国际妇产科学杂志 ›› 2022, Vol. 49 ›› Issue (4): 411-414.doi: 10.12280/gjfckx.20211024

• 妇科肿瘤研究:病例报告 • 上一篇    下一篇

甲磺酸阿帕替尼联合依托泊苷治疗铂耐药复发性卵巢癌二例

郭依琳, 王武亮()   

  1. 450014 郑州大学第二附属医院妇产科,妇科肿瘤临床医学研究中心
  • 收稿日期:2021-11-04 出版日期:2022-08-15 发布日期:2022-08-19
  • 通讯作者: 王武亮 E-mail:wangwuliang888@sina.com

Apatinib Mesylate Combined with Etoposide in the Treatment of Platinum Resistant Recurrent Ovarian Cancer: A Report of Two Cases

GUO Yi-lin, WANG Wu-liang()   

  1. Department of Obstetrics and Gynecology, Gynecological Oncology Clinical Medicine Research Center, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou 450014, China
  • Received:2021-11-04 Published:2022-08-15 Online:2022-08-19
  • Contact: WANG Wu-liang E-mail:wangwuliang888@sina.com

摘要:

卵巢癌是死亡率最高的妇科恶性肿瘤。由于大多数卵巢癌早期症状隐匿,70%患者发现时已为晚期。晚期卵巢癌的治疗方式是肿瘤细胞减灭术联合辅助化疗,但仍有高达75%的患者在完成了标准的初始治疗后出现疾病复发。几乎所有复发的卵巢癌患者最终都会对铂类药物产生耐药,治疗效果不佳,预后较差。甲磺酸阿帕替尼是一种小分子血管内皮生长因子受体2酪氨酸激酶抑制剂,可抑制肿瘤血管生成,减缓或阻止肿瘤生长和发展。现报告2例铂耐药复发性卵巢癌患者接受甲磺酸阿帕替尼(375 mg/次,1次/d,3周为1个治疗周期)联合依托泊苷(50 mg/次,1次/d,连续口服2周,停药1周,3周为1个治疗周期)治疗后。2例患者疗效评估均为部分缓解,1例患者无进展生存期达到11.7个月,另1例已治疗4.3个月,现仍在治疗中。药物不良反应均可耐受,以期为临床提供一种有效的治疗方案。

关键词: 抗肿瘤联合化疗方案, 卵巢肿瘤, 血管生成抑制剂, 病例报告, 复发性卵巢癌, 甲磺酸阿帕替尼

Abstract:

Ovarian cancer is the gynecological malignant tumor with the highest mortality rate. Because most of the early symptoms are hidden, 70% of patients are already at an advanced stage. The treatment of advanced ovarian cancer is cytoreductive surgery combined with adjuvant chemotherapy. While up to 75% of patients will meet the problem of disease recurrence after standard initial treatment. Almost all the patients with recurrent ovarian cancer will eventually develop resistance to platinum drugs, eventually leading to poor treatment effects and poor prognosis. Apatinib mesylate is a small molecule VEGFR-2 tyrosine kinase inhibitor, which can inhibit tumor angiogenesis and prevent tumor growth and development. This paper reports two cases of platinum resistant recurrent ovarian cancer patients who received Apatinib Mesylate (375 mg, qd, 3 weeks as a treatment cycle) combined with Etoposide (50 mg, qd, oral drugs for 2 weeks, stop drugs for 1 week, 3 weeks as a treatment cycle) treatment. Two cases were evaluated for partial response after treatment. One case had a progression-free survival period of 11.7 months, and the other case has received treatment for 4.3 months which is still under treatment now. Adverse drug reactions can be tolerated, in order to provide an effective treatment plan for clinic.

Key words: Antineoplastic combined chemotherapy protocols, Ovarian neoplasms, Angiogenesis inhibitors, Case reports, Recurrent ovarian neoplasms, Apatinib mesylate