Basu Bhakti, Basu Sandip
1 Molecular Biology Division, Bhabha Atomic Research Centre , Mumbai, India .
2 Radiation Medicine Centre , Bhabha Atomic Research Centre, Mumbai, India .
Cancer Biother Radiopharm. 2016 Apr;31(3):75-84. doi: 10.1089/cbr.2015.1922.
Recently, there has been an increasing interest in personalized approach in cancer management. Two developments could be regarded important for realization of this concept: (1) new biomarkers and (2) in vivo molecular tracers for both positron emission tomography and single photon emission computed tomography. Both approaches are successful in exploring tumor biology individually and can serve as tools to better stratify tumors for potential personalized medicine. The fundamental concept comes from the observation that one treatment does not work for all patients, even those with similar histopathology, essentially because of varying tumor genotype and phenotypic behavior pattern in each individual. Clinically validated biomarkers and tracers allow physicians to determine which patient may benefit from a particular therapy. Despite progress in the past decade, the concept is still in the early stages of clinical translation. In this review, the authors hypothesize the feasibility of integration of these two powerful techniques, which could lead to a faster translation and provide a more reliable basis toward the personalized approach in oncology. The authors believe that clinically validated biomarkers and tracers would allow physicians to determine which patients may benefit from personalized therapy. The logistics and implications of this combined approach for the day-to-day clinical oncology practice are discussed with special emphasis on neuroendocrine tumors, which demonstrates widely variable tumor biology. A logical way is also illustrated to explain how biomarkers and in vivo tracers could be complemented in a clinical workflow.
最近,癌症管理中的个性化方法越来越受到关注。对于实现这一概念而言,有两个进展可被视为重要因素:(1)新的生物标志物;(2)用于正电子发射断层扫描和单光子发射计算机断层扫描的体内分子示踪剂。这两种方法在单独探索肿瘤生物学方面都取得了成功,并且可以作为工具,更好地对肿瘤进行分层,以实现潜在的个性化医疗。其基本概念源于这样的观察结果:即使对于组织病理学相似的患者,一种治疗方法也并非对所有患者都有效,这主要是因为每个个体的肿瘤基因型和表型行为模式各不相同。经过临床验证的生物标志物和示踪剂使医生能够确定哪些患者可能从特定治疗中获益。尽管在过去十年中取得了进展,但这一概念仍处于临床转化的早期阶段。在本综述中,作者假设整合这两种强大技术的可行性,这可能会加快转化速度,并为肿瘤学中的个性化方法提供更可靠的基础。作者认为,经过临床验证的生物标志物和示踪剂将使医生能够确定哪些患者可能从个性化治疗中获益。本文讨论了这种联合方法在日常临床肿瘤学实践中的后勤保障和影响,并特别强调了神经内分泌肿瘤,这类肿瘤表现出广泛多样的肿瘤生物学特性。文中还阐述了一种合理的方式,以解释生物标志物和体内示踪剂在临床工作流程中如何相互补充。