Frontiers in Oncology (Nov 2023)

Circulating tumor DNA determining hyperprogressive disease after CAR-T therapy alarms in DLBCL: a case report and literature review

  • Jiajie He,
  • Jiajie He,
  • Jiajie He,
  • Rui Zou,
  • Rui Zou,
  • Rui Zou,
  • Liqing Kang,
  • Liqing Kang,
  • Lingzi Yu,
  • Lingzi Yu,
  • Lingzi Yu,
  • Peng Wang,
  • Peng Wang,
  • Yang Shao,
  • Junheng Liang,
  • Depei Wu,
  • Depei Wu,
  • Zhengming Jin,
  • Zhengming Jin,
  • Changju Qu,
  • Changju Qu

DOI
https://doi.org/10.3389/fonc.2023.1283194
Journal volume & issue
Vol. 13

Abstract

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Chimeric antigen receptor T-cell therapy (CAR-T) has been widely applied in the clinical practice of relapse/refractory (R/R) diffuse large B-cell lymphoma (DLBCL) due to its promising effects. Hyperprogressive disease (HPD) has gained attention for rapid tumor progression and has become a therapeutic and prognostic challenge. Here, we present a patient who had suffered from several recurrences previously and controlled well with a very small tumor lesion left was infused with CD19/CD22 bispecific CAR-T, with no immune effector cell-associated neurotoxicity syndrome, or cytokine release syndrome observed. However, rapid deterioration, subsequent imaging examination, circulating tumor DNA, and serum biomarkers detection identified HPD. The patient did not respond to salvage treatment and died 40 days after infusion. To our knowledge, only one case of HPD in DLBCL after CAR-T therapy has been reported. This fatal case alarmed the risk of HPD and the ctDNA profile monitoring we used was performed as a non-invasive method to diagnose HPD, providing far-reaching practical instruction for CAR-T therapy.

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