Retrospective Analysis of Intravascular Large B-Cell Lymphoma Treated With Rituximab-Containing Chemotherapy As Reported by the IVL Study Group in Japan

Kazuyuki Shimada(Nagoya University Hospital), Kosei Matsue(Nagoya University Hospital), Kazuhito Yamamoto(Nagoya University Hospital), Takuhei Murase(Nagoya University Hospital), Naoaki Ichikawa(Nagoya University Hospital), Masataka Okamoto(Nagoya University Hospital), Nozomi Niitsu(Nagoya University Hospital), Hiroshi Kosugi(Nagoya University Hospital), Norifumi Tsukamoto(Nagoya University Hospital), Hiroshi Miwa(Nagoya University Hospital), Hideki Asaoku(Nagoya University Hospital), Ako Kikuchi(Nagoya University Hospital), Morio Matsumoto(Nagoya University Hospital), Yoshio Saburi(Nagoya University Hospital), Yasufumi Masaki(Nagoya University Hospital), Motoko Yamaguchi(Nagoya University Hospital), Shigeo Nakamura(Nagoya University Hospital), Tomoki Naoe(Nagoya University Hospital), Tomohiro Kinoshita(Nagoya University Hospital)
Journal of Clinical Oncology
May 28, 2008
Cited by 277

Abstract

PURPOSE: To evaluate the safety and efficacy of rituximab-containing chemotherapies for intravascular large B-cell lymphoma (IVLBCL). PATIENTS AND METHODS: We retrospectively analyzed 106 patients (59 men, 47 women) with IVLBCL who received chemotherapy either with rituximab (R-chemotherapy, n = 49) or without rituximab (chemotherapy, n = 57) between 1994 and 2007 in Japan. The median patient age was 67 years (range, 34 to 84 years). The International Prognostic Index was high-intermediate/high in 97% of patients. RESULTS: The complete response rate was higher for patients in the R-chemotherapy group (82%) than for those in the chemotherapy group (51%; P = .001). The median duration of follow-up for surviving patients was 18 months (range, 1 to 95 months). Progression-free survival (PFS) and overall survival (OS) rates at 2 years after diagnosis were significantly higher for patients in the R-chemotherapy group (PFS, 56%; OS, 66%) than for patients in the chemotherapy group (PFS, 27% with P = .001; OS, 46% with P = 0.01). Multivariate analysis revealed that the use of rituximab was favorably associated with PFS (hazard ratio [HR], 0.45; 95% CI, 0.25 to 0.80; P = .006) and OS (HR, 0.42; 95% CI, 0.21 to 0.85; P = .016). Treatment-related death was observed in three patients (6%) who received R-chemotherapy and in five patients (9%) who received chemotherapy. CONCLUSION: Our data suggest improved clinical outcomes for patients with IVLBCL in the rituximab era. Future prospective studies of rituximab-containing chemotherapies are warranted.


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