Printer Friendly


Byline: Ayesha Khurshid, Saleem Ahmed Khan, Chaudhry Altaf, Hamid Saeed Malik, Muhammad Mukarram Bashir and Maria Altaf


Objective: To evaluate Immunophenotyping patterns in Mixed-Phenotype Acute Leukemias (MPAL).

Study Design: Descriptive study.

Place and Duration of Study: This study was carried out in the department of Hematology, Armed Forces Institute of Pathology Rawalpindi, from 1st Jan 2013 to 31st Jan 2017.

Material and Methods: After taking informed consent from the patients fulfilling the inclusion criteria, detailed history was taken and blood samples were drawn for blood complete picture. The patients suspected to have acute leukemia were subjected to bone marrow examination (aspiration and trephine biopsy) for further cytochemical staining (SBB) and Immunophenotyping.

Results: Total 680 new cases of acute leukemias on initial workup of either gender age were included. Patients of other haematological disorders were excluded from the study. Among 680 new cases of acute leukaemia, 23(3.4%) cases were of MPAL immunophenotyping using scoring system proposed by EGIL (European Group for the Immunological Characterization of Leukemias) classification. Among MPAL, 19(83%) cases were Biphenotypic [13(57%) cases of My/B-ALL, 5(22%) cases of My/T-ALL, and 1(4%) case of T/B-ALL]. 4(17%) cases were Bilineage (My/B-ALL). Most of the cases were diagnosed at less than 10 years of age.

Conclusion: My/B-ALL is the most common immunophenotype followed by My/T-ALL. Therefore immunophenotyping is indispensable for diagnosis and for therapy decisions of MPAL.

Keywords: Acute leukemia, Immunophenotype, Lineage, Lymphoid, Myeloid, Mixed phenotype acute leukemia.


Acute leukemia of ambiguous lineage are the type of leukemias in which the blasts demonstrate no clear evidence of differentiation along a single lineage1. This group includes those acute leukemias in which there is no associated expression of lineage-specific antigens (acute undifferentiated leukemia), as well as those in which there is expression of antigens associated with more than one lineage (mixed phenotype acute leukemias). The diagnosis of acute leukemias (AL) is based on clinical features, systemic examination bone marrow aspiration and trephine biopsy findings, immunophenotyping, cytogenetic and molecular investigations.

Acute leukemias are classified as having myeloid or B-lymphoid or T-lymphoid lineage, based on morphological features, as well as the expression of surface or cytoplasmic antigens on blast cells2. But there are rare cases of AL in which it is very difficult to classify the blasts, as they have morphologic, cytochemical and immunophenotypic characteristics of both myeloid and lymphoid lineages. This type of entity was defined as mixed-phenotypic AL (MPAL). Previously called biphenotypic acute leukemias (BALs), these neoplasms have been renamed mixed-phenotype acute leukemia (MPAL)3. BAL is characterized by one blast population that co-expresses several myeloid and lymphoid antigens in the same cells. In contrast, bilineage AL there are two separate blast populations, with each population expressing markers of a distinct lineage.

Mixed-phenotype acute leukemia (MPAL) is an uncommon clinical entity arising from a haemopoietic pluripotent stem cell, it is also known as mixed-lineage or hybrid acute leukemia4,5. Its incidence among acute leukemia account for approximately less than 5% of all acute leukemia6. Occurs in all age groups but are more frequent in adults7. Signs and symptoms of biphenotypic acute leukemias are similar to acute leukaemia. The diagnostic criteria were based on the scoring system proposed by the European Group for the Immunological characterization of Leukemias (EGIL) classification, that was adopted by the WHO 2001 classification8, as shown in table-I and by the 2008 WHO Classification of Tumors of Hematopoietic and Lymphoid Tissues9-11.

EGIL is based on lineage specific and lineage associated markers. Two marks are given to each of lineage specific markers and 0.5 and 1 mark is given to each of lineage associated markers. According to this scoring system, a case is considered as MPAL when point values are greater than two for the myeloid and one of the lymphoid lineages.

It is not unusual to identify two distinct blast populations in the same patient, one of small size with a high nucleus/cytoplasm ratio resembling lymphoblasts and the other larger with more abundant cytoplasm with or without granulation resembling myeloblasts.

