Homozygous A polymorphism of the complement C1qA276 correlates with prolonged overall survival in patients with diffuse large B cell lymphoma treated with R-CHOP.
Homozygous A polymorphism of the complement C1qA276 correlates with prolonged overall survival in patients with diffuse large B cell lymphoma treated with R-CHOP.
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补体 C1qA276 的纯合 A 多态性与接受 R-CHOP 治疗的弥漫性大 B 细胞淋巴瘤患者的总生存期延长相关
DOI:
10.1186/1756-8722-5-51
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发表时间:
2012-08-16
影响因子:
28.5
通讯作者:
Zhu J
中科院分区:
文献类型:
--
作者:
Jin X;Ding H;Ding N;Fu Z;Song Y;Zhu J
The precise mechanism of action for rituximab (R) is not fully elucidated. Besides antibody-dependent cellular cytotoxicity (ADCC), complements may also play an important role in the clinical response to rituximab-based therapy in diffuse large B cell lymphoma (DLBCL). The purpose of this study was to explore the relationship between C1qA[276] polymorphism and the clinical response to standard frontline treatment with R-CHOP in DLBCL patients. Genotyping for C1qA[276A/G] was done in 164 patients with DLBCL. 129 patients treated with R-CHOP as frontline therapy (R ≥ 4 cycles) were assessable for the efficacy. Patients with homozygous A were found to have a higher overall response rate than those with heterozygous or homozygous G alleles (97.3% vs. 83.7%,P = 0.068). The complete response rate in patients with homozygous A was statistically higher than that in AG and GG allele carriers (89.2% vs. 51.1%,P = 0.0001). The overall survival of patients with homozygous A was longer than that of the G allele carriers (676 days vs. 497 days, P = 0.023). Multivariate Cox regression analysis showed that C1qA A/A allele was an independent favorable prognostic factor for DLBCL patients treated with R-CHOP as first-line therapy. These results suggest that C1qA polymorphism may be a biomarker to predict response to R-CHOP as frontline therapy for DLBCL patients.
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影响因子:
10.9
作者:
Elbaz HA;Stueckle TA;Tse W;Rojanasakul Y;Dinu CZ
通讯作者:
Dinu CZ
影响因子:
28.5
作者:
Wang J;Ke XY
通讯作者:
Ke XY
影响因子:
51.1
作者:
Pfreundschuh, Michael;Trumper, Lorenz;Loeffler, Markus
通讯作者:
Loeffler, Markus
影响因子:
3.5
作者:
Stuart, GR;Lynch, NJ;Schwaeble, WJ
通讯作者:
Schwaeble, WJ
DOI:
10.1084/jem.188.12.2349
发表时间:
1998-12-21
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Pike SE;Yao L;Jones KD;Cherney B;Appella E;Sakaguchi K;Nakhasi H;Teruya-Feldstein J;Wirth P;Gupta G;Tosato G
通讯作者:
Tosato G