Characteristics of progressive multifocal leukoencephalopathy in hematological malignancies, With reference to HIV-infected patients
13 affiliations
- 1Blood Disorders Center, Aiiku Hospital, Sapporo, Japan
- 2Department of Diagnostic Imaging, Hokkaido University Hospital, Sapporo, Japan
- 3Department of Infection Control and Prevention, Hokkaido University Hospital, Sapporo, Japan
- 4Department of Hematology, Hokkaido University Hospital, Sapporo, Japan
- 5Department of Hematology, Sapporo Hokuyu Hospital, Sapporo, Japan
- 6Department of Hematology, Sapporo Kosei General Hospital, Sapporo, Japan
- 7Department of Hematology, Kushiro Rosai Hospital, Kushiro, Japan
- 8Department of Hematology, Sapporo Medical University Hospital, Sapporo, Japan
- 9Division of Hematology, Department of Internal Medicine, Asahikawa Medical University, Asahikawa, Japan
- 10Department of Hematology/Oncology, Asahikawa Kosei General Hospital, Asahikawa, Japan
- 11Department of Hematology, Kitami Red Cross Hospital, Kitami, Japan
- 12Division of Hematology and Oncology, Department of Internal Medicine, Iwate Medical University School of Medicine, Yahaba, Japan
- 13Department of Hematology, Faculty of Medicine, Hokkaido University, Sapporo, Japan
Abstract
Progressive multifocal leukoencephalopathy (PML) is a rare opportunistic infection of the central nervous system (CNS) observed in immunocompromised individuals. We retrospectively evaluated the clinical courses of PML in patients with hematological malignancies at North Japan Hematology Study Group institutions, using patients with human immunodeficiency virus (HIV) infection as a reference. Eight PML patients had hematological malignancies and 9 had HIV infection. CD4 + T cell counts were markedly low in patients with hematological malignancies (median 168/μl, range 48.4–330/μl) and did not differ significantly from those in patients with HIV infection (median 28/μl, range 8–225.4/μl). IgG levels were significantly lower in patients with hematological malignancies (median 643.5 mg/dL, range 205–2478 mg/dL) than in patients with with HIV infection (median 1691.5 mg/dL, range 1304–3014 mg/dL) (p < 0.01). Almost all patients with hematological malignancies died after progression of PML (median time from onset to death, 136 days). In contrast, seven patients with HIV infection were alive at the end of follow-up. The incidence of PML in patients with hematological malignancies may increase with the introduction of new antibody drugs and cellular therapies in future. Considering the poor prognosis, greater caution is warranted regarding this serious complication.
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BibTeX
@article{yokoyama2026characteristics,
title = {{Characteristics of progressive multifocal leukoencephalopathy in hematological malignancies, With reference to HIV-infected patients}},
author = {Emi Yokoyama and Taisuke Harada and Tomoyuki Endo and Hideki Goto and Junichi Sugita and Masayuki Aiba and Mutsumi Takahata and Takuto Miyagishima and Hajime Senjo and Satoshi Iyama and Shuichiro Takahashi and Masayo Yamamoto and Motohiro Shindo and Kazuya Sato and Junichi Hashiguchi and Tatsuo Oyake and Takanori Teshima},
journal = {International Journal of Hematology},
year = {2026},
month = jul,
doi = {10.1007/s12185-026-04256-5},
url = {https://doi.org/10.1007/s12185-026-04256-5},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Characteristics of progressive multifocal leukoencephalopathy in hematological malignancies, With reference to HIV-infected patients
AU - Emi Yokoyama
AU - Taisuke Harada
AU - Tomoyuki Endo
AU - Hideki Goto
AU - Junichi Sugita
AU - Masayuki Aiba
AU - Mutsumi Takahata
AU - Takuto Miyagishima
AU - Hajime Senjo
AU - Satoshi Iyama
AU - Shuichiro Takahashi
AU - Masayo Yamamoto
AU - Motohiro Shindo
AU - Kazuya Sato
AU - Junichi Hashiguchi
AU - Tatsuo Oyake
AU - Takanori Teshima
PY - 2026
DA - 2026/07/24
JO - International Journal of Hematology
DO - 10.1007/s12185-026-04256-5
UR - https://doi.org/10.1007/s12185-026-04256-5
AB - Progressive multifocal leukoencephalopathy (PML) is a rare opportunistic infection of the central nervous system (CNS) observed in immunocompromised individuals. We retrospectively evaluated the clinical courses of PML in patients with hematological malignancies at North Japan Hematology Study Group institutions, using patients with human immunodeficiency virus (HIV) infection as a reference. Eight PML patients had hematological malignancies and 9 had HIV infection. CD4 + T cell counts were markedly low in patients with hematological malignancies (median 168/μl, range 48.4–330/μl) and did not differ significantly from those in patients with HIV infection (median 28/μl, range 8–225.4/μl). IgG levels were significantly lower in patients with hematological malignancies (median 643.5 mg/dL, range 205–2478 mg/dL) than in patients with with HIV infection (median 1691.5 mg/dL, range 1304–3014 mg/dL) (p < 0.01). Almost all patients with hematological malignancies died after progression of PML (median time from onset to death, 136 days). In contrast, seven patients with HIV infection were alive at the end of follow-up. The incidence of PML in patients with hematological malignancies may increase with the introduction of new antibody drugs and cellular therapies in future. Considering the poor prognosis, greater caution is warranted regarding this serious complication.
SN - 0925-5710
SN - 1865-3774
ER -