Ratanatharathorn Voravit, Logan Brent, Wang Dan, Horowitz Mary, Uberti Joseph P, Ringden Olle, Gale Robert Peter, Khoury Hanna, Arora Mukta, Spellman Stephen, Cutler Corey, Antin Joseph, Bornhaüser Martin, Hale Gregory, Verdonck Leo, Cairo Mitchell, Gupta Vikas, Pavletic Steven
Blood and Marrow Transplantation Program, Karmanos Cancer Institute, Wayne State University, Detroit, MI 48201, USA.
Br J Haematol. 2009 Jun;145(6):816-24. doi: 10.1111/j.1365-2141.2009.07674.x. Epub 2009 Mar 26.
Prior therapy with rituximab might attenuate disparate histocompatibility antigen presentation by B cells, thus decreased the risk of acute graft-versus-host disease (GVHD) and improved survival. We tested this hypothesis by comparing the outcomes of 435 B-cell lymphoma patients who received allogeneic transplantation from 1999 to 2004 in the Center for International Blood and Marrow Transplant Research database: 179 subjects who received rituximab within 6 months prior to transplantation (RTX cohort) and 256 subjects who did not receive RTX within 6 months prior to transplantation (No-RTX cohort). The RTX cohort had a significantly lower incidence of treatment-related mortality (TRM) [relative risk (RR) = 0.68; 95% confidence interval (CI), 0.47-1.0; P = 0.05], lower acute grade II-IV (RR = 0.72; 95% CI, 0.53-0.97; P = 0.03) and III-IV GVHD (RR = 0.55; 95% CI, 0.34-0.91; P = 0.02). There was no difference in the risk of chronic GVHD, disease progression or relapse. Progression-free survival (PFS) (RR = 0.68; 95% CI 0.50-0.92; P = 0.01) and overall survival (OS) (RR = 0.63; 95% CI, 0.46-0.86; P = 0.004) were significantly better in the RTX cohort. Prior RTX therapy correlated with less acute GVHD, similar chronic GVHD, less TRM, better PFS and OS.
先前使用利妥昔单抗进行治疗可能会减弱B细胞呈现不同组织相容性抗原的能力,从而降低急性移植物抗宿主病(GVHD)的风险并提高生存率。我们通过比较1999年至2004年在国际血液和骨髓移植研究中心数据库中接受异基因移植的435例B细胞淋巴瘤患者的结局来验证这一假设:179例在移植前6个月内接受利妥昔单抗治疗的受试者(RTX队列)和256例在移植前6个月内未接受RTX治疗的受试者(非RTX队列)。RTX队列的治疗相关死亡率(TRM)显著更低[相对风险(RR)=0.68;95%置信区间(CI),0.47-1.0;P=0.05],急性II-IV级(RR=0.72;95%CI,0.53-0.97;P=0.03)和III-IV级GVHD(RR=0.55;95%CI,0.34-0.91;P=0.02)也更低。慢性GVHD、疾病进展或复发的风险没有差异。RTX队列的无进展生存期(PFS)(RR=0.68;95%CI 0.50-0.92;P=0.01)和总生存期(OS)(RR=0.63;95%CI,0.46-0.86;P=0.004)显著更好。先前的RTX治疗与更少的急性GVHD、相似的慢性GVHD、更低的TRM、更好的PFS和OS相关。