Table 1

Patient characteristics

IDSexAgeRai stageMutation statusALC (×109/L)%CD5+
cd19+
CytogeneticsTP53 mutationTreatment
1Male67IIMutated14993,2Del17p, trisomy 13, t(8;14)NDF, Chl
2Male68IUnmutatedNA90Del13q14NDR-CHOP, F
3Female55NDUnmutated46,697,2NDNDF, other lines unknown
4Male42NDUnmutated28799,7Del11qNDChl
5Male75IUnmutated12793Del13q14NDNo
6Male65NDND162,897,8NDNDF, other lines unknown
7Male76IIIUnmutated12091Del11qNDChl, CVP, F
8Male81NAND13697Del13q14NDChl, F
9Female630Polyclonal34,692,2NormalNDNo
10Male59NAMutated15587,9Del17p, trisomy 12NDChl, R-CVP, FCR, R
11Male70NAMutated322,6100Del13q14NDChl, FC,
12Male27NAUnmutated160,593,8Del13q14, Del11q, loss 6qTP53 WTNo
13Male600Mutated56,595,2NDNDNo
14Male75IIND73,496,6Del13q14TP53 WTNo
15Male52IUnmutated99,991,1Del17p, loss 5q, 5q, 6 p, 10q, 13q, 14q, 15q, 18 p, Gain 10q, 12q,NDFCR
16Male70NAUnmutated42292,8Del17pNDChl, CVP, FCR
17Female750ND28,592,9NDNDNo
18Female71IMutated31,790,5NDNDNo
19Female750Mutated43,494,1NDNDNo
20Male77IIMutated68,495,2Del13q14TP53 WTNo
21Male620Mutated80,192,1Del13q14TP53 WTNo
22Female600Unmutated65,391,2Trisomy 12TP53 WTNo
23Male75NAMutated84,191,8NDNDNo
24Female73IMutated36,989,9NDNDNo
25Female63IMutated110,392,6Del13q14, Trisomy 12NDNo
26Male630Unmutated250,9197,6Del11qNDNo
27Female51IIMutated122,7592,4Del13q14TP53 WTChl, Of
28Female790Mutated83,893,5NDTP53 WTNo
29Male67IVUnmutated333,796,8NormalTP53 WTNo
30Female54IMutated91,890,99loss XTP53 WTNo
31Male82NAUnmutated34,693,74NDNDNo
32Male69IIUnmutated41,894,04Del13q14, Del11qTP53 WTNo
33Male630ND44,691,3NDNDNo
34Female730Mutated20,992,08Del13q14TP53 WTNo
35Female91IND68,592,92NDNDNo
36Female690Mutated58,5192,26Del13q14NDNo
37Male66IMutated73,4191,98NormalNDNo
38Female800Unmutated37,2990,23NDNDNo
39Female86IMutated43,1495,36NDNDNo
40Male770Mutated52,2992,97Del13q14, 14q32-rearrangementNDNo
41Male700ND74,1197,29NDNDNo
42Female670ND95,6994,07NDNDNo
43Male82NDND83,6691,85NDNDNo
44Male66NDND49,695,08NDNDNo
45Female54NDMutated76,8494,52NDNDNo
46Female71IIUnmutated125,5596,36Del13q14TP53 mutChl +R, Venetoclax (resistant)
47Male80IND65,794Del13q14TP53 mutChl, Ibr (resistant)
48Male61NDND76,6591,7Del17pNDR-CVP, FCR, Ibr (resistant)
49Male66IIIND114,8296,39Del13q14, Del17pTP53 mutFCR
50Male70NDUnmutated36,4887,57Del17p, Del11q, gain of 3p14,3p14,1, 11q24,2q25TP53 mutNo
  • Treatment indications were in accordance with IWCLL criteria. Patients with no treatments were in a steady state under a ‘watch and wait’ regimen. Deletion of 17 p was determined by CGH-array. TP53 mutations were determined by Sanger sequencing. Chemorefractory samples were defined according to IWCLL 2008 criteria and were marked as refractory when patients did not respond or relapsed ≤6 months after fludarabine treatment. Ibrutinib and venetoclax refractory samples were obtained from patients that had an IWCLL-defined progression under maintenance treatment with ibrutinib or venetoclax.

  • ALC, Absolute leukocyte count; Chl, chlorambucil; F, fludarabine; FCR, fludarabine, cyclophosphamide and rituximab; Ibr, ibrutinib; ND, not determined; Of, ofatumumab; R, rituximab; R-CHOP, rituximab cyclophosphamide, doxorubicin, vincristine and prednisone; R-CVP, rituximab cyclophosphamide, vincristin and prednisone; WT, wild type.