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

Medicine (Baltimore). 2023 Dec 15;102(50):e36397. doi: 10.1097/MD.0000000000036397.

Abstract

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.

Publication types

  • Review
  • Case Reports

MeSH terms

  • Acute Disease
  • Antigens, CD19
  • Female
  • Humans
  • Immunotherapy, Adoptive / adverse effects
  • Leukemia, Myeloid, Acute* / etiology
  • Middle Aged
  • Phenotype
  • Receptors, Chimeric Antigen*
  • Treatment Outcome

Substances

  • Receptors, Chimeric Antigen
  • Antigens, CD19