Department of Pathology, University of Pittsburgh School of Medicine, UPMC Magee-Womens Hospital, Pittsburgh, Pennsylvania.
Department of Surgery, University of Pittsburgh School of Medicine, UPMC Magee-Womens Hospital, Pittsburgh, Pennsylvania.
Mod Pathol. 2024 Apr;37(4):100462. doi: 10.1016/j.modpat.2024.100462. Epub 2024 Feb 28.
The primary aim of this study was to determine the upgrade rates of variant lobular carcinoma in situ (V-LCIS, ie, combined florid [F-LCIS] and pleomorphic [P-LCIS]) compared with classic LCIS (C-LCIS) when diagnosed on core needle biopsy (CNB). The secondary goal was to determine the rate of progression/development of invasive carcinoma on long-term follow-up after primary excision. After institutional review board approval, our institutional pathology database was searched for patients with "pure" LCIS diagnosed on CNB who underwent subsequent excision. Radiologic findings were reviewed, radiologic-pathologic (rad-path) correlation was performed, and follow-up patient outcome data were obtained. One hundred twenty cases of LCIS were identified on CNB (C-LCIS = 97, F-LCIS = 18, and P-LCIS = 5). Overall upgrade rates after excision for C-LCIS, F-LCIS, and P-LCIS were 14% (14/97), 44% (8/18), and 40% (2/5), respectively. Of the total cases, 79 (66%) were deemed rad-path concordant. Of these, the upgrade rate after excision for C-LCIS, F-LCIS, and P-LCIS was 7.5% (5 of 66), 40% (4 of 10), and 0% (0 of 3), respectively. The overall upgrade rate for V-LCIS was higher than for C-LCIS (P = .004), even for the cases deemed rad-path concordant (P value: .036). Most upgraded cases (23 of 24) showed pT1a disease or lower. With an average follow-up of 83 months, invasive carcinoma in the ipsilateral breast was identified in 8/120 (7%) cases. Six patients had died: 2 of (contralateral) breast cancer and 4 of other causes. Because of a high upgrade rate, V-LCIS diagnosed on CNB should always be excised. The upgrade rate for C-LCIS (even when rad-path concordant) is higher than reported in many other studies. Rad-path concordance read, surgical consultation, and individualized decision making are recommended for C-LCIS cases. The risk of developing invasive carcinoma after LCIS diagnosis is small (7% with ∼7-year follow-up), but active surveillance is required to diagnose early-stage disease.
本研究的主要目的是确定在核心针活检(CNB)中诊断为变异型小叶原位癌(V-LCIS,即合并华丽型[F-LCIS]和多形型[P-LCIS])与经典小叶原位癌(C-LCIS)的升级率。次要目标是确定原发性切除后长期随访时浸润性癌进展/发展的发生率。在获得机构审查委员会批准后,我们对在 CNB 上诊断为“纯”LCIS 并随后进行切除的患者进行了机构病理学数据库搜索。回顾了影像学发现,进行了放射病理学(rad-path)相关性分析,并获得了随访患者的结果数据。在 CNB 上发现了 120 例 LCIS(C-LCIS=97 例,F-LCIS=18 例,P-LCIS=5 例)。切除后 C-LCIS、F-LCIS 和 P-LCIS 的总体升级率分别为 14%(14/97)、44%(8/18)和 40%(2/5)。在总病例中,79 例(66%)被认为是 rad-path 一致的。其中,C-LCIS、F-LCIS 和 P-LCIS 的切除后升级率分别为 7.5%(5/66)、40%(4/10)和 0%(0/3)。V-LCIS 的总体升级率高于 C-LCIS(P=.004),即使是被认为是 rad-path 一致的病例也是如此(P 值:.036)。大多数升级病例(24 例中的 23 例)显示 pT1a 疾病或更低。平均随访 83 个月后,在 120 例病例中发现同侧乳房浸润性癌 8 例(7%)。6 例患者死亡:2 例死于(对侧)乳腺癌,4 例死于其他原因。由于升级率较高,CNB 诊断的 V-LCIS 应始终切除。C-LCIS 的升级率(即使 rad-path 一致)高于许多其他研究报道。推荐对 C-LCIS 病例进行放射病理学一致性阅读、手术咨询和个体化决策。LCIS 诊断后发生浸润性癌的风险较小(7 年随访时为 7%),但需要进行主动监测以诊断早期疾病。