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两种 3 至 5 周同步推量适形调强放射治疗与标准 6 周乳房放射治疗急性和迟发性毒性比较。

Comparison of Acute and Late Toxicity of Two Regimens of 3- and 5-Week Concomitant Boost Prone IMRT to Standard 6-Week Breast Radiotherapy.

机构信息

Department of Radiation Oncology and Surgery, New York University School of Medicine, New York University Langone Medical Center New York, NY, USA.

出版信息

Front Oncol. 2012 May 8;2:44. doi: 10.3389/fonc.2012.00044. eCollection 2012.

Abstract

PURPOSE

Limited information is available comparing toxicity of accelerated radiotherapy (RT) to that of standard fractionation RT for early stage breast cancer. We report early and late toxicities of two prone regimens of accelerated intensity-modulated radiation therapy (IMRT) with a concomitant boost (CB) to the tumor bed delivered over 3 or 5 weeks as compared to standard 6 week RT with a sequential electron boost.

METHODS

From 2/2003 to 12/2007, 169 consecutive patients with Stage I-II breast cancer were offered the choice to undergo prone RT with either: a 6-week standard RT regimen of 46 Gy/23 fractions (fx) to the whole breast (WB), followed by a14 Gy sequential boost (SB) to the tumor bed (6wSB), a 5-week regimen of 50 Gy to WB with an IMRT CB of 6.25 Gy in 25 fx (5wCB); or a 3-week protocol of 40.5 Gy to WB with an IMRT CB of 7.5 Gy in 15 fx (3wCB). These regimens were estimated as biologically equivalent, based on alpha/beta = 4 for tumor control. Toxicities were reported using RTOG and LENT/SOMA scoring.

RESULTS

51/169 patients chose standard 6wSB, 28 selected 5wCB, and 90 enrolled in 3wCB protocol. Maximum acute toxicity was Grade 3 dermatitis in 4% of the patients in the 6wSB compared 1% in 3wCB. In general, acute complications (breast pain, fatigue, and dermatitis) were significantly less in the 3wCB than in the other schedules (P < 0.05). With a median follow-up of 61 months, the only Grade 3 late toxicity was telangiectasia in two patients: one in 3wCB and one in 5wCB group. Notably, fibrosis was comparable among the three groups (P = NS).

CONCLUSION

These preliminary data suggest that accelerated regimens of breast RT over 3 or 5 weeks in the prone position, with an IMRT tumor bed CB, result in comparable late toxicity to standard fractionation with a sequential tumor boost delivered over 6 weeks. As predicted by radiobiological modeling the shorter regimen was associated with less acute effects.

摘要

目的

早期乳腺癌加速放疗(RT)与标准分割 RT 的毒性比较信息有限。我们报告了两种俯卧位加速强度调制放疗(IMRT)方案的早期和晚期毒性,这些方案同时对肿瘤床进行了调强放疗(CB),治疗时间分别为 3 周和 5 周,与标准的 6 周 RT 序贯电子加量相比。

方法

从 2003 年 2 月至 2007 年 12 月,169 例 I 期-II 期乳腺癌患者可选择接受以下两种俯卧位 RT 方案:6 周标准 RT 方案,46Gy/23 次(fx)全乳(WB),随后 14Gy 序贯加量(SB)至肿瘤床(6wSB);5 周 50Gy 至 WB,同时进行 IMRT 调强放疗 CB 6.25Gy,共 25fx(5wCB);或 3 周 40.5Gy 至 WB,同时进行 IMRT 调强放疗 CB 7.5Gy,共 15fx(3wCB)。这些方案基于肿瘤控制的α/β=4 进行了生物学等效性估计。毒性采用 RTOG 和 LENT/SOMA 评分进行报告。

结果

169 例患者中,51 例选择标准 6wSB,28 例选择 5wCB,90 例选择 3wCB 方案。6wSB 组有 4%的患者出现最大急性毒性为 3 级皮炎,而 3wCB 组仅为 1%。一般来说,3wCB 组的急性并发症(乳房疼痛、疲劳和皮炎)明显少于其他方案(P<0.05)。中位随访 61 个月,仅出现 2 例 3 级晚期毒性,即 2 例患者均为毛细血管扩张症,其中 1 例为 3wCB 组,1 例为 5wCB 组。值得注意的是,三组之间的纤维化程度相当(P=NS)。

结论

这些初步数据表明,俯卧位 3 周或 5 周加速乳腺 RT 方案,同时对肿瘤床进行 IMRT 调强放疗 CB,与标准分割 6 周序贯肿瘤加量治疗的晚期毒性相当。正如放射生物学建模预测的那样,较短的治疗方案与较轻的急性副作用相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e22/3355878/0349efb54b8b/fonc-02-00044-g001.jpg

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