Xie Lu, Xu Jie, Sun Xin, Li Xiaowei, Liu Kuisheng, Liang Xin, Zhou Zuli, Zhuang Hongqing, Sun Kunkun, Wu Yiming, Gu Jin, Guo Wei
Musculoskeletal Tumor Center, Peking University People's Hospital, Beijing 100044, P.R. China.
Department of Thoracic Surgery, Peking University People's Hospital, Beijing 100044, P.R. China.
Oncol Lett. 2021 Jul;22(1):552. doi: 10.3892/ol.2021.12813. Epub 2021 May 24.
For osteosarcoma that progresses following first-line chemotherapy, prognosis remains poor although anti-angiogenesis tyrosine kinase inhibitors (TKIs) have been verified to prolong progression-free survival. Apatinib has led to positive responses in the treatment of refractory osteosarcoma. However, it demonstrates only short-lived activity, and the disease control rate of musculoskeletal lesions is worse compared with that of pulmonary lesions. This treatment failure has been partly overcome by the addition of ifosfamide and etoposide (IE). The present study retrospectively compared the activity of apatinib + IE in relapsed or refractory osteosarcoma in two sarcoma centres in China. The included patients had received a combination of apatinib 500 mg (orally) daily and the IE regimen (n=33) between June 3 2017 and July 17 2020. The tumour burden was considerable in these patients: 16/33 (48.5%) Patients had lung and musculoskeletal lesions, and 31/33 (93.9%) patients had progressed to two lines of therapies at baseline. With a median follow-up duration of 28.4 [interquartile range (IQR), 16.1-38.3] months, 21/33 (63.6%) patients had objective responses, and the median event-free survival was 11.4 (IQR, 6.7-18.4) months. The median overall survival time was 19.8 (IQR, 13.1-30.6) months. At the last follow-up, 16/33 patients had tumour downstaging, and all lesions had been completely resected. For osteosarcoma with multiple sites of metastasis, apatinib + IE demonstrated clinically meaningful antitumor activity and delayed disease progression in patients with recurrent or refractory osteosarcoma after failure of chemotherapy. This combination with manageable toxicity deserves further investigation in prospective trials.
对于一线化疗后进展的骨肉瘤,尽管抗血管生成酪氨酸激酶抑制剂(TKIs)已被证实可延长无进展生存期,但其预后仍然很差。阿帕替尼在难治性骨肉瘤的治疗中已产生阳性反应。然而,它仅显示出短期活性,与肺部病变相比,肌肉骨骼病变的疾病控制率更差。通过添加异环磷酰胺和依托泊苷(IE),部分克服了这种治疗失败的情况。本研究回顾性比较了阿帕替尼+IE在中国两个肉瘤中心对复发或难治性骨肉瘤的活性。纳入的患者在2017年6月3日至2020年7月17日期间接受了阿帕替尼500mg(口服)每日一次与IE方案联合治疗(n=33)。这些患者的肿瘤负荷相当大:16/33(48.5%)的患者有肺部和肌肉骨骼病变,31/33(93.9%)的患者在基线时已进展至二线治疗。中位随访时间为28.4[四分位间距(IQR),16.1 - 38.3]个月,21/33(63.6%)的患者有客观反应,中位无事件生存期为11.4(IQR,6.7 - 18.4)个月。中位总生存时间为19.8(IQR,13.1 - 30.6)个月。在最后一次随访时,16/33的患者肿瘤降期,所有病变均已完全切除。对于有多处转移的骨肉瘤,阿帕替尼+IE在化疗失败后的复发或难治性骨肉瘤患者中显示出具有临床意义的抗肿瘤活性并延迟了疾病进展。这种毒性可控的联合治疗值得在前瞻性试验中进一步研究。