Therapy-related acute myeloid leukemia with 24-month latency after CD19 CAR-T cell therapy in relapsed/refractory diffuse large B-cell lymphoma: a case report - Scorecard - MDSpire
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Acute Myeloid Leukemia Induced by Therapy with a 24-Month Latency Following CD19 CAR-T Cell Treatment for Relapsed/Refractory Diffuse Large B-Cell Lymphoma: A Case Study
Clinical Scorecard: Acute Myeloid Leukemia Induced by Therapy with a 24-Month Latency Following CD19 CAR-T Cell Treatment for Relapsed/Refractory Diffuse Large B-Cell Lymphoma: A Case Study
At a Glance
Category
Detail
Condition
Therapy-related Acute Myeloid Leukemia (t-AML)
Key Mechanisms
Biallelic loss of TP53 and prolonged genotoxic stress from CAR-T therapy
Target Population
Patients with relapsed/refractory diffuse large B-cell lymphoma (DLBCL) treated with CD19 CAR-T therapy
Care Setting
Oncology and hematology clinics
Key Highlights
Case of t-AML diagnosed 24 months post CD19 CAR-T therapy
Transition from wild-type TP53 to biallelic loss of TP53 observed
Patient achieved partial remission with azacitidine and venetoclax
DLBCL remained in remission during AML-directed therapy
Importance of ongoing hematologic monitoring emphasized
Guideline-Based Recommendations
Diagnosis
Bone marrow examination and flow cytometry for abnormal myeloid blasts
Genomic profiling to assess TP53 status
Management
Consider azacitidine and venetoclax for treatment of t-AML
Evaluate the need for allogeneic hematopoietic stem cell transplantation
Monitoring & Follow-up
Longitudinal genomic monitoring post CAR-T therapy
Hematologic monitoring beyond 12 months after CAR-T infusion
Risks
Potential for therapy-related myeloid neoplasms following CAR-T therapy
Increased risk of secondary malignancies due to prior treatments
Patient & Prescribing Data
65-year-old male with relapsed/refractory DLBCL
Combination therapy with azacitidine and venetoclax led to partial remission
Clinical Best Practices
Perform baseline CHIP screening before CAR-T therapy
Implement systematic longitudinal genomic profiling in patients post-CAR-T