Table 1.

Patient characteristics

Patient no.Age at first CLL treatment, yDefinition of high riskAnti-CD20 AbPrevious CLL therapy
61 hCKT  G, R FCR 
66 POD <1 year FCR 
52 del17p, TP53mut GIVe 
61 del17p, TP53mut GIVe 
74 del17p, TP53mut, CKT BIG 
92 del17p BIO 
70 del17p  MCP 
80 TP53mut, CKT  G, R BR 
86 hCKT  G, R BR 
10 74 CKT  G, R FCR 
11 74 del17p BIO 
12 63 POD <1 year FCR 
Patient no.Age at first CLL treatment, yDefinition of high riskAnti-CD20 AbPrevious CLL therapy
61 hCKT  G, R FCR 
66 POD <1 year FCR 
52 del17p, TP53mut GIVe 
61 del17p, TP53mut GIVe 
74 del17p, TP53mut, CKT BIG 
92 del17p BIO 
70 del17p  MCP 
80 TP53mut, CKT  G, R BR 
86 hCKT  G, R BR 
10 74 CKT  G, R FCR 
11 74 del17p BIO 
12 63 POD <1 year FCR 

hCKT included ≥5 cytogenetic aberrations, and CKT included ≥3 and <5 cytogenetic aberrations.

Ab, antibody; B, bendamustine; C, cyclophosphamide; CKT, complex karyotype; F, fludarabine; G, obinutuzumab; hCKT, high complex karyotype; I, ibrutinib; MCP, mitoxantrone, chlorambucil, and prednisolone; mut, mutated; O, ofatumumab; POD, progression of disease after end of therapy; R, rituximab; Ve, venetoclax.

High-risk features were assessed at clinical progression after induction treatment.

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