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安罗替尼与吉西他滨/多西他赛联合用于标准化疗失败的转移性骨肉瘤患者

The Combination of Anlotinib and Gemcitabine/Docetaxel in Patients with Metastatic Osteosarcoma Who Have Failed Standard Chemotherapy.

作者信息

Wang Tian, Lin Feng, Huang Yujing, Qian Guowei, Yu Wenxi, Hu Haiyan, Ji Tong, Tang Lina, Yao Yang

机构信息

The Eighth People's Hospital of Shanghai, Shanghai, People's Republic of China.

Shanghai Sixth People's Hospital, Shanghai Jiaotong University, Shanghai, People's Republic of China.

出版信息

Cancer Manag Res. 2022 Oct 4;14:2945-2952. doi: 10.2147/CMAR.S378264. eCollection 2022.

Abstract

PURPOSE

The options for the second-line treatment of metastatic osteosarcoma are still limited. Anlotinib is a multi-kinase inhibitor which has shown promising efficacy and good tolerability in various cancer types. This retrospective study was conducted to evaluate the efficacy and safety of anlotinib combined with gemcitabine/docetaxel (GD) in patients with metastatic osteosarcoma who have failed first-line chemotherapy.

PATIENTS AND METHODS

The data of patients who received anlotinib combined with GD or GD were collected. The primary endpoint was progression-free survival. Secondary endpoints included objective response rate and safety.

RESULTS

From July 2013 to November 2020, a total of 32 patients were enrolled, 13 received anlotinib combined with GD and 19 received GD. Median PFS was 9.0 months (95% CI 6.7-39.1) in the combination group and 5.0 months (95% CI 1.2-6.7) in the chemotherapy group. ORR were 38.4% and 15.8%, DCR were 69.2% and 38.1% in the combination and chemotherapy group, respectively. The most common adverse events included fatigue (78.9% in the combination group vs 69.2% in the chemotherapy group), hypertension (46.2% vs 10.5%), diarrhea (38.5% vs 21.1%), hypothyroidism (38.5% vs 15.8%), neutropenia (23.1% vs 36.8%) and AST elevation (30.8% vs 21.1%). The most common grade 3 or worse adverse events included hand-foot reaction (7.7% vs 5.3%), hypothyroidism (15.4% vs 0), neutropenia (0 vs 10.5%).

CONCLUSION

The combination of anlotinib and GD showed favorable efficacy with manageable toxicities compared with GD in the second-line treatment for metastatic osteosarcoma. This combination therapy deserves further investigations in patients with osteosarcoma.

摘要

目的

转移性骨肉瘤二线治疗的选择仍然有限。安罗替尼是一种多激酶抑制剂,已在多种癌症类型中显示出有前景的疗效和良好的耐受性。本回顾性研究旨在评估安罗替尼联合吉西他滨/多西他赛(GD)对一线化疗失败的转移性骨肉瘤患者的疗效和安全性。

患者与方法

收集接受安罗替尼联合GD或单纯GD治疗的患者数据。主要终点为无进展生存期。次要终点包括客观缓解率和安全性。

结果

2013年7月至2020年11月,共纳入32例患者,13例接受安罗替尼联合GD治疗,19例接受GD治疗。联合组的中位无进展生存期为9.0个月(95%CI 6.7 - 39.1),化疗组为5.0个月(95%CI 1.2 - 6.7)。联合组和化疗组的客观缓解率分别为38.4%和15.8%,疾病控制率分别为69.2%和38.1%。最常见的不良事件包括疲劳(联合组78.9%,化疗组69.2%)、高血压(46.2%对10.5%)、腹泻(38.5%对21.1%)、甲状腺功能减退(38.5%对15.8%)、中性粒细胞减少(23.1%对36.8%)和谷草转氨酶升高(30.8%对21.1%)。最常见的3级或更严重不良事件包括手足反应(7.7%对5.3%)、甲状腺功能减退(15.4%对0)、中性粒细胞减少(0对10.5%)。

结论

在转移性骨肉瘤的二线治疗中,与GD相比,安罗替尼联合GD显示出良好的疗效且毒性可控。这种联合治疗值得在骨肉瘤患者中进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ddc/9547547/550566d28181/CMAR-14-2945-g0001.jpg

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