PMID- 35846304 OWN - NLM STAT- MEDLINE DCOM- 20220719 LR - 20220802 IS - 1664-2392 (Print) IS - 1664-2392 (Electronic) IS - 1664-2392 (Linking) VI - 13 DP - 2022 TI - Efficacy and Safety of Lenvatinib in Anaplastic Thyroid Carcinoma: A Meta-Analysis. PG - 920857 LID - 10.3389/fendo.2022.920857 [doi] LID - 920857 AB - BACKGROUND: Lenvatinib has shown promising efficacy in targeted therapies that have been tested to treat anaplastic thyroid carcinoma (ATC) in both preclinical and clinical studies. The aim of this study was to evaluate the efficacy and safety of lenvatinib in the treatment of patients with ATC. METHODS: PubMed, the Cochrane Library, Embase, and ClinicalTrials.gov were searched for potential eligible studies from inception to February 1, 2022. The outcomes included partial response (PR), stable disease (SD), disease control rate (DCR), median progression-free survival (mPFS), and median overall survival (mOS). Effect sizes for all pooled results were presented with 95% CIs with upper and lower limit. RESULTS: Ten studies met the inclusion criteria. The aggregated results showed that the pooled PR, SD, and DCR were 15.0%, 42.0%, and 63.0%, respectively. The pooled mPFS and mOS were 3.16 (2.18-5.60) months and 3.16 (2.17-5.64) months, respectively. Furthermore, PFS rate at 3 months (PFSR-3m), PFSR-6m, PFSR-9m, PFSR-12m, and PFSR-15m were 52.0%, 22.5%, 13.9%, 8.4%, and 2.5%, respectively. Meanwhile, the 3-month OS rate (OSR-3m), OSR-6m, OSR-9m, OSR-12m, and OSR-15m were 64.0%, 39.3%, 29.7%, 18.9%, and 14.2%, respectively. The most common adverse events (AEs) of lenvatinib were hypertension (56.6%), proteinuria (32.6%), and fatigue (32%). CONCLUSIONS: This meta-analysis showed that lenvatinib has meaningful antitumor activity, but limited clinical efficacy in ATC. SYSTEMATIC REVIEW REGISTRATION: PROSPERO [https://www.crd.york.ac.uk/PROSPERO/], identifier [CRD42022308624]. CI - Copyright (c) 2022 Huang, Zhang, Zheng and Gao. FAU - Huang, Dongmei AU - Huang D AD - Department of Thyroid and Neck Tumor, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin's Clinical Research Center for Cancer, Tianjin, China. FAU - Zhang, Jinming AU - Zhang J AD - Department of Thyroid and Neck Tumor, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin's Clinical Research Center for Cancer, Tianjin, China. FAU - Zheng, Xiangqian AU - Zheng X AD - Department of Thyroid and Neck Tumor, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin's Clinical Research Center for Cancer, Tianjin, China. FAU - Gao, Ming AU - Gao M AD - Department of Thyroid and Neck Tumor, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin's Clinical Research Center for Cancer, Tianjin, China. AD - Department of Thyroid and Breast Surgery, Tianjin Union Medical Center, Tianjin, China. AD - Tianjin Key Laboratory of General Surgery Inconstruction, Tianjin Union Medical Center, Tianjin, China. LA - eng PT - Journal Article PT - Meta-Analysis PT - Research Support, Non-U.S. Gov't PT - Systematic Review DEP - 20220630 PL - Switzerland TA - Front Endocrinol (Lausanne) JT - Frontiers in endocrinology JID - 101555782 RN - 0 (Antineoplastic Agents) RN - 0 (Phenylurea Compounds) RN - 0 (Quinolines) RN - EE083865G2 (lenvatinib) SB - IM MH - *Antineoplastic Agents/adverse effects/therapeutic use MH - Humans MH - *Phenylurea Compounds/adverse effects/therapeutic use MH - *Quinolines/adverse effects/therapeutic use MH - *Thyroid Carcinoma, Anaplastic/drug therapy/pathology MH - *Thyroid Neoplasms/drug therapy/pathology PMC - PMC9279913 OTO - NOTNLM OT - anaplastic thyroid carcinoma OT - efficacy OT - lenvatinib OT - meta-analysis 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- 2022/07/19 06:00 MHDA- 2022/07/20 06:00 PMCR- 2022/01/01 CRDT- 2022/07/18 04:00 PHST- 2022/04/15 00:00 [received] PHST- 2022/05/31 00:00 [accepted] PHST- 2022/07/18 04:00 [entrez] PHST- 2022/07/19 06:00 [pubmed] PHST- 2022/07/20 06:00 [medline] PHST- 2022/01/01 00:00 [pmc-release] AID - 10.3389/fendo.2022.920857 [doi] PST - epublish SO - Front Endocrinol (Lausanne). 2022 Jun 30;13:920857. doi: 10.3389/fendo.2022.920857. eCollection 2022.