PMID- 35116347 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220205 IS - 2219-6803 (Electronic) IS - 2218-676X (Print) IS - 2218-676X (Linking) VI - 10 IP - 11 DP - 2021 Nov TI - Treatment beyond progression with chemo-immunotherapy in an advanced esophageal squamous cell carcinoma patient: a case report. PG - 4973-4978 LID - 10.21037/tcr-21-1395 [doi] AB - Esophageal cancer is an aggressive and common malignancy in Asian countries. Due to late diagnosis and limited treatments, the prognosis of esophageal cancer is still very poor. Although immune checkpoint inhibitors have become promising second-line treatments for esophageal cancer, there are limited evidences for first-line treatments. Here, we reported a case of successful treatment beyond progression with chemo-immunotherapy for esophageal squamous cell carcinoma (ESCC). Combined with local resection of several metastases during chemo-immunotherapy, the patient achieved a long survival time of 22 months and a good quality of life. Samples of the primary tumor and three metastases of testicle, skin nodule and left adrenal were obtained to perform whole exome sequencing (WES), RNA sequencing and immunohistochemistry. The skin nodule metastasis was resected after partial response, while the other two metastases of testicle and adrenal gland were removed after disease progression. Immunohistochemistry results exhibited low/negative PD-L1 expression and WES results showed intermediate TMB and MSI-L for all three lesions. However, RNA sequencing results presented a higher percentage of infiltrating CD8(+) T cells, higher signature scores of T cell status and higher expression level of human leukocyte antigen (HLA) genes in skin nodule metastasis than the other two metastases. This case provided a clinical evidence of beneficial treatment beyond progression with chemo-immunotherapy for ESCC. In addition, tumor microenvironment might be essential for clinical responses at the sampling time point. CI - 2021 Translational Cancer Research. All rights reserved. FAU - Peng, Ping AU - Peng P AD - Department of Oncology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. FAU - Xiao, Yajie AU - Xiao Y AD - YuceBio Technology Co., Ltd., Shenzhen, China. FAU - Zhao, Zhikun AU - Zhao Z AD - YuceBio Technology Co., Ltd., Shenzhen, China. FAU - Sun, Chao AU - Sun C AD - YuceBio Technology Co., Ltd., Shenzhen, China. FAU - Wu, Dongfang AU - Wu D AD - YuceBio Technology Co., Ltd., Shenzhen, China. FAU - Chen, Yuan AU - Chen Y AD - Department of Oncology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. FAU - Zhang, Li AU - Zhang L AD - Department of Oncology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. LA - eng PT - Case Reports PL - China TA - Transl Cancer Res JT - Translational cancer research JID - 101585958 PMC - PMC8798522 OTO - NOTNLM OT - Esophageal squamous cell carcinoma (ESCC) OT - case report OT - chemo-immunotherapy OT - treatment beyond progression OT - tumor microenvironment COIS- Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://dx.doi.org/10.21037/tcr-21-1395). PP, YC, and LZ report that since the initial planning of the work, this study was funded by the Wu Jieping Medical Foundation (320.6750.19078), Chinese Society of Clinical Oncology Foundation (Y-BMS2019-070) and Hubei Provincial Natural Science Foundation of China (grant No. 2019CFB544). No other funding or supports were obtained for the past 36 months. The other authors have no conflicts of interest to declare. EDAT- 2022/02/05 06:00 MHDA- 2022/02/05 06:01 PMCR- 2021/11/01 CRDT- 2022/02/04 05:48 PHST- 2021/07/23 00:00 [received] PHST- 2021/10/15 00:00 [accepted] PHST- 2022/02/04 05:48 [entrez] PHST- 2022/02/05 06:00 [pubmed] PHST- 2022/02/05 06:01 [medline] PHST- 2021/11/01 00:00 [pmc-release] AID - tcr-10-11-4973 [pii] AID - 10.21037/tcr-21-1395 [doi] PST - ppublish SO - Transl Cancer Res. 2021 Nov;10(11):4973-4978. doi: 10.21037/tcr-21-1395.