PMID- 35845479 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220719 IS - 2305-5839 (Print) IS - 2305-5847 (Electronic) IS - 2305-5839 (Linking) VI - 10 IP - 12 DP - 2022 Jun TI - Efficacy and safety of combined treatment with pembrolizumab in patients with locally advanced or metastatic esophageal squamous cell carcinoma in the real world. PG - 708 LID - 10.21037/atm-22-2779 [doi] LID - 708 AB - BACKGROUND: Treatments for patients with advanced esophageal cancer are still limited. Pembrolizumab has demonstrated antitumor activity in patients with advanced esophageal cancer in previous studies. Few studies have assessed safety and efficacy in routine clinical practice. We investigated the real-world outcomes of pembrolizumab for patients with advanced esophageal cancer. METHODS: This retrospective, observational study collected 57 advanced esophageal squamous cell carcinoma (ESCC) patients from October 1, 2019 to October 1, 2021, 57 who received different patterns of treatments according to the staging were collected. Briefly, patients diagnosed with locally advanced and surgically resectable ESCC received neoadjuvant therapy followed by surgery. For patients with locally advanced, unresectable ESCC, the treatment regimen including chemoradiotherapy combined with pembrolizumab was performed. Patients with metastatic ESCC or those not suitable for radiotherapy received pembrolizumab plus chemotherapy. Safety was assessed in all treated patients. The objective response rate (ORR) was used to evaluate the efficacy. RESULTS: The ORR was 74.1% (40/54) among all patients. The most common adverse events (AEs) were leukopenia (36.8%, 21/57), nausea (28.1%, 16/57), and thrombocytopenia (14%, 8/57). Grade III and higher AEs were observed in 9 of the 57 patients (15.8%). CONCLUSIONS: For patients with advanced ESCC, combined treatment with pembrolizumab was effective and safe. Multicenter studies should be carried out for further confirmation. CI - 2022 Annals of Translational Medicine. All rights reserved. FAU - Zhang, Pei AU - Zhang P AD - Department of Radiotherapy, The First Medical Center of Chinese PLA General Hospital, Beijing, China. FAU - Hou, Xiaobin AU - Hou X AD - Department of Thoracic Surgery, The First Medical Center of Chinese PLA General Hospital, Beijing, China. FAU - Cai, Boning AU - Cai B AD - Department of Radiotherapy, The First Medical Center of Chinese PLA General Hospital, Beijing, China. FAU - Yu, Wei AU - Yu W AD - Department of Radiotherapy, The First Medical Center of Chinese PLA General Hospital, Beijing, China. FAU - Chen, Jing AU - Chen J AD - Department of Radiotherapy, The First Medical Center of Chinese PLA General Hospital, Beijing, China. FAU - Huang, Xiang AU - Huang X AD - Department of Radiotherapy, The First Medical Center of Chinese PLA General Hospital, Beijing, China. FAU - Li, Ye AU - Li Y AD - Department of Radiotherapy, The First Medical Center of Chinese PLA General Hospital, Beijing, China. FAU - Zeng, Mingyue AU - Zeng M AD - Department of Radiotherapy, The First Medical Center of Chinese PLA General Hospital, Beijing, China. FAU - Ren, Zhipeng AU - Ren Z AD - Department of Thoracic Surgery, The First Medical Center of Chinese PLA General Hospital, Beijing, China. FAU - Gabriel, Emmanuel AU - Gabriel E AD - Department of Surgery, Division of Surgical Oncology, Mayo Clinic, Jacksonville, FL, USA. FAU - Qu, Baolin AU - Qu B AD - Department of Radiotherapy, The First Medical Center of Chinese PLA General Hospital, Beijing, China. FAU - Liu, Fang AU - Liu F AD - Department of Radiotherapy, The First Medical Center of Chinese PLA General Hospital, Beijing, China. LA - eng PT - Journal Article PL - China TA - Ann Transl Med JT - Annals of translational medicine JID - 101617978 PMC - PMC9279766 OTO - NOTNLM OT - Esophageal cancer OT - pembrolizumab OT - real-world analysis COIS- Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://atm.amegroups.com/article/view/10.21037/atm-22-2779/coif). The authors have no conflicts of interest to declare. EDAT- 2022/07/19 06:00 MHDA- 2022/07/19 06:01 PMCR- 2022/06/01 CRDT- 2022/07/18 03:50 PHST- 2022/04/01 00:00 [received] PHST- 2022/06/20 00:00 [accepted] PHST- 2022/07/18 03:50 [entrez] PHST- 2022/07/19 06:00 [pubmed] PHST- 2022/07/19 06:01 [medline] PHST- 2022/06/01 00:00 [pmc-release] AID - atm-10-12-708 [pii] AID - 10.21037/atm-22-2779 [doi] PST - ppublish SO - Ann Transl Med. 2022 Jun;10(12):708. doi: 10.21037/atm-22-2779.