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Outcomes of allogeneic hematopoietic stem cell transplantation for relapsed or refractory diffuse large B-cell lymphoma.
Kato, Koji; Sugio, Takeshi; Ikeda, Takashi; Yoshitsugu, Kanako; Miyazaki, Kana; Suzumiya, Junji; Yamamoto, Go; Kim, Sung-Won; Ikegame, Kazuhiro; Uehara, Yasufumi; Mori, Yasuo; Ishikawa, Jun; Hiramoto, Nobuhiro; Eto, Tetsuya; Nakazawa, Hideyuki; Kobayashi, Hikaru; Serizawa, Kentaro; Onizuka, Makoto; Fukuda, Takahiro; Atsuta, Yoshiko; Suzuki, Ritsuro.
Afiliação
  • Kato K; Department of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan. kato.koji.429@m.kyushu-u.ac.jp.
  • Sugio T; Department of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
  • Ikeda T; Division of Hematology and Stem Cell Transplantation, Shizuoka Cancer Center, Shizuoka, Japan.
  • Yoshitsugu K; Division of Hematology and Stem Cell Transplantation, Shizuoka Cancer Center, Shizuoka, Japan.
  • Miyazaki K; Department of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu, Japan.
  • Suzumiya J; Department of Hematology, Koga Community Hospital, Yaizu, Japan.
  • Yamamoto G; Department of Hematology, Federation of National Public Service Personnel Mutual Aid Associations Toranomon Hospital, Tokyo, Japan.
  • Kim SW; Department of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.
  • Ikegame K; Department of Hematology, Hyogo Medical University Hospital, Nishinomiya, Japan.
  • Uehara Y; Department of Hematology, Kitakyushu Municipal Medical Center, Kitakyushu, Japan.
  • Mori Y; Department of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
  • Ishikawa J; Department of Hematology, Osaka International Cancer Institute, Osaka, Japan.
  • Hiramoto N; Department of Hematology, Kobe City Medical Center General Hospital, Kobe, Japan.
  • Eto T; Department of Hematology, Hamanomachi Hospital, Fukuoka, Japan.
  • Nakazawa H; Department of Hematology and Medical Oncology, Shinshu University School of Medicine, Matsumoto, Japan.
  • Kobayashi H; Department of Hematology, Nagano Red Cross Hospital, Nagano, Japan.
  • Serizawa K; Division of Hematology and Rheumatology, Department of Internal Medicine, Kindai University Hospital, Osaka, Japan.
  • Onizuka M; Department of Hematology/Oncology, Tokai University School of Medicine, Isehara, Japan.
  • Fukuda T; Department of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.
  • Atsuta Y; Japanese Data Center for Hematopoietic Cell Transplantation, Nagakute, Japan.
  • Suzuki R; Department of Registry Science for Transplant and Cellular Therapy, Aichi Medical University School of Medicine, Nagakute, Japan.
Bone Marrow Transplant ; 59(3): 306-314, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38102209
ABSTRACT
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a currative treatment modality for diffuse large B-cell lymphoma (DLBCL) because of the intrinsic graft-versus-lymphoma effect. However, limited information is available regarding which patients with relapsed or refractory DLBCL are likely to benefit from allo-HSCT. We retrospectively analyzed data from 1268 DLBCL patients who received allo-HSCT. The overall survival and progression-free survival (PFS) rates were 30.3% and 21.6% at 3 years, respectively. Multivariate analysis revealed that stable or progressive disease at transplantation, male patient, poorer performance status at transplantation, and shorter intervals from previous transplantation were associated independently with a lower PFS. Four prognostic factors were used to construct a prognostic index for PFS, predicting 3-year PFS of 55.4%, 43.7%, 20.4% and 6.6%, respectively. The prognostic model predicted relapse rates following allo-HSCT accordingly (P < 0.0001), whereas did not predict transplantation-related mortality (P = 0.249). The prognostic index can identify a subgroup of DLBCL patients who benefit from allo-HSCT and it is worthwhile to evaluate whether this model is also applicable to patients undergoing allo-HSCT in cases of relapse after chimeric antigen receptor engineered T-cell therapy, although the application of allo-HSCT has been declining with the increase of novel immunotherapies.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Humans / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Humans / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article