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. Author manuscript; available in PMC: 2024 Oct 1.
Published in final edited form as: Genes Chromosomes Cancer. 2023 Apr 4;62(10):573–580. doi: 10.1002/gcc.23139

TABLE 3.

Management and clinical outcome of non-AML myeloid neoplasm patients with NPM1 mutations.

Management, follow-up and survival
Treatment Supportive treatment: 29% (10/34)
Other therapy: 65% (22/34)
• Hypomethylating agent: 55%
• Chemotherapy: 7%
• BM transplant: 24%
Lost to follow-up: 6% (2/34)
Transformation to AML or increase in blasts 9 patients transformed to AML
• 6MDS-EB
• 2 MDS-EB1
4 MDS-EB2
• 1CMML-2
• 1 MDS-MLD
• 1 MDS/MPN-U
1 patient had an increase in blasts (<20%)
• MDS(RCMD)
AML relapsea Positive: 78% (7/9)
Negative: 11% (1/9)
Not known: 11% (1/9)
Follow-up 29.5 months (median); 41.7 months (mean)
Survival Total median OS(n = 34): 70 months
OS in patients with progression to AML (n = 9): 20 monthsb
OS in patients without progression to AML (n = 25): 128 monthsb
a

Patients who progressed to AML and received appropriate treatment had disease relapse after initial response. Most patients received chemotherapy treatment.

b

log rank p = 0.05.