Division of Hematology, Mayo Clinic, Rochester, MN, USA.
Peking University Cancer Hospital & Institute, Beijing, PR China.
Future Oncol. 2020 May;16(15):991-999. doi: 10.2217/fon-2020-0176. Epub 2020 Apr 6.
While combination of rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone (R-CHOP) cures most patients with diffuse large B-cell lymphoma (DLBCL), those with high-risk international prognostic index disease have inferior survival. Enzastaurin as a potent inhibitor of PKC-β and PI3K/AKT pathway suppressor has been tested in many clinical trials including two key studies in DLBCL: Phase III maintenance study (Preventing Relapse in Lymphoma Using Daily Enzastaurin [PRELUDE]) and a first-line Phase II study (S028). DNA extracted from PRELUDE patients' blood samples was retrospectively genotyped identifying a novel genetic biomarker, DGM1 that showed high correlation with response to enzastaurin. A similar finding observed in the S028 study suggested that addition of enzastaurin to R-CHOP may significantly improve outcomes as frontline therapy for high-risk DGM1 positive DLBCL patients. ENGINE is a global, multicenter, placebo-controlled and randomized study to compare the effect of R-CHOP/enzastaurin as frontline treatment in high-risk DLBCL patients. The primary end point for this study is overall survival in patients who are DGM1 positive. Clinical Trial Registration Identifier: NCT03263026.
尽管利妥昔单抗、环磷酰胺、多柔比星、长春新碱和泼尼松(R-CHOP)联合治疗可治愈大多数弥漫性大 B 细胞淋巴瘤(DLBCL)患者,但具有高危国际预后指数疾病的患者生存预后较差。Enzastaurin 是一种有效的 PKC-β 和 PI3K/AKT 通路抑制剂,已在包括两项 DLBCL 关键研究在内的多项临床试验中进行了测试:III 期维持研究(使用每日 Enzastaurin 预防淋巴瘤复发[PRELUDE])和一线 II 期研究(S028)。从 PRELUDE 患者的血液样本中提取 DNA,进行回顾性基因分型,确定了一种新的遗传生物标志物 DGM1,该标志物与对 Enzastaurin 的反应高度相关。在 S028 研究中观察到了类似的发现,这表明在高危 DGM1 阳性 DLBCL 患者中,将 Enzastaurin 联合 R-CHOP 作为一线治疗可能显著改善预后。ENGINE 是一项全球性、多中心、安慰剂对照和随机研究,旨在比较 R-CHOP/Enzastaurin 作为高危 DLBCL 患者一线治疗的效果。该研究的主要终点是 DGM1 阳性患者的总生存。临床试验注册号:NCT03263026。