Zhang Lu-Ping, Liao Xing-Yun, Xu Yan-Mei, Yan Lv-Jun, Yan Gui-Fang, Wang Xin-Xin, Duan Yu-Zhong, Sun Jian-Guo
Cancer Institute of PLA, Xinqiao Hospital, Third Military Medical University, Chongqing, China.
Asian Pac J Cancer Prev. 2013;14(7):4255-9. doi: 10.7314/apjcp.2013.14.7.4255.
Soft tissue sarcomas (STS) are a heterogeneous group of tumors, and approximately 40-50% of patients with STS develop metastatic disease. The median overall survival of those patients was 12 months and their 5-year survival rate was 8%. Therefore, study on more effective treatment, especially the targeting therapies, is urgently needed.
To evaluate the efficacy and safety of Endostar® combined with chemotherapy in patients with advanced STS.
A retrospective case-series study was conducted in Cancer Institute of PLA, Xinqiao Hospital. A total of 71 patients suffering from advanced STS (IIB - IV) were included, of whom 49 cases treated with chemotherapy alone were defined as the control group and the rest 22 cases treated with the traditional chemotherapy combined with Endostar® were defined as the test group. The short-term therapeutic effects including objective response rate (ORR), disease control rate (DCR) and safety were evaluated in the two groups. In the follow-up, progression-free survival (PFS) and overall survival (OS) were also observed.
In the test and control groups, the ORR was 18.2% and 12.2%, respectively (P = 0.767), and the DCR was 86.4% and 61.2%, respectively (P=0.034). The median time to progression in the test and control groups was 120 days and 70 days with significant difference (P = 0.017), while the median overall survival was 452 days and 286 days without significant difference (P = 0.503). The one-year survival rate in the test group and control group was 56.2% and 35.4%, respectively, while the two-year survival rate was 30.2% and 26.5%, respectively. No significant difference in the side effects was found between the two groups.
Endostar® combined with chemotherapy resulted in a higher DCR and longer PFS in the patients with advanced STS, and the toxicity was tolerable.
软组织肉瘤(STS)是一组异质性肿瘤,约40%-50%的STS患者会发生转移性疾病。这些患者的中位总生存期为12个月,5年生存率为8%。因此,迫切需要研究更有效的治疗方法,尤其是靶向治疗。
评估恩度联合化疗治疗晚期STS患者的疗效和安全性。
在解放军总医院肿瘤研究所新桥医院进行一项回顾性病例系列研究。共纳入71例晚期STS(IIB-IV期)患者,其中49例单纯接受化疗的患者被定义为对照组,其余22例接受传统化疗联合恩度治疗的患者被定义为试验组。评估两组的短期治疗效果,包括客观缓解率(ORR)、疾病控制率(DCR)和安全性。在随访中,还观察了无进展生存期(PFS)和总生存期(OS)。
试验组和对照组的ORR分别为18.2%和12.2%(P = 0.767),DCR分别为86.4%和61.2%(P = 0.034)。试验组和对照组的中位疾病进展时间分别为120天和70天,差异有统计学意义(P = 0.017),而中位总生存期分别为452天和286天,差异无统计学意义(P = 0.503)。试验组和对照组的1年生存率分别为56.2%和35.4%,2年生存率分别为30.2%和26.5%。两组间副作用无显著差异。
恩度联合化疗可使晚期STS患者获得更高的DCR和更长的PFS,且毒性可耐受。