|Year : 2014 | Volume
| Issue : 2 | Page : 160-165
FLT3 and NPM-1 mutations in a cohort of acute promyelocytic leukemia patients from India
Suchitra Swaminathan1, Swati Garg2, Manisha Madkaikar2, Maya Gupta2, Farah Jijina3, Kanjaksha Ghosh2
1 Department of Pediatric Immunology and Leukocyte Biology, National Institute of Immunohaematology, Indian Council of Medical Research, K.E.M. Hospital, Parel, Mumbai, Maharashtra, India; Department of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA,
2 Department of Pediatric Immunology and Leukocyte Biology, National Institute of Immunohaematology, Indian Council of Medical Research, K.E.M. Hospital, Parel, Mumbai, Maharashtra, India,
3 Department of Hematology, K.E.M. Hospital, Parel, Mumbai, Maharashtra, India,
|Date of Web Publication||14-Oct-2014|
National Institute of Immunohaematology, Indian Council of Medical Research, 13th Floor, NMS building, K.E.M. Hospital, Parel, Mumbai - 400 012, Maharashtra, India
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Background: Acute promyelocytic leukemia (APL) with t (15;17) is a distinct category of acute myeloid leukemia (AML) and is reported to show better response to anthracyclin based chemotherapy. A favorable overall prognosis over other subtypes of AML has been reported for APL patients but still about 15% patients relapse.
Methods: This study evaluated the presence of Famus like tyrosine kinase-3 (FLT3) and nucleophosmin-1 (NPM1) gene mutations in a cohort of 40 APL patients. Bone marrow/peripheral blood samples from patients at the time of diagnosis and follow-up were processed for immunophenotyping, cytogenetic markers and isolation of DNA and RNA. Samples were screened for the presence of mutations in FLT3 and NPM1 genes using polymerase chain reaction followed by sequencing.
Results: Frequency of FLT3/internal tandem duplication and FLT3/tyrosine kinase domain was found to be 25% and 7% respectively. We observed a high frequency of NPM1 mutation (45%) in the present population of APL patients.
Keywords: Acute promyelocytic leukemia, famus like tyrosine kinase-3, nucleophosmin-1
|How to cite this article:|
Swaminathan S, Garg S, Madkaikar M, Gupta M, Jijina F, Ghosh K. FLT3 and NPM-1 mutations in a cohort of acute promyelocytic leukemia patients from India. Indian J Hum Genet 2014;20:160-5
|How to cite this URL:|
Swaminathan S, Garg S, Madkaikar M, Gupta M, Jijina F, Ghosh K. FLT3 and NPM-1 mutations in a cohort of acute promyelocytic leukemia patients from India. Indian J Hum Genet [serial online] 2014 [cited 2016 Aug 23];20:160-5. Available from: http://www.ijhg.com/text.asp?2014/20/2/160/142884
| Introduction|| |
Acute promyelocytic leukemia (APL) is a distinct subtype of acute myeloid leukemia (AML) and is treated differently than other types of AML.  It is characterized by the blast morphology,  specific coagulopathy,  fusion gene transcript promyelocyte leukemia retinoic acid receptor alpha (PML-RARα) t (15;17),  and is the most frequently curable acute leukemia in adults if promptly diagnosed and adequately treated.  Many studies have correlated the presence of activating mutations in Famus like tyrosine kinase-3 receptor (FLT3 mutation) with an adverse outcome in APL patients.  This receptor has been known to enhance the survival and proliferation of hematopoietic progenitors in response to its ligand.  Mostly, the mutations in FLT3 are the result of internal tandem duplication (ITD) of the intracellular juxtramembrane region of this molecule  which is known to contribute toward its constitutive expression;  FLT3/ITD has also been associated with leukocytosis in APL patients.  Many activating point mutations within the "a loop" of tyrosine kinase domain (TKD) have also been reported in AML patients ,, and their prognostic significance has been described. ,
Nucleophosmin-1 (NPM1) is a molecular chaperon of proteins, which facilitates the transport of ribosomal proteins through the nuclear membrane.  It is located in the nucleolus at a steady state  and known to contribute toward importantly cellular functions through protein-protein interactions. Mutation in NPM1 gene results in its cytoplasmic dislocation which has been implicated to play a critical role in leukemogenesis. , Evaluating transcript levels of NPM1 mutation has been suggested as a promising tool for minimal residual disease (MRD) monitoring in AML patients. 
