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局部晚期外阴癌的新辅助化疗。

Neoadjuvant chemotherapy in advanced vulvar cancer.

机构信息

Gynecology Department, Coimbra University Hospitals, Coimbra, Portugal.

出版信息

Int J Gynecol Cancer. 2010 Feb;20(2):294-8. doi: 10.1111/igc.0b013e3181c93adc.

Abstract

INTRODUCTION

Locally advanced tumors of the vulva represent approximately one third of all vulvar cancers. Therapeutic options include chemoradiation, radiotherapy, and neoadjuvant chemotherapy (NACT).

MATERIALS AND METHODS

Analysis of 3 NACT schemes, bleomicine, paclitaxel, and 5-fluorouracil/cisplatin, used in patients with locally advanced vulvar tumors in a 12-year period. The following parameters were evaluated and compared between regimens: age, initial tumor size, inguinal involvement, histological type, toxicities, response to treatment, surgery performed after NACT, and overall survival.

RESULTS

Of the 25 patients included, 10 underwent an NACT regimen with bleomicine (Group A); 5, with paclitaxel (Group B); and 10, with a combination of 5-fluorouracil/cisplatin (Group C). In Group A, there was a 60% response rate. Mortality was 70%, with an overall survival rate of 70%, 40%, and 30% at 12, 24, and 60 months, respectively. The mean (SD) survival was 46.7 (15.4) months. In Group B, the response rate was 40%, with an 80% mortality rate and a survival rate of 60% and 20% at 12 and 24 months, respectively. The mean (SD) survival was 17.0 (3.8) months. In Group C, 20% of the responses were observed and the mortality was 90%, with an overall survival rate of 10% at 12 and 24 months and a mean (SD) survival of 7.6 (2.0) months.

CONCLUSION

The best response and overall survival rates were achieved in Group A with the NACT scheme of bleomicine.

摘要

引言

外阴局部晚期肿瘤约占所有外阴癌的三分之一。治疗方案包括放化疗、放疗和新辅助化疗(NACT)。

材料和方法

分析了 12 年内 25 例局部晚期外阴肿瘤患者使用博来霉素、紫杉醇和 5-氟尿嘧啶/顺铂三种 NACT 方案的情况。评估并比较了方案之间的以下参数:年龄、初始肿瘤大小、腹股沟受累、组织学类型、毒性、治疗反应、NACT 后手术以及总生存率。

结果

25 例患者中,10 例接受博来霉素 NACT 方案(A 组);5 例接受紫杉醇(B 组);10 例接受 5-氟尿嘧啶/顺铂联合方案(C 组)。A 组的缓解率为 60%。死亡率为 70%,总生存率分别为 70%、40%和 30%,12、24 和 60 个月时。平均(SD)生存时间为 46.7(15.4)个月。B 组的缓解率为 40%,死亡率为 80%,12 和 24 个月时的生存率分别为 60%和 20%。平均(SD)生存时间为 17.0(3.8)个月。C 组观察到 20%的反应,死亡率为 90%,12 和 24 个月时的总生存率分别为 10%,平均(SD)生存时间为 7.6(2.0)个月。

结论

博来霉素 NACT 方案的 A 组获得了最佳的缓解率和总生存率。

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