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

Author:

Kobayashi Hirofumi1ORCID,Tsutsumi Hiroki1,Misaki Yukiko2,Maekawa Takashi3,Inoshita Naoko34,Kawamura Machiko15ORCID,Maseki Nobuo1ORCID

Affiliation:

1. Department of Hematology, Saitama Cancer Center, Saitama, Japan

2. Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan

3. Department of Pathology, Saitama Cancer Center, Saitama, Japan

4. Department of Pathology, Moriyama Memorial Hospital, Tokyo, Japan

5. Department of Clinical Laboratory Medicine, Saitama Cancer Center, Saitama, Japan

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.

Funder

Grant-in-Aid for Scientific Research

Publisher

Hindawi Limited

Subject

Cell Biology,Developmental Biology,Embryology,Anatomy

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