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Total hemoglobin changes in the breast tumors of patients undergoing neoadjuvant chemotherapy: a longitudinal analysis

机译:接受Neoadjuvant化疗的患者乳腺肿瘤的总血红蛋白变化:纵向分析

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Optical imaging techniques have emerged as a possible alternative to predict pathological complete response (pCR) in breast cancer patients undergoing neoadjuvant chemotherapy (NAC). Our team developed a so-called diffuse optical tomographic breast imaging system (DOTBIS) which does not require the use of contrast agents or compression and enables imaging of the whole breast volume using low intensity near infrared light capable to measure tissue concentration of total hemoglobin (ctTHb). In this retrospective study, we evaluated 55 stage Ⅱ-Ⅲ BC patients in the neoadjuvant setting who received weekly paclitaxel × 12. followed by dose-dense adriamycin/cyclophosphamidc every 2 weeks × 4. DOTBIS images were acquired from the patient whole breast volume at 6 different time points: at baseline (TP0); two weeks after the first taxane infusion (TP1): after four infusions of taxane (TP2); at the end of the taxane regimen and before starting AC cycle (TP3); after two AC infusions (TP4); and at the end of NAC and before surgery (TP5). In order to evaluate whether pCR status influences the change of ctTHb over time, we designed a multilevel mixed-effect model. pCR was defined as no invasive tumor cells from the breast and axillary tissue at surgery (ypT0 ypN0). Changes in ctTHb levels compared to baseline (TP0) values were statistically significant different between pCR (n = 20) and non-pCR (n=35) at all time points except at TP1 and at the end of the taxane cycle (TP3).
机译:光学成像技术已成为可能的替代方案,以预测接受新辅助化疗(NAC)的乳腺癌患者的病理完全反应(PCR)。我们的团队开发了一种所谓的弥漫性光学断层乳房成像系统(Dotbis),其不需要使用造影剂或压缩,并且可以使用能够测量总血红蛋白的组织浓度的近红外光线的低强度进行整体乳腺量的成像( CTTHB)。在这项回顾性研究中,我们在接受每周紫杉醇×12的新辅助设定中评估了55阶段Ⅱ-Ⅲ型BC患者。随后用剂量 - 致密的adriamycin /环膦Amidc每2周×4.达比特图像从患者的全乳腺量获得6不同的时间点:在基线(TP0);第一次紫杉烷输注后两周(TP1):在四个紫杉烷排名后(TP2);在紫杉烷方案结束时和在开始AC周期之前(TP3);两次交流输注(TP4)后;在NAC和手术前的结束时(TP5)。为了评估PCR状态是否会影响CTTHB的变化,我们设计了一种多级混合效应模型。 PCR定义为手术(YPT0 YPN0)的来自乳腺和腋中的侵入性肿瘤细胞。与基线(TP0)值相比的CTTHB水平的变化在除了TP1和紫杉烷循环的末端之外的PCR(n = 20)和非PCR(n = 35)之间的统计学上显着不同(TP3)。

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