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. 2020 May 30;34(7):1949–1953. doi: 10.1038/s41375-020-0890-1

Table 2.

Clinical characteristics of MPN according to the occurrence of infectious events.

Characteristics Total No Infection Infection p
Age
  >65 years—no. (%) 483 (51.0) 287 (59.4) 196 (40.6) 0.01
MPN subtype
  PV—no. (%) 287 (30.3) 144 (50.2) 143 (49.8) 0.75
  ET—no. (%) 388 (40.9) 204 (52.6) 184 (47.4) 0.11
  MF—no. (%) 223 (23.5) 95 (42.6) 128 (57.4) 0.022
  MPN-U—no. (%) 24 (2.5) 12 (50.0) 12 (50.0) 0.93
  CML—no. (%) 26 (2.8) 13 (50.0) 13 (50.0) 0.92
Driver mutation
  JAK2—no. (%) 682 (78.3) 342 (50.1) 340 (49.9) 0.45
  MPL—no. (%) 26 (3.0) 13 (50.0) 13 (50.0) 0.93
  CALR—no. (%) 131 (15.0) 62 (47.3) 67 (52.7) 0.64
  Triple negative—no. (%) 32 (3.7) 13 (40.6) 19 (59.4) 0.32
Therapy
  No medication—no. (%) 171 (18.0) 76 (44.4) 95 (55.6) 0.12
  HU—no. (%) 407 (42.9) 257 (63.1) 150 (36.9) 0.01
  Ruxolitinib—no. (%) 170 (17.9) 54 (31.8) 116 (68.2) 0.01
  Combination—no. (%) 53 (5.6) 16 (30.2) 37 (69.8) 0.04
  Interferon—no. (%) 57 (6.0) 22 (38.6) 35 (61.4) 0.09
  Other—no. (%) 90 (9.5) 44 (48.9) 46 (51.1) 0.94

Combination therapies included RUX plus either agent: hydroxyurea, pomalidomide, MDM2-inhibitors, BET-inhibitors, or interferon alpha.

no. number, PV polycythemia vera, ET essential thrombocythemia, MF myelofibrosis, MPN-U MPN unclassifiable, HU hydroxyurea.