Treatment of aggressive adult T-cell leukemia/lymphoma: a retrospective study in a hospital located in HTLV-1 highly endemic area.


Journal

International journal of hematology
ISSN: 1865-3774
Titre abrégé: Int J Hematol
Pays: Japan
ID NLM: 9111627

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 14 06 2019
accepted: 29 10 2019
revised: 21 10 2019
pubmed: 14 11 2019
medline: 11 8 2020
entrez: 14 11 2019
Statut: ppublish

Résumé

Adult T-cell leukemia/lymphoma (ATL) is a peripheral T-cell neoplasm associated with the human T-cell leukemia virus type-I (HTLV-1); prognosis still remains very poor. We retrospectively reviewed the treatment of 198 patients with acute-, lymphoma- and unfavorable chronic-type ATL (aggressive ATL) diagnosed from 2005 to 2014 in a hospital located in an area of Japan in which HTLV-1 is highly endemic. One-hundred forty-three, and 35 patients were treated using OPEC/MPEC and VCAP-AMP-VECP, respectively. OPEC/MPEC was mainly used until around 2010, and gradually switched to VCAP-AMP-VECP, especially for younger patients. The 2-year overall survival for patients treated by VCAP-AMP-VECP was significantly higher than that using OPEC/MPEC for patients < 70 years old (y.o.), but not for patients ≥ 70 y.o. A less intensive chemotherapy OPEC/MPEC could be performed without reducing dose intensity, even in elderly patients, and its therapeutic outcome is not inferior to that of VCAP-AMP-VECP. It is difficult to draw definite conclusion from this small retrospective study; however, OPEC/MPEC may represent an alternative option for elderly patients with aggressive ATL.

Identifiants

pubmed: 31721034
doi: 10.1007/s12185-019-02769-w
pii: 10.1007/s12185-019-02769-w
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

234-240

Commentaires et corrections

Type : ErratumIn

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Auteurs

Daisuke Nakamura (D)

Department of Hematology, Izuro Imamura Hospital, 17-1 Horie, Kagoshima, Japan. d5039@m3.kufm.kagoshima-u.ac.jp.
Department of Hematology and Rheumatology, Kagoshima University Hospital, 8-35-1 Sakuragaoka, Kagoshima, Japan. d5039@m3.kufm.kagoshima-u.ac.jp.

Makoto Yoshimitsu (M)

Department of Hematology and Rheumatology, Kagoshima University Hospital, 8-35-1 Sakuragaoka, Kagoshima, Japan.

Tomohisa Tabuchi (T)

Department of Hematology, Izuro Imamura Hospital, 17-1 Horie, Kagoshima, Japan.
Department of Hematology and Rheumatology, Kagoshima University Hospital, 8-35-1 Sakuragaoka, Kagoshima, Japan.

Naosuke Arima (N)

Department of Hematology, Izuro Imamura Hospital, 17-1 Horie, Kagoshima, Japan.
Department of Hematology and Rheumatology, Kagoshima University Hospital, 8-35-1 Sakuragaoka, Kagoshima, Japan.

Maiko Hayashida (M)

Department of Hematology, Izuro Imamura Hospital, 17-1 Horie, Kagoshima, Japan.
Department of Hematology and Rheumatology, Kagoshima University Hospital, 8-35-1 Sakuragaoka, Kagoshima, Japan.

Hirosaka Inoue (H)

Department of Hematology, Izuro Imamura Hospital, 17-1 Horie, Kagoshima, Japan.
Department of Hematology and Rheumatology, Kagoshima University Hospital, 8-35-1 Sakuragaoka, Kagoshima, Japan.

Kakushi Matsushita (K)

Department of Hematology, Izuro Imamura Hospital, 17-1 Horie, Kagoshima, Japan.
Department of Hematology and Rheumatology, Kagoshima University Hospital, 8-35-1 Sakuragaoka, Kagoshima, Japan.

Tadashi Matsumoto (T)

Department of Hematology, Izuro Imamura Hospital, 17-1 Horie, Kagoshima, Japan.

Naomichi Arima (N)

Department of Hematology and Rheumatology, Kagoshima University Hospital, 8-35-1 Sakuragaoka, Kagoshima, Japan.

Kenji Ishitsuka (K)

Department of Hematology and Rheumatology, Kagoshima University Hospital, 8-35-1 Sakuragaoka, Kagoshima, Japan.

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