PMID- 36742383 OWN - NLM STAT- MEDLINE DCOM- 20230207 LR - 20240102 IS - 1664-2392 (Print) IS - 1664-2392 (Electronic) IS - 1664-2392 (Linking) VI - 14 DP - 2023 TI - A real-world study of anlotinib combined with GS regimen as first-line treatment for advanced pancreatic cancer. PG - 1110624 LID - 10.3389/fendo.2023.1110624 [doi] LID - 1110624 AB - BACKGROUND: Anlotinib may boost the efficacy of pancreatic cancer (PC) treatment if timely added to the GS regimen (Gemcitabine, Tegafur-gimeracil-oteracil potassium); however, no data has been published. This study evaluated the safety and efficacy of anlotinib in combination with the GS regimen(hereafter referred to as the A+GS regimen) in the first-line treatment of patients with unresectable or metastatic PC. METHODS: Patients with unresectable or metastatic PC treated at Yueyang Central Hospital and Yueyang People's Hospital between October 2018 and June 2022 were enrolled in this retrospective real-world investigation. Treatment efficacy was evaluated based on the overall survival (OS), progression-free survival (PFS), disease control rate (DCR), and objective response rate (ORR), while the treatment safety was assessed by the frequency of major adverse events (AEs). RESULTS: Seventy-one patients were included in this study, 41 in the GS group and 30 in the A+GS group. The A+GS group had a longer mPFS than the GS group (12.0 months (95% CI, 6.0-18.0) and 6.0 months (95% CI, 3.0-8.1)), respectively (P = 0.005). mOS was longer in the GS+A group) when compared with the GS group (17.0 months (95%CI, 14.0-20.0) and 10.0 months (95% CI, 7.5-12.5)), respectively (P = 0.018). The GS+A group had higher ORR (50.0% vs 26.8%, P = 0.045) and DCR (83.3% vs 58.5%, P = 0.026). Furthermore, there were no grade 4-5 AEs and no treatment-related deaths, and no discernible increase in AEs in the GS+A group when compared with the GS group. CONCLUSION: The A+GS regimen therapy holds great promise in managing treatment-naive advanced PC, except that future prospective studies with larger sample sizes and multiple centers are required to determine its efficacy and safety. CI - Copyright (c) 2023 Zhan, Hu, Da, Weng, Zhou, Wen, Liu, Fang, Shen, Zhou, Luo, Xu, Zhan and Su. FAU - Zhan, Gouling AU - Zhan G AD - Department of Oncology, Yueyang Central Hospital, Yueyang, China. AD - Department of Oncology, Third Xiangya Hospital, Central South University, Changsha, China. FAU - Hu, Jianbing AU - Hu J AD - Department of Oncology, Yueyang Central Hospital, Yueyang, China. FAU - Da, Shijian AU - Da S AD - Department of Oncology, Yueyang Central Hospital, Yueyang, China. FAU - Weng, Jie AU - Weng J AD - Department of Oncology, Yueyang Central Hospital, Yueyang, China. FAU - Zhou, Chuanyi AU - Zhou C AD - Department of Oncology, Yueyang People's Hospital, Yueyang, China. FAU - Wen, Fang AU - Wen F AD - Department of Oncology, Yueyang Central Hospital, Yueyang, China. FAU - Liu, Songlian AU - Liu S AD - Department of Oncology, Yueyang Central Hospital, Yueyang, China. FAU - Fang, Fang AU - Fang F AD - Department of Oncology, Yueyang Central Hospital, Yueyang, China. FAU - Shen, Erdong AU - Shen E AD - Department of Oncology, Yueyang Central Hospital, Yueyang, China. FAU - Zhou, Qiang AU - Zhou Q AD - Department of Oncology, Yueyang Central Hospital, Yueyang, China. FAU - Luo, Pan AU - Luo P AD - Department of Oncology, Yueyang Central Hospital, Yueyang, China. FAU - Xu, Min AU - Xu M AD - Department of Hepatobiliary Surgery, Yueyang Central Hospital, Yueyang, China. FAU - Zhan, Dahe AU - Zhan D AD - Department of Oncology, Yueyang Central Hospital, Yueyang, China. FAU - Su, Yuqi AU - Su Y AD - Department of Oncology, Yueyang Central Hospital, Yueyang, China. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20230120 PL - Switzerland TA - Front Endocrinol (Lausanne) JT - Frontiers in endocrinology JID - 101555782 RN - 0 (anlotinib) RN - 1548R74NSZ (Tegafur) SB - IM MH - Humans MH - Prospective Studies MH - Retrospective Studies MH - *Tegafur/adverse effects MH - Antineoplastic Combined Chemotherapy Protocols/therapeutic use/adverse effects MH - *Pancreatic Neoplasms/pathology PMC - PMC9897321 OTO - NOTNLM OT - GS regimen OT - anlotinib OT - efficacy OT - overall survival OT - pancreatic cancer OT - progression-free survival OT - safety COIS- The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. EDAT- 2023/02/07 06:00 MHDA- 2023/02/08 06:00 PMCR- 2023/01/01 CRDT- 2023/02/06 03:45 PHST- 2022/11/29 00:00 [received] PHST- 2023/01/04 00:00 [accepted] PHST- 2023/02/06 03:45 [entrez] PHST- 2023/02/07 06:00 [pubmed] PHST- 2023/02/08 06:00 [medline] PHST- 2023/01/01 00:00 [pmc-release] AID - 10.3389/fendo.2023.1110624 [doi] PST - epublish SO - Front Endocrinol (Lausanne). 2023 Jan 20;14:1110624. doi: 10.3389/fendo.2023.1110624. eCollection 2023.