TY - JOUR
T1 - Retrospective analysis of primary gastric diffuse large B cell lymphoma in the rituximab era
T2 - A multicenter study of 95 patients in Japan
AU - Tanaka, Tsutomu
AU - Shimada, Kazuyuki
AU - Yamamoto, Kazuhito
AU - Hirooka, Yoshiki
AU - Niwa, Yasumasa
AU - Sugiura, Isamu
AU - Kitamura, Kunio
AU - Kosugi, Hiroshi
AU - Kinoshita, Tomohiro
AU - Goto, Hidemi
AU - Nakamura, Shigeo
N1 - Funding Information:
Funding This work was supported in part by a Grant-in-aid for Cancer Research from the Ministry of Education, Culture, Sports, Science and Technology, Japan, and a Grant-in-aid for delineation of molecular biological profile of the refractory lymphoid malignancy and the development of its tumor type-specific management from the Ministry of Health, Labor, and Welfare, Japan.
PY - 2012/3
Y1 - 2012/3
N2 - Primary gastric diffuse large B cell lymphoma (PG-DLBCL) is common subtype of extranodal non-Hodgkin lymphoma. The optimal treatment strategy for PG-DLBCL in the rituximab era still remains unknown. To evaluate clinical outcomes of PG-DLBCL in the rituximab era, we conducted a retrospective, multicenter analysis of 95 patients with PG-DLBCL. In 58 patients with localized disease, 3-year progression-free survival (PFS) and overall survival (OS) were 91% and 91% for patients with six cycles of rituximab plus CHOP (R-CHOP) and 92% and 95% for patients with three to four cycles of R-CHOP plus radiotherapy (Log-rank test, P = 0.595 and P = 0.278, respectively). In 37 patients with advanced disease, 3-year PFS and 3-year OS were 43% and 64% for patients with R-CHOP chemotherapy with or without radiotherapy. On multivariate analysis, advanced stage and elevated serum LDH levels were independent predictors of survival in patients with PG-DLBCL. One patient with localized disease relapsed in lymph node, and eight patients with advanced disease relapsed in lymph node (n = 3), stomach (n = 2), central nervous system (CNS; n = 2), and duodenum (n = 1). Intriguingly, CNS relapse developed within 6 months after initial series of treatment (4.9 and 5.8 months, respectively), and stomach relapse developed in later phase (27.2 and 32.9 months, respectively). Clinical outcomes of PG-DLBCL were extremely favorable for localized-stage patients in the rituximab era, although these might be poor for advanced-stage patients even in the rituximab era. Further prospective analyses are warranted.
AB - Primary gastric diffuse large B cell lymphoma (PG-DLBCL) is common subtype of extranodal non-Hodgkin lymphoma. The optimal treatment strategy for PG-DLBCL in the rituximab era still remains unknown. To evaluate clinical outcomes of PG-DLBCL in the rituximab era, we conducted a retrospective, multicenter analysis of 95 patients with PG-DLBCL. In 58 patients with localized disease, 3-year progression-free survival (PFS) and overall survival (OS) were 91% and 91% for patients with six cycles of rituximab plus CHOP (R-CHOP) and 92% and 95% for patients with three to four cycles of R-CHOP plus radiotherapy (Log-rank test, P = 0.595 and P = 0.278, respectively). In 37 patients with advanced disease, 3-year PFS and 3-year OS were 43% and 64% for patients with R-CHOP chemotherapy with or without radiotherapy. On multivariate analysis, advanced stage and elevated serum LDH levels were independent predictors of survival in patients with PG-DLBCL. One patient with localized disease relapsed in lymph node, and eight patients with advanced disease relapsed in lymph node (n = 3), stomach (n = 2), central nervous system (CNS; n = 2), and duodenum (n = 1). Intriguingly, CNS relapse developed within 6 months after initial series of treatment (4.9 and 5.8 months, respectively), and stomach relapse developed in later phase (27.2 and 32.9 months, respectively). Clinical outcomes of PG-DLBCL were extremely favorable for localized-stage patients in the rituximab era, although these might be poor for advanced-stage patients even in the rituximab era. Further prospective analyses are warranted.
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U2 - 10.1007/s00277-011-1306-0
DO - 10.1007/s00277-011-1306-0
M3 - Article
C2 - 21822617
AN - SCOPUS:84857370391
SN - 0939-5555
VL - 91
SP - 383
EP - 390
JO - Annals of Hematology
JF - Annals of Hematology
IS - 3
ER -