Immunophenotyping is essential for the diagnosis of mixed-phenotype acute leukaemia. MPAL is subdivided into four groups according to the expression of lymphoid and myeloid markers on the blasts. The most common are those in which the blasts co express myeloid and B-lymphoid, less often is myeloid and T-lymphoid antigens12,13. Trilineage differentiation with expression of B, T and myeloid markers is rare and coexistence of blasts expressing only B and T cell markers is very uncommon14. Most cases are terminal deoxynucleotidyl transferase (TdT) positive and express early hemopoietic markers such as CD34 and HLA-DR expression15,16.

The aim of our study is to evaluate Immunophenotyping patterns by flow cytometry in Mixed-Phenotype Acute Leukemias (MPAL) using scoring system proposed by EGIL.


This study was carried out in the department of Hematology, Armed Forces Institute of Pathology Rawalpindi. It was a descriptive, cross sectional study. The study was completed over a period of 4 years, from 1st Jan 2013 to 31st Jan 2017. Samples from patients of acute leukaemia on initial workup of either gender or age were included. Patients of other hematological malignancies were excluded from the study. A total of 680 patients of acute leukemia were included in this study. After taking informed consent from the patients fulfilling the inclusion criteria, detailed history was taken and blood samples were drawn for Blood complete picture. Sampling technique was non-probability consecutive sampling. In all cases MPAL we analyzed the laboratory values: white blood cell (WBC) count, hemoglobin (Hb) level, platelet count (Plt) and blast percentage.

Morphologic examination of peripheral blood (PB) and bone marrow (BM) smear and cytochemical staining (SBB) was performed after staining by standard technique with Leishman stain. Immunophenotyping of the patients suspected to have acute leukaemia was done.


Three ml of whole blood/0.5 ml bone marrow was collected and TLC, DLC was performed by Sysmex KX 21 automated hematology analyzer. Blood smear was examined for DLC and lymphocyte morphology. Carefully check the antibody panel required for the procedure. The monoclonal antibodies (MoAb) used for diagnosis of AL were: for B-lineage: CD19, CD22, CD20, CD10, for T-lineage: CD2, CD3, CD5, CD7, CD4, CD8, for myelo-monocytic lineage: CD13, CD33, CD11c, CD64, CD14, other cells surface markers: CD34, CD117, HLA-DR and intracellular MoAb: CD79a, CD3 and MPO. Each test tube (Falcon, BD) was labeled properly and placed in sequence. 10 u|of antibody was added in each tube as per defined panel, then 50 u|of whole blood/diluted bone marrow was added in each tube and thoroughly mixed. It was incubated in dark for 30 minutes at room temperature.

Dilution (1:10) of FACSLyse solution in distilled water was made. 2 ml of diluted FACSLyse was added in each tube. This was incubated in dark for 5 minutes at room temperature. Centrifuge at 300 g for 5 minutes at room temperature. Supernatant was discarded after centrifugation. 2 ml of RPMI 1640/PBS was added to each tube. Supernatant was discarded after centrifugation. Formalin (0.5 ml of 3.3%) was added to each test tube and kept at 4AoC until analysis on flow cytometer. The blast gate was identified on side scatter/CD45 dot plot. Data analysis were performed with Paint-a-Gate software. Surface antigen expression was considered positive if at least 20% of blasts showed a positive labeling. For cytoplasmic antigen expression, the threshold was 10%.

Table-I: European group for the immunological characterization of Leukemias (EGIL) classification.

Scoring###B lineage###T lineage###Myeloid Lineage

2 Points###CD79a, CD22, cyt IgM###CD3###MPO

1 Point###CD19, CD10, CD20###CD2, CD5###CD13, CD33, CD117,


0.5 Point###TdT###TdT, CD7###CD14, CD15, CD64,

###CD11b, CD11c

Table-II: Clinical and laboratory features of patients at diagnosis.


Age (yrs)###2###65###22

WBC (X109/L)###2.29###471###9.87

Hemoglobin mg/dl###4.8###12.5###9.4

Platelet count(X109/L)###5###392###33


Table-III: Comparison between My/B-ALL and My/T-ALL immunophenotype for age and sex.

###My/B-ALL (n=17)###My/T-ALL (n=5)###p-value

Age (30 yrs)###9###0




Data Analysis

All the collected data were entered and analyzed in Excel 2007. Median and range were calculated for quantitative variable like age, WBC count, haemoglobin, platelet count, percentege of blasts. Frequencies and percentages were calculated for qualitative variables like gender. Effect modifiers like age and gender were controlled by stratification. Post stratification chi-square test was applied, keeping p-value <0.05 as significant. Final data was shown by tables.


