|MINI SYMPOSIUM: MOLECULAR ONCOLOGY: ORIGINAL ARTICLE
|Year : 2015 | Volume
| Issue : 2 | Page : 91-94
Prognostic significance of cell surface phenotype in acute lymphoblastic leukemia
Shiek Aejaz Aziz1, Susheel Kumar Sharma1, Iram Sabah2, M Aleem Jan3
1 Department of Medical Oncology, Sher-I-Kashmir Institute of Medical Sciences, Srinagar, Jammu and Kashmir, India
2 Department of Clinical Pharmacology, Sher-I-Kashmir Institute of Medical Sciences, Srinagar, Jammu and Kashmir, India
3 Deaprtment of Clinical Hematology, Sher-I-Kashmir Institute of Medical Sciences, Srinagar, Jammu and Kashmir, India
|Date of Web Publication||22-Apr-2015|
Shiek Aejaz Aziz
Department of Medical Oncology, Sher-I-Kashmir Institute of Medical Sciences, Srinagar, Jammu and Kashmir
Source of Support: None, Conflict of Interest: None
Context: To find out the phenotypic character of lymphoblasts of acute lymphoblastic leukemia (ALL) patients in our study cohort and their possible effect on the prognosis. Aims: To investigate the phenotype in ALL in our demographic population and to prognosticate various upfront current protocols employed in our hospital. Settings and Design: The study spanned over a period of 4 years with retrospective and prospective data of January 2008 through December 2011. Materials and Methods: 159 patients of all age groups were enrolled for the study, of which flow cytometry was done in 144 patients. Statistical Analysis Used: Analysis was done using the variables on SPSS (statistical package for social sciences) software on computer. Survival curves were estimated by method of Kaplan-Meir. Results: Majority of the patients were of B-cell (68.1%) and 30.6% patients were of T-cell lineage. Of these, 80.6% patients were having cALLa positivity. Complete remission (CR) was achieved in 59.1%, 16.4% relapsed, and 20.1% patients died. Conclusions: Phenotyping has become an important and integral part of diagnosis, classification, management and prognosticating in ALL. B-cell has been found to have a better survival over T-cell lymphoblastic leukemia. cALLa antigen positivity has good impact in achieving CR in only B-cell lineage, myeloid coexpression has no significant effect on the outcome. BFM (Berlin-Frankfurt-Münster) based protocols though showed a higher CR and survival vis-a-vis UKALL-XII. However, patients enrolled in former group being of low risk category and lesser in numbers cannot be compared statistically with a fair degree of confidence.
Keywords: Acute lymphoblastic leukemia, flow cytometry, immunophenotype, India, Kashmir, leukemia, phenotype, prognosis
|How to cite this article:|
Aziz SA, Sharma SK, Sabah I, Jan M A. Prognostic significance of cell surface phenotype in acute lymphoblastic leukemia. South Asian J Cancer 2015;4:91-4
|How to cite this URL:|
Aziz SA, Sharma SK, Sabah I, Jan M A. Prognostic significance of cell surface phenotype in acute lymphoblastic leukemia. South Asian J Cancer [serial online] 2015 [cited 2019 Nov 17];4:91-4. Available from: http://journal.sajc.org/text.asp?2015/4/2/91/155696
| Introduction|| |
Acute lymphoblastic leukemia (ALL) is characterized by clonal proliferation, accumulation, and tissue infestation of neoplastic cells. It has bimodal distribution with initial peak at 1-4 years of age and second peak ≥60 years of age, a low but steady rise in incidence with increasing age.  Leukemic cells from patients of ALL express a variety of surface differentiation antigens which are also found on normal lymphocyte precursors at discrete stages of maturation. Therefore, ALL cells are thought to originate from normal lymphocyte precursors arrested at early stages of either B-cell or T-cell ontogeny. Majority of the leukemic cells express either B or T lineage differentiation antigen. However, a small fraction of the patients do express both T and B lineage antigens.
Previously, leukemias used to be diagnosed on the basis of morphology of the blasts. Though helpful, its accuracy in diagnosing acute leukemias was only around 80% and a significant number of patients were misdiagnosed and subjected to inadequate treatment, due to considerable overlap of morphological characters in myeloid and lymphoid cells. 
The sequence of events leading to the development of mature lymphoid cells is associated with cell surface modifications that can be easily analyzed by the use of monoclonal antibodies. Flow cytometry has increased the diagnostic accuracy to around 98%.  On this basis; patients can be divided into groups, depending upon the cell of origin like B-cell leukemia, T-cell leukemia. Further, B-cell leukemia can be subdivided into three categories early pre-B, pre-B, and mature B-cell leukemia.  Similarly, T-cell can be subdivided into pre-T cell and T-cell leukemia, according to stage of thymocyte differentiation receptor protein expression.  In addition, there are cells which express myeloid markers like CD-13 and CD-33 and is referred to as myeloid coexpression. The clinical significance of myeloid co expression has been widely debated. ,,,,,,,, The importance of the immunophenotypic analysis of ALL has been documented by numerous studies in adults and children. 
