| Literature DB >> 22969886 |
Yujin Kobayashi1, Yoshihiro Hatta, Atsuko Hojo, Yoshimasa Kura, Yoshihito Uchino, Hiromichi Takahashi, Satomi Kiso, Yukio Hirabayashi, Mai Yagi, Hitomi Kodaira, Daisuke Kurita, Toshitake Tanaka, Katsuhiro Miura, Noriyoshi Iriyama, Sumiko Kobayashi, Umihiko Sawada, Masahiko Sugitani, Jin Takeuchi.
Abstract
The addition of rituximab to cyclophosphamide, doxorubicin, vincristine and prednisone [CHOP (i.e., R-CHOP)] is considered to be the standard regimen for treating localized, primary gastric diffuse large B-cell lymphoma (PG-DLBCL). However, few studies have reported the long-term efficacy of R-CHOP therapy in the management of localized PG-DLBCL. In the present study, we performed a retrospective analysis of 11 patients with localized PG-DLBCL, who were treated with R-CHOP at Nihon University Itabashi Hospital and Kasukabe Municipal Hospital (Japan) from 2001 to 2008. Limited stage cancer was defined as stage I/II according to the Lugano staging system for gastrointestinal (GI) lymphomas. The relative dose intensity (RDI) of CHOP therapy was calculated for each patient. The median age of the patients was 68 years (range, 48-82). Gastralgia and anemia were common symptoms at initial presentation. All patients except 1 received 6 cycles of R-CHOP treatment without consolidative radiation therapy or prior surgery. RDI was maintained at over 80% in 9 out of 11 patients. All patients achieved complete remission and the estimated overall survival with a median follow-up of 54 months (range, 39-103) was 100%, without relapse or significant GI adverse effects, such as perforation or bleeding during R-CHOP treatment. No long-term adverse effects of rituximab were recorded during the observation period. Helicobacter pylori infection was diagnosed in 72.7% (8 cases) of the patients, but was eradicated in a limited number of patients. Our data suggest the feasibility and effectiveness of the addition of rituximab to conventional CHOP therapy in the management of localized PG-DLBCL.Entities:
Year: 2011 PMID: 22969886 PMCID: PMC3438714 DOI: 10.3892/etm.2011.387
Source DB: PubMed Journal: Exp Ther Med ISSN: 1792-0981 Impact factor: 2.447