FIP1L1-PDGFRA molecular analysis in the differential diagnosis of eosinophilia
© Loules et al; licensee BioMed Central Ltd. 2009
Received: 21 July 2008
Accepted: 02 February 2009
Published: 02 February 2009
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).
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.
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.
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.
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 [1–4]. 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) . 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 .
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, 8–11], they are dramatically sensitive to treatment with the tyrosine kinase inhibitor imatinib [5, 8–13]. 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.
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 [1–3] 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).
Detection of FIP1L1-PDGFRA fusion
The FIP1L1-PDGFRA rearrangement was analyzed by a modified nested reverse transcriptase-polymerase chain reaction (RT-PCR) protocol . In particular, RNA was extracted from BM or PB, and cDNA was reversed transcribed, as previously described . 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 , 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 .
Clinical and laboratory findings of the patients with primary eosinophilia
Duration of imatinib therapy
Result of imatinib therapy
Maculopapular rash, fatigue, peripheral neuropathy, splenomegaly
400 mg (I)
100 mg (M)
CHR, clinical, molecular remission
100 mg (I)
100 mg (M)
CHR, clinical, molecular remission
Abdominal pain, lymphadeno-pathy, fatigue, cough
Steroids for 6 mo
400 mg (I)
100 mg (M)
400 mg (I)
400 mg (M)
Malaise, arthralgia, gastritis, splenomagaly
for 2 y
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.
A more detailed clinical and laboratory presentation of patients carrying the FIP1L1-PDGFRA rearrangement is presented below:
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.
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.
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, 7–13, 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 . Moreover, Klion also noted that 10%–50% of patients meeting the classic definition of HES may be FIP1L1-PDGFRA-positive . 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 . 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 [2–4]. 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 , 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 . 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 . 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.
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.
The authors would like to thank Prof. AE Germenis and Dr. V Karanikas for critical appraisal of the manuscript.
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