM1, FLT3-ITD, c-kit, and CEBPA were analyzed, and polymerase chain reactions were performed as previously described.2,4,10 The expressions of CD34, CD33, HLA-DR, CD11c, CD13, CD14, CD15, CD123, CD7, CD56, and other surface markers were analyzed by flow cytometry.

Statistics

Chi-square test, independent sample t-test, or Mann–Whitney U-test, as appropriate for the type of data being analyzed, were used to assess the statistical significance of the difference between the two groups. Kaplan–Meier method was employed for survival analysis, and log-rank test was used to compare differential survival between groups. OS was defined as the time from day 1 of induction to death, HSCT, or last contact. RFS was the time from CR to relapse, death, HSCT, or last contact. P<0.05 was considered significant. SPSS software (Version 16.0; SPSS Inc., Chicago, IL, USA) was used to calculate statistically significant differences.

Results

FAB classification and cytogenetics

The most common subtype in the present cohort was M2 (42.90%, n=148), followed by M4 (21.45%, n=74), M5 (15.65%, n=54), and APL (13.33%, n=46). The frequency of other subtypes was <5% (M1: 2.90% [10/345] and M6: 3.19% [11/345]). Successful cytogenetic analyses were achieved in 298 (86.38%) patients, among whom 174 (58.39%) were considered cytogenetically normal.

Molecular mutations

Of the 345 patients, 59 (17.10%) were detected as CEBPA mutants, in which 47 cases were CEBPAdm and 12 were CEBPAsm. The frequency of CEBPA mutations was 25.29% (44/174) in those with a normal karyotype (NK). The incidence rates of NPM1 and FLT3-ITD mutations were 14.78% (51/345) and 13.62% (47/345), respectively. In those with an NK, the frequencies were 25.29% (44/174) and 18.39% (32/174) for NPM1 and FLT3-ITD mutations, respectively. Sixteen patients (4.69%, 16/345) with c-kit mutations were detected.

Clinical characteristics of patients with CEBPA mutations

Clinical characteristics of patients with or without CEBPA mutations are listed in Table 1. There was no significant difference in age or sex between patients with or without CEBPA mutations (P>0.05). Of the 59 cases with CEBPA mutations, 39 (66.10%) were M1 or M2. Patients with CEBPA mutations had a higher percentage of NK (89.80%, 44/49) than those without (52.21%, 130/249; χ2=23.808, P<0.001). Although the frequencies of NPM1, FLT3-ITD, and c-kit were lower in patients with CEBPA mutations than those without, no significant difference was detected for any such mutation (each P>0.05). Compared with those without mutations, expression of CD7 and HLA-DR was higher, whereas that of CD34 and CD56 was lower in patients with CEBPA mutations (each P<0.05). CEBPA-mutated patients presented with higher white blood cell counts and hemoglobin levels than those without such mutations (P<0.05 for each hemocytological analysis). Platelet counts of patients with CEBPA mutations tended to be lower than of those without CEBPA mutations; however, there was no significant difference (P=0.179).

Table 1 Clinical characteristics of patients with and without CEBPA mutations
Abbreviations: FAB, French–American–British; APL, acute promyelocytic leukemia; WBC, white blood cell.

Therapeutic response and outcomes

Of the 299 patients with non-APL, 39 did not choose chemotherapy and the remaining 260 were administered one course of chemotherapy, with 13 patients not being subsequently evaluated for this study. One-hundred and fifty cases achieved CR, a rate of 60.73% (150/247). Forty-one cases achieved partial remission, and the overall response rate was 77.33% (191/247). The CR rate was higher in patients with CEBPA mutations (75.0%, 42/56) than in those without CEBPA mutations (56.54%, 108/191; χ2=6.185, P=0.013). Two patients with CEBPA mutations and eight without CEBPA mutations received HSCT. The follow-up time ranged from 1 month to 34 months (median: 8 months). At the time of analyses, 34 patients (12.8%) relapsed and 13 (10.6%) had died. Two-year RFS was 66.1% in patients with CEBPAdm, which was higher than in those without such mutations (51.5%), but no significant difference was detected (P=0.145; Figure 1). Patients with CEBPAdm had superior OS compared with those without CEBPAdm (2-year OS: 88.9% versus 63.5%; P=0.034; Figure 2).

