The effectiveness of immunosuppressive therapy in patients with aplastic anaemia secondary to chemoradiotherapy for cancers.


Journal

British journal of haematology
ISSN: 1365-2141
Titre abrégé: Br J Haematol
Pays: England
ID NLM: 0372544

Informations de publication

Date de publication:
12 2021
Historique:
received: 15 05 2021
accepted: 14 08 2021
pubmed: 4 9 2021
medline: 4 1 2022
entrez: 3 9 2021
Statut: ppublish

Résumé

The outcome of immunosuppressive therapy (IST) and prognosis in patients with aplastic anaemia (AA) secondary to chemotherapy or radiotherapy for cancers remains unknown. A total of 43 of 2559 patients with AA referred to our hospital had previously received chemoradiotherapy for various types of solid tumours (n = 25) or haematological malignancies (n = 18). Their cancer status was complete remission (CR) in 27, non-CR in 13, and unknown in three. Small populations of glycosylphosphatidylinositol-anchored protein-deficient [GPI(-)] granulocytes were detected in 16 patients (37·2%). Of 18 patients who were treated with IST, 50% improved regardless of the presence of GPI(-) cells. The overall survival (OS) rate was significantly higher in patients with a history of solid tumours patients than in those of haematological malignancies (median OS, 87 vs. 11 months, P = 0·0003), and in patients treated with IST than in those of untreated patients (median OS, 115 vs. 20 months, P = 0·028). Cancer aggravation occurred in two of four patients who were treated with IST while in non-CR of their original cancers. Progression to myelodysplastic syndromes was observed in two patients not possessing GPI(-) cells. IST should thus be considered for patients with AA secondary to chemoradiotherapy for cancers, particularly when their original solid tumours are in CR.

Identifiants

pubmed: 34476805
doi: 10.1111/bjh.17802
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

770-780

Informations de copyright

© 2021 British Society for Haematology and John Wiley & Sons Ltd.

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Auteurs

Noriharu Nakagawa (N)

Department of Hematology, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Japan.
Department of Hematology, Toyama Prefectural Central Hospital, Toyama, Japan.

Ken Ishiyama (K)

Department of Hematology, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Japan.

Mikoto Tanabe (M)

Department of Hematology, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Japan.

Takeshi Yoroidaka (T)

Department of Hematology, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Japan.

Hiroki Mizumaki (H)

Department of Hematology, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Japan.

Tatsuya Imi (T)

Department of Hematology, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Japan.

Yoshitaka Zaimoku (Y)

Department of Hematology, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Japan.

Hiroyuki Maruyama (H)

Department of Hematology, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Japan.

Kohei Hosokawa (K)

Department of Hematology, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Japan.

Hirohito Yamazaki (H)

Department of Transfusion Medicine, Kanazawa University Hospital, Kanazawa, Japan.

Shinji Nakao (S)

Department of Hematology, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Japan.

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