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. Author manuscript; available in PMC: 2022 Apr 1.
Published in final edited form as: Am J Hematol. 2021 Jan 28;96(4):E103–E105. doi: 10.1002/ajh.26091

Table 1.

Response to Treatment

Patient no. (treated on study) Best Response Duration of Response (months) Ruxolitinib Discontinued Last Known Vital Status Adverse Events (Grade ≥2)**
1* CR 3.5 Yes (due to recurrence) Alive, without HLH Febrile neutropenia (Grade 4)
2* CR 23.5+ Yes (due to toxicity) Alive, without HLH Pain in extremity (Grade 2)
3* CR 35.5+ No Alive, without HLH Pneumonitis (Grade 2); Fatigue (Grade 3)
4* CR 17+ Yes (treatment no longer required) Alive, without HLH Nausea (Grade 2)
5* CR 17.5+ Yes (treatment no longer required) Alive, without HLH None
6 PR 12+ No Alive, without HLH None
Patient no. (treated off study)
7* PR 41.5+ No Alive, without HLH -
8* PR 34.5+ Yes (treatment no longer required) Alive, without HLH Headache
(Grade 2)
9 PR 16.5+ Yes (treatment no longer required) Alive, without HLH -
10 NR N/A N/A Died, with HLH (and disseminated candidiasis) -
11 PR 1.5 Yes (due to recurrence) Alive, without HLH -
12 NR N/A N/A Died, with HLH (and septic shock, VRE bacteremia, neutropenic colitis) -
13 NR N/A N/A Died, with HLH (and invasive sinus and pulmonary aspergillosis complicated by hemorrhagic and septic shock) -
*

Previously reported (3).

**

Unlikely, possibly, or probably related to ruxolitinib.

+

response ongoing at time of last follow-up

Abbreviations: complete response (CR), partial response (PR), no response (NR), not applicable (N/A)