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子宫内膜癌子宫切除术后单纯高剂量率近距离放疗

High-dose-rate brachytherapy alone post-hysterectomy for endometrial cancer.

作者信息

MacLeod C, Fowler A, Duval P, D'Costa I, Dalrymple C, Firth I, Elliott P, Atkinson K, Carter J

机构信息

Department of Radiation Oncology, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.

出版信息

Int J Radiat Oncol Biol Phys. 1998 Dec 1;42(5):1033-9. doi: 10.1016/s0360-3016(98)00292-2.

Abstract

PURPOSE

To evaluate the outcome of post-hysterectomy adjuvant vaginal high-dose-rate (HDR) brachytherapy.

METHODS AND MATERIALS

A retrospective analysis was performed on a series of 143 patients with endometrial cancer treated with HDR brachytherapy alone post-hysterectomy from 1985 to June 1993. Of these patients, 141 received 34 Gy in four fractions prescribed to the vaginal mucosa in a 2-week period. The median follow-up was 6.9 years. Patients were analyzed for treatment parameters, survival, local recurrence, distant relapse, and toxicity.

RESULTS

Five-year relapse free survival and overall survival was 100% and 88% for Stage 1A, 98% and 94% for Stage IB, 100% and 86% for Stage IC, and 92% and 92% for Stage IIA. The overall vaginal recurrence rate was 1.4%. The overall late-toxicity rate was low, and no RTOG grade 3, 4, or 5 complications were recorded.

CONCLUSION

These results are similar to reported international series that have used either low-dose-rate or HDR brachytherapy. The biological effective dose was low for both acute and late responding tissues compared with some of the HDR brachytherapy series, and supports using this lower dose and possibly decreasing late side-effects with no apparent increased risk of vaginal recurrence.

摘要

目的

评估子宫切除术后辅助性阴道高剂量率(HDR)近距离放射治疗的效果。

方法与材料

对1985年至1993年6月期间接受子宫切除术后单纯HDR近距离放射治疗的143例子宫内膜癌患者进行回顾性分析。其中,141例患者在2周内分4次给予阴道黏膜34 Gy的剂量。中位随访时间为6.9年。对患者的治疗参数、生存率、局部复发、远处转移和毒性进行分析。

结果

1A期患者的5年无复发生存率和总生存率分别为100%和88%,1B期为98%和94%,1C期为100%和86%,IIA期为92%和92%。总体阴道复发率为1.4%。总体晚期毒性率较低,未记录到RTOG 3级、4级或5级并发症。

结论

这些结果与已报道的使用低剂量率或HDR近距离放射治疗的国际系列研究结果相似。与一些HDR近距离放射治疗系列相比,急性和晚期反应组织的生物等效剂量较低,这支持使用较低剂量并可能减少晚期副作用,且阴道复发风险无明显增加。

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