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Acute toxicity of normofractionated intensity modulated radiotherapy with simultaneous integrated boost compared to three-dimensional conformal radiotherapy with sequential boost in the adjuvant treatment of breast cancer

机译:与乳腺癌佐剂治疗中的三维保形放射同时集成升压同时集成升压的急性毒性

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Intensity-modulated radiotherapy (IMRT) improves dose homogeneity and late toxicity compared to simple tangential techniques in adjuvant whole-breast radiotherapy for patients with breast cancer. Simultaneous-integrated boost (SIB) radiotherapy shortens the overall treatment time and improves dose homogeneity. However, prospective randomized trials regarding IMRT with SIB for adjuvant radiotherapy in breast cancer are lacking. The IMRT-MC2 (MINT) trial is a phase III prospective randomized controlled trial comparing IMRT with SIB (Arm A: whole breast 28?×?1.8?Gy, Boost 28?×?2.3?Gy) to 3D-conformal radiotherapy with a sequential boost (Arm B: whole breast 28?×?1.8?Gy, boost 8?×?2 Gy) in patients with breast cancer after BCS. Indication for boost radiotherapy was defined as age 70?years with presence of additional risk factors. This is a retrospective analysis of acute toxicity at one of two trial sites. Five hundred two patients were randomized, of which 446 patients were eligible for this analysis. There was no statistically significant difference in terms of any grade radiation dermatitis between the two treatment arms at the end of treatment (p?=?0.26). However, radiation dermatitis grade 2/3 (29.1% vs. 20.1 and 3.5% vs. 2.3%) occurred significantly more often in Arm A (p?=?0.02). Breast/chest wall pain at the first follow-up visit was significantly more common in patients treated on Arm B (p?=?0.02). Treatment on both arms was well tolerated, however there were some differences regarding radiodermatitis and breast pain. Further analyses are ongoing. clinicaltrials.gov , NCT01322854 , registered 24th March 2011.
机译:与乳腺癌患者辅助全乳房放射治疗的简单切向技术相比,强度调节放疗(IMRT)改善了剂量均匀性和晚期毒性。同时整理的增压(SIB)放射疗法缩短了整体治疗时间并提高了剂量均匀性。然而,缺乏关于乳腺癌中辅助放射治疗的ICRT的前瞻性随机试验。 IMRT-MC2(MINT)试验是一种相位III前瞻性随机对照试验,比较IMRT与SIB(ARM A:整个乳房28?×1.8?GY,促进28?×2.3?GY)到3D-保形放射疗法顺序提升(ARM B:整个乳房28?×1.8?GY,BCS后乳腺癌患者患有8?×2Gy)。促进放疗的迹象被定义为年龄70岁?有额外危险因素的年龄。这是两项试验网站之一对急性毒性的回顾性分析。五百名患者随机化,其中446名患者有资格进行此分析。在治疗结束时,两个治疗臂之间的任何级辐射皮炎的术语没有统计学意义(p?= 0.26)。然而,辐射皮炎2/3级(29.1%vs.10.1和3.5%vs.2.3%)在ARm A中经常发生显着频率(p?= 0.02)。在ARM在ARM(p≤x0.02)上的患者中,乳房/胸壁疼痛在第一次随访中的疼痛是更常见的(p?= 0.02)。两臂的治疗耐受良好,但有关淋巴炎和乳房疼痛存在一些差异。进一步分析正在进行中。 ClinicalTrials.gov,NCT01322854,2011年3月24日注册。

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