Despite recent progress in the management of ALL, prognosis is still guarded. If complete remission (CR) is achieved in 70%-80% of the patients, relapses occur frequently and long term disease survival does not exceed 25%-30% in most of the studies. ,,,,, It has been seen that patients with lymphoblast's of T-cell lineage have a much poorer prognosis than those with a reciprocal subset of non-T-cell lymphoblasts. ,, Cytogenetics t(9:22), t(4:11), t(1:9), and MLL (Mixed Lineage Leukemia) gene rearrangements have their own impact on outcome.
The present study aimed to investigate the phenotype in ALL in our demographic population and to prognosticate various upfront current protocols employed in our hospital. Also, comparative analysis of relevant available data was done. Impact of markers to subtype leukemias and treat with fair degree of confidence is an established norm. This being first from our state and the institution encouraged us to share our phenotype scenario of leukemias. In fact, this is the first and only study available in North India, depicting significant heterogeneity in phenotypic expression of ALL in India. We believe this could reflect different genotype and biology of our population, opening a window of opportunity for studying therapeutic variability.
| Materials and Methods|| |
Newly diagnosed cases of all age groups were enrolled and followed. Further, patients who were already enrolled since January 2008 were recruited retrospectively. Their data were retrieved from hospital database and those with incomplete recorded data were kept out of the study. Therefore, a 4-year study spanning from January 2008 to December 2011. Informed consent was taken from the patients or their guardians as eligible. Patients with incomplete data or improper follow-up were kept out of the study.
Heparinised bone marrow samples were used for flow cytometry using a panel of monoclonal antibodies to analyze blast cell population. Classification was based on expression of basic leukemia panel like CD3, CD5, CD7, CD8, CD10, CD19, CD20, CD21, CD22, CD13, CD33, CD117, CD79a, HLA-DR, cytoplasm, and surface immunoglobulins. For the markers to be positive, minimum of 20% of gated blast cells had to express the receptor. Patients were sub classified into early pre-B, pre-B, mature B-cell, pre-T, T-cell, mixed phenotype leukemia, or biphenotypic acute leukemia, according to the previously set World Health Organization criteria and European Group for the Immunological Characterization of Leukemias (EGIL) scoring system.
Patients were treated with different protocols like UKALL-XII, Modified BFM-90, pediatric BFM (intermediate and standard risk), and prophylactic cranial irradiation depending on defined risk category. High-risk patients and T-cell leukemias were treated usually with UKALL XII protocol. Also, prophylactic cranial irradiation was given in 65% cases.
Analysis was done using the variables on SPSS (statistical package for social sciences) software on computer. Survival curves were estimated by method of Kaplan-Meir.
| Results|| |
General Immunophenotypic characteristics of the study population [Table 1]
As shown, immunophenotyping was done in 144 patients out of 159. According to the criteria set, 98/144 (68.1%) were of B-cell lineage, which was further sub classified into early Pre-B cell 53/98 (36.8%), pre-B cell 42/98 (29.2%), and mature B-cell 3/98 (2%).
Out of 144 patients, 44 belonged to the T-cell lineage (30.6%). Of these, pre-T cell was seen in 6/44 (4.2%) and T-cell was seen in 38/44 (26.4%).
Also, 94/98 patients (95.6%) in B-cell lineage expressed cALLa antigen while only 50% of the T-cell cases were cALLa positive.
Myeloid co expression (mixed phenotype acute leukemia) was seen in 14/144 cases (9.7%) and biphenotypic acute leukemia was found in 2/144 patients (1.4%).
Comparative analysis of major immunophenotypic groups [Table 2]
T-cell ALL had CR in only 17% and 83% of the cases in this group relapsed or died, which was statistically significant.
cALLa antigen positivity had no significant impact on the outcome or prognosis of T-cell ALL cases.
Prognosis was significantly better in B-cell ALL group when compared with the T-cell group. Also, cALLa antigen positive B-cell cases had significantly more chances of achieving CR (76.6%) and lesser relapse with P value of 0.003.
Early pre-B cell leukemia was significantly associated with myeloid co expression (P = 0.025), whereas pre-B cell phenotype was negatively associated with myeloid co expression (P = 0.012). However, there was no significant effect on the prognosis due to myeloid co expression, neither was there any relation to cALLa antigen positivity.
