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FIP1L1-PDGFRA molecular analysis in the differential diagnosis of eosinophilia

Abstract

Background

Primary eosinophlia associated with the FIP1L1-PDGFRA rearrangement represents a subset of chronic eosinophilic leukaemia (CEL) and affected patients are very sensitive to imatinib treatment. This study was undertaken in order to examine the prevalence and the associated clinicopathologic and genetic features of FIP1L1-PDGFRA rearrangement in a cohort of 15 adult patients presenting with profound eosinophilia (> 1.5 × 109/L).

Methods

Reverse transcriptase-polymerase chain reaction (RT-PCR) was used for the detection of FIP1L1-PDGFRA rearrangement and the results confirmed by direct sequencing. C-KIT-D816V mutation was analysed retrospectively by PCR and restriction-fragment-length-polymorphism (PCR-RFLP), in all cases with primary eosinophilia.

Results

Two male patients with splenomegaly carried the FIP1L1-PDGFRA rearrangement, whilst 2 others were ultimately classified as suffering from idiopathic hypereosinophlic syndrome (HES) and one from systemic mastocytosis. These patients were negative for the C-KIT-D816V mutation and received imatinib (100–400 mg daily). Patients with CEL and HES responded to imatinib and remained in complete haematological, clinical and molecular (for carriers of FIP1L1-PDGFRA rearrangement) remission for a median of 28.2 months (range: 11–54), whilst the patient with systemic mastocytosis did not respond. Interestingly, in both patients with FIP1L1-PDGFRA rearrangement, the breakpoints into PDGFRA were located within exon 12 and fused with exons 8 and 8a of FIP1L1, respectively.

Conclusion

An early diagnosis of FIPIL1-PDGFRA-positive CEL and imatinib treatment offer to the affected patients an excellent clinical therapeutic result, avoiding undesirable morbidity. Moreover, although the molecular mechanisms underlying disease pathogenesis remain to be determined, imatinib can be effective in patients with idiopathic HES.

Peer Review reports

Background

Eosinophilia (> 0.5 × 109/L) is a common clinical finding that can be secondary to a large variety of diseases. When evaluation of eosinophilia fails to reveal an underlying disease, the diagnosis of hypereosinophilic syndrome (HES) is evocated. HES is defined by (1) eosinophilia (> 1.5 × 109/L) for more than 6 months; (2) exclusion of reactive eosinophilia caused by parasitic infections, allergies, or other known causes, as well as eosinophilia associated with neoplasias; and (3) evidence of end-organ damage [14]. Over the last decade, great progress has been made in understanding the molecular basis of HES that has resulted in the characterization of specific genetic alterations linked to clonal eosinophilia. The most frequent genetic aberration is the cryptic deletion of 4q12, i.e. del(4)(q12), producing the FIP1-like 1/platelet-derived growth factor receptor alfa (FIP1L1-PDGFRA) fusion transcript, which results in an eosinophilic, myeloproliferative disorder (chronic eosinophilic leukaemia, CEL) [5]. In addition, in a subset of patients with HES, eosinophilia is secondary to a primitive Th2 lymphoid disorder, overproducing interleukin-5 (IL-5), indicating the existence of lymphocyte-mediated HES [3].

The FIP1L1-PDGFRA fusion gene induces increased tyrosine kinase activity of PDGFRA [5, 6], and is present in approximately 10–15% of patients with HES [5, 7, 8]. Despite the fact that these patients appear to have a more severe disease phenotype, involving extensive end-organ pathology [5, 811], they are dramatically sensitive to treatment with the tyrosine kinase inhibitor imatinib [5, 813]. Thus, early detection of FIPIL1-PDGFRA rearrangement and the subsequent imatinib administration can offer to the affected patients an excellent clinical therapeutic outcome, avoiding undesirable morbidity and mortality.

This study was undertaken in order to examine both the prevalence and the associated clinicopathologic and genetic features of FIP1L1-PDGFRA rearrangement in a cohort of 15 adult patients presenting with eosinophilia and an absolute eosinophil count higher than 1.5 × 109/L.

