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Lymphodepletion chemotherapy revitalizes chimeric antigen receptor T cells contributing to regression of relapsed B-cell lymphoma: A case report.

AbstractINTRODUCTION:
Chimeric antigen receptor T cells (CAR-T) targeting CD19 have shown great potential for treatment of B-cell malignancies. For those patients who can not achieve complete remission (CR) or suffer from relapse after CAR-T therapy, further therapeutic strategies still remain elusive. Whether existing CAR-T cells can revitalize in vivo and eradicate tumor cells is still unknown.
PATIENT CONCERNS:
We report a case of diffused large B-cell lymphoma patient who had achieved CR after CD19 targeted CAR-T therapy but relapsed after 5 months.
DIAGNOSIS:
Five months after CAR-T cell infusion, the patient was confirmed a relapse by follow-up PET/CT scan and a mass biopsy. Flow cytometry showed a dramatically decreased percentage of CAR-T cells in peripheral blood (PB).
INTERVENTIONS:
A second anti-CD19 CAR-T therapy was planned with deliberation. Firstly, the patient received lymphodepletion chemotherapy with fludarabine (25 mg/m, d1-d3) and cyclophosphamide (500 mg/m d2-d3).
OUTCOMES:
After fludarabine and cyclophosphamide (FC) lymphodepletion chemotherapy, pre-existing CAR-T cells were revitalized and the patient developed grade 2 cytokine release syndrome (CRS) contributing to the regression of relapsed B-cell lymphoma.
CONCLUSIONS:
This case suggested that FC chemotherapy could revitalize CAR-T cells contributing to the regression of relapsed B-cell lymphoma. Nevertheless, further researches are required in the future as this report described only a single case.
AuthorsZuyu Liang, Hao Zhang, Mi Shao, Qu Cui, Zhao Wu, Lei Xiao, He Huang, Yongxian Hu
JournalMedicine (Medicine (Baltimore)) Vol. 99 Issue 43 Pg. e22510 (Oct 23 2020) ISSN: 1536-5964 [Electronic] United States
PMID33120740 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Antigens, CD19
  • Receptors, Chimeric Antigen
  • Cyclophosphamide
  • Vidarabine
  • fludarabine
Topics
  • Adult
  • Antigens, CD19 (immunology)
  • Antineoplastic Combined Chemotherapy Protocols (therapeutic use)
  • Cyclophosphamide (therapeutic use)
  • Cytokine Release Syndrome (etiology)
  • Humans
  • Lymphocyte Depletion
  • Lymphoma, Large B-Cell, Diffuse (drug therapy)
  • Male
  • Neoplasm Recurrence, Local (drug therapy)
  • Receptors, Chimeric Antigen (immunology)
  • Remission Induction
  • T-Lymphocytes (immunology)
  • Vidarabine (analogs & derivatives, therapeutic use)

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