Among 680 new cases of acute leukaemia, 23 cases were diagnosed with MPAL using scoring system proposed by EGIL classification. The overall incidence was 3.4% of MPAL. Among 23 patients of MPAL, 19 (83%) cases were biphenotypic [13(57%) cases of My/ B-ALL, 5 (22%) cases of My/T-ALL, and 1(4%) case of T/B-ALL]. 4(17%) cases were bilineage (My/B-ALL). In our study the CD34 was positive in 21 (91%) cases and negative in 2(9%) cases. Tdt was positive in 14(61%) patients, negative in 6 (26%) patients and not determined in 3 (13%) patients.

Immunophenotypic findings in patients of My/B-ALL, My/T-ALL, and T/B-ALL are shown in fig-1, 2 and 3 respectively.

Among the 23 cases of MPAL, 16 were males (70%) and 07 were females (30%). Male to female ratio was 2.3:1. Most of the cases were diagnosed at less than 10 years of age.

Most common symptom were fever and pallor. Hepatosplenomegaly was found in 20 (87%) patients and cervical lymphadenopathy was found in 10 (43%) patients. Anemia was present in 14 (56%) patients at the time of presentation.

All patients had variable number of blasts in the peripheral blood film and in bone marrow aspirate. Morphologically, in 8 (35%) cases the blasts had lymphoblastic morphology, in 11(48%) cases the blasts had myeloblastic morphology and 4(17%) cases had a dual population of small and large blasts difficult to classify by morphology. SBB positivity was seen 11 (48%), along with 3 weak positive cases, and 12 (52%) patients were SBB negative. Trephine biopsy sections showed diffuse and interstitial infiltration by blast cells in all the cases.

Focal and Diffuse fibrosis was seen in 20 (87%) cases, ranging from grade I to III by reticulin staining and unremarkable in 3 (13%) cases. The main clinical and laboratory features are summarized in table-II.

There were no significant differences between My/B-ALL and My/T-ALL immuno-phenotypes for age 30 years (p-value: 0.09) and gender (p-value: 0.228), shown in table-III. However one patient with the B/T-ALL immunophenotype was child (age 4 years). All 5 patients with a My/T-ALL were males and all females were of My/B-ALL immunophenotype.


Mixed-phenotype acute leukemia (MPAL) is a rare entity that comprises 0.5-4% of all acute leukemias17, in our laboratory 3.4% of acute leukemias were identified as MPAL. Prevalence of MPAL according to study by Xu et al, Owaldah et al, Mi et al is 4.6%, 3.4% and 3.4% respectively, which is comparable to our study. However in a study by Legrand et al prevalence of MPAL is 8% which is higher as compare to our study. There were heterogeneous population of blasts in our patients similar to other studies18.

Our study showed that out of total 680 patients of acute leukaemia 23(3.4%) were MPAL. Among MPAL, 16 were males (70%) and 07 were females (30%). Male to female ratio was 2.3:1. The male predominance in our study population is comparable with Legrand et al (France) (2.3:1)18, Mi et al (China) (2.2:1)19 and Aribi et al (USA) (2:1)20. In Xu et al (China) (1.3:1), Owaidah et al (Kingdom of Saudi Arabia) (1.6:1)21, Lee et al (Korea) (1.4:1)22, Weir et al (USA)(1.7:1)23 and other international studies male predominance is less significant. In his study (Xu et al), out of total 21 patients 12 (57%) were males and 9 (43%) were females. Male to female ratio was 1.3:1. However Matutes et al (UK), in their study has shown that out of total 100 patients 62(62%) were males and 38 (38%) were females7. Male to female ratio was 1.6:1.

The age of the patients with MPAL in our study ranged from 2 to 65 years with median age was 18 years. Xu et al (China) in their study has shown that age of patients with MPAL ranged from 15 to 73 years, with a median age of 41 years. In another study conducted in UK by Matutes et al (Blood 2011), twenty-eight (28%) patients were children, 2 of whom were infants (<1-year old) and 68 (68%) were adults (<15-years old) i-e; mostly the patients were adults but in contrast, in our study most of the patients were children <10 years old. In our population majority of MPAL patients are seen at younger age group, probably because Pakistan generally harbors younger population or there might be some biological variation of the disease in the sub-continent.

