Department of Radiation Oncology, University of Washington, Seattle, Washington.
Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Int J Radiat Oncol Biol Phys. 2015 Nov 1;93(3):622-30. doi: 10.1016/j.ijrobp.2015.07.006. Epub 2015 Jul 11.
PURPOSE: To evaluate locoregional recurrence (LRR) after mastectomy and impact of postmastectomy radiation (PMRT) by breast cancer subtype. METHODS AND MATERIALS: Between 2000 and 2009, 5673 patients with stage I to III breast carcinoma underwent mastectomy and nodal evaluation; 30% received PMRT. Isolated LRR (iLRR) and LRR were compared across groups defined by biological subtype and receipt of trastuzumab: luminal A (estrogen [ER]/progesterone [PR]+, HER2-, low/intermediate grade), luminal B (ER/PR+, HER2-, high grade), HER2 with trastuzumab, HER2 without trastuzumab, and triple negative (TN; ER-, PR-, HER2-). LRR hazard ratios (HR) were estimated with multivariable Fine and Gray models. The effect of PMRT on LRR was evaluated with Fine and Gray models stratified by propensity for PMRT. RESULTS: With a median follow-up time of 50.1 months, there were 19 iLRR and 109 LRR events. HER2 patients with trastuzumab had no iLRR and only a single LRR. Compared with luminal A patients, TN patients had significantly greater adjusted risk of iLRR (HR 14.10; 95% CI 2.97%-66.90%), with a similar trend among luminal B (HR 4.94; 95% CI 0.94%-25.82%) and HER2 patients without trastuzumab (HR 4.41; 95% CI 0.61%-32.11%). Although PMRT reduced LRR, the effect of PMRT varied by subgroup, with the greatest and smallest effects seen among luminal A (HR 0.17; 95% CI 0.05%-0.62%) and TN patients (HR 0.59; 95% CI 0.25%-1.35%), respectively. CONCLUSIONS: TN patients had the highest risk of LRR and the least benefit from PMRT; these patients may benefit from alternative treatment strategies. In contrast, in the era of HER2-directed therapy, the role of local therapy may need to be reassessed among HER2 patients.
目的:评估乳腺癌亚型术后局部区域复发(LRR)和术后放疗(PMRT)的影响。
方法与材料:2000 年至 2009 年间,5673 例 I 至 III 期乳腺癌患者接受了乳房切除术和淋巴结评估;30%的患者接受了 PMRT。通过生物亚型和曲妥珠单抗使用情况将孤立性 LRR(iLRR)和 LRR 进行比较: luminal A(雌激素[ER]/孕激素[PR]+,HER2-,低/中级别)、luminal B(ER/PR+,HER2-,高级别)、HER2 伴曲妥珠单抗、HER2 无曲妥珠单抗和三阴性(TN;ER-,PR-,HER2-)。采用多变量 Fine 和 Gray 模型估计 LRR 风险比(HR)。采用 Fine 和 Gray 模型分层分析 PMRT 倾向,评估 PMRT 对 LRR 的影响。
结果:中位随访时间为 50.1 个月,有 19 例 iLRR 和 109 例 LRR 事件。HER2 伴曲妥珠单抗的患者没有 iLRR,仅有 1 例 LRR。与 luminal A 患者相比,TN 患者调整后的 iLRR 风险显著更高(HR 14.10;95%CI 2.97%-66.90%),luminal B(HR 4.94;95%CI 0.94%-25.82%)和无曲妥珠单抗的 HER2 患者(HR 4.41;95%CI 0.61%-32.11%)也有类似的趋势。尽管 PMRT 降低了 LRR,但 PMRT 的效果因亚组而异,luminal A 患者的效果最大(HR 0.17;95%CI 0.05%-0.62%),而 TN 患者的效果最小(HR 0.59;95%CI 0.25%-1.35%)。
结论:TN 患者 LRR 风险最高,PMRT 获益最小;这些患者可能受益于替代治疗策略。相比之下,在曲妥珠单抗靶向治疗时代,HER2 患者的局部治疗作用可能需要重新评估。
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