Figure 1 Relapse-free survival in patients with and without CEBPA mutations.
Abbreviation: CEBPAdm, double mutation CEBPA.

Figure 2 Overall survival in patients with and without CEBPA mutations.
Abbreviation: CEBPAdm, double mutation CEBPA.

Discussion

AML is a heterogeneous disease. Cytogenetics and molecular markers play very important roles in diagnoses, treatment selections, and prognoses. However, ~60% of our AML patients had NK, and their prognoses can be further stratified according to molecular mutations; CEBPA mutations were such molecular markers for prognoses. However, there are limited data about the prevalence and prognostic significance of CEBPA mutations in AML patients from a Chinese population. No study has been performed to investigate the immunophenotype of Chinese AML patients with CEBPA mutations. In this study, we analyzed the clinical characteristics, therapeutic responses, and long-term outcome details in a consecutive cohort of Chinese patients.

The frequency of CEBPA mutations was 17.10% in this study, which was higher than that reported in populations from Switzerland (8.48%),5 the Netherlands (6.90%),6 the UK (7.0%),4 or France (8.0%),7 but was approximately the same as that reported in the scientific literature on a Chinese population (20.6%).11 Shen et al12 reported that the occurrence rate of CEBPA mutations was 12.2% in Chinese patients with AML. However, the proportion of APL was much higher in their cohort (32.7%) than in the present study (13.33%) or in other published reports. In this and previous studies on APL patients,12,13 the incidence rates of CEBPA mutations or NKs in Chinese patients were 25.29% and 22.0%–26.1%, respectively, which were higher than those reported in patients from the western world (10%–18%).13,8 Hence, the prevalence of CEBPA mutations may be higher in Chinese patients with AML than in their European counterparts, and further research is needed to validate.

Consistent with previous studies, CEBPA mutations were linked to morphologies M1 and M2 (66.10% of the mutated patients were M1 or M2).2,4 The correlation between M1 and M2 FAB subtypes and CEBPA mutations observed in this study and previous studies supports the critical role of the CEBPA gene in the intermediate stages of granulocytic differentiation. This also might be the case in patients with CEBPA mutations presenting with lower platelet counts, although no statistical significance to that effect was calculated in this study. We found that CEBPA-mutated patients presented with higher peripheral white blood cell counts, which was not previously observed in non-Chinese patients, but is consistent with one study on a population from the People’s Republic of China.12 This may be due to the following reasons: 1) higher CEBPA mutations were observed in this study and Shen et al’s study and 2) the frequency of NPM1 mutations, which was associated with higher peripheral leukocyte counts, was higher in patients with CEBPA mutations in this study (6.78% versus 0.0%–3.3% in previous studies2,8).

In the present study, we also analyzed the immunophenotype of leukemia cells from AML patients. Lin et al14 reported that positive rates (the cutoff value for positive result was defined as ≥20% cells) of CD7, CD34, CD15, and HLA-DR were significantly higher in patients with CEBPA mutations. We used the percentages of cells with clusters of differentiation markers as our immunophenotype criterion and found that the expression levels of CD7 and HLA-DR increased, whereas those of CD34 and CD56 decreased. There was some controversy for CD34 expression in CEBPA-mutated patients. One study from Germany2 supported the observation in this study, but another German study3 reported contrasting results. One relevant consideration is that the patients in these two German studies were those with NK.2,3

We also observed that CEBPA-mutated patients have higher CR rates similar to those of previous studies.8,12 Although we did not find a significant difference for RFS between patients with and without CEBPAdm, both this study and previous studies indicate that CEBPAdm patients had better OS compared with those without the mutation. We did not evaluate the influence of single or double CEBPA mutations on prognoses, owing to the small number of patients with the single mutation.

FLT3-ITD is an indicator of unfavorable prognoses in patients with AML. In this study, six patients with CEBPA mutations had the FLT3-ITD mutation. Three patients refused further treatment after induction therapy, including one with CR and two with NR, owing to personal reasons. The remaining three patients showed continued CR after four cycles of high-dose cytarabine consolidation, and they received maintenance therapy with biological cellular immune therapy or decitabine.

