Xu Bushu, Pan Qiuzhong, Pan Hua, Li Haomiao, Li Xianan, Chen Jing, Pang Danmei, Zhang Baoqing, Weng Desheng, Peng Ruiqing, Fang Meiyu, Zhang Xing
Melanoma and Sarcoma Medical Oncology Unit, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, China.
Department of Bone Oncology, The Third Affiliated Hospital of Southern Medical University, Guangzhou, China.
EClinicalMedicine. 2023 Sep 21;64:102240. doi: 10.1016/j.eclinm.2023.102240. eCollection 2023 Oct.
No standard maintenance treatment has been obtained to prolong the response duration of soft tissue sarcoma (STS) after first-line chemotherapy. In this study, we aimed to evaluate the efficacy and safety of anlotinib as a maintenance treatment after chemotherapy in STS.
In this multicentre, open-label, single-arm phase 2 trial, patients with advanced STS who achieved partial response or stable disease after first-line anthracycline-based chemotherapy were enrolled between April 2019 and January 2022. All patients received anlotinib as a maintenance treatment. The primary endpoint was progression-free survival (PFS) of anlotinib maintenance treatment. Other endpoints included overall survival (OS), objective response rate (ORR), disease control rate (DCR) and safety. This study is registered with ClinicalTrials.gov, NCT03890068.
At the data cut-off date (August 8, 2022), 49 patients were enrolled, including 17 with liposarcoma (35%) and 15 with leiomyosarcoma (31%). After a median follow-up of 17.1 months (IQR 9.0-27.2), the median PFS from the beginning of maintenance treatment was 9.1 months (95% CI 5.7-12.5), and the median OS was not reached, and the 1-year OS rate for anlotinib maintenance treatment was 98.0%. The best ORR and DCR were 16% (8/49, 95% CI 7-30) and 94% (46/49, 95% CI 83-99), respectively. Most of the treatment-related adverse events were grade 1-2. Of the grade 3-4 adverse events, the most common were hypertension (10%) and hand-foot syndrome reaction (6%).
Postchemotherapy maintenance treatment with anlotinib exhibits promising efficacy and tolerable toxicity in patients with advanced STS.
Chia Tai Tianqing Pharmaceutical Group Co., Ltd., the National Key Research and Development Program of China, and the National Natural Science Foundation of China.
目前尚未获得标准的维持治疗方案来延长软组织肉瘤(STS)一线化疗后的缓解持续时间。在本研究中,我们旨在评估安罗替尼作为STS化疗后维持治疗的疗效和安全性。
在这项多中心、开放标签、单臂2期试验中,2019年4月至2022年1月期间纳入了一线蒽环类化疗后达到部分缓解或疾病稳定的晚期STS患者。所有患者均接受安罗替尼作为维持治疗。主要终点是安罗替尼维持治疗的无进展生存期(PFS)。其他终点包括总生存期(OS)、客观缓解率(ORR)、疾病控制率(DCR)和安全性。本研究已在ClinicalTrials.gov注册,注册号为NCT03890068。
在数据截止日期(2022年8月8日),共纳入49例患者,其中17例为脂肪肉瘤(35%),15例为平滑肌肉瘤(31%)。中位随访17.1个月(IQR 9.0-27.2)后,从维持治疗开始的中位PFS为9.1个月(95%CI 5.7-12.5),中位OS未达到,安罗替尼维持治疗的1年OS率为98.0%。最佳ORR和DCR分别为16%(8/49,95%CI 7-30)和94%(46/49,95%CI 83-99)。大多数治疗相关不良事件为1-2级。在3-4级不良事件中,最常见的是高血压(10%)和手足综合征反应(6%)。
安罗替尼化疗后维持治疗在晚期STS患者中显示出有前景的疗效和可耐受的毒性。
正大天晴药业集团股份有限公司、中国国家重点研发计划和中国国家自然科学基金。