Presence of FLT3/ITD has been observed in 20-35% of APL cases ,,, where it has been correlated with shorter overall survival and poor postrelapse survival.  FLT3-D835Y has been reported in 7-20% APL patients ,, but its prognostic significance remains unclear in this subgroup of AML. Even though, about one-third patients with AML have been observed to be presented with mutation in NPM1 gene,  no significant incidence of NPM1 mutation in APL patients is reported. ,,
In the present study, we analyzed mutations in FLT3 and NPM1 gene in a cohort of 40 patients diagnosed with APL using combination of molecular techniques. This data were further analyzed for frequency of these mutations and then correlated with clinical characteristics at presentation, treatment and follow-up.
| Materials and Methods|| |
Patients and specimens
Overall, 54 patients were diagnosed with APL out of 276 AML patients referred to Department of Hematology, KEM Hospital, Parel, Mumbai from year 2004 to 2008 with approval of Institutional Ethical Committee. After informed consent, 3-5 ml bone marrow (BM) or/and peripheral blood specimen was collected in ethylenediaminetetraacetic acid tubes. Patients were classified according to French-American-British and WHO classification (>20% blasts in BM as established with morphological techniques; as the diagnostic criteria for acute leukemia). Cytogenetics was carried out as per standard protocols for identification of PML-RARα. Total 40 patients were included for the molecular diagnosis of FLT3 and NPM1 mutations.
Cytogenetic analysis was performed on BM/PB cells after short-term culture. Karyotypes, analyzed after G-banding, were described according to the International System for Human Cytogenetic Nomenclature.  Fluorescence in situ hybridization investigations for specific translocations were also carried out as previously described. 
DNA was isolated from BM/PB by the phenol chloroform method recommended by Sambrook et al.  from the nucleated cells frozen at −80°C. Polymerase chain reaction (PCR) amplifications using a specific set of primers for respective exons of each of the two genes (FLT3 and NPM1) were carried out with the appropriate set of primers (from Sigma Aldrich, USA) on PTC-225 thermal cycler (MJ Research, USA) and GeneAmp PCR System 9700 (Applied Biosystems, USA).
Famus like tyrosine kinase-3 gene screening was done by horizontal agarose gel electrophoresis as well as polyacrylamide gel electrophoresis.  D835Y point mutations in the TKD were detected by PCR-restriction fragment length polymorphism with enzyme EcoRV (Fermentas). Screening for another point mutation in this exon was carried out by PCR-single strand conformation polymorphism (SSCP) technique. Screening for NPM1 gene was done using genomic PCR amplification of exon 12 followed by SSCP was used to screen for mutation in this gene. 
The PCR product of all patients showing abnormal shifts in screening or presence of mutant bands from respective PCR of the two genes wassequenced for confirmation of the mutation.
Microsoft Excel 2007, Microsoft Inc. Washington DC and GraphPad InStat version 3.10 by GraphPad software Inc., CA, USA were used for all statistical analysis. Data have been reported as median (range). Student's t-test/Chi-square/Fisher's exact test has been run to demonstrate statistical significance wherever necessary. P < 0.05 was considered to be statistically significant.
| Results|| |
Frequency of mutations
A total of 40 patients were diagnosed with APL, out of which 21 were males, and 19 were females. There was no gender bias in any mutation frequency except FLT3/TKD where we found only three adult patients all females harboring D835Y mutation. Out of total 40 APL cases, 13 patients (30%) were found to be FLT3 mutation while 28 APL patients (70%) were FLT3wt. Frequency of FLT3/ITD was higher (77%) than that of FLT3/TKD (33%) in the present cohort, one adult female was found to harbor both FLT3/ITD and FLT3/TKD. Total 18 APL patients were found to harbor mutations in NPM1, 8 out of 18 (44%) patients were FLT3 mutation/NPM1 mutation, while 10 patients (56%) carried NPM1 mutation without any mutation in FLT3 [Table 1].
|Table 1: Frequency and clinical data of 40 APL patients across respective mutation groups|
Click here to view
All the patients in NPM1 mutation/FLT3 mutation group showed presence of Type A NPM1 mutation, which is the insertion of clustering-based adaptive genetic algorithm (CAGA), while this was present in about 70% patients of NPM1 mutation/FLT3wt. Two out of total 10 patients with NPM1 mutation without mutation in FLT3 had Type D mutation, that is, insertion of CAGG, complex mutation was observed in one patient [Table 2].
|Table 2: Types of NPM1 mutation in APL patients with and without mutation in FLT3|
Click here to view
Famus like tyrosine kinase-3 mutation patients was presented with a significantly higher total white blood cell counts at the presentation when compared with FLT3wt group (P < 0.05, unpaired t-test, confidence interval (CI 95%). Platelet count in the former group was slightly lower than the later, but was not significantly different. Patients with a mutation in NPM1 with FLT3 mutation were observed with significantly higher total counts when compared to those without the mutation in FLT3 (P < 0.05, unpaired t-test, CI 95%). Blast percentage, hemoglobin and platelet count were not significantly different in any group.
