TY - JOUR
T1 - Treatments and Outcomes of Newly Diagnosed CD5-Positive Diffuse Large B-Cell Lymphoma
T2 - A Multi-Institutional Observational Study
AU - Nato, Yuma
AU - Miyazaki, Kana
AU - Maruyama, Dai
AU - Takahashi, Hiroyuki
AU - Sunami, Kazutaka
AU - Murakami, Satsuki
AU - Negoro, Eiju
AU - Miyazawa, Yuri
AU - Choi, Ilseung
AU - Okada, Takahiro
AU - Takayama, Nobuyuki
AU - Tomita, Naoto
AU - Momose, Shuji
AU - Kaneda, Yuto
AU - Yoshida, Masahiro
AU - Gomyo, Hiroshi
AU - Toyama, Kohtaro
AU - Nishikori, Momoko
AU - Saito, Akio
AU - Hiraga, Junji
AU - Masunari, Taro
AU - Takahashi, Naoki
AU - Makiyama, Junya
AU - Suzuki, Tomotaka
AU - Tsunemine, Hiroko
AU - Takizawa, Jun
AU - Kato, Takeharu
AU - Masaki, Yasufumi
AU - Fukuhara, Noriko
AU - Okamoto, Masataka
AU - Tawara, Isao
AU - Asano, Naoko
AU - Ohshima, Koichi
AU - Izutsu, Koji
AU - Kato, Koji
AU - Suzuki, Ritsuro
AU - Yamaguchi, Motoko
N1 - Publisher Copyright:
© 2025 The Author(s). Hematological Oncology published by John Wiley & Sons Ltd.
PY - 2025/3
Y1 - 2025/3
N2 - CD5-positive diffuse large B-cell lymphoma (CD5+ DLBCL) is characterized by a poor prognosis and frequent central nervous system (CNS) relapse. Sandwich therapy comprising dose-adjusted (DA)-EPOCH-R (etoposide, prednisolone, vincristine, cyclophosphamide, doxorubicin, and rituximab) and high-dose methotrexate (HD-MTX) (DA-EPOCH-R/HD-MTX) showed excellent efficacy and manageable safety in a phase II study of patients diagnosed with stage II–IV CD5+ DLBCL. To validate the results of that study and elucidate the current state of treatment for CD5+ DLBCL, we retrospectively analyzed the outcomes of patients with CD5+ DLBCL diagnosed between 2016 and 2021 who received anthracycline-containing chemotherapy with rituximab. Among the 346 patients evaluated, 62 (18%) received DA-EPOCH-R/HD-MTX. The median follow-up time was 43 months. In 55 patients with stage II–IV disease treated with DA-EPOCH-R/HD-MTX, the 2-year overall survival (OS), progression-free survival, and cumulative incidence of CNS relapse were 87% (95% CI, 73%–94%), 76% (95% CI, 61%–86%), and 7.3% (95% CI, 2.4%–16%), respectively. There were no treatment-related deaths. Febrile neutropenia occurred in 18 (33%) patients. Multivariate analysis of the 346 patients identified elevated serum lactate dehydrogenase levels, multiple extranodal involvement, no intrathecal MTX (IT-MTX), and no DA-EPOCH-R/HD-MTX as independent risk factors for OS. Only one CNS relapse event was observed in 28 patients who received both HD-MTX and IT-MTX. Our study provides real-world data on the treatments and outcomes of a large number of patients. The favorable survival and manageable toxicity of DA-EPOCH-R/HD-MTX have been validated in clinical settings. The use of HD-MTX and IT-MTX might be effective for preventing CNS relapse in patients with CD5+ DLBCL.
AB - CD5-positive diffuse large B-cell lymphoma (CD5+ DLBCL) is characterized by a poor prognosis and frequent central nervous system (CNS) relapse. Sandwich therapy comprising dose-adjusted (DA)-EPOCH-R (etoposide, prednisolone, vincristine, cyclophosphamide, doxorubicin, and rituximab) and high-dose methotrexate (HD-MTX) (DA-EPOCH-R/HD-MTX) showed excellent efficacy and manageable safety in a phase II study of patients diagnosed with stage II–IV CD5+ DLBCL. To validate the results of that study and elucidate the current state of treatment for CD5+ DLBCL, we retrospectively analyzed the outcomes of patients with CD5+ DLBCL diagnosed between 2016 and 2021 who received anthracycline-containing chemotherapy with rituximab. Among the 346 patients evaluated, 62 (18%) received DA-EPOCH-R/HD-MTX. The median follow-up time was 43 months. In 55 patients with stage II–IV disease treated with DA-EPOCH-R/HD-MTX, the 2-year overall survival (OS), progression-free survival, and cumulative incidence of CNS relapse were 87% (95% CI, 73%–94%), 76% (95% CI, 61%–86%), and 7.3% (95% CI, 2.4%–16%), respectively. There were no treatment-related deaths. Febrile neutropenia occurred in 18 (33%) patients. Multivariate analysis of the 346 patients identified elevated serum lactate dehydrogenase levels, multiple extranodal involvement, no intrathecal MTX (IT-MTX), and no DA-EPOCH-R/HD-MTX as independent risk factors for OS. Only one CNS relapse event was observed in 28 patients who received both HD-MTX and IT-MTX. Our study provides real-world data on the treatments and outcomes of a large number of patients. The favorable survival and manageable toxicity of DA-EPOCH-R/HD-MTX have been validated in clinical settings. The use of HD-MTX and IT-MTX might be effective for preventing CNS relapse in patients with CD5+ DLBCL.
KW - CD5 antigen
KW - central nervous system neoplasms
KW - diffuse large B-cell lymphoma
KW - methotrexate
KW - retrospective study
UR - https://www.scopus.com/pages/publications/85218475857
UR - https://www.scopus.com/pages/publications/85218475857#tab=citedBy
U2 - 10.1002/hon.70047
DO - 10.1002/hon.70047
M3 - Article
C2 - 39937961
AN - SCOPUS:85218475857
SN - 0278-0232
VL - 43
JO - Hematological Oncology
JF - Hematological Oncology
IS - 2
M1 - e70047
ER -