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MRD-Negative Remission Induced in EP300-ZNF384 Positive B-ALL Patients by Tandem CD19/CD22 CAR T-Cell Therapy Bridging to Allogeneic Stem Cell Transplantation
- Source :
- OncoTargets and therapy
- Publication Year :
- 2021
- Publisher :
- Informa UK Limited, 2021.
-
Abstract
- Xin-Yue Zhang,1,2,* Hai-Ping Dai,1,2,* Ling Zhang,1,2 Si-Ning Liu,1,2 Yin Dai,1,2 De-Pei Wu,1,2 Xiao-Wen Tang1,2 1National Clinical Research Center for Hematologic Diseases, Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, 215006, Peopleâs Republic of China; 2Institute of Blood and Marrow Transplantation, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, 215123, Peopleâs Republic of China*These authors contributed equally to this workCorrespondence: De-Pei Wu; Xiao-Wen TangDepartment of Hematology, The First Affiliated Hospital of Soochow University, Jiangsu Institute of Hematology, Suzhou, Peopleâs Republic of ChinaTel +8651267781856Fax +8651265113556Email drwudepei@163.com; xwtang1020@163.comAbstract: EP300-ZNF384-positive B cell acute lymphoblastic leukemia (B-ALL) patients are reported to have a unique immunophenotype with high expression of CD19 and CD22, weak expression of CD20 and aberrant expression of CD13 and/or CD33, sensitivity to chemotherapy and a favorable outcome. To date, the cases of only 53 patients have been reported, albeit few reports on salvage therapy when conventional chemotherapies failed. Here, we describe two relapsed and refractory adult B-ALL patients with EP300-ZNF384 who achieved second remission through tandem CD19/CD22 CAR T-cell therapy. Grade 3 and 2 cytokine release syndrome were observed in cases 1 and 2, respectively. No immune effector cell-associated neurotoxicity syndrome was detected. Both patients underwent consolidate haploidentical hematopoietic stem cell transplantation (HSCT), and each maintained measurable residual disease-negative remission for 14 and 13 months, respectively. Our study suggests that CD19/CD22 CAR T-cell therapy bridging to allogeneic HSCT may be a viable option for EP300-ZNF384-positive B-ALL.Keywords: chimeric antigen receptor T-cells, CD19/CD22, EP300-ZNF384, acute lymphoblastic leukemia, relapsed/refractory
- Subjects :
- Oncology
medicine.medical_specialty
medicine.medical_treatment
Salvage therapy
CD19/CD22
acute lymphoblastic leukemia
Hematopoietic stem cell transplantation
OncoTargets and Therapy
relapsed/refractory
Cell therapy
immune system diseases
hemic and lymphatic diseases
Internal medicine
medicine
Case Series
Pharmacology (medical)
CD20
Chemotherapy
biology
business.industry
medicine.disease
chimeric antigen receptor T-cells
Transplantation
Cytokine release syndrome
biology.protein
EP300-ZNF384
Stem cell
business
Subjects
Details
- ISSN :
- 11786930
- Volume :
- 14
- Database :
- OpenAIRE
- Journal :
- OncoTargets and Therapy
- Accession number :
- edsair.doi.dedup.....5e80902414b0eadb98dd917442eb4524
- Full Text :
- https://doi.org/10.2147/ott.s324765