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. 2017 Sep;102(9):1511-1518.
doi: 10.3324/haematol.2017.165795. Epub 2017 May 4.

Characteristics and clinical significance of cytogenetic abnormalities in polycythemia vera

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Characteristics and clinical significance of cytogenetic abnormalities in polycythemia vera

Guilin Tang et al. Haematologica. 2017 Sep.

Abstract

Up to 20% of patients with polycythemia vera have karyotypic abnormalities at the time of the initial diagnosis. However, the cytogenetic abnormalities in polycythemia vera have not been well characterized and their prognostic impact is largely unknown. In this study, we aimed to address these issues using a large cohort of polycythemia vera patients with cytogenetic information available. The study included 422 patients, 271 in polycythemic phase, 112 with post-polycythemic myelofibrosis, 11 in accelerated phase, and 28 in blast phase. Abnormal karyotypes were detected in 139 (33%) patients, ranging from 20% in those in the polycythemic phase to 90% among patients in accelerated/blast phase. Different phases harbored different abnormalities: isolated del(20q), +8 and +9 were the most common abnormalities in the polycythemic phase; del(20q) and +1q were the most common abnormalities in post-polycythemic myelofibrosis; and complex karyotypes were the most common karyotypes in accelerated and blast phases. Patients with an abnormal karyotype showed a higher frequency of disease progression, a shorter transformation-free survival and an inferior overall survival compared with patients with a normal karyotype in the same disease phase. Cytogenetics could be effectively stratified into three risk groups, low- (normal karyotype, sole +8, +9 and other single abnormality), intermediate- (sole del20q, +1q and other two abnormalities), and high-risk (complex karyotype) groups. We conclude that cytogenetic changes in polycythemia vera vary in different phases of disease, and carry different prognostic impacts.

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Figures

Figure 1.
Figure 1.
Overall survival of patients in different stages. Patients in a higher stage had a significantly inferior overall survival. AP/BP: accelerated/blast phase; MF: post-polycythemic myelofibrosis; PP: polycythemic phase.
Figure 2.
Figure 2.
Transformation-free survival of patients with normal and abnormal karyotypes. Patients with an abnormal karyotype had a significantly shorter transformation-free survival. (A) Patients in polycythemic phase; (B) patients with post-polycythemic myelofibrosis.
Figure 3.
Figure 3.
Overall survival of patients with normal and abnormal karyotypes. Patients with an abnormal karyotype had a significantly inferior overall survival. (A) Patients in polycythemic phase; (B) patients with post-polycythemic myelofibrosis.
Figure 4.
Figure 4.
Overall survival of patients with low-, intermediate-, and high-risk cytogenetics. (A) Patients in polycythemic phase; (B) patients with post-polycythemic myelofibrosis.

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