| Literature DB >> 26547659 |
Masahiro Kitamura1, Motoki Akamatsu2, Masamitsu Kawanami3, Yasushi Furuichi4, Takeo Fujii5, Mari Mori4, Kazushi Kunimatsu6, Hidetoshi Shimauchi7, Yorimasa Ogata8, Matsuo Yamamoto9, Taneaki Nakagawa10, Shuichi Sato11, Koichi Ito11, Takefumi Ogasawara12, Yuichi Izumi13, Kazuhiro Gomi14, Kazuhisa Yamazaki15, Hiromasa Yoshie15, Mitsuo Fukuda16, Toshihide Noguchi17, Shogo Takashiba18, Hidemi Kurihara19, Toshihiko Nagata20, Takafumi Hamachi21, Katsumasa Maeda22, Makoto Yokota22, Ryuji Sakagami23, Yoshitaka Hara24, Kazuyuki Noguchi25, Toshi Furuuchi7, Takashi Sasano7, Enyu Imai26, Masatoshi Ohmae27, Hayuru Koizumi2, Mitsuru Watanuki2, Shinya Murakami1.
Abstract
We investigated the efficacy, safety, and clinical significance of trafermin, a recombinant human fibroblast growth factor (rhFGF)-2, for periodontal regeneration in intrabony defects in Phase III trials. Study A, a multicenter, randomized, double-blind, placebo-controlled study, was conducted at 24 centers. Patients with periodontitis with 4-mm and 3-mm or deeper probing pocket depth and intrabony defects, respectively, were included. A total of 328 patients were randomly assigned (2:1) to receive 0.3% rhFGF-2 or placebo, and 323 patients received the assigned investigational drug during flap surgery. One of the co-primary endpoints, the percentage of bone fill at 36 weeks after drug administration, was significantly greater in the rhFGF-2 group at 37.131% (95% confidence interval [CI], 32.7502 to 41.5123; n = 208) than it was in the placebo group at 21.579% (95% CI, 16.3571 to 26.8011; n = 100; p < 0.001). The other endpoint, the clinical attachment level regained at 36 weeks, was not significantly different between groups. Study B, a multicenter, randomized, blinded (patients and evaluators of radiographs), and active-controlled study was conducted at 15 centers to clarify the clinical significance of rhFGF-2. Patients with 6-mm and 4-mm or deeper probing pocket depth and intrabony defects, respectively, were included. A total of 274 patients were randomly assigned (5:5:2) to receive rhFGF-2, enamel matrix derivative (EMD), or flap surgery alone. A total of 267 patients received the assigned treatment during flap surgery. The primary endpoint, the linear alveolar bone growth at 36 weeks, was 1.927 mm (95% CI, 1.6615 to 2.1920; n = 108) in the rhFGF-2 group and 1.359 mm (95% CI, 1.0683 to 1.6495; n = 109) in the EMD group, showing non-inferiority (a prespecified margin of 0.3 mm) and superiority of rhFGF-2 to EMD. Safety problems were not identified in either study. Therefore, trafermin is an effective and safe treatment for periodontal regeneration in intrabony defect, and its efficacy was superior in rhFGF-2 compared to EMD treatments.Entities:
Keywords: CELL/TISSUE SIGNALING; CLINICAL TRIALS; CYTOKINES; DENTAL BIOLOGY; ENDOCRINE PATHWAYS
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Year: 2015 PMID: 26547659 DOI: 10.1002/jbmr.2738
Source DB: PubMed Journal: J Bone Miner Res ISSN: 0884-0431 Impact factor: 6.741