Literature DB >> 28652196

Efficacy of Escherichia coli-derived recombinant human bone morphogenetic protein-2 in posterolateral lumbar fusion: an open, active-controlled, randomized, multicenter trial.

Jae Hwan Cho1, Jae Hyup Lee2, Jin Sup Yeom3, Bong-Soon Chang4, Jae Jun Yang5, Ki Hyoung Koo5, Chang Ju Hwang1, Kwang Bok Lee6, Ho-Joong Kim3, Choon-Ki Lee4, Hyoungmin Kim4, Kyung-Soo Suk7, Woo Dong Nam8, Jumi Han9.   

Abstract

BACKGROUND CONTEXT: The efficacy and safety of recombinant human bone morphogenetic protein-2 (rhBMP-2) as a bone graft substitute in spinal fusion has been widely researched. However, no study of the efficacy and safety of Escherichia coli-derived rhBMP-2 (E.BMP-2) with a hydroxyapatite (HA) carrier has been proposed.
PURPOSE: This study aimed to compare the efficacy and safety of fusion materials between E.BMP-2 and autogenous iliac bone graft in posterolateral fusion (PLF). STUDY DESIGN/
SETTING: An open, active-controlled, randomized, multicenter trial was carried out. PATIENT SAMPLE: This study included 93 patients who underwent single-level lumbar or lumbosacral PLF. OUTCOME MEASURES: The primary outcome measure was computed tomography (CT)-based fusion rate at 12 and 24 weeks. Secondary outcome measures were fusion grade by radiographs and CT at 12 and 24 weeks and changes in Oswestry Disability Index (ODI), Short Form-36 (SF-36) Health Survey, and visual analogue scale (VAS).
METHODS: Patients who underwent 1-level PLF (between L1 and S1) for severe spinal stenosis or grade 1 spondylolisthesis were randomized to receive E.BMP-2 with an HA carrier (E.BMP-2 group) or autogenous iliac bone graft (AIBG group). Thin-section CT (<2 mm), VAS, ODI, and SF-36 were obtained pre- and postoperatively at 12 and 24 weeks. Outcome measures were compared between the groups.
RESULTS: A total of 100 patients were enrolled in this trial. Among them, 93 patients underwent planned surgery. Preoperative demographic and clinical data showed no difference between groups. CT-based fusion rates were 100.0% (41/41) for the E.BMP-2 group and 90.2% (46/51) for the AIBG group (p=.062) at 12 weeks and 100.0% (41/41) and 94.1% (48/51) (p=.251) at 24 weeks, respectively. Fusion grade based on radiographs and CT showed non-inferiority of the E.BMP-2 group compared with the AIBG group. All clinical parameters improved postoperatively. However, there was no difference in changes in VAS, ODI, or SF-36 between the groups. No serious adverse event related to E.BMP-2 was found.
CONCLUSIONS: The fusion rate of E.BMP-2 was comparable with that of AIBG following PLF. Good clinical efficacy and safety of E.BMP-2 in spinal fusion were also revealed. It was also suggested that HA shows suitability as a carrier for E.BMP-2. Thus, E.BMP-2 with an HA carrier can be an alternative bone graft material in spinal fusion.
Copyright © 2017 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Carrier; Clinical trial; E. coli; Hydroxyapatite; Iliac bone graft; Lumbar; Posterolateral fusion; rhBMP-2

Mesh:

Substances:

Year:  2017        PMID: 28652196     DOI: 10.1016/j.spinee.2017.06.023

Source DB:  PubMed          Journal:  Spine J        ISSN: 1529-9430            Impact factor:   4.166


  12 in total

1.  A meta-analysis of bone morphogenetic protein-2 versus iliac crest bone graft for the posterolateral fusion of the lumbar spine.

Authors:  Gonzalo Mariscal; Jorge H Nuñez; Carlos Barrios; Pedro Domenech-Fernández
Journal:  J Bone Miner Metab       Date:  2019-07-10       Impact factor: 2.626

2.  Evaluation of an increased strut porosity silicate-substituted calcium phosphate, SiCaP EP, as a synthetic bone graft substitute in spinal fusion surgery: a prospective, open-label study.

Authors:  Ciaran Bolger; Drew Jones; Steven Czop
Journal:  Eur Spine J       Date:  2019-03-05       Impact factor: 3.134

Review 3.  Therapeutics for enhancement of spinal fusion: A mini review.

Authors:  Yidan Zhang; Yu Jiang; Da Zou; Baozhi Yuan; Hua Zhu Ke; Weishi Li
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4.  BMP-2 Induced Signaling Pathways and Phenotypes: Comparisons Between Senescent and Non-senescent Bone Marrow Mesenchymal Stem Cells.

Authors:  Jae Hwan Cho; Jae Hyup Lee; Kyung Mee Lee; Choon-Ki Lee; Dong-Myung Shin
Journal:  Calcif Tissue Int       Date:  2021-10-29       Impact factor: 4.333

5.  Safety and Efficacy of Recombinant Human Bone Morphogenetic Protein-2 in Multilevel Posterolateral Lumbar Fusion in a Prospective, Randomized, Controlled Trial.

Authors:  Ho Yong Choi; Seung-Jae Hyun; Chang Hyun Lee; Ji Hyun Youn; Mi Young Ryu; Ki-Jeong Kim
Journal:  Neurospine       Date:  2022-09-30

6.  Bone Morphogenetic Protein in Anterior Lumbar Interbody Fusions: A Propensity-Matched Medicare Outcome Analysis.

Authors:  Syed I Khalid; Ravi S Nunna; Rachyl M Shanker; Kyle B Thomson; Rown Parola; Owoicho Adogwa; Ankit I Mehta
Journal:  Int J Spine Surg       Date:  2022-06-14

7.  Effectiveness and Feasibility of Injectable Escherichia coli-Derived Recombinant Human Bone Morphogenetic Protein-2 for Anterior Lumbar Interbody Fusion at the Lumbosacral Junction in Adult Spinal Deformity Surgery: A Clinical Pilot Study.

Authors:  Sang-Kyu Im; Jung-Hee Lee; Ki Young Lee; Seung-Jin Yoo
Journal:  Orthop Surg       Date:  2022-05-27       Impact factor: 2.279

8.  Superiority Claims for Spinal Devices: A Systematic Review of Randomized Controlled Trials.

Authors:  S Raymond Golish; Michael W Groff; Ali Araghi; Jason A Inzana
Journal:  Global Spine J       Date:  2019-06-07

9.  Comparative Clinical Effectiveness and Safety of Bone Morphogenetic Protein Versus Autologous Iliac Crest Bone Graft in Lumbar Fusion: A Meta-analysis and Systematic Review.

Authors:  Shichao Liu; Yinqing Wang; Zeyan Liang; Maochao Zhou; Chunmei Chen
Journal:  Spine (Phila Pa 1976)       Date:  2020-06-15       Impact factor: 3.241

Review 10.  Bone regeneration strategies: Engineered scaffolds, bioactive molecules and stem cells current stage and future perspectives.

Authors:  Antalya Ho-Shui-Ling; Johanna Bolander; Laurence E Rustom; Amy Wagoner Johnson; Frank P Luyten; Catherine Picart
Journal:  Biomaterials       Date:  2018-07-11       Impact factor: 12.479

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