Favorable response of a patient with primary B/myeloid mixed phenotype acute Leukemia to CD19-CAR-T: Case report and literature review

Authors:Wang, Lixin; Pang, Yanbin; Fang, Chuling; Zhao, Weiqiang; Xu, Yuanyuan; Guo, Xiao; Qiao, Jingqiao; Mei, Junhui; Wang, Hongxin; Yu, Chuan; Li, Yisheng; Tang, Zhixiong; Yu, Li*
Source:Medicine; analytical reviews of general medicine, neurology, psychiatry, dermatology, and pediatries, 2023, 102(50): e36397.
DOI:10.1097/MD.0000000000036397

Summary

Rationale:Mixed phenotype acute leukemia (MPAL) is a rare and heterogeneous type of leukemia known for its poor prognosis. The optimal treatment strategy for this condition currently lacks consensus, leaving uncertainty in its management. Nonetheless, a potential therapeutic option for patients with refractory MPAL who express target antigens is donor-derived chimeric antigen receptor T (CAR-T) cell therapy.Patient concerns:We recently reported a 61-year-old woman with MPAL and elucidated its diagnosis and treatment.Diagnosis:The diagnosis of MPAL was established based on the classification of World Health Organization in 2016.Interventions:Despite undergoing 3 different acute lymphoblastic leukemia (ALL) regimens and 1 acute myelogenous leukemia (AML) regimen, the patient did not achieve remission. Subsequently, the patient received human CD19-targeted CAR-T cell therapy.Outcomes:The patient achieved a successful and complete remission after CAR-T cell therapy. Tragically, 8 months after CAR-T infusion, the patient experienced a relapse characterized by CD19-negative disease and ultimately passed away.Lessons:This case underscores the potential efficacy and safety of human-derived CD19 CAR-T cell therapy in treating refractory MPAL. While this particular patient outcome was unfortunate, it suggests that CAR-T cell therapy may still hold promise as a viable treatment option for MPAL patients unresponsive to other therapies. Further research in this field is warranted to determine the most effective treatment strategies for managing this challenging disease.

  • Institution
    南方医科大学

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