Methods

Patients

Peripheral blood (PB) and/or bone marrow (BM) from 15 patients (male/female: 7/8, mean age: 45.2 years, range: 22–72 years) with eosinophilia (eosinophils > 1.5 × 109/L), without an unambiguous history of allergic diseases, were referred to the Immunology Lab and examined for the presence of FIP1L1-PDGFRA rearrangement. Regardless of the molecular analysis, a complete clinical and laboratory examination was also performed. The diagnosis of idiopathic HES, systemic mastocytosis and/or CEL was based either on standard diagnostic criteria [13] or on the result of the molecular analysis. Cytogenetic analysis was performed in all, but one, patients with primary eosinophilia and in two patients, for which ultimately another diagnosis was made. Flow cytometric analysis for the demonstration of CD3-CD4+ or CD3+CD4-CD8- clones, implicated in lymphocyte-mediated HES, was performed in all patients, but serum vitamin B12, IL-5 and mast cell tryptase levels were not assayed. Detection of C-KIT-D816V mutation was performed retrospectively in all cases with primary eosinophilia.

Written informed consent was obtained from all patients and the study was approved by the Institutional Review Board of both hospitals (University Hospital of Larissa and Papageorgiou General Hospital, Greece).

Molecular analyses

Detection of FIP1L1-PDGFRA fusion

The FIP1L1-PDGFRA rearrangement was analyzed by a modified nested reverse transcriptase-polymerase chain reaction (RT-PCR) protocol [14]. In particular, RNA was extracted from BM or PB, and cDNA was reversed transcribed, as previously described [15]. One sixth of the synthesized cDNA was used in a first PCR reaction of 30 μL, using 62.5 μM of each deoxynucleoside triphosphate, 20 pmol of each primer (sense: 5'-ACCTGGTGCTGATCTTTCTGAT-3' and antisense: 5'-TGAGAGCTTGTTTTTCACTGGA-3'), 1.6 mM MgCl2 and 1.4 μL of Taq Elongase (Invitrogen, UK) in a PCR buffer supplied by the manufacturer. Thereafter, 1 uL of the first PCR product was used as template for the nested PCR reaction (30 uL), along with 62.5 μM of each deoxynucleoside triphosphate, 10 pmol of each primer (sense: 5'-AAAGAGGATACGAATGGGACTTG-3' and antisense: 5'-GGGACCGGCTTAATCCATAG-3'), 1.5 mM MgCl2 and 0.5 U of Taq Polymerase (Invitrogen, UK) in a PCR buffer supplied by the manufacturer. The primary PCR conditions were: 2 min at 94°C followed by 32 cycles (94°C for 45 sec, 56°C for 45 sec, 68°C for 75 sec) followed by 5 min at 68°C. The conditions for the nested PCR were: 2 min at 94°C followed by 25 cycles (94°C for 30 sec, 60°C for 30 sec, 72°C for 60 sec) followed by 5 min at 72°C after the last cycle. All PCR amplifications were carried out in the PCR-engine apparatus PTC-200, MJ Research (Watertown-Mass., USA). The first and nested PCR products were analyzed in 2.5% TBE agarose gels. The cell line EOL-1 (with known FIP1L1-PDGFRA rearrangement) served as positive control in our experiments.

For the confirmation of nested PCR results, PCR products with suspected FIP1L1-PDGFRA rearrangement were purified by QIAquick gel extraction kit (Qiagen, UK) and directed sequenced using an ABI Prism 310 Genetic Analyzer (Applied Biosystems, Foster City, CA) and a Big Dye Terminator DNA sequencing kit (Applied Biosystems).

Mutational analysis of C-KIT

The C-KIT-D816V mutation was analysed at the genomic DNA level. In particular, DNA was extracted using the QIAamp DNA Blood Mini kit (Qiagen, UK), according to the manufacturer's instructions. Semi-nested PCR was performed, as previously described [16], with some modifications. In particular, the first PCR was performed in a final volume of 30 μL containing 100 uM of each dNTP, 1.5 mM MgCl2, and 0.5 U Taq polymerase (Invitrogen, UK), and 10 pmol of each primer (sense: 5'-CACAGAGACTTGGCAGCCAG-3' and antisense: 5'-CAGGATTTACATTATGAAAGTCACGG-3'). Aliquots of 1 μL of the PCR product served as template for the semi-nested PCR, using the same concentrations as above. The primers for the nested PCR were: sense 5'-ATCCTCCTTACTCATGGTCGGATC-3' and the same antisense used for the primary PCR. Each PCR cycle consisted of 30 seconds denaturation at 94°C, 30 sec annealing at 56°C, and 45 sec extension at 72°C. The first cycle was preceded by two minutes denaturation at 94°C. The last cycle was extended by a five minute elongation at 72°C. The first PCR run for 30 cycles and nested-PCR for 25 cycles. All PCR amplifications were carried out in the PCR-engine apparatus PTC-200, MJ Research (Watertown-Mass., USA).