Treatment and follow-up
Of a total 40 APL patients, 25 underwent chemotherapy while 15 did not receive treatment at our center. Treatment regimen for these patients included arsenic trioxide as described earlier for an Indian study.  Patients who were untreated either could not opt for treatment due to insufficient finances or they chose to take treatment at other centers and, therefore, follow-up of these patients could not be done. Mostly follow-up was done till the first remission. Frequency with which FLT3 mutation patients achieved complete remission (22%) was significantly lower than that of FLT3wt (69%) patients (P < 0.05, Fisher's exact test, CI 95%, the relative risk 1.6). Presence of NPM1 mutation with FLT mutation showed a better complete remission frequency of 40% that was quite comparable to the NPM1 mutation group without mutation in FLT3 (50%) [Table 3].
| Discussion|| |
Despite of a favorable cytogenetic risk group, patients with APL still relapse with an approximate rate of 15-20%.  Evaluation of MRD by quantifying transcript levels of PML-RARα or NPM1 been sought by research groups. , Characterization of recurring molecular defects such as mutations in FLT3, NPM1, Ras etc., has enhanced our understanding toward basic mechanism of leukemogenesis in past few years. The present study evaluates a cohort of 40 APL patients from India belonging to heterogeneous population of different ethnicity and culture. Frequency of FLT3/ITD and FLT3/TKD (D835Y) in the present population is observed to be 25% and 7% respectively, which in accordance with the previous studies from various populations. ,,, However, NPM1 mutation is present in about 50% of the current population of APL patients which has never been observed as a significant incident in other reports. ,, Median age of patients with FLT3/ITD is about 23 years, which is quite comparable to the median age value of 28 years reported by an Indian study,  but not to a Japanese study where it has been reported as 56 years,  median age of FLT3/TKD is 45 years as observed in the previous studies. ,,, However, FLT3-D835Y is completely female biased in the current cohort when compared to the reported predominance in males,  reason for which could not be established.
One striking observation in the present study is the higher incident rate of NPM1 mutations, which have never been reported at this frequent rate in APL patients and suggested to be less frequent in Asians as compared to Caucasian in a Thai study.  All the patients with NPM1 mutation/FLT3 mutation harbor "Type A" mutation, which is characterized by insertion of CAGA whereas patients with only NPM1 mutation without FLT3 mutation harbor "Type A" and "Type D" mutation, "Type B" mutation is not observed in the present population.
Clinical features at the presentation for the current cohort of APL patients with or without mutation in FLT3 gene are quite similar to those reported in the other studies. Moreover, presence of NPM1 mutation with FLT3 mutation shows a higher total count when compared to NPM1 mutation with FLTwt, which contributes toward the poor prognosis of former group as already been described by several studies in AML. ,,
Sixty-three percent (25/40) of the total diagnosed APL patients underwent chemotherapy, follow-up data until the first remission is available and is correlated with the incidence of specific mutations. Complete remission was achieved by only 22% of FLT3 mutation patients compared with 68% of FLT3wt APL patients. This observation is quite in accordance with previous studies where complete remission was achieved by 23-40% APL patients with FLT mutation. , A better frequency of remission is seen in patients with NPM mutation/FLT3wt which is in accordance with the previous studies deriving results from Asian APL patients , and is as good as the remission frequency of NPMwt/FLT3wt group that is, 60% and 75%, respectively.
One of the questions from the present study is why we have lower remission rates in APL in contrast to what has been described in the literature. Though we cannot be sure but it may not be out of place to mention here that general population in large part of India are exposed to arsenic either through ground water contamination or through industrial pollution. This may have produced underlying arsenic resistance situation. However, this hypothesis needs to be conformed through larger well-designed epidemiological studies.
| Conclusion|| |
The present cohort of APL patients shows a higher frequency of FLT3/ITD and a female biased incidence of FLT3/TKD. The high frequency of mutation in NPM1 gene of APL patients here is a novel observation where presence of NPM1 mutation with FLT3 mutation shows a better remission as observed in our previous study on AML patients, but the remission is better in APL patients with NPM1wt/FLT3wt than the group with only NPM1 mutation.  We suggest that a better understanding toward mutation in FLT3 and NPM1 gene in APL patients might help in overcoming the relapse in this favorable group of AML.
| References|| |
Stock W, Najib K, Moser BK, Powell BL, Holowka N, Gulati K, et al
. High incidence of FLT3 mutations in adults with Acute Promyelocytic Leukemia (APL): Correlation with diagnostic features and treatment outcome (CALGB 9710). J Clin Oncol 2008;26:374.
