接受新辅助治疗的患者在乳腺磁共振成像中发现新的或可疑磁共振成像结果的频率和结果。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-10-26 DOI:10.1007/s10549-024-07511-7
Sona A Chikarmane, Averi Gibson, Allyson L Chesebro, Catherine S Giess
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引用次数: 0

摘要

目的:评估新辅助治疗(NAT)患者乳腺 MRI 上与指标原发肿瘤无关的不确定增强结果的频率和结果:这项回顾性研究确定了我院在 2017 年至 2020 年期间为评估 NAT 反应而进行的所有诊断性乳腺 MRI。所有与指标肿瘤无关的不确定增强结果(BI-RADS 3-5)、建议进行后续成像或组织诊断的检查均被纳入其中。缺乏治疗前磁共振成像的病例或随访不足的病例被排除在外。对所有 NAT 后乳腺 MRI 的成像进行重新审查。对电子病历进行审查,以评估患者和病变特征及结果:2017年至2020年期间,为评估对NAT的反应,进行了614/4042(15.2%)次乳腺MRI检查。排除后,这些检查中有 38 次(6.2%)发现了 42 个与指标肿瘤无关的不确定增强结果,建议进行后续成像(15 次)或组织诊断(23 次)。与治疗前的基线 MRI 相比,42 项检查结果中有 15 项(35.7%)是新发现的,8/42(19.0%)有所增加,19/42(45.2%)在治疗前的 MRI 中就存在。大多数检查结果出现在指数肿瘤的对侧(28 例,66.7%)。检查结果包括肿块(17 例,40.4%)、病灶(15 例,35.7%)和非肿块增强(10 例,23.8%)。在 42 项检查结果中,19 项(45.2%)进行了经皮活检,10 项(23.8%)进行了手术活检或乳房切除术,13 项(31%)进行了造影检查。37例为良性病变,4例为未升级的高危病变(非典型导管增生、非典型小叶增生和乳头状瘤病伴非典型导管增生),1例(2.4%)为恶性病变(浸润性小叶癌),治疗前的核磁共振成像显示为非肿块增强:结论:为评估新辅助化疗反应而进行的乳腺磁共振成像检查中,与指标肿瘤无关的不确定增强病灶并不常见。这些病变一旦出现,其恶性的可能性极低,尤其是与治疗前的磁共振成像相比:临床意义:由于新辅助化疗后随访时乳腺 MRI 上的偶发不确定增强病变很少是恶性的,因此放射科医生在建议对新辅助化疗后的此类病变进行随访或组织诊断时应审慎行事。
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Frequency and outcomes of new or suspicious MRI findings on breast MRI for patients on neoadjuvant therapy.

Purpose: To assess the frequency and outcomes of indeterminate enhancing findings on breast MRI unrelated to the index primary tumor(s) in patients on neoadjuvant therapy (NAT).

Materials and methods: This retrospective review identified all diagnostic breast MRIs performed to evaluate response to NAT at our institution between 2017 and 2020. All exams with indeterminate enhancing findings (BI-RADS 3-5) unrelated to the index tumor(s) for which follow-up imaging or tissue diagnosis was recommended were included. Cases lacking a pre-treatment MRI or those with insufficient follow-up were excluded. Imaging of all post-NAT breast MRIs were re-reviewed. The electronic medical record was reviewed to evaluate patient and lesion characteristics and outcomes.

Results: Between 2017 and 2020, 614/4042 (15.2%) breast MRIs were performed to evaluate response to NAT. After exclusions, 38 of these exams (6.2%) identified 42 indeterminate enhancing findings unrelated to the index tumor for which follow-up imaging (15 exams) or tissue diagnosis (23 exams) was recommended. Fifteen of 42 (35.7%) of the findings were new compared to the pre-treatment baseline MRI, 8/42 (19.0%) increased and 19/42 (45.2%) were present on pre-treatment MRI. Most findings were contralateral to the index tumor (28, 66.7%). Findings were masses (17, 40.4%), focus (15, 35.7%), and non-mass enhancement (10, 23.8%). Of the 42 findings, 19 (45.2%) underwent percutaneous biopsy, 10 (23.8%) underwent surgical biopsy or mastectomy, and 13 (31%) were followed by imaging. Thirty-seven were benign, 4 were high-risk lesions without upgrade (atypical ductal hyperplasia, atypical lobular hyperplasia, and papillomatosis with atypical ductal hyperplasia), and one (2.4%) was malignant (invasive lobular carcinoma), which was non-mass enhancement present on the pre-treatment MRI.

Conclusion: Indeterminate enhancing lesions unrelated to the index tumor(s) on breast MRIs performed to assess response to neoadjuvant chemotherapy are uncommon. When present, these lesions have an extremely low likelihood of malignancy, especially when new compared to the pre-treatment MRI.

Clinical relevance: Because incidental indeterminate enhancing lesions on breast MRI at post-NAT follow-up are rarely malignant, radiologists should be judicious in recommending follow-up or tissue diagnosis for such lesions after NAT.

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