Clinical and biological characterization of patients with low (0.1-2%) JAK2V617F allele burden at diagnosis.

Detection of the JAK2V617F mutation is of major help in the diagnosis of myeloproliferative neoplasms (MPNs). Techniques using allele-specific quantitative PCR (AS-qPCR) can reliably and consistently detect down to 0.001% mutated alleles. Moreover, a study of healthy blood donors has shown that the maximum JAK2V617F value in 200 subjects was 0.035%. In practice, a positivity threshold of 1% is commonly accepted. The generalization of highly sensitive techniques revealed that the detection of very small clones (around and below 1% JAK2V617F) is far from exceptional and the interpretation of this is sometimes challenging. In particular, one may question the clinical interest in detecting such minor clones in untreated patients. Molecular biologists and clinicians involved in MPN management in the Myeloproliferative Neoplasms and Related Disorders European Network (MPN&MPNr-EuroNet) have collected and analyzed clinical and biological data from 36 patients presenting with 0.1-2% JAK2V617F at diagnosis. All patients had provided an informed written consent in accordance with the Declaration of Helsinki for the use of remnant DNA for investigational purposes. Local ethics committees approved the study. Eight molecular biology laboratories members of the MPN&MPNr-EuroNet were sent DNA standards containing 0.1 % and 1% JAK2V617F prepared and provided by IPSOGEN (now QiagenMarseille, France) to calibrate local assays. With the help of these standards, 36 patients were selected who fulfilled the following criteria: JAK2V617F determined at least twice with at least two months between the two determinations; one determination found between 0.1% and 2% JAK2V617F in the absence of cytotoxic therapy; sufficient clinical and biological characterization to confirm or rule out the diagnosis of MPN; sufficient DNA for centralized assessment of JAK2V617F allele burden and search for additional mutations. Each center first used their own JAK2V617F quantification technique and sent DNA to the CHU de Bordeaux where the allele burden was centrally determined using a "sense" and an "anti-sense" primerbased allele-specific qPCR as described (Figure 1). For patients with erythrocytosis, JAK2 exon 12 mutations were screened by high resolution melting curve analysis (HRM) followed by sequencing. For patients with thrombocytosis or suspicion of myelofibrosis, MPL exon 10 and CALR mutations were detected by HRM or fragment analysis and confirmed by sequencing. Patients were subdivided into four groups depending on the reason for which they underwent JAK2V617F mutation detection: erythrocytosis (n=15), unusual thrombosis (n=3), thrombocytosis (n=11) or suspicion of myelofibrosis (circulating immature granulocytes, anemia and/or splenomegaly; n=7). The correlation between the allele burdens determined locally and in the central laboratory was not perfect, a few results being under-estimated in local laboratories (Table 1). However, all positive results were confirmed positive by central determination. This underlines the technical difficulty of precisely assessing low burdens and the usefulness of centralized assessment of low JAK2V617F quantification results. Among the 15 patients explored for erythrocytosis, only 3 had a final diagnosis of polycythemia vera (PV) according to WHO criteria (omitting the JAK2V617F mutation). Of these, one (E4) had an additional mutation in exon 14, just upstream (5') of the G1849T (V617F) substitution, thus interfering with the annealing of the primer and resulting in an underestimation of the JAK2V617F burden when assessed with a "sense" qPCR. These cases can be detected by using an "anti-sense" qPCR with the specific primer located 3' of the mutation (Figure 1). For patient E4, the alternative PCR revealed a significant mutated clone (10% JAK2V617F). The same phenomenon applies to patient M7; in this case, the "sense" qPCR indicated a JAK2V617F burden of 0.6% while the “anti-sense” revealed a high burden (73%). Thus, an unexpectedly low JAK2V617F burden should first prompt a search for additional mutations that might be hampering correct primer annealing. Another PV patient (E8) had a mutation in the exon 12 of JAK2 in addition to the small (1.5%) JAK2V617F clone. The third patient with a PV phenotype (E14) did not fulfill WHO criteria of PV at the time of diagnosis because he had a normal EPO level and bone marrow histology was not consistent with PV. However, when JAK2V617F was later reassessed, it was found to have slightly increased levels (from 0.6% to 1.5%) and the EPO level was then found below the lower limit. Thus, in this case, enough criteria were gathered to establish the diagnosis of PV based on the WHO recommendations. In the 12 remaining patients with erythrocytosis, none had sufficient criteria to confirm the diagnosis of PV. Three (patients E1, E2 and E10) had secondary erythrocytosis attributed to a respiratory condition (chronic obstructive pulmonary disease). Three others (patients E3, E9 and E13) had probable secondary erythrocytosis with high levels of EPO. Two (patients E11 and E15) had a false erythrocytosis diagnosed on the basis of a normal isotopic red cell mass, and one (patient E12) had a transitory erythrocytosis that resolved spontaneously. Three others (patients E5, E6 and E7) had idiopathic erythrocytosis of whom 2 remained stable without treatment. Two of these 3 patients did not have a bone marrow biopsy, so a diagnosis of MPN could not be definitively ruled out. None of the patients explored for erythrocytosis evolved towards myelofibrosis or leukemia. For the 3 patients tested for unusual thromboses (which did not include splanchnic thromboses), no sign of MPN was found and blood counts remained normal. For the 11 patients presenting with thrombocytosis, a clear diagnosis of MPN could be made in 5, either because the bone marrow histology was in favor of MPN, and/or because an additional mutation was found in the MPL (Tc3) or CALR (Tc5 and 11) genes. For the other patients, even though the bone marrow histology was not available (Tc6 and Tc9), or was reported as normal (Tc1, Tc2, Tc7 and Tc8), the persistence of high platelet counts in the absence of any reactive cause of thrombocytosis made the diagnosis of essential thrombocythemia (ET) highly probable. For patients tested for suspicion of myelofibrosis, a hematologic malignancy was always confirmed: 3 primary myelofibrosis (PMF), 3 myelodysplastic syndromes, and one overlapping syndrome (atypical chronic myeloid leukemia). The evolution of these patients was mostly pejorative. These results indicate that when a low JAK2V617F burden is found, one should first eliminate the possibility that the %JAK2V617F is under-estimated because of an additional mutation hampering correct primer or probe annealing. Secondly, the existence of another mutation should be searched for, either in JAK2 exon 12 for patients with erythrocytosis or in the CALR or MPL genes for other