ENGINE: a Phase III randomized placebo controlled study of enzastaurin/R-CHOP as frontline therapy in high-risk diffuse large B-cell lymphoma patients with the genomic biomarker DGM1

Author:

Nowakowski Grzegorz S1,Zhu Jun2,Zhang Qingyuan3,Brody Joshua4,Sun Xiuhua5,Maly Joseph6,Song Yuqin2,Rizvi Syed7,Song Yongping8,Lansigan Frederick9,Jing Hongmei10,Cao Junning11,Lue Jennifer K12,Luo Wen13,Zhang Lei13,Li Ling13,Han Isabel13,Sun Joan13,Jivani Manoj13,Liu Young13,Heineman Thomas13,Smith Stephen D14

Affiliation:

1. Division of Hematology, Mayo Clinic, Rochester, MN, USA

2. Peking University Cancer Hospital & Institute, Beijing, PR China

3. Harbin Medical University Cancer Hospital, Harbin, PR China

4. Icahn School of Medicine at Mount Sinai, New York, NY, USA

5. The Second Hospital of Dalian Medical University, Dalian, PR China

6. Norton Cancer Institute, Louisville, KY, USA

7. University of Texas Southwestern Medical Center, Dallas, TX, USA

8. Affliliated Cancer Hospital of Zhengzhou University, Zhengzhou, PR China

9. Dartmouth-Hitchcock Medical Center, Lebanon, NH

10. Peking University Third Hospital, Beijing, PR China

11. Fudan University Shanghai Cancer Center, Shanghai, PR China

12. Columbia University Medical Center, New York, NY, USA

13. Denovo Biopharma LLC, San Diego, CA, USA

14. University of Washington/Fred Hutchinson Cancer Center, Seattle, WA, USA

Abstract

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

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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