Clinical observation of local intervention combined with camrelizumab and apatinib in the treatment of metastatic soft-tissue sarcoma

阿帕蒂尼 医学 软组织肉瘤 不利影响 软组织 肉瘤 临床终点 内科学 外科 无进展生存期 射频消融术 联合疗法 离格 实体瘤疗效评价标准 肿瘤科 进行性疾病 总体生存率 化疗 烧蚀 放射治疗 病理 随机对照试验
作者
Yan Li,Hailiang Li,Hongtao Hu,Shanshan Shao,Cheng Chen,Chenyang Guo,Yan Zhao,Quan-Jun Yao
出处
期刊:Journal of Cancer Research and Therapeutics [BioMed Central]
卷期号:17 (7): 1718-1718 被引量:2
标识
DOI:10.4103/jcrt.jcrt_1310_21
摘要

The study aimed to investigate the effectiveness and safety of the combination of immune checkpoint inhibitor, local interventional therapy, and anti-angiogenic therapy in patients with metastatic soft-tissue sarcoma (mSTS).We retrospectively evaluated the medical records of patients with mSTS who started treatment between September 2018 and June 2020 at our hospital.Overall, 33 patients with different subtypes of mSTS were included. Most primary tumors originated from the lungs, and the rest were scattered throughout the body. All patients were treated with camrelizumab combined with apatinib within 5 days of local interventional therapy using transarterial chemoembolization (TACE) or radiofrequency ablation (RFA). Primary end point was progression-free survival (PFS), and secondary end points were objective response rate (ORR), disease control rate (DCR), and patient safety.The median PFS, median overall survival (OS), ORR, and DCR were 8.8 months, 18.5 months, 36.4%, and 75.8%, respectively. Patients (n = 20) treated with RFA combined with TACE showed better responses than those treated with RFA alone (n = 13), with mPFS of 9.3 and 7.9 months (P = 0.044) and mOS of 19.0 and 16.2 months (P = 0.043), respectively. Patients (n = 8) with alveolar soft part sarcomas showed excellent efficacy, with ORR, DCR, mPFS, and mOS of 62.5%, 87.5%, 11.5 months, and 22.5 months, respectively. Grades 3 or 4 treatment-related adverse events occurred in 12 of 33 patients.Local intervention therapy combined with camrelizumab and apatinib is effective and safe for patients with mSTS and should be investigated in future clinical trials.

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