Department of Biomedical Sciences, Humanitas University, Milan, Italy.
IRCCS Humanitas Research Hospital, Via Manzoni 56, 20089 Rozzano, Milan, Italy.
AJR Am J Roentgenol. 2022 Dec;219(6):884-894. doi: 10.2214/AJR.22.27756. Epub 2022 Jun 22.
Contrast-enhanced mammography (CEM) is rapidly expanding as a credible alternative to MRI in various clinical settings. The purpose of this study was to compare CEM and MRI for neoadjuvant therapy (NAT) response assessment in patients with breast cancer. This prospective study included 51 patients (mean age, 46 ± 11 [SD] years) with biopsy-proven breast cancer who were candidates for NAT from May 2015 to April 2018. Patients underwent both CEM and MRI before, during, and after NAT (pre-NAT, mid-NAT, and post-NAT, respectively). Post-NAT CEM included a 6-minute delayed acquisition. One breast radiologist with experience in CEM reviewed CEM examinations; one breast radiologist with experience in MRI reviewed MRI examinations. The radiologists assessed for the presence of an enhancing lesion; if an enhancing lesion was detected, its size was measured. RECIST version 1.1 response assessment categories were derived. Pathologic complete response (pCR) was defined as absence of both invasive cancer and ductal carcinoma in situ (DCIS). Of 51 patients, 16 achieved pCR. CEM yielded systematically lower size measurements compared with MRI (mean difference, -0.2 mm for pre-NAT, -0.7 mm for mid-NAT, and -0.3 mm for post-NAT). All post-NAT imaging tests yielded systematically larger size measurements compared with pathology (mean difference, 0.8 mm for CEM, 1.2 mm for MRI, and 1.9 mm for delayed CEM). Of 12 patients with residual DCIS, an enhancing lesion was detected in seven on post-NAT CEM, eight on post-NAT MRI, and nine on post-NAT delayed CEM. Agreement of RECIST response categories between CEM and MRI, expressed as kappa coefficient, was 0.791 at mid-NAT and 0.871 at post-NAT. For detecting pCR by post-NAT imaging, sensitivity and specificity were 81% and 83% for CEM, 100% and 86% for MRI, and 81% and 89% for delayed CEM. Sensitivity was significantly higher for MRI than CEM ( = .001) and delayed CEM ( = .002); remaining comparisons were not significant ( > .05). After NAT for breast cancer, CEM and MRI yielded comparable assessments of lesion size (both slightly overestimated vs pathology) and RECIST categories and showed no significant difference in specificity for pCR. MRI had higher sensitivity for pCR. Delayed CEM acquisition may help detect residual DCIS. Although MRI remains the preferred test for NAT response monitoring, the findings support CEM as a useful alternative when MRI is contraindicated or not tolerated.
对比增强乳腺摄影(CEM)作为 MRI 在各种临床环境中的可靠替代方案正在迅速发展。本研究的目的是比较 CEM 和 MRI 在接受新辅助治疗(NAT)的乳腺癌患者中的疗效评估。这项前瞻性研究纳入了 51 名(平均年龄,46±11[SD]岁)经活检证实患有乳腺癌并符合 NAT 条件的患者,这些患者于 2015 年 5 月至 2018 年 4 月期间接受治疗。患者在接受 NAT 前(pre-NAT)、期间(mid-NAT)和之后(post-NAT)分别接受了 CEM 和 MRI 检查。post-NAT CEM 包括 6 分钟延迟采集。一位有 CEM 检查经验的乳腺放射科医师评估了 CEM 检查;一位有 MRI 检查经验的乳腺放射科医师评估了 MRI 检查。放射科医师评估增强病变的存在;如果检测到增强病变,则测量其大小。根据 RECIST 1.1 标准评估治疗反应类别。无浸润性癌和导管原位癌(DCIS)的完全病理缓解(pCR)定义为不存在。51 名患者中,16 名达到 pCR。与 MRI 相比,CEM 系统地提供了更低的大小测量值(pre-NAT 时的平均差异为-0.2mm,mid-NAT 时为-0.7mm,post-NAT 时为-0.3mm)。所有 post-NAT 成像检查与病理相比系统地提供了更大的大小测量值(CEM 为 0.8mm,MRI 为 1.2mm,延迟 CEM 为 1.9mm)。在 12 名残留 DCIS 的患者中,7 名患者在 post-NAT CEM 上,8 名患者在 post-NAT MRI 上,9 名患者在 post-NAT 延迟 CEM 上检测到增强病变。CEM 和 MRI 之间的 RECIST 反应类别之间的一致性,用kappa 系数表示,在 mid-NAT 时为 0.791,在 post-NAT 时为 0.871。对于通过 post-NAT 成像检测 pCR,CEM 的敏感性和特异性分别为 81%和 83%,MRI 为 100%和 86%,延迟 CEM 为 81%和 89%。MRI 的敏感性明显高于 CEM(=0.001)和延迟 CEM(=0.002);其余比较无显著性差异(>0.05)。乳腺癌接受新辅助治疗后,CEM 和 MRI 对病变大小(均略高于与病理相比)和 RECIST 类别进行了相似的评估,并且 pCR 的特异性无显著差异。MRI 对 pCR 的敏感性更高。延迟 CEM 采集可能有助于检测残留的 DCIS。尽管 MRI 仍然是 NAT 反应监测的首选检查,但这些发现支持 CEM 作为 MRI 禁忌或不耐受时的有用替代方案。