RWE: CIBMTR
Efficacy
PFS by JULIET eligibility
OS at 12 months
60%
ORR
57%
CR
42%
Safety | |
---|---|
CRSGrade ≥3 | 8% |
ICANSGrade ≥3 | 8% |
67% of CIBMTR patients would have been ineligible for the JULIET trial. Similar outcomes were shown in JULIET eligible and ineligible patients
- Reference: 1. Landsburg DJ et al. American Society of Hematology Annual Meeting, 11–14 December 2021, Atlanta, GA. Abstract 429.
Efficacy
PFS by JULIET eligibility
ORR
%
CR
%
OS at 24 months
%
Safety | |
---|---|
CRSGrade ≥3 | % |
ICANSGrade ≥3 | % |
Patients with comorbidities (~44%) derived similar benefit to those without, with comparable safety1
- Reference: 1. Landsburg DJ et al. American Society of Hematology Annual Meeting, 10–13 December 2022, New Orleans, LA. Presentation 656.
Data collection1
May 2018–May 2022
US, Canada and Israel
Median follow-up
~ years1
No. of patients infused with tisa-cel1
(968 in efficacy set)
Median age (range) yearsPatients ≥65 years | 66.5 (14–91)55% |
Gender (male) | 59% |
ECOG ≥2 | 5% |
IPI | NR |
HG lymphoma (double or triple hit) | 13%11% |
DLBCL | 81% |
Transformed lymphoma | 28% |
Comorbidities | 55% |
LDH elevated | NR |
Prior therapies (median)≥2 lines | 3 (0–11)84% |
Primary refractoryRefractory to last lineRelapsed | 38%NR54% |
Prior SCTAutoAllo | 26%2% |
Bridging therapy | NR |
Median time from receipt of apheresis product at manufacturing site to shipment | 26 days |
- Patient characteristics shown are from 17-month follow-up2 as data are missing from 2 year follow-up.
- References: 1. Landsburg DJ et al. American Society of Hematology Annual Meeting, 10–13 December 2022, New Orleans, LA. Presentation 656.
- 2. Landsburg DJ et al. American Society of Hematology Annual Meeting, 11–14 December 2021, Atlanta, GA. Abstract 429.
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