Median WBC count in the MPAL in our study was 9.87 x 109/L. Minimum WBC was 2.29 x 109/L and maximum was 471 x 109/L. Xu et al showed median WBC of 19.4 x 109/L. Minimum WBC was 0.7 x 109/L and maximum was 450 x 109/L, which is comparable to our study. A study done by Lee et al22 showed that median WBC of 7.4 x 109/L. Minimum WBC was 0.5 x 109/L and maximum was 520 x 109/L, which is also comparable to our study.

The most frequent immunophenotype was B-lymphoid + myeloid followed by T-lymphoid + myeloid immunophenotype. In a study from China (Xu et al) author compared, 9 other published studies containing from 19 to 63 cases of MPAL. They concluded that the most frequent type of MPAL involves the co-expression of markers of myeloid and B-lineage, between 47 and 72% (My/B-ALL). MPAL with myeloid and T-lineage markers are next in frequency (24%) (My/T-ALL), while both B/T and triple myeloid/B/T BAL are rare.

In Matutes et al, immunophenotyping showed that 59 (59%) cases had a B-lymphoid + myeloid immunophenotype (My/B-ALL), 35 (35%) had T-lymphoid + myeloid immunopheno-type (My/T-ALL), 4 (4%) had B + T-lymphoid immunophenotype (B/T-ALL), and in the remaining 2 cases (2%) there was evidence of trilineage concomitant expression (myeloid, B, and T lymphoid) (My/B/T-ALL).

In our study My/B-ALL immunophenotype was 13(57%), My/T-ALL was 5(22%) and B/T-ALL was only 1(4%). Four (17%) cases were bilineage (My/B-ALL). No case of trilineage expression (myeloid, B, T lymphoid) is reported in our study. The results of our study are comparable to international studies. The origin of blasts cells in MPAL is unknown, most probably this leukemia arises in a very early hemopoietic progenitor cells with potential to undergo either lymphoid or myeloid differentiation or rarely B-and T-cell differentiation7. Most cases of MPAL show expression of early hemopoietic stem cell marker CD3417, MPAL without CD34 are rare. Beata et al2 showed that out of total 8 cases of MPAL, CD34 was positive in 7 (88%) cases and 1 (12%) was negative for CD343. In a study by Xu et al 17 (81%) patients were positive for CD34 and 4 (19%) patients were negative for CD34.

In our study the CD34 was positive in 21 (91%) cases and negative in 2 (9%) cases. Thus CD34 positivity in our study is similar to international studies.

In Xu et al, Tdt was positive in 15 (71%) patients and negative in 6 (29%) patients. In Matutes et al, Tdt was positive in 81 (89%) out of 91 cases and negative in 10 (11%) cases. In our study Tdt was positive in 14 (61%) patients, negative in 6 (26%) patients and not determined in 3 (13%) patients, similar to international studies.


My/B-ALL is the most common immuno-phenotype followed by My/T-ALL. Therefore immunophenotyping is indispensable for diagnosis and for therapy decisions of MPAL.


This study has no conflict of interest to declare by any author.


1. Manola KN. Cytogenetic abnormalities in acute leukaemia of ambiguous lineage: an overview. Br J Haematol 2013; 163: 24-39.

2. Porwit A, Bene MC. Acute Leukemias of Ambiguous Origin. Am J Clin Pathol 2015; 144(3): 361-76.

3. Beata JK, Benedek, Erzsebet B, Eniko K, Aliz T, Monica I. The Role of Immunophenotyping in Diagnosis of Biphenotypic Acute Leukemias. AMM 2011; 57(3): 218-21.

4. Ye Z, Wang S. Mixed phenotype acute leukemia. Chin Med J (Engl) 2014; 127(16): 2999-3003.

5. Sarma A, Sharma DJ, Bhuyan C, Hazarika M, Kataki CA. A Biphenotypic (Mixed Phenotypic) Acute Leukemia: Report of two cases with immunophenotypic study. OJBD 2013; 3(2): 65-8.

6. Van den Ancker W, Westers TM, de Leeuw DC, van der Veeken YF, Loonen A, van Beckhoven E, et al. A threshold of 10% for myeloperoxidase by flow cytometry is valid to classify acute leukemia of ambiguous and myeloid origin. Cytometry B Clin Cytom 2013; 84(2): 114-8.

7. Matutes E, Pickl WF, Van't Veer M, Morilla R, Swansbury J, Strobl H, et al. Mixed-phenotype acute leukemia: clinical and laboratory features and outcome in 100 patients defined according to the WHO 2008 classification. Blood 2011; 117(11): 3163-71.

