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[FLT3-ITD mutation-positive acute myeloid leukemia undergoing clonal transition with PTPN11 mutation at relapse].
Kurihara, Kazuya; Sadato, Daichi; Najima, Yuho; Hirama, Chizuko; Haraguchi, Kyoko; Kato, Kana; Kondo, Kaori; Sadaga, Yasutaka; Kato, Chika; Sakai, Satoshi; Kambara, Yasuhiro; Nabe, Yoshimi; Teshima, Koh; Asano, Kazuya; Jinguji, Atsushi; Shimabukuro, Masashi; Ouchi, Fumihiko; Inai, Kazuki; Koi, Satoshi; Shingai, Naoki; Toya, Takashi; Shimizu, Hiroaki; Kobayashi, Takeshi; Oboki, Keisuke; Harada, Hironori; Okuyama, Yoshiki; Harada, Yuka; Doki, Noriko.
Afiliación
  • Kurihara K; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Sadato D; Clinical Research Support Center, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Najima Y; Tokyo Metropolitan Institute of Medical Science.
  • Hirama C; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Haraguchi K; Clinical Research Support Center, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Kato K; Tokyo Metropolitan Institute of Medical Science.
  • Kondo K; Division of Transfusion and Cell Therapy, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Sadaga Y; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Kato C; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Sakai S; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Kambara Y; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Nabe Y; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Teshima K; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Asano K; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Jinguji A; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Shimabukuro M; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Ouchi F; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Inai K; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Koi S; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Shingai N; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Toya T; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Shimizu H; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Kobayashi T; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Oboki K; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Harada H; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Okuyama Y; Tokyo Metropolitan Institute of Medical Science.
  • Harada Y; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
  • Doki N; Laboratory of Oncology, School of Life Science, Tokyo University of Pharmacy and Life Sciences.
Rinsho Ketsueki ; 65(2): 63-68, 2024.
Article en Ja | MEDLINE | ID: mdl-38447999
ABSTRACT
A 28-year-old man was diagnosed with acute myelomonocytic leukemia. He achieved complete remission (CR) after two cycles of induction therapy. However, after consolidation therapy, bone marrow aspiration performed to prepare for allogeneic hematopoietic stem cell transplantation revealed disease relapse. Companion diagnostics confirmed the presence of the FLT3-ITD mutation. The patient received gilteritinib monotherapy and achieved CR. Subsequently, he underwent unrelated allogeneic bone marrow transplantation. One year after transplantation, the patient relapsed, and gilteritinib was resumed. However, the leukemia progressed, and panel sequencing using a next-generation sequencer showed that the FLT3-ITD mutation disappeared. A mutation in PTPN11, which regulates the RAS/MAPK signaling pathway, was also detected. Gilteritinib was discontinued, and the patient achieved CR with salvage chemotherapy. He underwent related haploidentical peripheral blood stem cell transplantation but died of relapse. This was a case in which genetic analysis revealed clonal transition and acquisition of resistance to treatment.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Leucemia Mieloide Aguda Límite: Adult / Humans / Male Idioma: Ja Revista: Rinsho Ketsueki Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Leucemia Mieloide Aguda Límite: Adult / Humans / Male Idioma: Ja Revista: Rinsho Ketsueki Año: 2024 Tipo del documento: Article