Suppr超能文献

调强近距离放疗联合间质热疗在同期放化疗治疗局部晚期宫颈癌患者中的应用:一项 III 期研究

HDR brachytherapy combined with interstitial hyperthermia in locally advanced cervical cancer patients initially treated with concomitant radiochemotherapy--a phase III study.

机构信息

Department of Brachytherapy, The Maria Skłodowska-Curie Memorial Cancer Center and Institute of Oncology, Warsaw, Poland.

出版信息

Radiother Oncol. 2013 Nov;109(2):194-9. doi: 10.1016/j.radonc.2013.04.011. Epub 2013 May 14.

Abstract

BACKGROUND AND PURPOSE

The aim of this randomised trial was to investigate whether hyperthermia (HT) combined with interstitial brachytherapy (ISBT) has any influence on local control (LC), disease-free survival (DFS), or acute and late side effects in patients with advanced cervical cancer.

MATERIALS AND METHODS

After radiochemotherapy, consecutive patients with cervical cancer (FIGO stage II-III) were randomly assigned to two treatment groups, either ISBT alone or ISBT combined with interstitial hyperthermia (ISHT). A total of 205 patients were included in the statistical analysis. Once a week, HT, at a temperature above 42.5°C, was administered for 45min before and during the HDR BT.

RESULTS

The median follow-up time was 45months (range 3-72months). An effect of hyperthermia was not detected for disease-free survival (DFS) (log-rank test: p=0.178) or for local control (LC) (p=0.991). According to Cox's analysis, HT did not significantly influence failure or interactions with potential prognostic factors for LC or DFS. Statistical differences were not observed for the distribution of early and late complications between the HT and non HT groups.

CONCLUSIONS

ISHT is well-tolerated and does not affect treatment-related early or late complications. Improvements in DFS and LC were not observed following the addition of ISHT to ISBT.

摘要

背景与目的

本随机试验旨在研究热疗(HT)联合间质近距离放疗(ISBT)是否会对晚期宫颈癌患者的局部控制(LC)、无病生存(DFS)或急性和晚期副作用产生影响。

材料与方法

在放化疗后,连续的宫颈癌患者(FIGO 分期 II-III 期)被随机分配到 ISBT 单独治疗组或 ISBT 联合间质内热疗(ISHT)组。共有 205 例患者纳入统计分析。每周一次,在 HDR BT 之前和期间,将温度升至 42.5°C 以上的 HT 施用于患者 45 分钟。

结果

中位随访时间为 45 个月(范围 3-72 个月)。HT 对无病生存(DFS)(对数秩检验:p=0.178)或局部控制(LC)(p=0.991)没有影响。根据 Cox 分析,HT 对 LC 或 DFS 的潜在预后因素的失败或相互作用没有显著影响。HT 和非 HT 组之间的早期和晚期并发症分布没有观察到统计学差异。

结论

ISHT 耐受良好,不会影响与治疗相关的早期或晚期并发症。在 ISBT 中加入 ISHT 并未改善 DFS 和 LC。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验