Bennett JM, Catovsky D, Daniel MT, Flandrin G, Galton DA, Gralnick HR, et al.
Proposals for the classification of the acute leukaemias. French-American-British (FAB) co-operative group. Br J Haematol 1976;33:451-8.
Tallman MS, Kwaan HC. Reassessing the hemostatic disorder associated with acute promyelocytic leukemia. Blood 1992;79:543-53.
de Thé H, Lavau C, Marchio A, Chomienne C, Degos L, Dejean A. The PML-RAR alpha fusion mRNA generated by the t (15;17) translocation in acute promyelocytic leukemia encodes a functionally altered RAR. Cell 1991;66:675-84.
Parmar S, Tallman MS. Acute promyelocytic leukaemia: A review. Expert Opin Pharmacother 2003;4:1379-92.
Stock W, Najib K, Moser BK, Powell BL, Holowka N, Gulati K, et al.
High incidence of FLT3 mutations in adults with Acute Promyelocytic Leukemia (APL): Correlation with diagnostic features and treatment outcome (CALGB 9710). J Clin Oncol 2008;26:374.
Muench MO, Roncarolo MG, Menon S, Xu Y, Kastelein R, Zurawski S, et al.
FLK-2/FLT-3 ligand regulates the growth of early myeloid progenitors isolated from human fetal liver. Blood 1995;85:963-72.
Nakao M, Yokota S, Iwai T, Kaneko H, Horiike S, Kashima K, et al.
Internal tandem duplication of the flt3 gene found in acute myeloid leukemia. Leukemia 1996;10:1911-8.
Kiyoi H, Towatari M, Yokota S, Hamaguchi M, Ohno R, Saito H, et al.
Internal tandem duplication of the FLT3 gene is a novel modality of elongation mutation which causes constitutive activation of the product. Leukemia 1998;12:1333-7.
Kiyoi H, Naoe T, Yokota S, Nakao M, Minami S, Kuriyama K, et al.
Internal tandem duplication of FLT3 associated with leukocytosis in acute promyelocytic leukemia. Leukemia Study Group of the Ministry of Health and Welfare (Kohseisho). Leukemia 1997;11:1447-52.
Yamamoto Y, Kiyoi H, Nakano Y, Suzuki R, Kodera Y, Miyawaki S, et al.
Activating mutation of D835 within the activation loop of FLT3 in human hematologic malignancies. Blood 2001;97:2434-9.
Liang DC, Shih LY, Hung IJ, Yang CP, Chen SH, Jaing TH, et al.
FLT3-TKD mutation in childhood acute myeloid leukemia. Leukemia 2003;17:883-6.
Sheikhha MH, Awan A, Tobal K, Liu Yin JA. Prognostic significance of FLT3 ITD and D835 mutations in AML patients. Hematol J 2003;4:41-6.
Fröhling S, Schlenk RF, Breitruck J, Benner A, Kreitmeier S, Tobis K, et al.
Prognostic significance of activating FLT3 mutations in younger adults (16 to 60 years) with acute myeloid leukemia and normal cytogenetics: A study of the AML Study Group Ulm. Blood 2002;100:4372-80.
Callens C, Chevret S, Cayuela JM, Cassinat B, Raffoux E, de Botton S, et al.
Prognostic implication of FLT3 and Ras gene mutations in patients with acute promyelocytic leukemia (APL): A retrospective study from the European APL Group. Leukemia 2005;19:1153-60.
Borer RA, Lehner CF, Eppenberger HM, Nigg EA. Major nucleolar proteins shuttle between nucleus and cytoplasm. Cell 1989;56:379-90.
Falini B, Bolli N, Liso A, Martelli MP, Mannucci R, Pileri S, et al.
Altered nucleophosmin transport in acute myeloid leukaemia with mutated NPM1: Molecular basis and clinical implications. Leukemia 2009;23:1731-43.
Falini B, Martelli MP, Bolli N, Sportoletti P, Liso A, Tiacci E, et al.
Acute myeloid leukemia with mutated nucleophosmin (NPM1): Is it a distinct entity? Blood 2011;117:1109-20.
Verhaak RG, Goudswaard CS, van Putten W, Bijl MA, Sanders MA, Hugens W, et al.
Mutations in nucleophosmin (NPM1) in acute myeloid leukemia (AML): Association with other gene abnormalities and previously established gene expression signatures and their favorable prognostic significance. Blood 2005;106:3747-54.
