TY - JOUR
T1 - The effect of adding rituximab to CHOP-based therapy on clinical outcomes for Japanese patients with diffuse large B-cell lymphoma
T2 - A propensity score matching analysis
AU - Nishimori, Hisakazu
AU - Matsuo, Keitaro
AU - Maeda, Yoshinobu
AU - Nawa, Yuichiro
AU - Sunami, Kazutaka
AU - Togitani, Kazuto
AU - Takimoto, Hidetaka
AU - Hiramatsu, Yasushi
AU - Kiguchi, Toru
AU - Yano, Tomofumi
AU - Yamane, Hiromichi
AU - Tabayashi, Takayuki
AU - Takeuchi, Makoto
AU - Makita, Masanori
AU - Sezaki, Nobuo
AU - Yamasuji, Yoshiko
AU - Sugiyama, Haruko
AU - Tabuchi, Takahiro
AU - Kataoka, Itaru
AU - Fujii, Nobuharu
AU - Ishimaru, Fumihiko
AU - Shinagawa, Katsuji
AU - Ikeda, Kazuma
AU - Hara, Masamichi
AU - Yoshino, Tadashi
AU - Tanimoto, Mitsune
PY - 2009/4
Y1 - 2009/4
N2 - 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.
AB - 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.
KW - CHOP
KW - DLBCL
KW - Non-Hodgkin's lymphoma
KW - Rituximab
KW - Survival
UR - http://www.scopus.com/inward/record.url?scp=67649159580&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=67649159580&partnerID=8YFLogxK
U2 - 10.1007/s12185-009-0259-8
DO - 10.1007/s12185-009-0259-8
M3 - Article
C2 - 19326060
AN - SCOPUS:67649159580
SN - 0925-5710
VL - 89
SP - 326
EP - 331
JO - International Journal of Hematology
JF - International Journal of Hematology
IS - 3
ER -