To detect the presence of the C-KIT-D816V mutation, the semi-nested PCR products were digested with the endonuclease HinfI (New England Biolabs, USA) and the restriction products were analysed by electrophoresis on a 4% agarose TBE gels. The C-KIT-D816V mutation creates a second restriction site within the semi-nested PCR products. The predicted sizes for the wild-type sequence were 121 bp and 68 bp, and for the mutated sequence 121 bp, 68 bp, 54 bp, and 14 bp [16].

Results

Amongst the 15 patients with eosinophilia, only two were positive for the FIP1L1-PDGFRA rearrangement (13,3%). Two others were classified as idiopathic HES and another as systemic mastocytosis, after bone marrow and lymph node biopsies, indicating mast cell infiltration. A summary of the clinical and laboratory findings for these patients is presented in Table 1.

Table 1 Clinical and laboratory findings of the patients with primary eosinophilia

Within the remaining patients, one suffered from eosinophilic gastroenteritis, two from asthma (all responded to steroids), two from atypical myeloproliferative syndrome (one was also positive to JAK2-V617F mutation and both responded to hydroxyurea therapy), one from dermatomyocytis, one from bronchiectasis, and one from chronic idiopathic urticaria. In two cases, the eosinophilia was not permanent and ascribed to possible allergic causes (also responded to steroids). Notably, only the patient with eosinophilic gastroenteritis displayed eosinophilia for more than 6 months.

All patients with primary eosinophilia (CEL, HES and systemic mastocytosis) were negative for the C-KIT-D816V mutation, while cytogenetic analysis in all, but one patient (case 2 of Table 1), due to dry-tap on bone marrow aspiration, was normal. Moreover, a clonal interleukin-5-producing T-cell population was not detected by flow cytometry in any of the above patients.

All patients with primary eosinophilia negative for the FIP1L1-PDGFRA rearrangement, displayed eosinophilia for more than 6 months (mean: 7 months, range: 6–8). Amongst them, one with idiopathic HES was receiving imatinib as first line therapy and the others were receiving imatinib after failure of their previous treatment (Table 1). The patients with idiopathic HES responded to imatinib in a dosage of 400 mg per day, displaying CHR and clinical remission, and continue on imatinib, till now (Table 1). The last patient, suffering from systemic mastocytosis with eosinophilia, was negative to FIP1L1-PDGFRA rearrangement, as well as to the C-KIT-D816V mutation, but did not respond to imatinib treatment. Interestingly, she had initially received IFN-alfa subcutaneously for 2 years, with no response, and then received imatinib (400 mg per day), for which she was also not sensitive.

Considering the patients carrying the FIP1L1-PDGFRA rearrangement, they were males, exhibiting splenomagaly. Both patients displayed more than one isoforms of the fusion gene (Figure 1), similar to the majority of the affected patients, as described in the literature. The RT-PCR results were confirmed in both cases by sequencing analysis. Interestingly enough, as for all patients reported in the literature, the breakpoint into the PDGFRA gene was located in exon 12 (different for each patient), that was fused with exon 8 of the FIP1L1 gene for the first patient and exon 8a for the second (Figure 1). Moreover, the connection site between the genes was the same for the isoforms of each patient, and their different length was due to deletions in the FIP1L1 gene (for example in case 1 of Table 1, one isoform was characterized by deletion of the whole exon 7a of the FIP1L1 gene).

Figure 1
figure 1

Molecular analyses of patients with FIP1L1-PDFGRA rearrangement. A. Reverse transcriptase-polymerase chain reaction (RT-PCR) analysis of the FIP1L1-PDFGRA fusion gene isolated from bone marrow and peripheral blood of patients with chronic eosinophilic leukaemia at diagnosis. M: 100 bp ladder molecular weight marker (Invitrogen, UK); Lane 1: case 1; Lane 2: case 2; Lane 3: cell line EOL-1 (positive control), Lane 4: negative PCR control (blank). It is noteworthy that both patients, as well as the cell line EOL-1 (positive control), display more than one mRNA isoforms of the fusion gene. B. Sequence variants for each patient with the fusion gene. FIP1L1 sequences are shown in lowercase and in blue, and PDGFRA sequences are shown in uppercase and in black. Exon numbering in FIP1L1 is based on a complementary DNA (cDNA) clone (GenBank accession number NM_030917). The amino acid sequence of the chimeric protein in site of fusion is indicated in green. C. Schematic representation of the FIP1L1-PDGFRA fusion protein. In both cases the breakpoints in PDGFRA are located within the juxtamembrane region, between the two tryptophan (W) residues of the putative WW-domain.

