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阴道近端的放射耐受剂量。

The irradiation tolerance dose of the proximal vagina.

作者信息

Au Samuel P, Grigsby Perry W

机构信息

Radiation Oncology Department, Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO, USA.

出版信息

Radiother Oncol. 2003 Apr;67(1):77-85. doi: 10.1016/s0167-8140(02)00384-5.

Abstract

PURPOSE

The purpose of this investigation was to determine the irradiation tolerance level and complication rates of the proximal vagina to combined external irradiation and low dose rate (LDR) brachytherapy. Also, the mucosal tolerance for fractionated high dose rate (HDR) brachytherapy is further projected based on the biological equivalent dose (BED) of LDR for an acceptable complication rate.

MATERIALS AND METHODS

Two hundred seventy-four patients with stages I-IV cervical carcinoma treated with irradiation therapy alone from 1987 to 1997 were retrospectively reviewed for radiation-associated late sequelae of the proximal vagina. All patients received LDR brachytherapy and 95% also received external pelvic irradiation. Follow-up ranged from 15 to 126 months (median, 43 months). The proximal vagina mucosa dose from a single ovoid (single source) or from both ovoids plus the tandem (all sources), together with the external irradiation dose, were used to derive the probability of a complication using the maximum likelihood logistic regression technique. The BED based on the linear-quadratic model was used to compute the corresponding tolerance levels for LDR or HDR brachytherapy.

RESULTS

Grades 1 and 2 complications occurred in 10.6% of patients and Grade 3 complications occurred in 3.6%. There were no Grade 4 complications. Complications occurred from 3 to 71 months (median, 7 months) after completion of irradiation, with over 60% occurring in the first year. By logistic regression analysis, both the mucosal dose from a single ovoid or that from all sources, combined with the external irradiation dose, demonstrate a statistically significant fit to the dose response complication curves (both with P=0.016). The single source dose was highly correlated with the all source dose with a cross-correlation coefficient 0.93. The all source dose was approximately 1.4 times the single source dose. Over the LDR brachytherapy dose rate range, the complication rate was relatively stable to small variations of the underlying tumor biological characteristics and the dose rate. The complication rates change approximately an absolute 1% over the range of the alpha-beta ratio (alpha/beta) from 2 to 4 Gy and repair constant (mu) of 0.46/h to 0.60/h. The complication rates increased an absolute 2% over the mucosa dose rate from 1.75 to 3.50 Gy/h. They markedly increased as the dose rate increased above 3.00 Gy/h as in HDR brachytherapy. The projected HDR Grade 3 tolerance varied from 25 Gy for one fraction to 57 Gy for six fractions in addition to 20 Gy external irradiation for nominal 3-5% complication rates. The traditional LDR tolerance dose of 150 Gy was shown to yield nominal 11% and 4% Grades 1 and 2 and Grade 3 sequelae, respectively.

CONCLUSIONS

The traditional 150 Gy LDR tolerance dose (single source plus external irradiation) can be relaxed to 175 Gy or equivalently a full mucosal dose of 238 Gy (all sources plus external irradiation) for a nominal 5% Grade 3 complication rate. Higher fractionation is necessary with four to six fractions in HDR therapy for similar rates of sequelae. The mucosal surface dose from a single ovoid, which can be readily computed, remains a convenient tolerance check for treatment planning purposes.

摘要

目的

本研究旨在确定近端阴道对体外照射与低剂量率(LDR)近距离放射治疗联合治疗的耐受水平及并发症发生率。此外,基于LDR的生物等效剂量(BED),针对可接受的并发症发生率,进一步推算分次高剂量率(HDR)近距离放射治疗的黏膜耐受情况。

材料与方法

回顾性分析1987年至1997年间仅接受放射治疗的274例I-IV期宫颈癌患者近端阴道的放射性晚期后遗症。所有患者均接受LDR近距离放射治疗,95%的患者还接受了盆腔体外照射。随访时间为15至126个月(中位时间43个月)。利用最大似然逻辑回归技术,根据单个卵形体(单源)或两个卵形体加施源器(所有源)的近端阴道黏膜剂量以及体外照射剂量,推算并发症发生概率。基于线性二次模型的BED用于计算LDR或HDR近距离放射治疗的相应耐受水平。

结果

10.6%的患者发生1级和2级并发症,3.6%的患者发生3级并发症。无4级并发症。并发症发生于放疗结束后3至71个月(中位时间7个月),超过60%的并发症发生在第一年。通过逻辑回归分析,单个卵形体的黏膜剂量或所有源的黏膜剂量与体外照射剂量相结合,均显示出与剂量反应并发症曲线具有统计学意义的拟合度(P均=0.016)。单源剂量与所有源剂量高度相关,交叉相关系数为0.93。所有源剂量约为单源剂量的1.4倍。在LDR近距离放射治疗剂量率范围内,并发症发生率相对稳定,不受基础肿瘤生物学特性和剂量率微小变化的影响。在α/β比值从2至4 Gy以及修复常数(μ)从0.46/h至0.60/h的范围内,并发症发生率变化约为绝对1%。随着黏膜剂量率从1.75 Gy/h增加到3.50 Gy/h,并发症发生率增加绝对2%。当剂量率高于3.00 Gy/h时,如在HDR近距离放射治疗中,并发症发生率显著增加。对于名义上3%-5%的并发症发生率,推算的HDR 3级耐受剂量从单次分割的25 Gy到六次分割的57 Gy不等,外加20 Gy的体外照射。传统的LDR耐受剂量150 Gy显示出名义上分别有11%和4%的1级和2级以及3级后遗症。

结论

对于名义上5%的3级并发症发生率,传统的150 Gy LDR耐受剂量(单源加体外照射)可放宽至175 Gy,或等效于全黏膜剂量238 Gy(所有源加体外照射)。对于类似的后遗症发生率,HDR治疗需要四至六次分割。单个卵形体的黏膜表面剂量易于计算,仍是治疗计划中方便的耐受检查指标。

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