RealPatient

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 years66.5 (14–91)55%
Gender (male)59%
ECOG ≥25%
IPINR
HG lymphoma
(double or triple hit)
13%11%
DLBCL81%
Transformed lymphoma28%
Comorbidities55%
LDH elevatedNR
Prior therapies (median)≥2 lines3 (0–11)84%
Primary refractoryRefractory to last lineRelapsed38%NR54%
Prior SCTAutoAllo26%2%
Bridging therapyNR
Median time from receipt of apheresis product at manufacturing site to shipment26 days

Largest RWE source but with some limitations: No information on bridging therapy, ECOG data missing for 15%, some data issues

  • 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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