8. Bene MC, Castoldi G, Knapp W, Ludwig WD, Matutes E, Orfao A et al. Proposals for the immunological classification of acute leukemias. European group for the immunological characterization of leukemias (EGIL). Leukemia 1995; 9: 1783-86.

9. Pomerantz A, Rodriguez-Rodriguez S, Demichelis-Gomez R, Barrera-Lumbreras G, Barrales-Benitez O, Lopez-Karpovitch X, et al. Mixed-phenotype acute leukemia: Suboptimal treatment when the 2008/2016 WHO classification is used. Blood Res 2016; 51(4): 233-41.

10. Matutes E, Morilla R, Farahat N, Carbonell F, Swansbury J, Dyer M, et al. Definition of acute biphenotypic leukemia. Haematologica 1997; 82: 64-66.

11. Borowitz MJ, Bene MC, Harris NL, Porwit A, Matutes E. Acute leukemias of ambiguous lineage. In: Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, Thiele J, Vardiman JW (Eds.): WHO classification of tumors of haematopoietic and lymphoid tissues. IARC: Lyon 2008. 149-55.

12. Gajendra S, Sachdev R, Dorwal P, Goel S, Jha B, Sahni T. Mixed-phenotypic acute leukemia: cytochemically myeloid and pheno-typically early T-cell precursor acute lymphoblastic leukemia. Blood Res 2014; 49(3): 196-98.

13. Chen W. Case study interpretation-New Orleans: case 2. Mixed phenotype acute leukemia, T/myeloid. Cytometry B Clin Cytom 2013; 84: 342-345.

14. Kohla SA, Sabbagh AA, Omri HE, Ibrahim FA, Otazu I B, Alhajri H, et al. Mixed Phenotype Acute Leukemia with Two Immunophenotypically Distinct B and T Blasts Populations, Double Ph+ Chromosome and Complex Karyotype: Report of an Unusual Case.Clin Med Insights Blood Disord 2015; 8: 25-31.

15. Wolach O, Stone RM. Mixed-phenotype acute leukemia: current challenges in diagnosis and therapy. Curr Opin Hematol 2017; 24(2): 139-145.

16. Rahman K, George S, Tewari A, Mehta A. Mixed phenotypic acute leukemia with two immunophenotypically distinct blast populations: Report of an unusual case. Cytometry B Clin Cytom 2013; 84(3): 198-201.

17. Xu XQ, Wang JM, Lu SQ, Chen Li, Yang JM, Zhang JP et al. Clinical and biological characteristics of adult biphenotypic acute leukemia in comparison with that of acute myeloid leukemia and acute lymphoblastic leukemia: A case series of a Chinese population. Haematologica 2009; 94: 919-27.

18. Legrand O, Perrot JY, Simonin G, Baudard M, Cadiou M, Blanc C, et al. Adult biphenotypic acute leukaemia: an entity with poor prognosis which is related to unfavourable cytogenetics and P-glycoprotein over expression. Br J Haematol 1998; 100: 147-55.

19. Mi Y, Bian S, Meng Q, Xue Y, Yu M, Chen G, et al. Study on the clinical characteristics of biphenotypic acute leukemia. Zhonghua Xue Ye Xue Za Zhi 2000; 21(7): 352-4.

20. Aribi A, Bueso-Ramos C, Estey E, Estrov Z, O'Brien S, Giles F, et al. Biphenotypic acute leukaemia: A case series. Br J Haematol 2007; 138(2): 213-6.

21. Owaidah TM, Al Beihany A, Iqbal MA, Elkum N, Roberts GT. Cytogenetics, molecular and ultrastructural characteristics of biphenotypic acute leukemia identified by the EGIL scoring system. Leukemia 2006; 20(4): 620-6.

22. Lee JH, Min YH, Chung CW, Kim BK, Yoon HJ, Jo DY, et al. Korean Society of Hematology AML/MDS Working Party. Prognostic implications of the immunophenotype in biphenotypic acute leukemia. Leuk Lymphoma 2008; 49(4): 700-9.

23. Weir EG, Ali Ansari-Lari M, Batista DA, Griffin CA, Fuller S, Smith BD, et al. Acute bilineal leukemia: a rare disease with poor outcome. Leukemia 2007; 21(11): 2264-70.
COPYRIGHT 2017 Asianet-Pakistan
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2017 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Publication:Pakistan Armed Forces Medical Journal
Article Type:Report
Date:Dec 31, 2017

Terms of use | Privacy policy | Copyright © 2020 Farlex, Inc. | Feedback | For webmasters