Subject characteristics and therapy
Sample . | Diagnosis . | Age, y . | WBC, ×109/L . | Hg B, g/dL . | HCT, % . | Platelets, ×109/L . | Cytogenetics . | Rx . | V617F . | Proliferation at 100 nM, % . | Inhibited . |
---|---|---|---|---|---|---|---|---|---|---|---|
648 | CIMF | 66 | 24.2 | 8.2 | 28 | 455 | 46,XY,del(13)(q12q14)[10]/46,XY[7] | THAL/PRED | ++ | 47.20 | I |
694 | CIMF | 66 | 23.8 | 9.2 | 28 | 353 | 46,XY,del(13)(q12q14)[10]/46,XY[7] | EPO | ++ | 37.63 | I |
695 | CIMF | 41 | 7 | 10.8 | 33 | 582 | 46,XX | ASA | − | 66.90 | N |
699 | CIMF | 45 | 3.5 | 8 | 24 | 123 | ND | None | − | 31.92 | I |
692 | ET | 40 | 5.6 | 13.9 | ND | 409 | 46,XX[11] | HU | + | 21.56 | I |
703 | ET | 47 | 8.4 | 14 | 41 | 563 | 46,XX[25] | HU | + | 20.75 | I |
708 | ET | 67 | 6.3 | 13.5 | 38 | 186 | ND | HU, ASA | + | 39.21 | I |
713 | ET | 52 | 5.2 | 11.4 | 34 | 509 | ND | HU, ASA | + | 4.22 | I |
777 | ET | 73 | 9.8 | ND | 48 | 1065 | 46,XY[8] | None | + | 14.80 | I |
675 | ET | 73 | 4.4 | 13.2 | 39 | 383 | 46,XX[25] | HU | − | 31.86 | I |
688 | ET | 75 | 7.5 | 14.1 | 41 | 1143 | 46,XY | ASA | − | 43.47 | I |
704 | ET | 53 | 6 | 12.1 | 35 | 575 | 46,XX | HU, ASA | − | 34.16 | I |
707 | ET | 57 | 4.5 | 14 | 259 | ND | HU | − | 20 | I | |
706 | ET | 41 | 8 | 11.6 | 36 | 602 | ND | HU, ASA | − | 85.45 | N |
700 | PV | 69 | 8 | 11.7 | 33 | 732 | ND | HU, ASA | + | 27.89 | I |
739 | PV | 56 | 6.3 | 13.2 | 39 | 369 | ND | HU, PB, ASA | + | 22.42 | I |
724 | PV | 76 | 8.3 | 15 | 44 | 372 | ND | PB, ASA | + | 57.75 | N |
742 | PV→ AML | 63 | 53.5 | 8.7 | 27 | 549 | ND | HU | ++ | 15.38 | I |
NBM1 | CONTROL | ND | ND | ND | ND | ND | ND | ND | − | 60.57 | N |
NBM2 | CONTROL | ND | ND | ND | ND | ND | ND | ND | − | 65.49 | N |
NBM3 | CONTROL | ND | ND | ND | ND | ND | ND | ND | − | 89.38 | N |
Sample . | Diagnosis . | Age, y . | WBC, ×109/L . | Hg B, g/dL . | HCT, % . | Platelets, ×109/L . | Cytogenetics . | Rx . | V617F . | Proliferation at 100 nM, % . | Inhibited . |
---|---|---|---|---|---|---|---|---|---|---|---|
648 | CIMF | 66 | 24.2 | 8.2 | 28 | 455 | 46,XY,del(13)(q12q14)[10]/46,XY[7] | THAL/PRED | ++ | 47.20 | I |
694 | CIMF | 66 | 23.8 | 9.2 | 28 | 353 | 46,XY,del(13)(q12q14)[10]/46,XY[7] | EPO | ++ | 37.63 | I |
695 | CIMF | 41 | 7 | 10.8 | 33 | 582 | 46,XX | ASA | − | 66.90 | N |
699 | CIMF | 45 | 3.5 | 8 | 24 | 123 | ND | None | − | 31.92 | I |
692 | ET | 40 | 5.6 | 13.9 | ND | 409 | 46,XX[11] | HU | + | 21.56 | I |
703 | ET | 47 | 8.4 | 14 | 41 | 563 | 46,XX[25] | HU | + | 20.75 | I |
708 | ET | 67 | 6.3 | 13.5 | 38 | 186 | ND | HU, ASA | + | 39.21 | I |
713 | ET | 52 | 5.2 | 11.4 | 34 | 509 | ND | HU, ASA | + | 4.22 | I |
777 | ET | 73 | 9.8 | ND | 48 | 1065 | 46,XY[8] | None | + | 14.80 | I |
675 | ET | 73 | 4.4 | 13.2 | 39 | 383 | 46,XX[25] | HU | − | 31.86 | I |
688 | ET | 75 | 7.5 | 14.1 | 41 | 1143 | 46,XY | ASA | − | 43.47 | I |
704 | ET | 53 | 6 | 12.1 | 35 | 575 | 46,XX | HU, ASA | − | 34.16 | I |
707 | ET | 57 | 4.5 | 14 | 259 | ND | HU | − | 20 | I | |
706 | ET | 41 | 8 | 11.6 | 36 | 602 | ND | HU, ASA | − | 85.45 | N |
700 | PV | 69 | 8 | 11.7 | 33 | 732 | ND | HU, ASA | + | 27.89 | I |
739 | PV | 56 | 6.3 | 13.2 | 39 | 369 | ND | HU, PB, ASA | + | 22.42 | I |
724 | PV | 76 | 8.3 | 15 | 44 | 372 | ND | PB, ASA | + | 57.75 | N |
742 | PV→ AML | 63 | 53.5 | 8.7 | 27 | 549 | ND | HU | ++ | 15.38 | I |
NBM1 | CONTROL | ND | ND | ND | ND | ND | ND | ND | − | 60.57 | N |
NBM2 | CONTROL | ND | ND | ND | ND | ND | ND | ND | − | 65.49 | N |
NBM3 | CONTROL | ND | ND | ND | ND | ND | ND | ND | − | 89.38 | N |
A sample was inhibited (I) if proliferation at 100 nM was less than 50% control (vehicle treated) cells, and not inhibited (N) if proliferation was more than 55% control. By this determination, 15 of 18 MPD samples are inhibited by lestaurtinib versus 0 of 3 control samples. All samples were from different subjects with the exception of samples 648 and 694, which were from the same subject at different points in time. The presence of the JAK2 V617F substitution was determined for each sample, and is listed in column 10.
WBC indicates white blood cells; Hg B, hemoglobin B; HCT, hematocrit; Rx, prescription; −, a sample where the mutation was not detected; +, a sample positive for the mutation; ++, a sample considered homozygous for the V617F mutation, as determined by a complete resistance to restriction enzyme digestion with BsaXI; I, inhibited; and N, not inhibited.