A more detailed clinical and laboratory presentation of patients carrying the FIP1L1-PDGFRA rearrangement is presented below:

Case 1

The first patient presented maculo-papular rash on lower extremities and abdomen and an absolute eosinophil count of 2 × 109/L, one and half year before admission to the hospital. Initially the rash was considered to be of allergic etiology and the patient received local corticosteroids by a dermatologist. Nevertheless, a progressive deterioration of the rash was observed, and the patient also complained of fatigue and muscle weakness accompanied by hypaesthesia of the peripheral parts of the lower extremities that led to the weakness of walk, one week prior to admission. At that time, the laboratory tests showed that the eosinophils increased to 11.4 × 109/L and moreover, a mild anaemia (Hb: 12.5 gr/dl) was present. Clinical examination revealed splenomegaly (palpable spleen 8 cm below the left costal margin), vesicular exanthema on the abdomen and the low extremities and absent deep tendon reflexes. Bone marrow aspiration and biopsy revealed an extensive eosinophil infiltration (68%), whilst the cytogenetic analysis was normal. Molecular analysis excluded the presence of BCR-ABL transcript, while a FIP1L1-PDGFRA rearrangement was documented (Figure 1A). Imatinib was initiated at a dosage of 400 mg and after 14 days of treatment, the eosinophil count significantly declined along with a dramatic reduction of splenomegaly. Imatinib was well tolerated with an initial decrease of Hb levels to 9 gr/dl, that was resolved by reducing the imatinib dosage to 200 mg per day and administrating 150 mcg of darbepoetin alfa, twice weekly subcutaneously. The mobility and the hypaesthesia were recovered 2 months later and PB and BM molecular signal of the FIP1L1-PDGFRA fusion gene were undetectable 4 months after treatment. Six months later, the imatinib dosage further declined to 100 mg per day, and the patient is currently followed-up as an outpatient.

Case 2

The second patient displayed eosinophilia (10.2 × 109/L) and mild anaemia (Hb: 13.1 gr/dl) during a routine laboratory examination. A clinical examination revealed only splenomegaly (palpable spleen 2 cm below the left costal margin). Bone marrow aspiration was dry-tap, and for this reason cytogenetic analysis was not performed. However bone marrow biopsy revealed an extensive infiltration (80%) by eosinophils. Molecular analysis revealed the presence of the FIP1L1-PDGFRA rearrangement. Imatinib was started at a dosage of 100 mg two weeks after the estimation of eosinophilia and after 14 days of treatment, the eosinophil count become normal (0.3 × 109/L) and the spleen was not palpable below the left costal margin. Imatinib was well tolerated without side effects, and PB and BM molecular signal of the FIP1L1-PDGFRA fusion gene was undetectable 3 months after treatment.

Discussion

In this study we describe our experience for the diagnostic utility of the detection of FIP1L1-PDGFRA rearrangement in patients with profound eosinophilia. In our cohort, the prevalence of FIP1L1-PDGFRA rearrangement was 13.3% in the total analysed group and 40% among patients with primary eosinophilia. Till now, the recorded proportion of FIP1L1-PDGFRA-positive cases among such patients varies widely, ranging from 0% to 56%, probably reflecting small sample sizes, as in our cohort, and variable inclusion criteria [5, 713, 17]. In the study, with the largest cohort, Pardanani and co-workers screened 741 patients with moderate to severe eosinophilia and reported a 3% prevalence of FIP1L1-PDGFRA fusion positivity [12]. Moreover, Klion also noted that 10%–50% of patients meeting the classic definition of HES may be FIP1L1-PDGFRA-positive [18]. It is obvious, that a subsequent meta-analysis, taking into account all published studies, could clarify the true prevalence of FIP1L1-PDGFRA rearrangement in patients with idiopathic eosinophilia and HES.

