国际肿瘤学杂志 ›› 2014, Vol. 41 ›› Issue (8): 620-623.doi: 10.3760/cma.j.issn.1673-422X.2014.08.019

• 论著 • 上一篇    下一篇

白蛋白结合型紫杉醇联合贝伐珠单抗二线治疗晚期胰腺癌的临床观察

黄少江   

  1. 400037 重庆,第三军医大学新桥医院肿瘤科
  • 收稿日期:2014-02-27 修回日期:2014-04-25 出版日期:2014-08-15 发布日期:2014-08-14
  • 通讯作者: 黄少江,E-mail:jinshatanwo@163.com E-mail:jinshatanwo@163.com

Clinical observation of albumin bound paclitaxel plus bevacizumab as second line therapy in patients with advanced pancreatic cancer

Huang Shaojiang     

  1. Department of Oncology, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, China
  • Received:2014-02-27 Revised:2014-04-25 Online:2014-08-15 Published:2014-08-14
  • Contact: Huang Shaojiang E-mail:jinshatanwo@163.com

摘要: 目的 探讨白蛋白结合型紫杉醇联合贝伐珠单抗二线治疗晚期胰腺癌疗效、不良反应和生存情况。方法 应用白蛋白结合型紫杉醇联合贝伐珠单抗二线治疗晚期胰腺癌27例,具体方案:第1天白蛋白结合型紫杉醇130 mg/m2、贝伐珠单抗7.5 mg/m2,21 d为1个周期,最少化疗2个周期,每个周期评价不良反应,2个周期评价疗效。结果27例患者均可进行疗效评价,无完全缓解病例,部分缓解2例,稳定14例,进展11例,有效率为7.41%,临床获益率为59.26%,中位无进展生存期为4个月(95%CI为3.004~4.996个月),中位生存期为8个月(95%CI为5.900~10.100个月)。主要不良反应为骨髓抑制、胃肠道反应、乏力、脱发、皮疹及外周神经毒性,不良反应多为1~2级,患者能够耐受,未发生治疗相关性死亡。结论 白蛋白结合型紫杉醇联合贝伐珠单抗二线治疗晚期胰腺癌可以控制病情进展,不良反应可以耐受,但仍需要扩大样本深入研究。

关键词: 胰腺肿瘤, 白蛋白结合型紫杉醇, 贝伐珠单抗

Abstract: ObjectiveTo investigate the efficacy, adverse reaction and survival condition of albuminbound paclitaxel combined with bevacizumab as secondline therapy in patients with advanced pancreatic cancer. MethodsTwentyseven cases of advanced pancreatic cancer were enrolled to receive albuminbound paclitaxel combined with bevacizumab regimen. The dose of the drugs was as follows: albuminbound paclitaxel 130 mg/m2, d1, bevacizumab 7.5 mg/m2, d1. Twentyone days were a cycle for each regimen, and the least chemotherapy cycle was 2. The adverse reactions were evaluated for each cycle and the objective response was evaluated for 2 cycles. ResultsThe 27 patients could be evaluated. None was in complete remission, 2 cases were in partial remission, 14 cases were in stabilization, 11 cases were in progress. The response rate (RR) was 7.41%, and the disease control rate (DCR) was 59.26%. The median progress free survival (PFS) was 4 months (95%CI: 3.0044.996 months), and the median overall survival (OS) was 8 months (95%CI: 5.90010.100 months). The main adverse reactions included myelosuppression, gastrointestinal reaction, fatigue, lipsotrichia, erythra, peripheral neurotoxicity, etc, most of which were 12 grade. The adverse effect was well tolerated, and there was no treatmentrelated death. ConclusionThe albuminbound paclitaxel combined with bevacizumab as secondline therapy in patients with advanced pancreatic cancer shows slow progress and low adverse effect and needs further study.

Key words: Pancreatic neoplasms, Albumin bound paclitaxel, Bevacizumab