Gilteritinib Monotherapy as a Transplant Bridging Option for a Patient with FLT3-Mutated Acute Promyelocytic Leukemia Who Developed a Second Relapse after All-Trans Retinoic Acid + Chemotherapy, Arsenic Trioxide, and High-Dose Cytarabine Therapy.

IF 0.7 Q4 HEMATOLOGY Case Reports in Hematology Pub Date : 2023-12-13 eCollection Date: 2023-01-01 DOI:10.1155/2023/8568587
Hirofumi Kobayashi, Hiroki Tsutsumi, Yukiko Misaki, Takashi Maekawa, Naoko Inoshita, Machiko Kawamura, Nobuo Maseki
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Abstract

We report a case of FLT3-mutated APL who developed disease relapse despite all-trans retinoic acid (ATRA) + chemotherapy, and re-induction chemotherapy with arsenic trioxide (ATO) and high-dose (HD) cytarabine (Ara-C) therapy failed to yield complete remission. Because the leukemic cells were resistant to all the aforementioned therapies, we started the patient on monotherapy with gilteritinib, a selective FLT3-inhibitor, as an alternative re-induction treatment option rather than further intensive chemotherapy. The patient showed complete hematologic remission in response to this therapy. This case serves as supporting evidence for the use of single-agent therapy with gilteritinib as a bridge to transplantation in patients with refractory FLT3-mutated APL.

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吉利替尼单药疗法作为FLT3突变急性早幼粒细胞白血病患者的移植过渡方案,该患者在接受全反式维甲酸+化疗、三氧化二砷和大剂量阿糖胞苷治疗后再次复发。
我们报告了一例FLT3突变的APL患者,该患者在接受全反式维甲酸(ATRA)+化疗后病情复发,使用三氧化二砷(ATO)和高剂量(HD)阿糖胞苷(Ara-C)进行再诱导化疗也未能获得完全缓解。由于白血病细胞对上述所有疗法均产生耐药性,我们开始对患者使用吉特替尼(一种选择性FLT3抑制剂)进行单药治疗,作为替代强化化疗的再诱导治疗方案。患者在接受这种治疗后,血液学症状得到完全缓解。该病例为吉特替尼单药治疗作为难治性FLT3突变APL患者移植的桥梁提供了佐证。
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