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- Luming Zheng, Ling Li, Qingqing He, Meng Wang, Yunhan Ma, Jian Zhu, Yanchen Li, Xiaokang Fu, and Yaxuan Zhang.
- Department of General Surgery, 960th Hospital of the People's Liberation Army, Jinan, Shandong, P. R. China.
- Medicine (Baltimore). 2021 Aug 13; 100 (32): e26138e26138.
RationaleAnaplastic thyroid carcinoma (ATC) is an aggressive malignancy that is almost always fatal and lacks effective systemic treatment options. Current treatments of ATC include surgery, radiation, and chemotherapy, used in combination when possible. In the aspect of immunotherapy, the biomarker of TMB-H and MSI-H may suggest that patients benefit from pembrolizumab. Programmed cell death-ligand 1 (PD-L1) is highly expressed in ATC but has not been written into the guidelines or approved by the FDA as a biomarker for thyroid cancer immunotherapy.Patient ConcernsA 55-year-old woman was admitted to our hospital because of a slight right-sided neck enlargement in November 2019.DiagnosesThe clinical diagnosis was ATC, pT3bN0M0, and stage IVB.InterventionsOral administration of apatinib (250 mg 3 times daily) was initiated after surgery, but some unpleasant side effects emerged after 1 month of treatment. Next-generation sequencing revealed that the tumor harbored 2 mutations, HRAS p.Q61R and TP53 p.P278S, and PD-L1 staining was positive with a high expression. Thus, camrelizumab (programmed cell death protein 1 inhibitor) was combined with apatinib, and apatinib was changed to 250 mg once a day from March 2020.OutcomesNo adverse reactions were observed after the treatment immunotherapy combined with antiangiogenic drugs. Currently, the survival time of patients is more than 11 months, and the quality of life is not affected.ConclusionThis case suggests that immunotherapy in patients with ATC based upon PD-L1 evaluation provides a therapeutic option. Targeting programmed cell death protein 1/PD-L1 may provide a much-needed treatment option for patients with advanced ATC.Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc.
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