The detection of FIP1L1-PDGFRA rearrangement in the second patient, directly after the estimation of eosinophilia, resulted in the early diagnosis of CEL, with a profound impact on the patient's clinical course and outcome. Thus, it is not unreasonable to speculate that the usage of molecular techniques for the early diagnosis of suspected FIP1L1-PDGFRA-positive leukemias, can modify the diagnostic criteria of hypereosinophilic syndrome with significant impact in undesirable morbidity and mortality.

Interestingly, in both patients with FIP1L1-PDGFRA rearrangement, the breakpoints into PDGFRA were located in exon 12 and fused with exons 8 and 8a of FIP1L1, respectively. Till now, all described breakpoints occurred in an FIP1L1 intron (spread from 7 to 10 at genomic DNA level) and in exon 12 of PDGFRA [5, 9]. Although in all reported cases, the PDGFRA breakpoints were variable, they were limited to exon 12 and more specifically within the region encoding a WW-like domain [2]. A similar finding was also observed in our patients (Figure 1). There is strong evidence that the result of FIP1L1-PDGFRA rearrangement is an interrupted PDGFRA juxtamembrane region, due to an interstitial deletion of a tryptophan (W) residue of the putative WW-domain (Figure 1). This domain is believed to be a negative regulator of kinase activity and serves as an auto-inhibitory domain. Thus, the interruption of the juxtamembrane region of PDGFRA may serve as the primary mode of constitutive kinase activation and the leukemic transformation of the affected cells [2, 19].

In our study, both patients with FIP1L1-PDGFRA rearrangement were male and exhibited splenomegaly, similar to the majority of the positive patients reported in the literature. It is noteworthy that one patient displayed rash as a presenting sign, considering that skin involvement is rare in CEL [11, 20]. Moreover, this patient displayed undesirable morbidity due to initial misdiagnosis, while the second one was diagnosed early after the demonstration of eosinophilia in routine laboratory examination, without reference to the diagnostic criteria of HES [24]. This point should be highlighted, considering that even in such patients, cardiac damage can be irreversible. On the other hand, 2 HES patients were also sensitive to imatinib treatment, and remained in CHR, receiving imatinib 9 and 50 months, respectively, after diagnosis. It has been reported that up to 40% of imatinib responding patients lack the FIP1L1-PDGFRA fusion [5, 11, 17, 20], suggesting the activation of other, still unknown, tyrosine kinases that may contribute to disease pathogenesis and phenotype. Although in a recent report, Baccarani and coworkers reported that such patients need higher doses of imatinib and usually relapse [11], this does not appear to be absolutely the rule [5, 17], since in our cohort 2 HES patients remain in CHR and clinical remission, receiving 100 and 400 mg of imatinib, respectively, as maintenance treatment.

Moreover, we treated another patient with primary eosinophilia, whose diagnosis was ultimately systemic mastocytosis. Regardless of the presence or absence of FIP1L1-PDGFRA or C-KIT-D816V, patients with SM may present with eosinophilia [21]. It is well documented today that some of these patients carry the FIP1L1-PDGFRA rearrangement and are sensitive to imatinib treatment, suggesting that the molecular pathogenesis for this subset of patients is similar to that of CEL [14, 21]. Indeed, it has been recently proposed that these patients should be appropriately classified as systemic mastocytosis-CEL [21]. However, our patient was negative for the FIP1L1-PDGFRA rearrangement, as well as for the C-KIT-D816V mutation, and did not respond to imatinib treatment.

Conclusion

An early diagnosis of FIP1L1-PDGFRA-positive CEL and imatinib treatment can offer to affected patients an excellent clinical therapeutic result, avoiding undesirable morbidity and mortality. Moreover, although the molecular mechanisms underlying disease pathogenesis and phenotype remain to be determined, imatinib can also be effective in patients with idiopathic HES.

References

  1. Chusid MJ, Dale DC, West BC, Wolff SM: The hypereosinophilic syndrome: analysis of fourteen cases with review of the literature. Medicine (Baltimore). 1975, 54: 1-27. 10.1097/00005792-197501000-00001.

    Article  CAS  Google Scholar 

  2. Cools J, Stover EH, Wlodarska I, Marynen P, Gilliland DG: The FIP1L1-PDGFRα kinase in hypereosinophilic syndrome and chronic eosinophilic leukemia. Curr Opin Hematol. 2003, 11 (1): 51-57. 10.1097/00062752-200401000-00008.

