Published online 25 August 2008
Haematologica, Vol 93, Issue 11, 1723-1727 doi:10.3324/haematol.13081
Copyright © 2008 by Ferrata Storti Foundation

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Brief Reports

Frequent reduction or absence of detection of the JAK2-mutated clone in JAK2V617F-positive patients within the first years of hydroxyurea therapy

François Girodon^1,2, Céline Schaeffer¹, Cédric Cleyrat³, Morgane Mounier², Ingrid Lafont⁴, Frédéric Dos Santos¹, Aurélie Vidal¹, Marc Maynadié¹, Sylvie Hermouet^3,5

¹ Laboratoire d’Hématologie, Centre Hospitalier Universitaire (CHU) de Dijon, Dijon
² Registre des hémopathies malignes de Côte d’Or, EA Université de Bourgogne, Dijon
³ INSERM U892, Centre de Recherche en Cancérologie Nantes/Angers, Nantes
⁴ Service d’Hématologie Clinique, CHU de Dijon, Dijon and
⁵ Laboratoire d’Hématologie, Centre Hopitalier Universitaire, Nantes, France

Correspondence: François Girodon, Laboratoire d’Hématologie, Hôpital du Bocage, CHU de Dijon, Dijon, France. E-mail:francois.girodon{at}chu-dijon

ABSTRACT

We analyzed the effect of hydroxyurea on the JAK2V617F allelic ratio (%JAK2V617F), measured in purified blood granulocytes, of patients with polycythemia vera and essential thrombocythemia. Thirty-six patients were examined sequentially prior to and after start of hydroxy-urea therapy (8 polycythemia vera, 17 essential thrombocythemia), or while remaining untreated (2 polycythemia vera, 9 essential thrombocythemia). Hydroxyurea therapy (median duration: 15 months) reduced the %JAK2V617F by >30% in 13/25 patients (4 polycythemia vera, 9 essential thrombocythemia). For 3 patients, JAK2V617F remained undetectable for 3–27 months. In addition, a single time point study of two large cohorts of patients, examined either at the time of diagnosis (99 polycythemia vera, 178 essential thrombocythemia) or while receiving hydroxyurea (36 polycythemia vera, 98 essential thrombocythemia; median length of therapy: 32 months), confirmed reduction of %JAK2V617F in the hydroxyurea-treated group (24% vs. 33% JAK2V617F at diagnosis, p<0.01). Prospective studies are needed to determine the prognostic value of reduced JAK2V617F allele burden under cytoreductive therapy.

Key words: JAK2V617F, hydroxyurea, myeloproliferative neoplasm, polycythemia vera, essential thrombocythemia, allele-specific real time quantitative PCR.

Introduction

Detection of the V617F mutation of JAK2 (JAK2V617F), recently discovered as specifically expressed in the majority of BCR-ABL-negative myeloproliferative diseases (MPDs), has become a main diagnostic test for polycythemia vera (PV) and essential thrombocythemia (ET).^1–3 In contrast, the relevance of the JAK2V617F mutation load for predicting the risk of thrombosis, myelofibrosis or leukemic transformation remains controversial.^4–9 The lack of consensus may be explained by heterogeneity in techniques and materials (purified cells, whole blood, genomic DNA, cDNA) used to quantify JAK2V617F, and by the cohorts of patients studied. Indeed, since the JAK2V617F load is currently thought not to be affected by conventional treatments, most of the published studies of the JAK2V617F mutation load have mixed treated and untreated patients. However, the insensitivity of the JAK2V617F-mutated clone to conventional therapy has never been proven. So far the JAK2V617F allelic ratio (%JAK2V617F) has usually been analyzed at a single time point. Studies analyzing the %JAK2V617F sequentially are rare: Passamonti et al. described an increase in %JAK2V617F in a cohort of 8 patients over a mean period of 17 months.¹⁰ Kiladjian et al. reported a high molecular response rate in PV patients treated with interferon -2a (IFN-2a).¹¹ Using sequential %JAK2V617F analyses, Barosi et al. described transformation from heterozygous to homozygous forms of primary myelofibrosis.¹² Surprisingly, the effect of hydroxyurea (HU), an inexpensive drug widely used in MPDs, on the JAK2V617F mutation load is still unknown. To address this question, we quantified JAK2V617F in purified blood granulocytes from three distinct cohorts of PV and ET patients. A first group of patients was examined at diagnosis then followed as they remained untreated (11 patients) or received HU (25 patients), then two large cohorts of patients, either at the time of diagnosis or under treatment with HU, were studied retrospectively.