Comparison of the protocol used to the prognosis [Table 3]
There was significant difference in slow early response (SER), CR, relapse, failure and death between different protocols used.
|Table 3: Protocols received and outcome in patients in whom immunophenotyping was done|
Click here to view
| UKALL-XII|| |
Around half of the patients were put on this protocol (49.9%). First marrow after induction in patients on this protocol showed that 41.4% had SER, whereas 58.6% had CR. Marrow examination after complete treatment revealed that CR was maintained in 41.4%, relapse in 22.9%, failure in 5.7%, and 28.6% patients died during the course of study. Overall survival rate was 71.4% at the end of the study.
Modified BFM 90 protocol
A total of 25.8% cases were put on this protocol. After induction, marrow showed CR in 84.2% and SER in 15.8% patients. At the end of study 71.1% maintained CR, 7.9% patients relapsed, and 21.1% cases died. Thus, overall survival at the end of study in this group was 78.9%.
Pediatric BFM (intermediate risk)
A total of 11.3% patients received this protocol. CR was achieved in 87.5% cases in first marrow after induction and same percentage was maintained till end of study. This rate was significantly higher than UKALL XII and Modified BFM 90 protocols. However, before making any generalizations, it should be noted that significantly less number of cases were on this protocol and that patients in other protocols were of high-risk category and were expected to have poor outcome.
Similarly, around 92.3% cases achieved and maintained CR on pediatric BFM (standard risk) but only a minority of patients were on this group and were of low risk category.
Mean follow up period of the cases was maximum of (23.0 ± 11.5) months in pediatric BFM (standard risk) and least in modified BFM-90 protocol (14.1 ± 9.5) months. There was no significant difference in the complications during treatment with different protocols.
The mean and median survival in age less than or equal to 18 years was 21 months each with standard error of 1, while that in the age group more than 18 years was 24 months respectively. There were more early deaths in the adult age group but was not statistically significant.
Male gender had slightly better survival than females but was not statistically significant.
Overall, UKALL XII protocol maintained high survival with a steady decline, whereas BFM-based protocols showed higher initial mortality but had subsequent better survival and tolerability.
| Discussion|| |
Impact of markers to subtype leukemias and treat with fair degree of confidence is an established norm. This being first from our state and the institution encouraged us to share our phenotype scenario of leukemias. Infact, this is the first and only study available in North India, depicting significant heterogeneity in phenotypic expression of ALL in India. We believe this could reflect different genotype and biology of our population, opening a window of opportunity for studying therapeutic variability.
A total of 69.8% of our study population was less than or equal to 18 years. F:M ratio in this group was 1:0.93, whereas it was 1:1.17 in those more than 18 years. Mean age of presentation was (15.9 ± 12.0) years. Majority of our cases were of B-cell lineage (68.1%), while T-cell leukemia was seen in 30.6% patients, which was higher than most Western data but comparable to South Indian studies. T-cell leukemias had poorer prognosis when compared with B-cell leukemia. cALLa positivity had significant bearing on CR in B-cell ALL but not in T-cell ALL. Myeloid co expression had no significant effect on prognosis. Biphenotypic acute leukemia was seen in 1.4% cases.
Majority of the patients were treated with UKALL XII protocol and the rest with BFM-based protocols. Patients on UKALL XII protocol maintained a high survival with a steady decline, whereas those on BFM-based protocols had higher initial deaths but better subsequent survival, exceeding significantly from that in UKALL XII protocol. There was no significant difference in the complications seen across different protocol groups. However, treatment interruption because of nutritional status and hepatitis did occur.
We conclude that phenotyping has become an important and integral part of diagnosis, classification, management, and prognosticating in ALL. B-cell lineage leukemia has been found to have a better survival over T-cell lymphoblastic leukemia. While cALLa antigen positivity has good impact in achieving CR in only B-cell lineage, myeloid co expression has no significant effect on the outcome. BFM-based protocols though showed a higher CR and survival vis-a-vis UKALL-XII. However, patients enrolled in former group being of low-risk category and lesser in numbers cannot be compared statistically with a fair degree of confidence.
| Acknowledgment|| |
The authors thank the patients and their families for their support, cooperation and patience. We would also like to thank the staff of the departments associated with care and management of the patients.
| References|| |
Dores GM, Devesa SS, Curtis RE, Linet MS, Morton LM. Acute leukemia incidence and patient survival among children and adults in the United States, 2001-2007. Blood 2012;119:34-43.
Pui CH, Evans WE. Acute lumphoblastic leukemia. N. Engl J Med 1998:339:605-15.
