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Clinical significance of late CMV disease in adult patients who underwent allogeneic stem cell transplant.
Shimizu, Hiroaki; Najima, Yuho; Kako, Shinichi; Tanaka, Masatsugu; Fujiwara, Shin-Ichiro; Mori, Takehiko; Usuki, Kensuke; Gotoh, Moritaka; Hagihara, Maki; Tsukada, Nobuhiro; Oniduka, Makoto; Takada, Satoru; Sakaida, Emiko; Fujisawa, Shin; Onoda, Masahiro; Aotsuka, Nobuyuki; Yano, Shingo; Ohashi, Kazuteru; Takahashi, Satoshi; Okamoto, Shinichiro; Kanda, Yoshinobu.
  • Shimizu H; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, Japan; Department of Medicine and Clinical Science, Gunma University, Gunma, Japan. Electronic address: hiroakis0825@icloud.com.
  • Najima Y; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, Japan.
  • Kako S; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan.
  • Tanaka M; Department of Hematology, Kanagawa Cancer Center, Yokohama, Japan.
  • Fujiwara SI; Division of Hematology, Department of Medicine, Jichi Medical University, Shimotsuke, Japan.
  • Mori T; Division of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
  • Usuki K; Department of Hematology, NTT Medical Center Tokyo, Tokyo, Japan.
  • Gotoh M; Department of Hematology, Tokyo Medical University, Tokyo, Japan.
  • Hagihara M; Department of Hematology and Clinical Immunology, Yokohama City University Hospital, Yokohama, Japan.
  • Tsukada N; Department of Hematology, Japanese Red Cross Medical Center, Tokyo, Japan.
  • Oniduka M; Department of Hematology and Oncology, Tokai University School of Medicine, Kanagawa, Japan.
  • Takada S; Leukemia Research Center, Saiseikai Maebashi Hospital, Gunma, Japan.
  • Sakaida E; Division of Hematology, Department of Hematology, Chiba University Hospital, Chiba, Japan.
  • Fujisawa S; Department of Hematology, Yokohama City University Medical Center, Yokohama, Japan.
  • Onoda M; Department of Internal Medicine, Chiba Aoba Municipal Hospital, Chiba, Japan.
  • Aotsuka N; Department of Hematology, Japanese Red Cross Narita Hospital, Narita, Japan.
  • Yano S; Division of Clinical Oncology and Hematology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.
  • Ohashi K; Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, Japan.
  • Takahashi S; Division of Molecular Therapy, The Advanced Clinical Research Center, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
  • Okamoto S; Division of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
  • Kanda Y; Division of Hematology, Jichi Medical University Saitama Medical Center, Saitama, Japan; Division of Hematology, Department of Medicine, Jichi Medical University, Shimotsuke, Japan.
J Infect Chemother ; 29(12): 1103-1108, 2023 Dec.
Article en En | MEDLINE | ID: mdl-37532223
ABSTRACT

INTRODUCTION:

Late cytomegalovirus (CMV) disease, which was defined as CMV disease occurring >100 days post-transplant, remains an important complication among allogeneic stem cell transplant recipients, even now that the prophylactic strategy using ganciclovir preemptive therapy has been established. Due to the recent expansion of donor sources and conditioning regimens, it is therefore appropriate to reevaluate the incidence, risk factors, and clinical impacts of late CMV disease.

METHODS:

This study included the 1295 adult patients, who underwent transplant for the first time from 2008 to 2015, without underlying disease relapse or CMV disease within 100 days post-transplant. There were no restrictions on underlying diseases or transplant procedures.

RESULTS:

During the median follow-up period of 48.4 months, 21 patients developed late CMV disease and the 5-year cumulative incidence of late CMV disease was 1.6%. By multivariate analysis, haploidentical related donor, adult T-cell leukemia lymphoma, and preemptive therapy before 100 days post-transplant were extracted as independent risk factors. Late CMV disease negatively affected transplant outcomes, and was identified as an independent risk factor for the non-relapse mortality rate (hazard ratio 3.83, p < 0.001) and overall survival rate (hazard ratio 4.01, p < 0.001). Although 17 of 21 patients with late CMV disease died, the main causes of death were not related to CMV, except in three patients with CMV pneumonia.

CONCLUSIONS:

Although the incidence of late CMV disease is low in transplant recipients, this complication negatively affects clinical courses. Therefore, transplant recipients with these risk factors should be more carefully managed.
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Año: 2023 Tipo del documento: Article