Dose-adjusted EPOCH with or without rituximab for aggressive lymphoma patients: real world data.


Journal

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

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 11 03 2020
accepted: 25 08 2020
revised: 11 08 2020
pubmed: 4 9 2020
medline: 26 11 2020
entrez: 4 9 2020
Statut: ppublish

Résumé

CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisolone) -/+ rituximab (R) is the standard chemotherapeutic regimen for aggressive lymphoma, but is insufficient for aggressive lymphoma with adverse prognostic factors. Dose-adjusted (DA)-EPOCH (etoposide, doxorubicin, cyclophosphamide, vincristine, and prednisolone) -/+ R demonstrates excellent efficacy against some aggressive lymphoma. Thus, we conducted a retrospective study to evaluate the feasibility and efficacy of this therapy in clinical practice. We enrolled 149 patients from 17 institutions diagnosed between 2007 and 2015. The median follow-up period for survivors was 27 months (range 0.2-123). The complete response (CR) rate of newly diagnosed patients was 79% (95% CI 68-87%). All patients were hospitalized to receive this therapy and 94% of patients also received granulocyte-colony-stimulating factor support. There were no treatment-related deaths. Febrile neutropenia (FN) and grade 3 or 4 infection occurred in 55% and 28% of patients, respectively. There were no significant differences in FN or infection between young (≤ 65 years) and elderly patients (> 65 years). In newly diagnosed diffuse large B-cell lymphoma-not otherwise specified patients (n = 46), the CR rate was 80% (95% CI 64-91%) and the 2-year OS rate was 81% (95% CI 66-90%). In the present study, DA-EPOCH -/+ R exhibited excellent efficacy and feasibility for aggressive lymphoma.

Identifiants

pubmed: 32880824
doi: 10.1007/s12185-020-02984-w
pii: 10.1007/s12185-020-02984-w
doi:

Substances chimiques

Granulocyte Colony-Stimulating Factor 143011-72-7
Rituximab 4F4X42SYQ6
Vincristine 5J49Q6B70F
Etoposide 6PLQ3CP4P3
Doxorubicin 80168379AG
Cyclophosphamide 8N3DW7272P
Prednisone VB0R961HZT

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

807-816

Subventions

Organisme : Japan Agency for Medical Research and Development (JP)
ID : JP18ck0106439, J.S.

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Auteurs

Shinichiro Matsuda (S)

Innovative Cancer Center/Oncology-Hematology, Shimane University Hospital, 89-1 Enya, Izumo, Shimane, 693-8501, Japan.

Ritsuro Suzuki (R)

Innovative Cancer Center/Oncology-Hematology, Shimane University Hospital, 89-1 Enya, Izumo, Shimane, 693-8501, Japan.

Tsutomu Takahashi (T)

Innovative Cancer Center/Oncology-Hematology, Shimane University Hospital, 89-1 Enya, Izumo, Shimane, 693-8501, Japan.

Youko Suehiro (Y)

Department of Hematology, National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan.

Naoto Tomita (N)

Department of Hematology, St. Marianna University School of Medicine, Kawasaki, Japan.

Koji Izutsu (K)

Department of Hematology, Toranomon Hospital, Tokyo, Japan.

Noriko Fukuhara (N)

Department of Hematology, Tohoku University Hospital, Sendai, Japan.

Yoshitaka Imaizumi (Y)

Department of Hematology, Nagasaki University, Nagasaki, Japan.

Kazuyuki Shimada (K)

Department of Hematology, Nagoya University Hospital, Nagoya, Japan.

Tomonori Nakazato (T)

Department of Hematology, Yokohama Municipal Citizens Hospital, Yokohama, Japan.

Isao Yoshida (I)

Department of Hematologic Oncology, National Hospital Organization Shikoku Cancer Center, Ehime, Japan.

Kana Miyazaki (K)

Department of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu, Japan.

Motoko Yamaguchi (M)

Department of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu, Japan.

Junji Suzumiya (J)

Innovative Cancer Center/Oncology-Hematology, Shimane University Hospital, 89-1 Enya, Izumo, Shimane, 693-8501, Japan. suzumiya@med.shimane-u.ac.jp.

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