F. Hoffmann-La Roche, Basel, Switzerland.
Roche Pharma AG, Grenzach-Wyhlen, Germany.
Curr Med Res Opin. 2019 Dec;35(12):2079-2087. doi: 10.1080/03007995.2019.1649378. Epub 2019 Aug 13.
To compare the efficacy of emicizumab prophylaxis with that of factor VIII (FVIII) prophylaxis in patients with hemophilia A without inhibitors using two approaches: network meta-analyses (NMA) and additional sub-group analyses from the HAVEN 3 trial. The NMA used data from trials identified using a systematic literature review and compared bleed rates in patients receiving emicizumab prophylaxis and patients receiving FVIII prophylaxis using a Bayesian, random effects generalized linear model with log link Poisson likelihood. Additional sub-groups of the HAVEN 3 trial included here were defined as patients whose dose-taking behavior met either European label or World Federation of Hemophilia guidelines. A negative binomial regression model was used to conduct an intra-patient comparison of bleed rates within the sub-groups, during treatment with FVIII prophylaxis before entering HAVEN 3 and treatment with emicizumab prophylaxis during HAVEN 3. Four studies were included in the base-case NMA. Evidence showed that the total treated bleed rate was lower with emicizumab prophylaxis compared with FVIII prophylaxis (rate ratio [RR] = 0.36 [95% credible interval (CrI) = 0.13-0.95]). Similar associations were observed in sensitivity analyses. The additional HAVEN 3 analyses also showed lower rates of treated bleeds with emicizumab prophylaxis than with FVIII prophylaxis (RRs [95% confidence interval (CI)] = 0.380 [0.186-0.790] and 0.472 [0.258-0.866] in two sub-groups). These results confirm the original HAVEN 3 intra-patient comparison findings. Combined findings from NMA and additional sub-group analyses of HAVEN 3 support the superiority of emicizumab prophylaxis over FVIII prophylaxis in patients with hemophilia A without inhibitors.
比较无抑制剂的血友病 A 患者使用依米珠单抗预防与使用 FVIII 预防的疗效:网络荟萃分析(NMA)和 HAVEN 3 试验的附加亚组分析。NMA 使用系统文献综述中确定的试验数据,并使用贝叶斯、随机效应广义线性模型与对数链接泊松似然比较接受依米珠单抗预防和接受 FVIII 预防的患者的出血率。这里包含的 HAVEN 3 试验的附加亚组定义为剂量依从性符合欧洲标签或世界血友病联合会指南的患者。使用负二项回归模型在亚组内进行患者内比较,比较 FVIII 预防治疗前进入 HAVEN 3 治疗和 HAVEN 3 期间依米珠单抗预防治疗的出血率。四项研究被纳入基础 NMA。证据表明,依米珠单抗预防的总治疗出血率低于 FVIII 预防(率比[RR] = 0.36 [95%可信区间(CrI)= 0.13-0.95])。敏感性分析也观察到了类似的关联。额外的 HAVEN 3 分析还表明,依米珠单抗预防的治疗出血率低于 FVIII 预防(RRs [95%置信区间(CI)] = 0.380 [0.186-0.790]和 0.472 [0.258-0.866]在两个亚组中)。这些结果证实了原始 HAVEN 3 患者内比较的发现。NMA 和 HAVEN 3 的附加亚组分析的综合结果支持依米珠单抗预防在无抑制剂的血友病 A 患者中优于 FVIII 预防。