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Decision analysis of allogeneic bone marrow transplantation versus immunosuppressive therapy for young adult patients with aplastic anemia.
Kanda, Yoshinobu; Usuki, Kensuke; Inagaki, Mitsuhiro; Ohta, Akiko; Ogasawara, Yoji; Obara, Naoshi; Kako, Shinichi; Kurokawa, Mineo; Shimada, Naoki; Suzuki, Takahiro; Hama, Asahito; Yamaguchi, Hiroki; Nakao, Shinji; Yamazaki, Hirohito.
Afiliação
  • Kanda Y; Division of Hematology, Department of Medicine, Jichi Medical University, 3311-1 Yakushiji, Shimotsuke, Tochigi, 329-0498, Japan. ycanda-tky@umin.ac.jp.
  • Usuki K; Jichi Medical University Saitama Medical Center, Saitama, Japan. ycanda-tky@umin.ac.jp.
  • Inagaki M; NTT Medical Center Tokyo, Tokyo, Japan.
  • Ohta A; Hiroshima Red Cross Hospital & Atomic-Bomb Survivors Hospital, Hiroshima, Japan.
  • Ogasawara Y; Saitama Medical University, Saitama, Japan.
  • Obara N; The Jikei University School of Medicine, Tokyo, Japan.
  • Kako S; University of Tsukuba, Tsukuba, Ibaraki, Japan.
  • Kurokawa M; Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Shimada N; The University of Tokyo, Tokyo, Japan.
  • Suzuki T; International University of Health and Welfare, Otawara, Tochigi, Japan.
  • Hama A; Kitasato University, Kanagawa, Japan.
  • Yamaguchi H; Japanese Red Cross Aichi Medical Center Nagoya First Hospital, Nagoya, Japan.
  • Nakao S; Nippon Medical School, Tokyo, Japan.
  • Yamazaki H; Kanazawa University Hospital, Kanazawa, Japan.
Int J Hematol ; 117(5): 660-668, 2023 May.
Article em En | MEDLINE | ID: mdl-36595144
ABSTRACT

BACKGROUND:

Allogeneic bone marrow transplantation (BMT) from an HLA-matched sibling donor is recommended as an initial treatment for young patients. However, immunosuppressive therapy (IST) with cyclosporine and anti-thymocyte globulin may be a viable option even when an HLA-identical sibling donor is available.

METHODS:

We constructed a Markov model to simulate the 10-year clinical course of patients aged 21-40 years with newly diagnosed severe aplastic anemia. Immediate BMT and IST were compared as an initial treatment assuming the availability of an HLA-identical sibling donor. Transition probabilities after treatment were determined based on a registry data analysis for BMT and a long-term prospective study for IST.

RESULTS:

Quality-adjusted life years (QALYs) after treatment selection were 6.77 for BMT and 6.74 for IST. One-way sensitivity analysis revealed that the utility for being alive without GVHD after BMT, that for being alive with partial response after IST, and the response rate after initial IST strongly affected the results.

CONCLUSIONS:

BMT and IST produced similar QALY for young patients with severe aplastic anemia. An estimation of the response rate to the initial IST may enable an individualized comparison between BMT and IST.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro / Anemia Aplástica Tipo de estudo: Etiology_studies / Health_economic_evaluation / Observational_studies / Prognostic_studies Aspecto: Patient_preference Limite: Adult / Humans Idioma: En Revista: Int J Hematol Assunto da revista: HEMATOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro / Anemia Aplástica Tipo de estudo: Etiology_studies / Health_economic_evaluation / Observational_studies / Prognostic_studies Aspecto: Patient_preference Limite: Adult / Humans Idioma: En Revista: Int J Hematol Assunto da revista: HEMATOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Japão
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