TY - JOUR
T1 - Prospective therapeutic studies of disseminated extranodal large B-cell lymphoma including intravascular large B-cell lymphoma
AU - Sakai, Tomoyuki
AU - Ueda, Yusuke
AU - Yanagisawa, Hiroto
AU - Arita, Kotaro
AU - Iwao, Haruka
AU - Yamada, Kazunori
AU - Mizuta, Shuichi
AU - Kawabata, Hiroshi
AU - Fukushima, Toshihiro
AU - Tai, Katsunori
AU - Kishi, Shinji
AU - Morinaga, Koji
AU - Murakami, Jun
AU - Takamatsu, Hiroyuki
AU - Terasaki, Yasushi
AU - Yoshio, Nobuyuki
AU - Kondo, Yukio
AU - Okumura, Hirokazu
AU - Matano, Sadaya
AU - Yamaguchi, Masaki
AU - Tsutani, Hiroshi
AU - Masaki, Yasufumi
N1 - Publisher Copyright:
© 2021, National Center for Global Health and Medicine. All rights reserved.
PY - 2024
Y1 - 2024
N2 - This study aimed to establish a standard treatment for disseminated extranodal large B-cell lymphoma, including intravascular large B-cell lymphoma (DEN-LBCL/IVL), and to validate the clinical diagnostic criteria we proposed. Between 2006 and 2016, 22 patients were enrolled in a clinical trial conducted by the Hokuriku Hematology Oncology Study Group. The first cycle of chemotherapy consisted of dose-reduced cyclophosphamide, doxorubicin, vincristine, and prednisolone (CHOP) with delayed administration of rituximab. From the second to the sixth cycle, patients received conventional rituximab and CHOP therapy. The primary endpoint was overall survival (OS), while the secondary endpoints included the complete response (CR) rate and time to treatment failure (TTF). The results showed a CR rate of 73%, a median OS of 65 months, and a median TTF of 45 months. These findings indicate that patients with DEN-LBCL/IVL were effectively treated with our new chemoimmunotherapy regimen. Our clinical diagnostic criteria are useful for identifying patients who require early intervention.
AB - This study aimed to establish a standard treatment for disseminated extranodal large B-cell lymphoma, including intravascular large B-cell lymphoma (DEN-LBCL/IVL), and to validate the clinical diagnostic criteria we proposed. Between 2006 and 2016, 22 patients were enrolled in a clinical trial conducted by the Hokuriku Hematology Oncology Study Group. The first cycle of chemotherapy consisted of dose-reduced cyclophosphamide, doxorubicin, vincristine, and prednisolone (CHOP) with delayed administration of rituximab. From the second to the sixth cycle, patients received conventional rituximab and CHOP therapy. The primary endpoint was overall survival (OS), while the secondary endpoints included the complete response (CR) rate and time to treatment failure (TTF). The results showed a CR rate of 73%, a median OS of 65 months, and a median TTF of 45 months. These findings indicate that patients with DEN-LBCL/IVL were effectively treated with our new chemoimmunotherapy regimen. Our clinical diagnostic criteria are useful for identifying patients who require early intervention.
KW - R-CHOP
KW - clinical diagnostic criteria
KW - intravascular large B-cell lymphoma
KW - random skin biopsy
UR - http://www.scopus.com/inward/record.url?scp=105002235027&partnerID=8YFLogxK
U2 - 10.35772/ghm.2024.01021
DO - 10.35772/ghm.2024.01021
M3 - 学術論文
AN - SCOPUS:105002235027
SN - 2434-9186
VL - 6
SP - 277
EP - 281
JO - Global Health and Medicine
JF - Global Health and Medicine
IS - 4
ER -