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紫杉醇联合卡铂和顺铂同期放化疗治疗高危或晚期子宫内膜癌。

Concomitant paclitaxel plus carboplatin and radiotherapy for high-risk or advanced endometrial cancer.

机构信息

Zhejiang Cancer Hospital, Hangzhou, China.

出版信息

Int J Gynecol Cancer. 2013 May;23(4):685-9. doi: 10.1097/IGC.0b013e3182808232.

DOI:10.1097/IGC.0b013e3182808232
PMID:23615571
Abstract

OBJECTIVE

The objective of this study was to evaluate the outcome and feasibility of concurrent chemotherapy with paclitaxel plus carboplatin and radiotherapy (RT) in patients with high-risk or advanced endometrial cancer.

METHODS

A retrospective analysis of patients treated between January 2003 and December 2009 was conducted. Adjuvant therapy consisted of external beam radiation to the pelvis (45-48.6 Gy) and weekly administration of paclitaxel (40 mg/m(2)) plus carboplatin with an area under the curve of 2 administered intravenously during RT. Two further cycles of paclitaxel (175 mg/m(2)) and carboplatin (area under the curve, 5), separated by 4 weeks, were administered at the end of RT for advanced stage disease. Para-aortic RT and/or vault brachytherapy were added at the discretion of the physicians.

RESULTS

A total of 31 patients with a median age of 56 years (31-69 years) were evaluated. The majority had stage III disease (58%), and the most common histology was endometrioid adenocarcinoma (78%). All patients completed the planned RT. The median follow-up time was 64 months (12-86 months). Five patients' conditions progressed, and all 5 died of the disease. Most of the 5 patients were with serous histologic type and advanced stage disease. There was no local recurrence. The 2-, 3-, and 5-year progression-free survival rates were 87%, 84%, and 79%, respectively. The 2-, 3-, and 5-year overall survival rates were 94%, 87%, and 83%, respectively. Toxicity included grade 3/4 neutropenia in 45.2% of patients, gastrointestinal toxicity in 32.3% of patients, and grade 1/2 sensory neuropathy in 38.7% of patients.

CONCLUSIONS

Concomitant paclitaxel plus carboplatin and radiation was feasible and well tolerated and resulted in excellent local-regional control. However, distant metastases continued to occur in more advanced-stage patients. This regimen appears reasonable to be tested for efficacy in randomized studies.

摘要

目的

本研究旨在评估紫杉醇联合卡铂化疗并同步放疗(RT)治疗高危或晚期子宫内膜癌患者的疗效和可行性。

方法

对 2003 年 1 月至 2009 年 12 月期间接受治疗的患者进行回顾性分析。辅助治疗包括盆腔外照射(45-48.6Gy)和每周紫杉醇(40mg/m²)联合卡铂(RT 期间静脉注射 AUC2)。对于晚期疾病,在 RT 结束时再给予紫杉醇(175mg/m²)和卡铂(AUC5)两个周期,每 4 周 1 次。根据医生的判断,还可以进行腹主动脉放疗和/或穹窿近距离放疗。

结果

共 31 例患者,中位年龄 56 岁(31-69 岁),大多数患者为 III 期疾病(58%),最常见的组织学类型为子宫内膜样腺癌(78%)。所有患者均完成了计划的 RT。中位随访时间为 64 个月(12-86 个月)。5 例患者病情进展,均死于疾病。这 5 例患者大多为浆液性组织学类型和晚期疾病。无局部复发。2、3、5 年无进展生存率分别为 87%、84%和 79%。2、3、5 年总生存率分别为 94%、87%和 83%。毒性反应包括 45.2%的患者出现 3/4 级中性粒细胞减少、32.3%的患者出现胃肠道毒性和 38.7%的患者出现 1/2 级感觉神经毒性。

结论

紫杉醇联合卡铂和放疗是可行的,且患者耐受性良好,可获得良好的局部区域控制。然而,晚期患者仍持续出现远处转移。该方案在随机研究中测试疗效似乎是合理的。

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