Design and Methods

Patients
Patients from two centers diagnosed with MPD according to the WHO criteria were studied as three groups. Thirty-six patients from center 1 (10 PV, 26 ET) were examined first at diagnosis then sequentially without (11 patients) or with HU treatment (25 patients). In a second, retrospective study, two distinct groups of patients were examined at a single time point: group A (n=277; 99 PV, 178 ET; 124 from center 1, 153 from center 2) was examined at the time of diagnosis; group B (n=134; 36 PV, 98 ET; 51 from center 1, 83 from center 2), while under treatment with HU. The study was approved by the institutional ethics committee on human experimentation, Comité de Protection des Personnes Est I and informed consent was provided according to the Declaration of Helsinki.

Analysis of %JAK2V617F
Purified blood granulocytes were prepared in the two centers as described.¹³ Cytospins, stained with May-Grünwald-Giemsa, confirmed the purity (>95%) of the granulocyte preparations. Genomic DNA was prepared using QIAamp DNA mini-kits (Qiagen). In both centers, levels of expression of JAK2 wild-type (WT) or mutated (V617F) were determined in duplicate using the same sensitive (0.15% JAK2V617F) allele-specific quantitative PCRs (AS-qPCR) with the specificity based on sense forward primers.¹³ Copy numbers were determined by comparison with serial dilutions of plasmids.¹³ Absence of significant inter-center variability in the AS-qPCR assay was verified by parallel analysis in both centers of 70 DNA samples (data not shown). To limit inter-assay variability, sequential samples from a same patient were analyzed in the same AS-qPCR run. Whenever the JAK2V617F allele burden decreased by >30% or became undetectable during treatment, quantification was repeated on the same sample, then on new samples. A second AS-qPCR assay with the specificity based on anti-sense reverse primers was developed to verify the JAK2V617F allelic ratio in HU-treated patients. Sequences of primers and probes were: forward primer, 5'-GCGCGTGCATCTTTATTATGGCAGA-3' JAK2 wild-type reverse primer, 5'-CCCGTTACTCTCGTCTCCACAGAC-3'; JAK2V617F reverse primer, 5'-GCCGTTACTCTCGTCTCCACAGAA-3' and probe, 5' 6FAM-GAGAAAGC TTGCTCATCATACTTGCTGC-3' TAMRA.

Statistical analysis
Mean comparison one-sided parametrical test was used to compare different groups of patients, and Fisher’s exact or ² tests to compare proportions. Analysis of sequential %JAK2V617F was made with a t-test. Data were analyzed using the Stata software. p<0.05 was considered statistically significant.

Results and Discussion

The effect of HU on the JAK2V617F-mutated clone was studied with sequential assessment of %JAK2V617F in 36 patients. These patients (10 PV, 26 ET) had at least two determinations of the JAK2V617F mutation load, at the time of diagnosis and after a median period of 16 months of follow-up, with or without HU (Figure 1). Twenty-five patients were treated with HU (8 PV, 17 ET) with a 15-month median duration of treatment at the time of the second assessment of the %JAK2V617F; 11 patients (2 PV, 9 ET) did not receive cytoreductive therapy (median follow-up: 16 months; range: 1–47 months). The group of ET patients to whom HU was prescribed had higher platelet counts at diagnosis than patients who were not given HU (758 vs. 620 G/L, p=0.0289). Consistent with aggressive forms of MPD justifying cytoreductive therapy, they also had a higher %JAK2V617F at diagnosis (PV, 64%; ET, 34%) than patients who remained untreated (PV, 43%; ET, 20%). In the group of untreated patients, the %JAK2V617F remained stable (Figure 1A). In contrast, treatment with HU resulted in decreased %JAK2V617F, from 43% at diagnosis to 24% during HU-treatment (p<0.0001). The decrease in %JAK2V617F was significant in PV (from 64 to 40%, p=0.0141) and in ET (from 34 to 16.7%, p<0.01) (Figure 1B, C). Of note, a >30% decrease was noted in 13 patients (5 females, 8 males). JAK2V617F became undetectable in 4 ET patients (1 female, 3 males) after a 5–55 month period of treatment, and remained undetectable for a 3–27 month period of follow-up. Decreases in %JAK2V617F were confirmed by a second AS-qPCR assay (Table 1). Importantly, 3 of the 4 ET patients found negative for JAK2V617F while receiving HU were confirmed negative by the second AS-qPCR assay; the fourth patient was found positive, but with 1% JAK2V617F only.

