Bachour Petra C, Sonis Stephen T
Harvard School of Dental Medicine, Boston.
Brigham and Women's Hospital and the Dana-Farber Cancer Institute, Boston.
Curr Opin Support Palliat Care. 2018 Jun;12(2):198-210. doi: 10.1097/SPC.0000000000000339.
The goals of this review are to describe the complexity of factors influencing the risk of cancer regimen-related mucosal injury (CRRMI), to evaluate the contribution of the innate immune response to CRRMI risk, to compare the concordance of genome analytics in describing mechanism and risk, and to determine if common biological pathways are noted when CRRMI is compared to a disease with a similar phenotype.
The pathogenesis of and risk for CRRMI are complex and influenced by multiple intrinsic and extrinsic factors. It is incumbent on analyses to recognize the likelihood that the interplay and cross-talk of synergistically expressed factors is critical and that the contributing weights of these factors is not uniform from patient to patient. Genomically derived analyses imply final common pathways are implicit in phenotype expression.
The identification of specific factors (both genomic and otherwise) which contribute to CRRMI risk represents an important opportunity to apply principles of precision medicine to the management of regimen-related toxicities.
本综述的目标是描述影响癌症治疗相关黏膜损伤(CRRMI)风险的因素的复杂性,评估先天免疫反应对CRRMI风险的作用,比较基因组分析在描述机制和风险方面的一致性,并确定将CRRMI与具有相似表型的疾病进行比较时是否能发现共同的生物学途径。
CRRMI的发病机制和风险很复杂,受多种内在和外在因素影响。分析工作必须认识到协同表达的因素之间的相互作用和相互影响很关键,而且这些因素对不同患者的影响权重并不一致。基因组分析表明最终的共同途径隐含在表型表达中。
确定导致CRRMI风险的特定因素(包括基因组因素及其他因素)是将精准医学原则应用于治疗相关毒性管理的重要契机。