    Article  Google Scholar 

  3. Wilkins HJ, Crane MM, Copeland K, Williams WV: Hypereosinophilic syndrome: An update. Am J Hematol. 2005, 80: 148-157. 10.1002/ajh.20423.

    Article  PubMed  Google Scholar 

  4. Fletcher S, Bain B: Diagnosis and treatment of hypereosinophilic syndromes. Curr Opin Hematol. 2007, 14: 37-42. 10.1097/00062752-200701000-00008.

    Article  CAS  PubMed  Google Scholar 

  5. Cools J, DeAngelo DJ, Gotlib J, Stover EH, Legare PD, Cortes J, Kutok J, Clark J, Galinsky I, Griffin JD, Cross NCP, Tefferi A, Malone J, Alam R, Schrier SL, Schmid J, Rose M, Vandenberghe P, Verhoef G, Boogaerts M, Wlodarska I, Kantarjian H, Marynen P, Coutre SE, Stone R, Gilliland G: A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome. N Engl J Med. 2003, 348: 1201-1214. 10.1056/NEJMoa025217.

    Article  CAS  PubMed  Google Scholar 

  6. Griffin JH, Leung J, Bruner RJ, Caligiuri MA, Briesewitz R: Discovery of a fusion kinase in EOL-1 cells and idiopathic hypereosinophilic syndrome. Proc Natl Acad Sci USA. 2003, 100: 7830-7835. 10.1073/pnas.0932698100.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. La Starza R, Specchia G, Cuneo A, Beacci D, Nozzoli C, Luciano L, Aventin A, Sambani C, Testoni N, Foppoli M, Invernizzi R, Marynen P, Martelli MF, Mecucci C: The hypereosinophilic syndrome: fluorescence in situ hybridization detects the del(4)(q12)-FIP1L1/PDGFRA but not genomic rearrangements of other tyrosine kinases. Haematologica. 2005, 90: 596-601.

    CAS  PubMed  Google Scholar 

  8. Pardanani A, Brockman SR, Paternoster SF, Flynn HC, Ketterling RP, Lasho TL, Ho CL, Li CY, Dewald GW, Tefferi A: FIP1L1-PDGFRA fusion: prevalence and clinicopathologic correlates in 89 consecutive patients with moderate to severe eosinophilia. Blood. 2004, 104: 3038-3045. 10.1182/blood-2004-03-0787.

    Article  CAS  PubMed  Google Scholar 

  9. Vandenberghe P, Wlodarska I, Michaux L, Zachee P, Boogaerts M, Vanstraelen D, Herregods MC, Van Hoof A, Selleslag D, Roufosse F, Maerevoet M, Verhoef G, Cools J, Gilliland DG, Hagemeijer A, Marynen P: Clinical and molecular features of FIP1L1-PDFGRA (+) chronic eosinophilic leukemias. Leukemia. 2004, 18: 734-742. 10.1038/sj.leu.2403313.

    Article  CAS  PubMed  Google Scholar 

  10. Klion AD, Noel P, Akin C, Law MA, Gilliland DG, Cools J, Metcalfe DD, Nutman TB: Elevated serum tryptase levels identify a subset of patients with a myeloproliferative variant of idiopathic hypereosinophilic syndrome associated with tissue fibrosis, poor prognosis, and imatinib responsiveness. Blood. 2003, 101: 4660-4666. 10.1182/blood-2003-01-0006.

    Article  CAS  PubMed  Google Scholar 

  11. Baccarani M, Cilloni D, Rondoni M, Ottaviani E, Messa F, Merante S, Tiribelli M, Buccisano F, Testoni N, Gottardi E, de Vivo A, Giugliano E, Iacobucci I, Paolini S, Soverini S, Rosti G, Rancati F, Astolfi C, Pane F, Saglio G, Martinelli G: The efficacy of imatinib mesylate in patients with FIP1L1-PDGFRa-positive hypereosinophilic syndrome. Results of a multicenter prospective study. Haematologica. 2007, 92: 1173-1179. 10.3324/haematol.11420.