Channa J, Shamsi T, Hashmi K. Role of immunophenotyping in diagnosis of acute leukemia. J Coll Physicians Surg Pak 2000;10:158-60.
Pui CH. Childhood leukemias. N Engl J Med 1995:332:1618-30.
Sobol RE, Mick R, Royston I, Davey FR, Ellison RR, Newman R, et al
. Clinical importance of myeloid antigen expression in adult acute lymphoblastic leukemia. N Engl J Med 1987;316:1111-7.
Crist W, Pullen J, Boyett J, Falleta J, van Eys J, Borowitz M, et al.
Acute lymphoid leukemia in adolescents: Clinical and biologic features predict a poor prognosis. A Pediatric Oncology Group study. J Clin Oncol 1988;6:34-43.
Bradstock KF, Kirk J, Grimsley PG, Kabral A, Hughes WG. Unusual immunophenotypes in acute leukaemias: Incidence and clinical correlations. Br J Haematol 1989;72:512-8.
Childs CC, Hirsch-Ginsberg C, Walters RS, Anderson BS, Reuben J, Trujillo JM, et al.
Myeloid surface antigen-positive acute lymphoblastic leukemia (My + ALL): Immunophenotypic, ultrastructural, cytogenetic and molecular characteristics. Leukemia 1989;11:777-83.
Ludwig WD, Bartram CR, Harbott J, Koller U, Haas OA, Hansen-Hagge T, et al
. Phenotypic and genotypic heterogeneity in infant acute leukemia I. acute lymphoblastic leukemia. Leukemia 1989;6:431-9.
Guyotat D, Campos L, Shi ZH, Charrin C, Treille D, Magaud JP, et al
. Myeloid surface antigen expression in adult acute lymphoblastic leukemia. Leukemia 1990;9:664-6.
Pui CH, Behm FG, Singh B, Rivera GK, Schell MJ, Roberts WM, et al
. Myeloid-associated antigen expression lacks prognostic value in childhood acute lymphoblastic leukemia treated with intensive multiagent chemotherapy. Blood 1990;75:198-202.
Wiersma SR, Ortega J, Sobel E, Weinberg KI. Clinical importance of myeloid-antigen expression in acute lymphoblastic leukemia of childhood. N Engl J Med 1991;324:800-8.
Pui CH, Behm FG, Crist WM. Clinical and biologic relevance of immunologic marker studies in childhood acute lymphoblastic leukemia. Blood 1993;82:343-62.
Greaves MF, Brown C, Rapson NT, Lister A. Antisera to acute lymphoblastic leukemia cells. Clin Immunol Immunopathol 1975;4:67-84.
Hoelzer D, Thiel E, Loffler H, Buchner T, Ganser A, Heil G, et al.
Prognostic factors in a multicenter study for treatment of acute lymphoblastic leukemia in adults. Blood 1988;71:123-31.
Hoelzer D. High-dose chemotherapy in adult acute lymphoblastic leukemia. Semin Hematol 1991;28:84-9.
Berman E, Weiss M, Kempin S, Gee T, Bertino J, Clarkson B. Intensive therapy for adult acute lymphoblastic leukemia. Semin Hematol 1991;28:72-5.
Linker CA, Levitt LJ, O′Donnell M, Forman SJ, Ries CA. Treatment of adult acute lymphoblastic leukemia with intensive cyclical chemotherapy: A follow-up report. Blood 1991;78:2814-22.
Blume KG, Forman SJ, Snyder DS, Nademanee AP, O′Donne1 MR, Fahey JL, et al
. Allogeneic bone marrow transplantation for acute lymphoblastic leukemia during first complete remission. Transplantation 1987;43:389-92.
Weisdorf DJ, McGlave PB, Ramsay NK, Miller WJ, Nesbit ME, Woods WG, et al
. Allogeneic bone marrow transplantation for acute leukemia: Comparative outcomes for adults and children. Br J Haematol 1988;69:351-8.
Tsukimoto I, Wong HY, Lampkin BC. Surface markers and prognostic factors in acute lymphoblastic leukemia. N Engl J Med 1976;294:245-8.
Chessells IM, Hardisty RM, Rapson NT, Greaves MF. Acute lymphoblastic leukaemia in children: Classification and prognosis. Lancet 1977;2:1307-9.
Borella L, Sen L, Dow LW, Casper IT. Cell differentiation antigens versus tumor-related antigens in childhood acute lymphoblastic leukemia (ALL). Clinical significance of leukemia markers. In: Thierfelder S, Rod H, Thiel E, editors. Immunological Diagnosis of Leukemias and Lymphomas. Vol. 20. Berlin: Springer-Verlag; 1977. p. 77 -86.
[Table 1], [Table 2], [Table 3]