Table 1.

Patient characteristics

Pt no.Age, yTime: CLL Dx to RS, moHistologyPertinent genetic aberrations by FISHCKIGHV mutational statusClonally relatedNo. of prior TxMost recent prior line of Tx*Time on BTKi prior to leuka-pheresis, dTime from RT diagnosis to leuka-pheresis, dConcurrent BTKiDisease status at leuka-pheresisMax CRS gradeMax ICANS gradeGrade 3/4 eventsBest response (Lugano)Time to best response, dFollow-up, dClinical status
50 24 Non-GCB Del(13q) Yes Unable to assess Unable to assess RDHAP/ RDHAX N/A 1111 No PR No CR 72 345 Ongoing CR 
2 46 38 Non-GCB Del(11q), MYC Yes Unmutated Unable to assess BTKi 51 182 Yes PD No CR 92 296 Received consolidation with MUD PBSCT, with ongoing CR 
64 197 Non-GCB del(13q), del(17p), MYC Yes Unmutated Yes BTKi 24 50 Yes PR No CR 93 210 Ongoing CR, continues on BTKi 
76 89 HGBCL del(11q), del(13q), del(17p) Yes Unable to assess Unable to assess REPOCH 119 Yes PD Yes PR 107 210 Relapsed disease at day 201 
70 109 Non-GCB MYC Yes Unmutated Yes BTKi 98 124 Yes§ PD Yes N/A N/A 49 Died of infection 
72 36 Non-GCB del(11q) Not done Mutated Yes BTKi N/A 30 Yes|| SD Yes PR 64 183 Ongoing PR, continues on BTKi 
40 131 Non-GCB MYC Not done Mutated Unable to assess REPOCH N/A 120 Yes SD No PR 37 155 Ongoing PR 
63 157 GCB None Not done Unmutated Yes BTKi 120 143 Yes PD No CR 81 86 Ongoing CR, continues BTKi 
69 117 HGBCL Del (17p) Yes Unmutated Yes REPOCH N/A 215 No PR No CR 92 93 Ongoing CR 
Pt no.Age, yTime: CLL Dx to RS, moHistologyPertinent genetic aberrations by FISHCKIGHV mutational statusClonally relatedNo. of prior TxMost recent prior line of Tx*Time on BTKi prior to leuka-pheresis, dTime from RT diagnosis to leuka-pheresis, dConcurrent BTKiDisease status at leuka-pheresisMax CRS gradeMax ICANS gradeGrade 3/4 eventsBest response (Lugano)Time to best response, dFollow-up, dClinical status
50 24 Non-GCB Del(13q) Yes Unable to assess Unable to assess RDHAP/ RDHAX N/A 1111 No PR No CR 72 345 Ongoing CR 
2 46 38 Non-GCB Del(11q), MYC Yes Unmutated Unable to assess BTKi 51 182 Yes PD No CR 92 296 Received consolidation with MUD PBSCT, with ongoing CR 
64 197 Non-GCB del(13q), del(17p), MYC Yes Unmutated Yes BTKi 24 50 Yes PR No CR 93 210 Ongoing CR, continues on BTKi 
76 89 HGBCL del(11q), del(13q), del(17p) Yes Unable to assess Unable to assess REPOCH 119 Yes PD Yes PR 107 210 Relapsed disease at day 201 
70 109 Non-GCB MYC Yes Unmutated Yes BTKi 98 124 Yes§ PD Yes N/A N/A 49 Died of infection 
72 36 Non-GCB del(11q) Not done Mutated Yes BTKi N/A 30 Yes|| SD Yes PR 64 183 Ongoing PR, continues on BTKi 
40 131 Non-GCB MYC Not done Mutated Unable to assess REPOCH N/A 120 Yes SD No PR 37 155 Ongoing PR 
63 157 GCB None Not done Unmutated Yes BTKi 120 143 Yes PD No CR 81 86 Ongoing CR, continues BTKi 
69 117 HGBCL Del (17p) Yes Unmutated Yes REPOCH N/A 215 No PR No CR 92 93 Ongoing CR 

BTKi, Bruton tyrosine kinase inhibitor; CR, complete response; del/Del, deletion; Dx, diagnosis; FISH, fluorescent in situ hybridization; GCB, germinal center B; HGBCL, high-grade B-cell lymphoma; IGHV, immunoglobulin heavy chain variable region; Max, maximum; MUD PBSCT, matched unrelated donor peripheral blood stem cell transplant; MYC, MYC gene rearrangement; N/A, not applicable; PD, progressive disease; PR, partial response; Pt, patient; RDHAP, rituximab, dexamethasone, cytarabine, cisplatin; RDHAX, rituximab, dexamethasone, cytarabine, oxaliplatin; REPOCH, rituximab, etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin; SD, stable disease; Tx, treatment.

*

Denotes prior line of therapy immediately preceding leukapheresis.

Patient received prior CAR-T therapy for CLL before developing RS.

Stopped BTKi when patient received MUD PBSCT.

§

Stopped BTKi 5 days after axi-cel due to toxicity.

||

Started on BTKi after leukapheresis and continued.

Started on BTKi after leukapheresis stopped prior to axi-cel infusion.

Close Modal

or Create an Account

Close Modal
Close Modal