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. Author manuscript; available in PMC: 2020 Aug 1.
Published in final edited form as: Br J Haematol. 2019 Mar 11;186(3):e31–e35. doi: 10.1111/bjh.15861

Table I.

Characteristics of patients with post-chemotherapy CHIP, and specific mutations identified.

Age (years) Sex Race Cancer Chemo-therapy Months from treatment CHIP-associated mutations
49 F W Breast ACT 20 DNMT3A
50 F W Breast ACT 7 DNMT3A (x2)
54 F B Lymphoma ABVD 23 DNMT3A
59 F W Breast ACT 9 GNAS
61 F W Lymphoma ABVD 91 DNMT3A
62 F W Breast ACT 18 ASXL1, DNMT3A, TET2
64 M W Lymphoma RCHOP 57 DNMT3A, TP53
65 F W Lymphoma RCHOP 44 TET2
67 M W Lymphoma RCHOP 119 KIT, SRSF2
67 F W Lymphoma RCHOP 8 TET2
69 F W Breast ACT 10 ASXL1, DNMT3A
69 M W Lymphoma RCHOP 100 ASXL1, BCORL1, SRSF2, ZRSR2
71 F W Breast AC 53 DNMT3A (x2)
71 F W Breast ACT 59 DNMT3A
75 F W Lymphoma CHOP 67 DNMT3A, TET2

ABVD: doxorubicin, bleomycin, vinblastine, and dacarbazine; AC: doxorubicin and cyclophosphamide; ACT: doxorubicin, cyclophosphamide and paclitaxel; B: black; CHIP: clonal haematopoiesis of indeterminate potential; CHOP: cyclophosphamide, doxorubicin, vincristine and prednisone; F: female; M: male; RCHOP: rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; W: white non-Hispanic.