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Immune-related dissociated response as a specific atypical response pattern in solid tumors with immune checkpoint blockade

杜瓦卢马布 阿替唑单抗 无容量 医学 彭布罗利珠单抗 易普利姆玛 免疫疗法 阿维鲁单抗 免疫检查点 实体瘤疗效评价标准 封锁 肿瘤科 银耳霉素 免疫系统 内科学 临床试验 免疫学 临床研究阶段 受体
作者
Yaping Guan,Dongfeng Feng,Beibei Yin,Kun Li,Jun Wang
出处
期刊:Therapeutic Advances in Medical Oncology [SAGE Publishing]
卷期号:14: 17588359221096877-17588359221096877 被引量:27
标识
DOI:10.1177/17588359221096877
摘要

Immune checkpoint blockade using immune checkpoint inhibitors, including cytotoxic T-lymphocyte-associated antigen–4 and programmed cell death protein-1/programmed cell death ligand–1 inhibitors, has revolutionized systematic treatment for advanced solid tumors, with unprecedented survival benefit and tolerable toxicity. Nivolumab, pembrolizumab, cemiplimab, avelumab, durvalumab, atezolizumab, and ipilimumab are currently approved standard treatment options for various human cancer types. The response rate to immune checkpoint inhibitors, however, is unsatisfactory, and unexpectedly, atypical radiological responses, including delayed responses, pseudoprogression, hyperprogression, and dissociated responses (DRs), are observed in a small subgroup of patients. The benefit of immunotherapy for advanced patients who exhibit atypical responses is underestimated according to the conventional response evaluation criteria in solid tumors (RECIST). In particular, DR is considered a mixed radiological or heterogeneous response pattern when responding and nonresponding lesions or new lesions coexist simultaneously. The rate of DR reported in different studies encompass a wide range of 3.3–47.8% based on diverse definition of DR. Although DR is also associated with treatment efficacy and a favorable prognosis, it is different from pseudoprogression, which has concordant progressive lesions and can be regularly captured by immune RECIST. This review article aims to comprehensively determine the frequency, definition, radiological evaluation, probable molecular mechanisms, prognosis, and clinical management of immune-related DR and help clinicians and radiologists objectively and correctly interpret this specific atypical response and better understand and manage cancer patients with immunotherapy and guarantee their best clinical benefit.
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