| Literature DB >> 19326060 |
Hisakazu Nishimori1, Keitaro Matsuo2, Yoshinobu Maeda1, Yuichiro Nawa3, Kazutaka Sunami4, Kazuto Togitani5, Hidetaka Takimoto6, Yasushi Hiramatsu7, Toru Kiguchi8, Tomofumi Yano9, Hiromichi Yamane10, Takayuki Tabayashi11, Makoto Takeuchi12, Masanori Makita13, Nobuo Sezaki14, Yoshiko Yamasuji1, Haruko Sugiyama1, Takahiro Tabuchi1, Itaru Kataoka1, Nobuharu Fujii1, Fumihiko Ishimaru1, Katsuji Shinagawa1, Kazuma Ikeda1, Masamichi Hara3, Tadashi Yoshino15, Mitsune Tanimoto16.
Abstract
We conducted a retrospective analysis to evaluate the impact on clinical outcomes of adding rituximab to cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) treatment for diffuse large B-cell lymphoma (DLBCL) patients in Japan. A propensity score method was used to compensate for the non-randomized study design. From January 2000 to December 2004, 378 patients who were newly diagnosed with DLBCL at 13 institutes were enrolled: 123 in the rituximab plus CHOP-based chemotherapy (R+) group, and 255 in the CHOP-based chemotherapy only (R-) group. The complete response rate was significantly higher in the R+ group than in the R- group (77.7 vs. 69.4%, P < 0.001). The progression-free survival (PFS) at 2 years was 62.4% in the R+ group and 57.0% in the R- group. The 2-year overall survival (OS) was 76.9% for the R+ group and 70.5% for the R- group. A multivariate analysis revealed that the addition of rituximab was a strong independent prognostic factor for PFS (hazard ratio 0.64, 95% CI 0.43-0.96, P = 0.031). A subgroup analysis revealed that R+ particularly benefited younger patients (hazard ratio 0.25, 95% CI 0.08-0.75, P = 0.013). IPI also showed significant impact for PFS (hazard ratio 1.82, 95% CI 1.55-2.14 for one score increase, P < 0.001) as well as OS (hazard ratio 2.10, 95% CI 1.71-2.57, P < 0.001). In summary, the addition of rituximab to CHOP-based chemotherapy results in better outcomes for Japanese DLBCL patients, particularly younger patients.Entities:
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Year: 2009 PMID: 19326060 DOI: 10.1007/s12185-009-0259-8
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490