4.6 Article

Case Report: Successful therapy with all-trans retinoic acid combined with chemotherapy followed by hematopoietic stem cell transplantation for acute promyelocytic leukemia carrying the BCOR-RARA fusion gene

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FRONTIERS IN ONCOLOGY
卷 12, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2022.1013046

关键词

acute promyelocytic leukemia; variant; BCOR-RARA; all-trans retinoic acid; allogeneic hematopoietic stem cell transplantation

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资金

  1. National Natural Science Foundation of China
  2. Science and Technology Commission of Shanghai Municipality
  3. [81800141]
  4. [81890994]
  5. [81770144]
  6. [81870110]
  7. [19DZ1910702]

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This study reported a rare case of BCOR-RARA variant APL and suggested that allo-HSCT after ATRA combined with chemotherapy is the optimal choice for vAPL patients with a high risk of relapse.
Acute promyelocytic leukemia (APL) is characterized by the balanced translocation of chromosomes 15 and 17, resulting in the formation of PML-RARA fusion gene. More than 98% of APL have PML-RARA fusion, and less than 2% have other types of RARA gene partners, which named variant APL (vAPL). In the present study, we reported a vAPL with BCOR-RARA, which was the third case of BCOR-RARA APL published. The patient achieved complete remission (CR) with all-trans retinoic acid (ATRA) monotherapy, and molecular CR with ATRA plus standard chemotherapy. After that, he underwent allogeneic hematopoietic stem cell transplantation (allo-HSCT) and ATRA maintenance and maintained a molecular CR status. This case provided valuable insights into the accurate identification of vAPL. Moreover, ATRA combined with chemotherapy followed by allo-HSCT was suggested as an optimal choice for those vAPL patients who had a high risk of relapse.

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