Department of Medical Oncology, Fujian Medical University Union Hospital, No. 29 Xinquan Road, Fuzhou 350001, Fujian, People's Republic of China.
J Cancer Res Clin Oncol. 2012 Mar;138(3):425-30. doi: 10.1007/s00432-011-1109-7. Epub 2011 Dec 11.
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.
通过回顾性分析,评价依托泊苷、长春新碱、多柔比星和地塞米松(EVAD)联合化疗作为一线化疗失败的晚期 AIDS 相关卡波西肉瘤(AIDS-KS)患者的二线治疗的疗效和毒性。
88 例高危 AIDS-KS 患者接受 EVAD 联合化疗:依托泊苷 100mg/m2,连续 3 天;长春新碱 1.4mg/m2,最大单剂量 2.0mg,第 1 天;多柔比星 30mg/m2,第 1 天;地塞米松 40mg,连续 3 天,每 3 周为 1 个周期。所有合格患者在接受多柔比星、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 2 至 6 个周期后均复发或进展。
对所有患者的反应进行了评估。总客观缓解率为 59.1%(95%CI 48.83-69.37%),完全缓解 5 例,部分缓解 47 例。其余患者观察到 26 例稳定疾病和 10 例进展疾病。中位随访时间为 27 个月(范围 8-52 个月)。中位无进展生存期为 6.80 个月(95%CI 2.04-11.56 个月),中位总生存期为 14.24 个月(95%CI 10.26-18.22 个月)。92.0%的患者出现白细胞减少,其中 20 例为 3 级,12 例为 4 级。
EVAD 联合化疗为治疗晚期 AIDS 相关 KS 提供了一种新的、有效和安全的治疗方法。