Abstract GS4-05: Dose escalated simultaneous integrated boost radiotherapy for women treated by breast conservation surgery for early breast cancer: 3-year adverse effects in the IMPORT HIGH trial (CRUK/06/003)

C. Coles, C. Griffin, A. Kirby, J. Haviland, J. Titley, K. Benstead, A. Brunt, C. Chan, L. Ciurlionis, O. Din, E. Donovan, D. Eaton, A. Harnett, P. Hopwood, M. Jefford, P. Jenkins, CE. Lee, M. McCormack, L. Sherwin, I. Syndikus, Y. Tsang, N. Twyman, R. Ventikaraman, S. Wickers, M. Wilcox, J. Bliss, J. Yarnold
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引用次数: 14

Abstract

Background IMPORT HIGH is a randomised, multi-centre phase III trial testing dose escalated simultaneous integrated boost (SIB) against sequential boost each delivered by intensity modulated radiotherapy (IMRT) for early stage breast cancer with higher risk of local relapse. The primary endpoint was initially breast induration at 3 years, requiring 840 patients; accrual was extended (target 2568) with the new primary endpoint of local relapse. We report adverse effects (AE) at 3 years. Methods Women age ≥18 after breast conservation surgery for pT1-3 pN0-pN3a M0 invasive carcinoma were eligible. Randomisation was 1:1:1 between 40Gy/15F to whole breast (WB) + 16Gy/8F sequential photon boost to tumour bed (40+16Gy), 36Gy/15F to WB, 40Gy to partial breast + 48Gy (48Gy) or + 53Gy (53Gy) in 15F SIB to tumour bed. AEs were assessed annually by clinicians in all patients and in a planned sub-set (840) of patients by photographs at 3 years and by patients at 6 months, 1 and 3 years. AE scores were dichotomised as none/mild vs marked for photographs and none/mild vs moderate/marked for patients and clinicians. Fisher9s exact tests compared groups; principal comparison (protocol-specified) between 53Gy and 48Gy (p Results 2617 women consented between 03/2009 and 09/2015 from 39 UK radiotherapy centres. Median follow-up was 49.1 (IQR 36.8-63.2) months. Median age was 49 (IQR 44-56); 9%, 38% & 53% were tumour grade 1, 2 & 3 respectively; 30% were node positive. 66% received chemotherapy and 73% endocrine therapy. 3-year AE data were available for 2017 clinician assessments, 641 photographs and 842 patient assessments. Proportions of patients with marked AEs were low overall. Rates of moderate/marked AEs at 3 years were broadly similar between the randomised groups; with a suggestion of a slightly increased risk for breast induration in 53Gy compared with control (borderline significance). Conclusions These results represent the largest and most mature reported AE outcomes of breast SIB within a clinical trial. At 3 years, rates of moderate/marked AEs were similar between SIB IMRT and WB + sequential boost IMRT delivered over 3 and 4.5 weeks respectively. Citation Format: Coles CE, Griffin CL, Kirby AM, Haviland JS, Titley JC, Benstead K, Brunt AM, Chan C, Ciurlionis L, Din OS, Donovan EM, Eaton DJ, Harnett AN, Hopwood P, Jefford ML, Jenkins PJ, Lee CE, McCormack M, Sherwin L, Syndikus I, Tsang Y, Twyman NI, Ventikaraman R, Wickers S, Wilcox MH, Bliss JM, Yarnold JR. Dose escalated simultaneous integrated boost radiotherapy for women treated by breast conservation surgery for early breast cancer: 3-year adverse effects in the IMPORT HIGH trial (CRUK/06/003) [abstract]. In: Proceedings of the 2018 San Antonio Breast Cancer Symposium; 2018 Dec 4-8; San Antonio, TX. Philadelphia (PA): AACR; Cancer Res 2019;79(4 Suppl):Abstract nr GS4-05.
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GS4-05:在IMPORT HIGH试验(CRUK/06/003)中,剂量递增同时综合增强放疗对早期乳腺癌保乳手术患者的3年不良反应。
IMPORT HIGH是一项随机、多中心III期试验,测试剂量递增的同步综合增强(SIB)与强度调节放疗(IMRT)对局部复发风险较高的早期乳腺癌的顺序增强。主要终点是最初的3年乳房硬化,需要840例患者;随着局部复发这一新的主要终点,累积时间延长(目标2568)。我们报告了3年的不良反应(AE)。方法选择年龄≥18岁的pT1-3 - pN0-pN3a M0浸润性癌保乳术后患者。40Gy/15F到全乳房(WB) +16Gy /8F连续光子增强到肿瘤床(40+16Gy), 36Gy/15F到WB, 40Gy到部分乳房+ 48Gy (48Gy)或15F SIB到肿瘤床+ 53Gy (53Gy)的随机分组为1:1:1。临床医生每年对所有患者进行ae评估,并在计划的患者亚组(840名)中对3年、6个月、1年和3年的患者进行照片评估。AE评分分为无/轻度vs标记照片,无/轻度vs中度/标记患者和临床医生。fisher 9的精确测试比较各组;53Gy和48Gy的主要比较(方案指定)(p)结果:2009年3月至2015年9月期间,来自39个英国放疗中心的2617名妇女同意接受放疗。中位随访时间为49.1个月(IQR 36.8-63.2)。中位年龄49岁(IQR 44-56);1级、2级和3级分别占9%、38%和53%;30%为淋巴结阳性。66%接受化疗,73%接受内分泌治疗。2017年临床医生评估、641张照片和842例患者评估均可获得3年AE数据。明显ae患者的比例总体较低。3年中度/显著ae发生率在随机分组之间大致相似;与对照组相比,53Gy时乳房硬化的风险略有增加(临界意义)。这些结果代表了临床试验中报道的最大和最成熟的乳腺SIB AE结果。在3年时,SIB IMRT和WB +顺序增强IMRT分别在3周和4.5周内进行,中度/显著ae的发生率相似。引用格式:Coles CE, Griffin CL, Kirby AM, Haviland JS, Titley JC, Benstead K, brent AM, Chan C, Ciurlionis L, Din OS, Donovan EM, Eaton DJ, Harnett AN, Hopwood P, Jefford ML, Jenkins PJ, Lee CE, McCormack M, Sherwin L, Syndikus I, Tsang Y, Twyman NI, Ventikaraman R, Wickers S, Wilcox MH, Bliss JM, Yarnold JR。早期乳腺癌保乳手术患者同步提升放疗剂量的研究:IMPORT HIGH试验3年不良反应(CRUK/06/003)[摘要]。2018年圣安东尼奥乳腺癌研讨会论文集;2018年12月4-8日;费城(PA): AACR;癌症杂志,2019;79(4增刊):摘要nr GS4-05。
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