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. 2022 Nov 24;37(2):255–264. doi: 10.1038/s41375-022-01767-y

Table 1.

Prognostication in myelofibrosis includes diverse disease-specific variables that contribute to clinical heterogeneity.

Lille IPSS DIPSS DIPSSplus MIPSS70 GIPSS MYSEC-PM
Age X X X X
Leukocytosis Xa X X X X
Anemia X X X X X X
Symptoms X X X X X
Circulating blasts X X X X X
Thrombocytopenia X X X
RBC transfusion dependent X
Adverse Karyotypeb X X X
BMF X
Non-CALR type 1 X X X
HMR = 1 Xc Xd
HMR > 1 Xc

IPSS International Prognostic Scorcing System, DIPSS Dynamic International Prognsotic Scoring System, MIPSS Mutation-Enhanced International Prognostic Scoring System 70, GIPSS Genetically Inspired Prognostic Scoring System, MYSEC-PM Myelofibrosis Secondary to PV and ET-Prognostic Model, RBC red blood cell, BMF bone marrow fibrosis, HMR high molecular risk.

aLeukocytosis and leukopenia are variables in the Lille prognostic Model.

bComplex karyotype or abnormalities including +8, -7/7q-, i(17q), -5/5q-, 12p-, inv(3) or 11q23 rearrangement.

cHMR mutations in MIPSS70: ASXL1, EZH2, IDH1/2, SRSF2.

dHMR mutations in GIPSS: ASXL1, SRSF2, U2AF1Q157.