Haris Mohammad, Bagga Puneet, Hariharan Hari, McGettigan-Croce Bevin, Johnson Laura A, Reddy Ravinder
Center for Magnetic Resonance and Optical Imaging (CMROI), Department of Radiology, Perelman School of Medicine at the University of Pennsylvania, B1 Stellar-Chance Laboratories, 422 Curie Boulevard, Philadelphia, PA, 19104-6100, USA.
Translational Medicine, Sidra Medical and Research Center, Doha, Qatar.
J Transl Med. 2017 Jun 19;15(1):140. doi: 10.1186/s12967-017-1240-6.
While many decades of scientific research studies have gone into harnessing the power of the immune system to fight cancer, only recently have cancer immunotherapeutic approaches begun to show robust clinical responses in patients with a variety of cancers. These treatments are adding to the current arsenal of cancer treatments; surgery, radiation and chemotherapy, and increasing the therapeutic options for cancer patients. Despite these advances, issues associated with these therapies include that not all patients respond to these therapies, and some patients who respond experience varying degrees of toxicities. One of the major issues affecting immunotherapy is the inability to evaluate trafficking of activated T-cells into sites of tumor. The current diagnostic imaging based on conventional anatomic imaging, which is the mainstay to monitor response to cytotoxic chemotherapy or radiation, is not adequate to assess initial response to immunotherapy or disease evolution. Patients' prognosis by histological analysis has limited use in regards to immunotherapy. Thus, there is a crucial need for noninvasive biomarkers for screening patients that show long term response to therapy. Here, we provide a brief account of emerging molecular magnetic resonance imaging biomarkers that have potential to exploit the metabolism and metabolic products of activated T cells.
尽管数十年来一直在进行科学研究,以利用免疫系统的力量对抗癌症,但直到最近,癌症免疫治疗方法才开始在患有各种癌症的患者中显示出强大的临床反应。这些治疗方法正在增加当前的癌症治疗手段,如手术、放疗和化疗,并为癌症患者增加了治疗选择。尽管取得了这些进展,但与这些疗法相关的问题包括并非所有患者都对这些疗法有反应,而且一些有反应的患者会经历不同程度的毒性。影响免疫治疗的主要问题之一是无法评估活化T细胞向肿瘤部位的迁移。基于传统解剖成像的当前诊断成像,是监测对细胞毒性化疗或放疗反应的主要手段,但不足以评估对免疫治疗的初始反应或疾病进展。通过组织学分析判断患者的预后在免疫治疗方面的用途有限。因此,迫切需要用于筛选对治疗有长期反应的患者的非侵入性生物标志物。在此,我们简要介绍新兴的分子磁共振成像生物标志物,这些生物标志物有可能利用活化T细胞的代谢和代谢产物。