Prognostically informative mutations of most frequent detection in patients with MPN
Gene . | Polycythemia vera . | Essential thrombocythemia . | Primary myelofibrosis . | “Secondary” myelofibrosis . |
---|---|---|---|---|
JAK2 V617F | • Higher risk of thrombosis (included in revised IPSET) | • Intermediate prognosis and higher risk of thrombosis compared to patients with CALR mutation | ||
CALR | • Lower risk of thrombosis compared to JAK2 mutated | • CALR type 1/like: improved survival compared to JAK2 V617F and “triple negative” • Improved outcome after SCT • Absence of CALR type 1/like included in MIPSS70/plus v2.0 • Absence of CALR mutation included in MYSEC-PM and MTSS scores | • Improved OS compared to JAK2 V617F and “triple negative” • Improved outcome after SCT • Absence of CALR mutation included in MYSEC-PM and MTSS scores | |
MPL W515 | • Intermediate prognosis and higher risk of thrombosis compared to patients with CALR mutation | |||
“Triple negative” | • Inferior OS and LFS compared to JAK2/CALR mutation (especially in pre-PMF) | |||
JAK2 exon 12 | • Similar rates of thrombosis, evolution to post–PV-MF and BP, and survival to JAK2 V617F | |||
ASXL1 | • “Adverse variant” associated with inferior OS and MFS • Included in MIPSS-PV | • “HMR variant” associated with inferior OS/LFS, lower PFS following SCT • Included in MIPSS70/plus v2.0 and GIPSS | ||
EZH2 | • “Adverse variant” associated with inferior OS/LFS | • “HMR variant” associated with inferior OS • Included in MIPSS70/plus v2.0 | ||
IDH1 IDH2 | • IDH1: “adverse variant” associated with inferior OS and LFS | • IDH2: “adverse variant” associated with inferior OS | • “HMR variants” associated with inferior OS/LFS and as lower PFS following SCT • Included in MIPSS70/plus v2.0 | • “Adverse variant” associated with lower PFS following SCT |
SRSF2 | • “Adverse variant” associated with inferior OS • Included in MIPSS-PV | • “Adverse variant” associated with inferior OS/LFS • Included in MIPSS-ET | • “HMR variant” associated with inferior OS/LFS • Included in MIPSS70/plus v2.0 and GIPSS | |
U2AF1 Q157 | • “HMR variant” associated inferior OS • Included in MIPSS70/plus v2.0 and GIPSS | |||
U2AF1 or DNMT3A or CBL | • U2AF1: “adverse variant” associated with inferior OS/MFS • Included in MIPSS-ET | • “Adverse variant” associated with worse OS in SCT | • “Adverse variant” associated with worse OS in SCT | |
RUNX1 | • “Adverse variant” associated with inferior OS and LFS | • “Adverse variant” associated with inferior OS/LFS | ||
TP53 | • “Adverse variant” associated with inferior LFS | • “Adverse variant” associated with inferior OS/LFS • Included in MIPSS-ET | • “Adverse variant” associated with leukemic transformation | |
LNK (SH2B3) | • “Adverse variant” associated with inferior OS | |||
SF3B1 | • “Adverse variant” associated with inferior OS and MFS • Included in MIPSS-ET | |||
RAS | • “Adverse variant” associated with inferior OS • Associated with JAKi-refractoriness |
Gene . | Polycythemia vera . | Essential thrombocythemia . | Primary myelofibrosis . | “Secondary” myelofibrosis . |
---|---|---|---|---|
JAK2 V617F | • Higher risk of thrombosis (included in revised IPSET) | • Intermediate prognosis and higher risk of thrombosis compared to patients with CALR mutation | ||
CALR | • Lower risk of thrombosis compared to JAK2 mutated | • CALR type 1/like: improved survival compared to JAK2 V617F and “triple negative” • Improved outcome after SCT • Absence of CALR type 1/like included in MIPSS70/plus v2.0 • Absence of CALR mutation included in MYSEC-PM and MTSS scores | • Improved OS compared to JAK2 V617F and “triple negative” • Improved outcome after SCT • Absence of CALR mutation included in MYSEC-PM and MTSS scores | |
MPL W515 | • Intermediate prognosis and higher risk of thrombosis compared to patients with CALR mutation | |||
“Triple negative” | • Inferior OS and LFS compared to JAK2/CALR mutation (especially in pre-PMF) | |||
JAK2 exon 12 | • Similar rates of thrombosis, evolution to post–PV-MF and BP, and survival to JAK2 V617F | |||
ASXL1 | • “Adverse variant” associated with inferior OS and MFS • Included in MIPSS-PV | • “HMR variant” associated with inferior OS/LFS, lower PFS following SCT • Included in MIPSS70/plus v2.0 and GIPSS | ||
EZH2 | • “Adverse variant” associated with inferior OS/LFS | • “HMR variant” associated with inferior OS • Included in MIPSS70/plus v2.0 | ||
IDH1 IDH2 | • IDH1: “adverse variant” associated with inferior OS and LFS | • IDH2: “adverse variant” associated with inferior OS | • “HMR variants” associated with inferior OS/LFS and as lower PFS following SCT • Included in MIPSS70/plus v2.0 | • “Adverse variant” associated with lower PFS following SCT |
SRSF2 | • “Adverse variant” associated with inferior OS • Included in MIPSS-PV | • “Adverse variant” associated with inferior OS/LFS • Included in MIPSS-ET | • “HMR variant” associated with inferior OS/LFS • Included in MIPSS70/plus v2.0 and GIPSS | |
U2AF1 Q157 | • “HMR variant” associated inferior OS • Included in MIPSS70/plus v2.0 and GIPSS | |||
U2AF1 or DNMT3A or CBL | • U2AF1: “adverse variant” associated with inferior OS/MFS • Included in MIPSS-ET | • “Adverse variant” associated with worse OS in SCT | • “Adverse variant” associated with worse OS in SCT | |
RUNX1 | • “Adverse variant” associated with inferior OS and LFS | • “Adverse variant” associated with inferior OS/LFS | ||
TP53 | • “Adverse variant” associated with inferior LFS | • “Adverse variant” associated with inferior OS/LFS • Included in MIPSS-ET | • “Adverse variant” associated with leukemic transformation | |
LNK (SH2B3) | • “Adverse variant” associated with inferior OS | |||
SF3B1 | • “Adverse variant” associated with inferior OS and MFS • Included in MIPSS-ET | |||
RAS | • “Adverse variant” associated with inferior OS • Associated with JAKi-refractoriness |
LFS, leukemia-free survival; MFS, myelofibrosis-free survival; PFS, progression-free survival.