    Article  CAS  PubMed  Google Scholar 

  12. Pardanani A, Ketterling RP, Li CY, Patnaik MM, Wolanskyj AP, Elliott MA, Camoriano JK, Butterfield JH, Dewald GW, Tefferi A: FIP1L1-PDGFRA in eosinophilic disorders: prevalence in routine clinical practice, long-term experience with imatinib therapy, and a critical review of the literature. Leuk Res. 2006, 30: 965-970. 10.1016/j.leukres.2005.11.011.

    Article  CAS  PubMed  Google Scholar 

  13. Helbig G, Stella-Holowiecka B, Grosicki S, Bober G, Krawczyk M, Wojnar J, Reiter A, Hochhaus A, Holowiecki J: The results of imatinib therapy for patients with primary eosinophilic disorders. Eur J Haematol. 2006, 76: 535-536. 10.1111/j.1600-0609.2006.00652.x.

    Article  PubMed  Google Scholar 

  14. Pardanani A, Ketterling RP, Brockman SR, Flynn HC, Paternoster SF, Shearer BM, Reeder TL, Li CY, Cross NCP, Cools J, Gilliland DG, Dewald GW, Tefferi A: CHIC2 deletion, a surrogate for FIP1L1-PDGFRA fusion, occurs in systemic mastocytosis associated with eosinophilia and predicts response to imatinib mesylate therapy. Blood. 2003, 102: 3093-3096. 10.1182/blood-2003-05-1627.

    Article  CAS  PubMed  Google Scholar 

  15. Speletas M, Kioumi A, Loules G, Hytiroglou P, Tsitouridis J, Christakis J, Germenis AE: Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV. Blood Cells Mol Dis. 2008, 40 (3): 353-359. 10.1016/j.bcmd.2007.09.011.

    Article  CAS  PubMed  Google Scholar 

  16. Sotlar K, Marafioti T, Griesser H, Theil J, Aepinus C, Jaussi R, Stein H, Valent P, Horny HP: Detection of c-kit mutation Asp 816 to Val in microdissected bone marrow infiltrates in a case of systemic mastocytosis associated with chronic myelomonocytic leukaemia. Mol Pathol. 2000, 53 (4): 188-193. 10.1136/mp.53.4.188.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Dahabreh IJ, Giannouli S, Zoi C, Zoi K, Voulgarelis M, Moutsopoulos HM: Management of hypereosinophilic syndrome. A prospective study in the era of molecular genetics. Medicine (Baltimore). 2007, 86: 344-354.

    Article  CAS  Google Scholar 

  18. Klion AD: Recent advances in the diagnosis and treatment of hypereosinophilic syndromes. Hematology Am Soc Hematol Educ Program. 2005, 209-214.

    Google Scholar 

  19. Stover EH, Chen J, Folens C, Lee BH, Mentens N, Marynen P, Williams IR, Gilliland DG, Cools J: Activation of FIP1L1-PDGFRalpha requires disruption of the juxtamembrane domain of PDGFRalpha and is FIP1L1-independent. Proc Natl Acad Sci USA. 2006, 103: 8078-83. 10.1073/pnas.0601192103.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Gotlib J, Cools J, Malone JM, Schrier SL, Gilliland DG, Coutre SE: The FIP1L1-PDGFRa fusion tyrosine kinase in hypereosinophilic syndrome and chronic eosinophilic leukemia: implications for diagnosis, classification, and management. Blood. 2004, 103: 2879-2891. 10.1182/blood-2003-06-1824.

    Article  CAS  PubMed  Google Scholar 

  21. Valent P, Akin C, Metcalfe DD: FIP1L1/PDGFRA is a molecular marker of chronic eosinophilic leukaemia but not for systemic mastocytosis. Eur J Clin Invest. 2007, 37: 153-154. 10.1111/j.1365-2362.2007.01757.x.

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

The authors would like to thank Prof. AE Germenis and Dr. V Karanikas for critical appraisal of the manuscript.

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Correspondence to Matthaios Speletas.

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MS was primarily responsible for this work, from conception to submission of the manuscript and wrote the paper. GL carried out the molecular genetic studies and helped drafting of the manuscript. FK carried out the flow cytometric analyses and contributed to the data interpretation. NG, EP and PM participated in study design and the collection and interpretation of data. All authors read and approved the final manuscript.

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Loules, G., Kalala, F., Giannakoulas, N. et al. FIP1L1-PDGFRA molecular analysis in the differential diagnosis of eosinophilia. BMC Hematol 9, 1 (2009). https://doi.org/10.1186/1471-2326-9-1

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