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安罗替尼联合阿霉素和异环磷酰胺作为不可切除软组织肉瘤转化治疗的评估

Evaluation of Anlotinib Combined with Adriamycin and Ifosfamide as Conversion Therapy for Unresectable Soft Tissue Sarcomas.

作者信息

Long Zuoyao, Lu Yajie, Li Minghui, Fu Zhanli, Akbar Yunus, Li Jing, Chen Guojing, Zhang Hong-Mei, Wang Qi, Xiang Liangbi, Wang Zhen

机构信息

Xijing Hospital, The Air Force Military Medical University, Xi'an 710000, China.

General Hospital of Northern Theater Command, Shenyang 110000, China.

出版信息

Cancers (Basel). 2023 Jan 23;15(3):700. doi: 10.3390/cancers15030700.

Abstract

(1) Background: This study investigated the safety and efficiency of adriamycin and ifosfamide combined with anlotinib (AI/AN) as a neoadjuvant conversion therapy in uSTS. (2) Methods: Patients with uSTS were eligible to receive AI/An, including adriamycin (20 mg/m/d) and ifosfamide (3 g/m/d) for the first to the third day combined with anlotinib (12 mg/d) for 2 weeks on/1 week off, all of which combine to comprise one cycle. Surgery was recommended after four cycles of treatment. (3) Results: A total of 28 patients were enrolled from June 2018 to December 2020. The best tumor responses included eight patients with partial responses and 20 with a stable disease. Patients with synovial sarcoma and liposarcoma had a significant decrease in the number of tumors compared with fibrosarcoma ( = 0.012; = 0.042). The overall response rate and disease control rate were 28.57% and 100%, respectively. In total, 24 patients received surgery, while the rates of limb salvage and R0 resection were 91.67% ( = 22/24) and 87.50% ( = 21/24), respectively. Until the last follow-up visit, the mean PFS and RFS were 21.70 and 23.97 months, respectively. During drug administration, 67.87% of patients had grade ≥3 AEs. No treatment-related death occurred. (4) Conclusions: AI/AN followed by surgery showed favorable efficiency and manageable safety in patients with uSTS. A randomized controlled study with a large cohort should be performed for further investigations.

摘要

(1) 背景:本研究探讨了阿霉素和异环磷酰胺联合安罗替尼(AI/AN)作为肢体软组织肉瘤(uSTS)新辅助转化治疗的安全性和有效性。(2) 方法:uSTS患者 eligible to receive AI/An,包括阿霉素(20mg/m²/d)和异环磷酰胺(3g/m²/d),第1至3天使用,联合安罗替尼(12mg/d),2周用药/1周停药,所有这些构成一个周期。建议在四个周期治疗后进行手术。(3) 结果:2018年6月至2020年12月共纳入28例患者。最佳肿瘤反应包括8例部分缓解患者和20例疾病稳定患者。滑膜肉瘤和脂肪肉瘤患者的肿瘤数量与纤维肉瘤相比有显著减少(P = 0.012;P = 0.042)。总缓解率和疾病控制率分别为28.57%和100%。共有24例患者接受了手术,保肢率和R0切除率分别为91.67%(22/24)和87.50%(21/24)。直到最后一次随访,平均无进展生存期(PFS)和无复发生存期(RFS)分别为21.70个月和23.97个月。在给药期间,67.87%的患者发生≥3级不良反应。未发生与治疗相关的死亡。(4) 结论:AI/AN序贯手术在uSTS患者中显示出良好的疗效和可管理的安全性。应进行一项大样本队列的随机对照研究以作进一步调查。

“eligible to receive”直译为“有资格接受”,这里意译为“适合接受”可能更通顺,但按要求未添加其他解释说明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a01/9913396/669b473f4dbc/cancers-15-00700-g001.jpg

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