Table 1

Occurrence of CSF3R mutations in patients with CN and development of secondary malignancies

Patient groupNo CSF3R nonsense mutation, no. (%)CSF3R nonsense mutation, no. (%)Total no.
CN without Mo7/MDS/leukemia 82 (66) 43 (34) 125 
CN with Mo7/MDS/leukemia 5 (22) 18 (78) 23 
    CN/Mo7 
    CN/MDS 
    CN/AML 13 
    CN/ALL 
    CN/CMML 
Total CN 87 (59) 61 (41) 148 
Patient groupNo CSF3R nonsense mutation, no. (%)CSF3R nonsense mutation, no. (%)Total no.
CN without Mo7/MDS/leukemia 82 (66) 43 (34) 125 
CN with Mo7/MDS/leukemia 5 (22) 18 (78) 23 
    CN/Mo7 
    CN/MDS 
    CN/AML 13 
    CN/ALL 
    CN/CMML 
Total CN 87 (59) 61 (41) 148 

The correlation between occurrence of CSF3R mutations and the development of secondary malignancies was highly significant using the Pearson chi-square test (P = 8.6 × 10−5).

CN indicates congenital neutropenia; Mo7, monosomy 7; MDS, myelodysplastic syndrome; AML, acute myeloid leukemia; ALL, acute lymphoblastic leukemia; CMML, chronic myelomonocytic leukemia.

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