...
首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Etoposide, vincristine, doxorubicin and dexamethasone (EVAD) combination chemotherapy as second-line treatment for advanced AIDS-related Kaposi's sarcoma.
【24h】

Etoposide, vincristine, doxorubicin and dexamethasone (EVAD) combination chemotherapy as second-line treatment for advanced AIDS-related Kaposi's sarcoma.

机译:依托泊苷,长春新碱,阿霉素和地塞米松(EVAD)联合化疗是晚期艾滋病相关的卡波西氏肉瘤的二线治疗。

获取原文
获取原文并翻译 | 示例

摘要

To evaluate through retrospective analysis the efficacy and toxicity of combination chemotherapy with etoposide, vincristine, doxorubin and dexamethasone (EVAD) as second-line therapy in patients with advanced AIDS-related Kaposi's sarcoma (AIDS-KS) after failure of first-line chemotherapy.Eighty-eight patients with poor-risk AIDS-KS were treated intravenously with combination chemotherapy with EVAD; etoposide at a dose of 100 mg/m(2) on three consecutive days, vincristine 1.4 mg/m(2) with a maximum single dosage of 2.0 mg on day one, doxorubicin 30 mg/m(2) on day one and dexamethasone 40 mg on three consecutive days, with a three week cycle. All eligible patients had relapsed or progressed after prior two to six cycles of combination chemotherapy with doxorubicin, bleomycin and vincristine (ABV) or bleomycin and vincristine (BV).Assessment of the response of all the patients was made. The overall objective response rate was 59.1% (95% CI 48.83-69.37%), with five complete responses and 47 partial responses. Twenty-six cases of stable disease and 10 of progressive disease were observed in the remaining patients. The median follow-up period was 27 months (range 8-52 months). The median time to progression was 6.80 months (95% CI 2.04-11.56 months), and the median overall survival was 14.24 months (95% CI 10.26-18.22 months). Leucopenia was seen in 92.0% of patients, of which 20 patients had grade 3 and 12 had grade 4. Conclusions Combination chemotherapy with EVAD offers a new, active and safe therapeutic approach for the treatment of advanced AIDS-related KS.
机译:通过回顾性分析来评估依托泊苷,长春新碱,阿霉素和地塞米松(EVAD)联合化疗作为一线化疗失败后与艾滋病相关的卡波西肉瘤(AIDS-KS)晚期患者的二线治疗的疗效和毒性。对88例AIDS-KS低危患者进行了EVAD联合化疗的静脉内治疗。依托泊苷,连续三天剂量为100 mg / m(2),长春新碱1.4 mg / m(2),第一天最大单剂量为2.0 mg,阿霉素30 mg / m(2),第一天为地塞米松连续三天服用40毫克,每三个星期服用一次。所有符合条件的患者在接受阿霉素,博来霉素和长春新碱(ABV)或博来霉素和长春新碱(BV)联合化疗之前的2至6个周期后均复发或进展,并对所有患者的反应进行了评估。总体客观缓解率为59.1%(95%CI为48.83-69.37%),其中有5项完全缓解和47项部分缓解。在其余患者中观察到26例稳定疾病和10例进行性疾病。中位随访期为27个月(8-52个月)。中位进展时间为6.80个月(95%CI 2.04-11.56个月),中位总体生存期为14.24个月(95%CI 10.26-18.22个月)。 92.0%的患者出现白细胞减少症,其中20例3级患者和12例4级患者。结论EVAD联合化疗为治疗晚期艾滋病相关的KS提供了一种新的,有效且安全的治疗方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号