Conclusion

Both this study and previous studies suggest a higher prevalence of CEBPA mutations in AML patients from Chinese population than that in AML patients from populations of western countries, and CEBPAdm had a favorable impact on prognoses in AML patients.

Acknowledgments

The authors thank the Department of Hematology and Oncology of The First Hospital, Bethune Medical College of Jilin University, for their assistance in this work. This work was supported by the Fifth Youth Developmental Foundation of The First Hospital of Jilin University (no JDYY52014004).

Disclosure

The authors report no conflicts of interest in this work.


References

1.

Fröhling S, Schlenk RF, Stolze I, et al. CEBPA mutations in younger adults with acute myeloid leukemia and normal cytogenetics: prognostic relevance and analysis of cooperating mutations. J Clin Oncol. 2004;22(4):624–633.

2.

Dufour A, Schneider F, Metzeler KH, et al. Acute myeloid leukemia with biallelic CEBPA gene mutations and normal karyotype represents a distinct genetic entity associated with a favorable clinical outcome. J Clin Oncol. 2010;28(4):570–577.

3.

Marcucci G, Maharry K, Radmacher MD, et al. Prognostic significance of, and gene and microRNA expression signatures associated with, CEBPA mutations in cytogenetically normal acute myeloid leukemia with high-risk molecular features: a Cancer and Leukemia Group B Study. J Clin Oncol. 2008;26(31):5078–5087.

4.

Green CL, Koo KK, Hills RK, Burnett AK, Linch DC, Gale RE. Prognostic significance of CEBPA mutations in a large cohort of younger adult patients with acute myeloid leukemia: impact of double CEBPA mutations and the interaction with FLT3 and NPM1 mutations. J Clin Oncol. 2010;28(16):2739–2747.

5.

Pabst T, Eyholzer M, Fos J, Mueller BM. Heterogeneity within AML with CEBPA mutations; only CEBPA double mutations, but not single CEBPA mutations are associated with favorable prognosis. Br J Cancer. 2009;100(18):1343–1346.

6.

Wouters BJ, Löwenberg B, Erpelinck-Verschueren CA, van Putten WL, Valk PJ, Delwel R. Double CEBPA mutations, but not single CEBPA mutations, define a subgroup of acute myeloid leukemia with a distinctive gene expression profile that is uniquely associated with a favorable outcome. Blood. 2009;113(13):3088–3091.

7.

Renneville A, Boissel N, Gachard N, et al. The favorable impact of CEBPA mutations in patients with acute myeloid leukemia is only observed in the absence of associated cytogenetic abnormalities and FLT3 internal duplication. Blood. 2009;113(21):5090–5093.

8.

Taskesen E, Bullinger L, Corbacioglu A, et al. Prognostic impact, concurrent genetic mutations, and gene expression features of AML with CEBPA mutations in a cohort of 1182 cytogenetically normal AML patients: further evidence for CEBPA double mutant AML as a distinctive disease entity. Blood. 2011;117(8):2469–2475.

9.

Shaffer LG, Slovak ML, Campbell LJ, editors. ISCN 2009: An International System for Human Cytogenetic Nomenclature (2009). Basel: Karger; 2009.

10.

Rulina AV, Spirin PV, Prassolov VS. Activated leukemic oncogenes AML1-ETO and c-kit: role in development of acute myeloid leukemia and current approaches for their inhibition. Biochemistry (Mosc). 2010;75(13):1650–1666.

11.

Ruan GR, Niu JH, Li LD, et al. DNA fragment length analysis for screening of CEBPA mutations in acute myeloid leukaemia. Clin J Clin. 2011;5(1):64–69.

12.

Shen Y, Zhu YM, Fan X, et al. Gene mutation patterns and their prognostic impact in a cohort of 1185 patients with acute myeloid leukemia. Blood. 2011;118(20):5593–5603.

13.

Ruan GR, Jiang B, Niu JH, et al. Detection of CEBPA gene mutations in acute myeloid leukaemia and its clinic significance. Clin J Clin. 2011;5(17):4987–4991.

14.

Lin LI, Chen CY, Lin DT, et al. Characterization of CEBPA mutations in acute myeloid leukemia: most patients with CEBPA mutations have biallelic mutations and show a distinct immunophenotype of the leukemic cells. Clin Cancer Res. 2005;11(4):1372–1379.

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