[Efficacy and safety of Anlotinib in the treatment of advanced sarcoma].

Q Yan, W T Yao, X H Du, L Y Guo, Y C Fan
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引用次数: 0

Abstract

Objective: Patients with advanced sarcomas have a dismal prognosis with few effective therapies. The purpose of this study was to evaluate the efficacy and safety of anlotinib in the treatment of advanced sarcoma and to explore the relationship between adverse events (AEs) and efficacy. Methods: Data from 45 advanced sarcoma patients who received anlotinib monotherapy at Affiliated Cancer Hospital of Zhengzhou University between June 2018 and August 2021 were retrospectively analyzed. According to Response Evaluation Criteria In Solid Tumors (RECIST) Version 1.1, the objective remission rate (ORR) and disease control rate (DCR) were calculated, and the progression free survival (PFS) and treatment-related AEs were recorded and analyzed. Survival analysis was conducted using the Kaplan-Meier survival rates were compared using the Log rank test. Results: Forty patients were treated for more than 1.5 months and received efficacy evaluation. The ORR and DCR after 3 months were 7.5%(3/40) and 80.0%(32/40), respectively. The overall ORR was 2.5%(1/40), the total DCR was 27.5%(11/40), and the median progression-free survival (m-PFS) was 6.70 months; The m-PFS of alveolar soft tissue sarcoma (ASPS) was 10.27 months, which was significantly longer than that of other subtypes of sarcoma (P=0.048). In addition, the DCR of ASPS and synovial sarcoma (SS) was significantly better than that of osteosarcoma (P<0.05). The most common AEs were elevated thyroid stimulating hormone (17.8%, 8/45), anemia (15.6%, 7/45), fatigue (11.1%, 5/45). Five patients developed grade 3 AEs after treatment; The PFS of patients with hand-foot syndrome after treatment was significantly longer than that of patients without hand-foot syndrome (14.10 vs 6.00, P=0.024). Conclusions: The efficacy of anlotinib in the treatment of ASPS and SS is better than that of other subtypes. The PFS in the group with hand-foot syndrome was significantly longer than that of the group without hand-foot syndrome.

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安洛替尼治疗晚期肉瘤的疗效和安全性。
目的:晚期肉瘤患者预后不佳,缺乏有效的治疗方法。本研究的目的是评估安洛替尼治疗晚期肉瘤的疗效和安全性,并探讨不良事件(AE)与疗效之间的关系。方法:回顾性分析2018年6月至2021年8月在郑州大学附属癌症医院接受安洛替尼单药治疗的45例晚期肉瘤患者的数据。根据实体瘤疗效评估标准(RECIST)1.1版,计算客观缓解率(ORR)和疾病控制率(DCR),并记录和分析无进展生存期(PFS)和治疗相关AE。使用Kaplan-Meier进行生存分析,使用Log秩检验比较生存率。结果:40例患者治疗时间超过1.5个月,并接受了疗效评价。3个月后ORR和DCR分别为7.5%(3/40)和80.0%(32/40)。总ORR为2.5%(1/40),总DCR为27.5%(11/40),中位无进展生存期(m-PFS)为6.70个月;肺泡软组织肉瘤(ASPS)的m-PFS为10.27个月,明显长于其他亚型肉瘤(P=0.048)。此外,ASPS和滑膜肉瘤(SS)的DCR明显优于骨肉瘤(P=0.024)。结论:安洛替尼治疗ASPS和SS的疗效优于其他亚型。手足综合征组的PFS明显长于无手足综合征的组。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
中华肿瘤杂志
中华肿瘤杂志 Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
10433
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