CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:(18)F FDG PET/CT and Novel Molecular Imaging for Directing Immunotherapy in Cancer.
(18)F FDG PET/CT and Novel Molecular Imaging for Directing Immunotherapy in Cancer.
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免疫治疗已经改变了多种癌症的治疗格局,在既往预后不良的疾病中实现了持久缓解。患者选择仍然是一个挑战,预测性生物标志物是亟待满足的临床需求。当前的预测性生物标志物,包括程序性死亡配体1(PD-L1)(通过免疫组织化学检测),并不完美。有前景的生物标志物,包括肿瘤突变负荷和TIL(肿瘤浸润淋巴细胞)密度,未能一致地预测缓解,且尚未转化为常规临床实践。病灶内部和病灶之间免疫反应的异质性构成了进一步挑战,而氟18氟脱氧葡萄糖PET/CT在评估缓解、分层治疗以及检测和监测免疫相关毒性方面具有潜在作用。新型放射性药物也提供了独特机会,可界定免疫肿瘤微环境,以更好地预测哪些患者可能对治疗产生缓解,例如通过体内全身PD-L1和CD8+ T细胞表达成像。
此外,纵向分子成像可能有助于进一步界定动态变化,尤其是在免疫治疗耐药的情况下,帮助指导更个性化的治疗策略。本综述重点介绍了分子成像在临床需求领域中对分子动力学和治疗反应进行分层、预测和监测的当前及新兴应用。
Immunotherapy has transformed the treatment landscape of many cancers, with durable responses in disease previously associated with a poor prognosis. Patient selection remains a challenge, with predictive biomarkers an urgent unmet clinical need. Current predictive biomarkers, including programmed death-ligand 1 (PD-L1) (measured with immunohistochemistry), are imperfect. Promising biomarkers, including tumor mutation burden and tumor infiltrating lymphocyte density, fail to consistently predict response and have yet to translate to routine clinical practice.
Heterogeneity of immune response within and between lesions presents a further challenge where fluorine 18 fluorodeoxyglucose PET/CT has a potential role in assessing response, stratifying treatment, and detecting and monitoring immune-related toxicities. Novel radiopharmaceuticals also present a unique opportunity to define the immune tumor microenvironment to better predict which patients may respond to therapy, for example by means of in vivo whole-body PD-L1 and CD8+ T cell expression imaging.
In addition, longitudinal molecular imaging may help further define dynamic changes, particularly in cases of immunotherapy resistance, helping to direct a more personalized therapeutic approach. This review highlights current and emerging applications of molecular imaging to stratify, predict, and monitor molecular dynamics and treatment response in areas of clinical need.
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