Lalla Rajesh V
Section of Oral Medicine, University of Connecticut Health Center, 263, Farmington Avenue, Farmington, CT 06030-1605, USA.
Expert Rev Gastroenterol Hepatol. 2015 Feb;9(2):127-8. doi: 10.1586/17474124.2015.965146. Epub 2014 Oct 1.
Oral and gastrointestinal mucositis has emerged as an important toxicity of cancer therapy. In addition to supportive care measures, agents for the prevention or treatment of mucositis in specific patient populations are described in the evidence-based clinical practice guidelines published by the Multinational Association of Supportive Care in Cancer/International Society of Oral Oncology. However, there still remains an unmet clinical need for preventive and therapeutic agents in several patient populations. The successful development of such agents will rely on our improved understanding of the pathogenic mechanisms underlying mucositis. Studies are also underway on novel delivery mechanisms and risk prediction models that can facilitate the selective use of interventions for mucositis in a targeted and cost-effective manner. A large number of agents are at various stages in the clinical development pipeline. Enhanced management of this dose-limiting toxicity will allow the delivery of optimal cancer therapy and improve patient prognosis.
口腔和胃肠道黏膜炎已成为癌症治疗的一种重要毒性反应。除支持性护理措施外,多国癌症支持治疗协会/国际口腔肿瘤学会发布的循证临床实践指南中描述了用于特定患者群体预防或治疗黏膜炎的药物。然而,在一些患者群体中,对预防和治疗药物仍存在未满足的临床需求。此类药物的成功研发将依赖于我们对黏膜炎潜在致病机制的深入理解。目前也正在开展关于新型给药机制和风险预测模型的研究,这些研究能够以有针对性且具成本效益的方式促进黏膜炎干预措施的选择性使用。大量药物正处于临床开发的不同阶段。加强对这种剂量限制性毒性的管理将有助于提供最佳的癌症治疗并改善患者预后。