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Figure 1. Evolution of the %JAK2V617F in treated and untreated polycythemia vera and essential thrombocythemia patients. (A) Patients who did not receive any cytoreductive treatment. (B) essential thrombocythemia patients who were treated with hydroxyurea for the indicated time (expressed in months). (C) polycythemia vera patients who were treated with hydroxyurea for the indicated time (expressed in months). There was no significant change in %JAK2V617F in untreated patients. The %JAK2V617F was significantly decreased for both essential thrombocythemia and polycythemia vera patients who received HU (p<0.05). (- -) female patients; (–) male patients.

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Table 1. %JAK2V617F analysis in patients tested before and during hydroxyurea treatment.

The effect of HU on the %JAK2V617F was then investigated in a retrospective study of large cohorts of PV and ET patients, using two distinct groups of patients tested at a single time point. Patients of group A were examined at the time of diagnosis. JAK2V617F was not detected in granulocytes of 5/99 PV patients (5%) and 51/178 ET patients (29%) (Table 2). These cohorts of PV and ET patients were comparable to those previously described.¹³ Mean %JAK2V617F in patients carrying the mutation was 54% in PV and 18% in ET. A minority of PV (13/99, 13%) had <25% JAK2V617F and a minority of ET (10/178, 6%) had >40% JAK2V617F. JAK2V617F -positive ET patients were older, with lower platelet counts and higher hematocrit and hemoglobin levels (controlled for gender) than JAK2V617F-negative ET patients. The proportion of male patients was 51% for PV and 40% for ET. There was no difference in JAK2V617F mutation load between male and female patients; this was true in both the PV and ET groups.

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Table 2. Hematologic and clinical features of patients.

Patients of group B, a distinct cohort, had been treated with HU for a median duration of 32 months (same median duration of treatment for PV and ET patients), with no significant difference in treatment duration between male and female patients. The mean ages of PV and ET patients were similar in groups A and B; the proportions of male patients in group B were 50% for PV and 40% for ET. As expected, hematocrit, hemoglobin level, white blood cell (WBC) and platelet counts were significantly lower in the treated group (for both PV and ET) than in the group at diagnosis (Table 2). HU-treated patients had a significantly lower JAK2V617F allelic ratio (24%) than patients at diagnosis (33%, p<0.01). JAK2V617F was not detected in granulocytes from 5/36 treated PV patients (14%) and 34/98 treated ET patients (35%); these proportions were not significantly different from those of group A.

Interestingly, under HU treatment, PV patients with <25% JAK2V617F (15/36, 7 males, 8 females) represented a higher percentage than in the PV cohort at diagnosis (42% vs. 13%, p<0.001). Consistently, treated PV patients had a lower %JAK2V617F than PV patients at diagnosis (44% vs. 54%, p=0.0257). There was no difference in %JAK2V617F for the group of ET patients under treatment compared to those tested at time of diagnosis. However, analysis of ET data by gender revealed a lower %JAK2V617F during HU therapy for female patients (p<0.01). The same analysis of PV also showed that the decrease in %JAK2V617F associated with HU treatment was significant only in women (39% with HU vs. 53% at diagnosis, p=0.0249), suggesting that the JAK2V617F-mutated clone may be more sensitive to HU in female than in male MPD patients. A similar gender difference had previously been reported by Pemmaraju et al.⁷ in a series of 80 ET patients that included treated patients.

