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eMAP – electronic EHA Medical HemAtology Program

Patient Characteristics          =12mo       <12mo         P                                           Patients with poorer survival (<12 months) were associated with
                                 26          109                                                       a higher proportion being ineligible for ZUMA1, being less likely
Survival                         56 (20-79)  57 (21-83)    n.s.                                        to be bridging responders, and having had an early relapse
n                                15 (71%)    73 (65%)      n.s.                                        (within 30 days of CAR T). Those with better survival (=12
Median age                       11 (42%)    62 (57%)      n.s.                                        months) had a higher proportion of bridging responders, were
Male                             12 (46%)    68 (62%)      n.s.                                        more likely to have a later relapse (after 100 days post-CAR
IPI high/high-intermediate @ LD  19 (73%)    104 (95%)     0.0019                                      T), and were more likely to receive allogeneic HSCT. Note that
LDH >Normal @ LD                 15 (58%)    28 (27%)      0.0047                                      of the 40 patients who proceeded to allogeneic HSCT post-
ZUMA1 ineligible                                                                                       relapse/progression, the 12-month OS was 34%.
Bridging responders / no         1/24 (4%)   17/103 (17%)  n.s.
bridging                         24 (92%)    76 (70%)      0.023                                       The study authors concluded that long-term survival after failure
ECOG =2 @ LD                     7 (27%)     34 (31%)      n.s.                                        of CAR T therapy is possible in about 20% of patients with
=3 Treatment lines               15 (58%)    71 (65%)      n.s                                         LBCL, with predictors of favourable survival including good-
Prior SCT                        1 (4%)      26 (24%)      0.027                                       risk pre-CAR T features and a long interval between CAR T
Tisa-cel                         12 (46%)    22 (20%)      0.011                                       therapy and relapse. Of important note, allogenic HSCT for
REL after CAR-T =30d             13 (50%)    26 (24%)      0.015                                       consolidation of treatment responses post-relapse/progression
REL after CAR-T >100d            9 (35%)     30 (28%)      n.s.                                        may improve outcomes of CAR T failure.
alloHSCT performed               4 (15%)     8 (7%)        n.s.
1st salvage Pola-based           1 (4%)      7 (6%)        n.s.
1st salvage CPi-based
1st salvage Lena-based

CAR, chimeric antigen receptor; CPi, checkpoint inhibitor; ECOG, Eastern Cooperative Oncology Group;
HSCT, hematopoietic stem cell transplantation; IPI, International Prognostic Index score; LD, limited
disease; LDH, lactate dehydrogenase; Lena, lenalidomide; Pola, polatuzumab vedotin; REL, relapse/
progression; SCT, stem cell transplant.

     WATCH                                                                                                  WATCH
DR. KURUVILLA’S IN-DEPTH PRESENTATION OF THIS                                                          DR. KURUVILLA’S THOUGHTS ON THE RELEVANCE OF
ABSTRACT (~4 MINUTES)                                                                                  THESE DATA TO CANADIAN PRACTICE (~2 MINUTES)

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