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Association details:
Evidence:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
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Title:

huJCAR014 CAR-T Cells in Treating Adult Patients With Relapsed or Refractory B-Cell Non-Hodgkin Lymphoma or Acute Lymphoblastic Leukemia

Excerpt:
...- Evidence of CD19 expression by immunohistochemistry or flow cytometry on any prior or current tumor specimen or high likelihood of CD19 expression based on disease histology...
Trial ID:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

JCAR014 and Durvalumab in Treating Patients With Relapsed or Refractory B-cell Non-Hodgkin Lymphoma

Excerpt:
...- Evidence of CD19 expression on any prior or current tumor specimen or a high likelihood of CD19 expression based on disease histology...
Trial ID:
More C2 evidence
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

Laboratory Treated T Cells in Treating Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia, Non-Hodgkin Lymphoma, or Acute Lymphoblastic Leukemia

Excerpt:
...- Patients with CD19 expressing acute lymphoblastic leukemia (ALL), chronic lymphocytic leukemia (CLL) or non-Hodgkin lymphoma (NHL)...
Trial ID:
Less C2 evidence
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

CAR T-Cell Therapy for Relapsed or Refractory Large B-Cell Lymphoma Using a Fully Human CD19-Targeted Single Chain Variable Fragment: Results of a First-in-Human Phase I/II Study

Published date:
11/03/2022
Excerpt:
In the efficacy-evaluable set (n=23), the overall (OR) and complete response (CR) rates at day 28 were 74% and 52%, respectively. After a median follow-up of 15 months, the 12-month progression-free survival (PFS) and overall survival (OS) were 43% and 86%, respectively. In pts in CR at day 28, the 12-month PFS was 71% (Figure A). In responders with subsequent disease progression, CD19 expression was confirmed in 3 of 3 of pts with available data (100%)...JCAR021, a fully-human scFv CD19-targeted CAR T-cell product, was dose-escalated to the RP2D with manageable toxicities in pts with R/R LBCL.
Secondary therapy:
cyclophosphamide + fludarabine oral
DOI:
https://doi.org/10.1182/blood-2022-157826
Trial ID: