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. 2021 Sep 15;11(9):4470–4484.

Table 1.

Patients’ characteristics: CML samples used for in vitro studies and response to ‘asciminib+ponatinib’

Patient no. Age (years) Gender Source CML phase BCR-ABL1 mutations Therapy before cell sampling ‘asciminib+ponatinib’
#1 54 f PB CP n.t. none Synergistic (p); Cooperative CD34+/CD38- (a-fc)
#2 27 m PB CP n.t. none Synergistic (p) Cooperative CD34+/CD38- (a-fc)
#3 19 m PB CP n.t. none Synergistic (p); Cooperative CD34+/CD38- (a-fc)
#4 34 f PB CP n.t. none Synergistic (p)
#5 36 m PB CP n.t. none Synergistic (p)
#6 25 f PB CP n.t. Imatinib (dis.) Synergistic (p)
#7 46 f PB CP n.t. none Synergistic (p)
#8 52 f PB CP n.t. none Cooperative (p)
#9 31 m BM BP T315I Imatinib (res.) Cooperative CD34+/CD38- (a-fc)
Dasatinib (res.)
#10 48 f BM BP T315I Dasatinib (res.) Cooperative CD34+/CD38- (a-fc)
#11 43 m PB BP V299L/F317L Imatinib (res.) Synergistic CD34+/CD38- (a-fc)
Dasatinib (res.)
CHT+GO HSCT

No., number; f, female; m, male; PB, peripheral blood; BM, bone marrow; CP, chronic phase; BP, blast phase; n.t.: not tested; dis: discontinued by the patient; res, resistant; CHT: polychemotherapy; GO: gemtuzumab ozogamycin; HSCT: hematopoietic stem cell transplantation. The in vitro response of leukemic cells to the combination ‘asciminib+ponatinib’ was assessed by 3H-thymidine uptake experiments (cell proliferation: p) and/or by determination of apoptotic CD34+/CD38- stem-cells by Annexin V-FITC/DAPI staining and flow cytometry (a-fc).