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作 者:Hong-Yu Yang Yu-Xuan Du Yu-Jia Hou Dian-Rong Lu Peng Xue
机构地区:[1]Department of Oncology,Wangjing Hospital,China Academy of Chinese Medical Sciences,Beijing 100000,China [2]Department of Oncology,Tianjin University of Chinese Medicine,Tianjin 300000,China [3]Traditional Chinese Medical Science,Tianjin University of Chinese Medicine,Tianjin 300000,China
出 处:《World Journal of Clinical Cases》2023年第28期6841-6849,共9页世界临床病例杂志
基 金:Supported by the National Natural Science Foundation,No.81973640.
摘 要:BACKGROUND Immune checkpoint inhibitors,including programmed death-ligand 1(PD-L1)and programmed death-1(PD-1)have recently been approved to treat locally advanced and metastatic urothelial carcinoma(UC).However,some patients experience rapid tumor progression rather than any clinical benefit from anti-PDL1/PD-1 therapy.CASE SUMMARY A 73-year-old woman with bladder UC showed the progression of multiple metastases after surgery and chemotherapy for over 12 mo.The patient could not tolerate further chemotherapy.Next-generation sequencing was performed,and the results indicated that the tumor mutational burden was 6.4 mutations/Mb.The patient received the anti-PD-L1 agent toripalimab combined with albuminbound paclitaxel.Compared with the baseline staging before immunotherapy,the patient had a treatment failure time of<2 mo,an increase in tumor burden of>50%,and a>2-fold increase in progression,indicating hyperprogression.CONCLUSION Selecting patients most likely to respond to treatment with immunotherapeutic agents remains challenging.For older patients with advanced UC who have already exhausted multi-line chemotherapy options,immunotherapy should be used prudently if no effective biomarker is available.Further studies are required to clarify the causes and mechanisms of hyperprogression.
关 键 词:Bladder urothelial carcinoma Hyperprogression IMMUNOTHERAPY Toripalimab Case report
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