The finding that HU, the drug most commonly used in MPDs, reduces and occasionally renders the JAK2V617F-mutated clone undetectable with sensitive (0.15%) AS-qPCR assays underlines the importance of detecting and quantifying JAK2V617F before initiating cytoreductive therapy. This is necessary in order to rule out false negatives under treatment. In this regard, JAK2V617F-negative should be applied solely to patients for whom the V617F mutation was not detectable prior to treatment. Furthermore, molecular response to HU, in addition to assay sensitivity, may explain the differences in ratios of JAK2V617F-positivity for ET reported in studies mixing treated and untreated patients (usually 50% JAK2V617F-positive) compared to studies of patients at diagnosis (70–75% JAK2V617F-positive).^7,8,13,14

The delay and length of response of the JAK2-mutated clone to HU therapy could not be evaluated in this mostly retrospective study. However, all but 2 patients who responded to HU had been treated for <3 years (median: 18 months) and decreases in JAK2V617F allele burden were observed in 2 patients with <6 months of treatment, suggesting that reduction of the JAK2V617F -mutated clone likely occurs within the first year of HU therapy. This could explain the apparent contradictions between our study and others, which reported no change in %JAK2V617F in sequential analysis of treated MPD patients, likely under HU-therapy for several years when first tested for JAK2V617F.¹⁵ We tried to compare patients with molecular response to HU with those who did not respond. The only difference between ET patients responding to HU with decreased %JAK2V617F and those with no variation was younger age (mean age: 60 vs. 71 years respectively, p<0.05). There was no difference in blood parameters (WBC, platelet counts, Ht, Hb) at the time of diagnosis. Similarly, blood counts of patients for whom JAK2V617F became undetectable with HU treatment did not differ from those with moderate or no decrease in %JAK2V617F.

Finally, it is important to determine whether one should aim towards complete molecular response in JAK2V617F-positive patients. As treatment affects the (mutated) granulocyte/(non-mutated) lymphocyte ratio, accurate assessment of the molecular response of treated patients – quantification of low levels of JAK2V617F – can only be achieved using purified granulocytes, not whole blood.¹⁶ However, the prognostic value of the disappearance of the JAK2V617F-mutated clone during treatment is currently not known. We and others previously reported sharp decreases and disappearance of JAK2V617F-mutated clones in PV and ET patients in association with transformation into acute myeloid leukemia.¹⁷ In the present series, none of the patients who became JAK2V617F-negative with HU therapy showed signs of leukemic transformation for as long as 27 months. Prospective studies with sequential assessments of %JAK2V617F – taking into account gender – are needed to determine whether obtaining a molecular response has a favorable influence on MPD evolution, compared to patients for whom the JAK2V617F load remains stable.

Acknowledgments

we wish to thank Mrs. Dominique Bouchot, Marie-Christine Boursier, Martine Courtois, Laetitia Ergand, Isabelle Helot, Fabienne Perrault-Hu and Danielle Pineau, for excellent technical help. We are indebted to our colleagues from the Departments of Clinical Hematology of the hospitals of Dijon, Châlon sur Saône, Nantes and La Roche sur Yon for providing patient samples.

Footnotes

Funding: this work was sponsored by the University Hospital of Dijon for regulatory and ethic submission, and was supported by a grant from the Lions Club Châlon Tulipes Contre le Cancer to FG, and by a grant from the Comité Grand Ouest of the Ligue Nationale contre le Cancer to SH.

Authorship and Disclosures

FG and SH conceived the study, analyzed the data, wrote the paper and created Table 2; CC performed AS-qPCRs; MM carried out statistical analyses, CS collected and analyzed the data, created Table 1 and Figure 1; FDS and AV collected the data; IL enrolled patients, MM enrolled patients and revised the manuscript, FG is responsible for the patient database.

All the individuals listed as co-authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship as detailed in the ICMJE website: http://www.icmje.org/#author. The authors reported no potential conflicts of interest.

Received for publication March 18, 2008. Revision received May 29, 2008. Accepted for publication June 4, 2008.

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