Owosho Adepitan A, DeColibus Katherine A, Okhuaihesuyi Osariemen, Levy Layne C
Department of Diagnostic Sciences, College of Dentistry/Department of Otolaryngology-Head & Neck Surgery, College of Medicine, The University of Tennessee Health Sciences Center, 875 Union Avenue, Memphis, TN 38163, USA.
Department of Diagnostic Sciences, College of Dentistry, The University of Tennessee Health Sciences Center, Memphis, TN 38163, USA.
Dent J (Basel). 2024 Mar 22;12(4):83. doi: 10.3390/dj12040083.
Osteoradionecrosis of the jaw is a morbid complication of radiotherapy in patients with oral and oropharyngeal cancers that may be precipitated by dental extractions. Pentoxifylline and tocopherol (PENTO) has been utilized in the management of osteoradionecrosis and as prophylaxis for post-radiated head and neck oncology patients requiring an invasive dental procedure. This observational study aims to report the outcome of the prophylactic use of PENTO in the prevention of osteoradionecrosis of the jaw after dental extractions in post-radiated oral and oropharyngeal cancer patients and to review the current literature on this topic. Four post-radiated oral and oropharyngeal oncology patients were referred to the dental oncology clinic of the University Dental Practice, University of Tennessee Health Sciences Center for dental extractions. All four patients were prescribed pentoxifylline 400 mg BID (twice a day) and tocopherol 400 IU BID (oral tablets) for 2 weeks before extraction(s) and for 6 weeks after extraction(s). All patients were followed up every week after the second week post-extraction if feasible until the extraction site(s) healed (covered by mucosa). The assessment endpoint was defined as 6 weeks post-extraction with the outcomes assessed as using four categories determined by the area of exposed bone: complete healing (complete mucosal coverage of extraction site); partial healing (reduction in size of extraction site); no change; and progression (increase in size of the extraction site). At the assessment endpoint, all patients had complete healing of all extraction sites. The ORN rate at the patient level (0/4) and individual tooth level (0/8) was 0%. All patients tolerated the PENTO medications and no adverse effects from the use of these medications were reported. This limited study in addition to the other reviewed studies estimates the rate of ORN at the patient level as 3.2% (14/436) for post-radiated head and neck oncology patients after dental extractions/invasive oral procedures. In conclusion, this PENTO regimen can reduce/prevent the incidence of ORN in post-radiated head and neck oncology patients. This safe and cost-effective protocol (PENTO regimen) should be further evaluated as prophylaxis for post-radiated head and neck oncology patients requiring an invasive dental procedure. We recommend large prospective studies to be carried out to further validate these findings.
颌骨放射性骨坏死是口腔和口咽癌患者放疗后的一种严重并发症,拔牙可能会诱发该病。己酮可可碱和生育酚(PENTO)已被用于治疗颌骨放射性骨坏死,并作为需要进行侵入性牙科手术的放疗后头颈肿瘤患者的预防用药。这项观察性研究旨在报告预防性使用PENTO预防放疗后口腔和口咽癌患者拔牙后颌骨放射性骨坏死的效果,并回顾关于该主题的现有文献。四名放疗后的口腔和口咽肿瘤患者被转诊至田纳西大学健康科学中心大学牙科诊所的牙科肿瘤科进行拔牙。所有四名患者在拔牙前2周和拔牙后6周均被开了己酮可可碱400毫克,每日两次(一天两次)和生育酚400国际单位,每日两次(口服片剂)。如果可行,所有患者在拔牙后第二周后每周进行随访,直至拔牙部位愈合(被黏膜覆盖)。评估终点定义为拔牙后6周,结果根据暴露骨面积分为四类进行评估:完全愈合(拔牙部位完全被黏膜覆盖);部分愈合(拔牙部位尺寸缩小);无变化;进展(拔牙部位尺寸增大)。在评估终点,所有患者的所有拔牙部位均完全愈合。患者层面(0/4)和单个牙齿层面(0/8)的ORN发生率均为0%。所有患者都耐受PENTO药物,未报告使用这些药物产生的不良反应。除其他综述研究外,这项有限的研究估计,放疗后头颈肿瘤患者拔牙/侵入性口腔手术后患者层面的ORN发生率为3.2%(14/436)。总之,这种PENTO方案可以降低/预防放疗后头颈肿瘤患者ORN的发生率。这种安全且具有成本效益的方案(PENTO方案)应作为需要进行侵入性牙科手术的放疗后头颈肿瘤患者的预防措施进行进一步评估。我们建议开展大型前瞻性研究以进一步验证这些发现。