A recent publication by Antonioli et al. shows that the continuous use of hydroxyurea (HU) does not appreciably reduce JAK2 V617F allele burden in patients with polycythemia vera (PV) or essential thrombocythemia (ET).1 Our results confirm and extend these data. To assess the effects of a cytoreductive treatment on the JAK2-V617F allelic ratio, a single center retrospective study in myeloproliferative neoplasm (MPN) patients was performed. The effect of HU on the JAK2-V617F allele burden was evaluated in at least two sequential samples of 21 patients with PV or ET submitted to HU therapy and referred for molecular diagnosis. The JAK2V617F allele load was measured by an allele-specific PCR with fluorescent primers in DNA of density gradient purified granulocytes according to Jones et al.2 with slight modifications.3 As standards, serial dilutions of plasmids carrying the wild-type and V617F mutated JAK2 sequences were used. JAK2-V617F allele burden was determined based on availability of serial samples of genomic DNA, laboratory data and clinical records of the 8 PV and 13 ET (one of them transforming to acute leukemia) patients, as shown in Figure 1. The JAK2-V617F allele burden was evaluated before and/or after initiation of HU therapy and compared to the last sample that was available during treatment.
We herein correlate changes in the JAK2-V617F allele burden with HU dose variation; hematocrit (Ht) and platelet counts during HU treatment for PV (Figure 2A) and ET patients (Figure 2B). Hydroxyurea usage was consistently associated with hematologic changes over time (Table 1). However, while HU dosage importantly impacted Ht (PV patients 3, 7, and 63) and platelet count (ET patients 4, 6, 10, 11 and 31), JAK2-V617F allele burden did not necessarily vary according to changes in HU doses. Although 3 PV patients (1, 2, and 3) and 5 ET patients (18, 31, 34, 51 and 54) evolved with JAK2 fluctuations, these oscillations did not significantly impact allele burden over time. In general, the percentage of JAK2-V617F allele burden tended to remain stable through HU treatments.
While fluctuations with reductions of JAK2-V617F allele burden were seen when comparing pre-treatment JAK2-V617F allele load with the latest sample, patients with longer follow ups evolved with a stable allelic burden despite variations in hematologic counts and HU doses (median period of follow up of 20 months for PV and 21 months for ET).
The relationship between the kinetics of HU-mediated response and clone size of JAK2-V617V in MPN is still not clear. Although changes in the JAK2-V617F allele burden were reported at HU initiation or termination for individual PV or ET patients,4,5,6,7 and during short follow ups,4,6 it appears that after a certain threshold of JAK2 allele burden is achieved, only slight fluctuations are seen.4,6 Reports on long-term evaluation of patients receiving HU treatment, which show slight variations or stabilization of a certain value of JAK2-V617F allele load variable from patient to patient seem to reinforce this concept.4,6,7
It is noteworthy that patients who presented broader fluctuations of JAK2-V617F allele burden (those changing from a former assigned quartile to another) were those with intermediate ratios of JAK2-V617F allele burden (2 and 3 quartile). In contrast, patients situated in the boundaries of a JAK2-V617F mutation ratio scale (1 and 4 quartile) showed no major modification of JAK2 V617F allele burden in response to HU variations (Figure 2 and Table 1).
Our study has limitations owing to the small size of the sample and the short follow up. Nevertheless, the results reinforce the idea that hematologic parameters are deeply impacted by HU dosage, as evidenced by the decrease in platelet and red blood cell counts in response to HU dose elevation and the increase under HU dose reduction. Moreover, it suggests that, in the lower and upper extremes (1 or 4 quartile) of allele burden detection, the variation of JAK2-V617F allele burden is less evident.
The findings herein lead to interesting questions regarding the effect of HU in hematologic compartments (as those seen in Ht or platelet counts in our data) as compared to its effect on JAK2-V617F positive cells. The kinetics of JAK2-V617F versus Ht in PV or platelet counts in ET suggest that JAK2-V617F allele burden is, at least to some extent, dissociated from HU effects on the hematologic parameters. Since pharmacological JAK inhibition has been shown to impact spleen size in MPN patients,8 it will be of great interest to observe the effect of JAK inhibitor dose oscillations on JAK2-V617F allele burden.
References
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