Current Status of Recombinant Human Bone Morphogenetic Protein-2 (rhBMP-2) in Maxillofacial Surgery: Should It Be Continued?

Recombinant human bone morphogenetic protein-2 (rhBMP-2) has shown potential in maxillofacial surgery owing to its osteoinductive properties. However, concerns about its safety and high cost have limited its widespread use. This review presents the status of rhBMP-2 use in maxillofacial surgery, focusing on its clinical application, efficacy, safety, and limitations. Studies have demonstrated rhBMP-2's potential to reduce donor site morbidity and increase bone height in sinus and ridge augmentation; however, it may not outperform autogenous bone grafts. In medication-related osteonecrosis of the jaw treatment, rhBMP-2 has been applied adjunctively with promising results, although its long-term safety requires further investigation. However, in maxillofacial trauma, its application is limited to the restoration of large defects. Safety concerns include postoperative edema and the theoretical risk of carcinogenesis. Although postoperative edema is manageable, the link between rhBMP-2 and cancer remains unclear. The limitations include the lack of an ideal carrier, the high cost of rhBMP-2, and the absence of an optimal dosing regimen. In conclusion, rhBMP-2 is a promising graft material for maxillofacial surgery. However, it has not yet become the gold standard owing to safety and cost concerns. Further research is required to establish long-term safety, optimize dosing, and develop better carriers.

Automated summary

This review presents the current status of recombinant human bone morphogenetic protein-2 (rhBMP-2) in maxillofacial surgery, including its clinical application, efficacy, safety, and limitations. Studies have shown that rhBMP-2 has potential in reducing donor site complications and increasing bone height, but it may not be as effective as autogenous bone grafts. In the treatment of medication-related osteonecrosis of the jaw, rhBMP-2 has promising results but requires further investigation for long-term safety. In maxillofacial trauma, it is limited to large defect restoration. Safety concerns include postoperative edema and the theoretical risk of carcinogenesis. Limitations include the lack of an ideal carrier, high cost, and optimal dosing regimen.