Krönke J, Schlenk RF, Jensen KO, Tschürtz F, Corbacioglu A, Gaidzik VI, et al.
Monitoring of minimal residual disease in NPM1-mutated acute myeloid leukemia: A study from the German-Austrian acute myeloid leukemia study group. J Clin Oncol 2011;29:2709-16.
Hasan SK, Sazawal S, Dutta P, Pillai LS, Kumar B, Chaubey R, et al.
Impact of FLT3 internal tandem duplications on Indian acute promyelocytic leukemia patients: Prognostic implications. Hematology 2007;12:99-101.
Mathews V, Thomas M, Srivastava VM, George B, Srivastava A, Chandy M. Impact of FLT3 mutations and secondary cytogenetic changes on the outcome of patients with newly diagnosed acute promyelocytic leukemia treated with a single agent arsenic trioxide regimen. Haematologica 2007;92:994-5.
Noguera NI, Breccia M, Divona M, Diverio D, Costa V, De Santis S, et al.
Alterations of the FLT3 gene in acute promyelocytic leukemia: Association with diagnostic characteristics and analysis of clinical outcome in patients treated with the Italian AIDA protocol. Leukemia 2002;16:2185-9.
Falini B, Mecucci C, Tiacci E, Alcalay M, Rosati R, Pasqualucci L, et al.
Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype. N Engl J Med 2005;352:254-66.
Falini B, Mecucci C, Saglio G, Lo Coco F, Diverio D, Brown P, et al.
NPM1 mutations and cytoplasmic nucleophosmin are mutually exclusive of recurrent genetic abnormalities: A comparative analysis of 2562 patients with acute myeloid leukemia. Haematologica 2008;93:439-42.
Mukda E, Pintaraks K, Sawangpanich R, Wiangnon S, Pakakasama S. FLT3 and NPM1 gene mutations in childhood acute myeloblastic leukemia. Asian Pac J Cancer Prev 2011;12:1827-31.
Mitelman F. ISCN 1995: An International System for Human Cytogenetic Nomenclature. Basel, Switzerland: Karger; 1995.
Crescenzi B, Fizzotti M, Piattoni S, La Starza R, Matteucci C, Carotti A, et al.
Interphase FISH for Y chromosome, VNTR polymorphisms, and RT-PCR for BCR-ABL in the monitoring of HLA-matched and mismatched transplants. Cancer Genet Cytogenet 2000;120:25-9.
Sambrook J, Fritschi EF, Maniatis T. Molecular cloning: A laboratory manual. 6.4 Isolation of High-molecular-weight DNA from Mammalian Cells Using Proteinase K and Phenol. 2 nd
ed. New York: Cold Spring Harbor Laboratory Press; 1989.
Mathews V, George B, Lakshmi KM, Viswabandya A, Bajel A, Balasubramanian P, et al.
Single-agent arsenic trioxide in the treatment of newly diagnosed acute promyelocytic leukemia: Durable remissions with minimal toxicity. Blood 2006;107:2627-32.
Tobal K, Moore H, Macheta M, Yin JA. Monitoring minimal residual disease and predicting relapse in APL by quantitating PML-RARalpha transcripts with a sensitive competitive RT-PCR method. Leukemia 2001;15:1060-5.
Chillón MC, Santamaría C, García-Sanz R, Balanzategui A, Sarasquete ME, Alcoceba M, et al
. Long FLT3 internal tandem duplications and reduced PML-RARα expression at diagnosis characterize a high-risk subgroup of acute promyelocytic leukemia patients. Haematologica 2010;95:745-51.
Boonthimat C, Thongnoppakhun W, Auewarakul CU. Nucleophosmin mutation in Southeast Asian acute myeloid leukemia: Eight novel variants, FLT3 coexistence and prognostic impact of NPM1/FLT3 mutations. Haematologica 2008;93:1565-9.
Dunna NR, Rajappa S, Digumarti R, Vure S, Kagita S, Damineni S, et al.
Fms like tyrosine kinase (FLT3) and nucleophosmin 1 (NPM1) mutations in de novo normal karyotype acute myeloid leukemia (AML). Asian Pac J Cancer Prev 2010;11:1811-6.
Ghosh K, Swaminathan S, Madkaikar M, Gupta M, Kerketta L, Vundinti B. FLT3 and NPM1 mutations in a cohort of AML patients and detection of a novel mutation in tyrosine kinase domain of FLT3 gene from Western India. Ann Hematol 2012;91:1703-12.
[Table 1], [Table 2], [Table 3]