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多变量模型识别在核心针活检诊断为非典型导管增生后癌症升级风险低的女性。

Multivariate model to identify women at low risk of cancer upgrade after a core needle biopsy diagnosis of atypical ductal hyperplasia.

机构信息

Department of Surgery, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, 55905, USA.

出版信息

Breast Cancer Res Treat. 2017 Jul;164(2):295-304. doi: 10.1007/s10549-017-4253-1. Epub 2017 May 4.

Abstract

PURPOSE

Atypical ductal hyperplasia (ADH) identified on percutaneous breast biopsy represents a high-risk lesion, upgrading to cancer with surgical excision in ~7-45.8% of cases. Routine excision is questioned due to potential overtreatment and cost. This study evaluates clinical, imaging, and histologic features to predict the risk of upgrade.

METHODS

With IRB approval, a single-institution retrospective review was performed of patients who underwent surgical excision of ADH diagnosed by core biopsy from June 2005 to June 2013. We reviewed electronic medical records, breast imaging, and biopsy slides. Multiple imputation was used for missing data. Association of various features with cancer upgrade was assessed using logistic regression.

RESULTS

Among 399 cases, the upgrade rate to cancer was 16.0%, (95% CI: 12.8-20.0%), with nine invasive cancers and 55 ductal carcinoma in situ (DCIS) only. Via a logistic regression approach, we defined a subgroup with low risk for upgrade: women whose biopsies showed no individual cell necrosis, and either a) 1 focus of ADH with ≥50% removal, or b) 2-3 foci with ≥90% removal. Cases meeting these criteria had an upgrade rate of 4.9% (95% CI: 1.0-8.9%), compared to 21.4% (16.4-26.3%) in cases that did not meet this low-risk definition.

CONCLUSIONS

ADH on core biopsy with low risk of upgrade to cancer is defined by lack of individual cell necrosis, number of foci of ADH, and percent of imaging lesion removed. If these findings are validated, women whose biopsies meet low-risk criteria might be considered for prevention therapy and surveillance without surgical excision.

摘要

目的

经皮乳腺活检中发现的非典型导管增生(ADH)是一种高危病变,在 ~7-45.8%的病例中,通过手术切除可升级为癌症。由于潜在的过度治疗和成本问题,常规切除受到质疑。本研究评估了临床、影像学和组织学特征,以预测升级风险。

方法

经机构审查委员会批准,对 2005 年 6 月至 2013 年 6 月期间通过核心活检诊断为 ADH 并接受手术切除的患者进行了单机构回顾性研究。我们查阅了电子病历、乳腺影像学和活检切片。对于缺失数据,使用了多重插补。使用逻辑回归评估各种特征与癌症升级的相关性。

结果

在 399 例病例中,癌症升级率为 16.0%(95%CI:12.8-20.0%),其中 9 例为浸润性癌,55 例为导管原位癌(DCIS)。通过逻辑回归方法,我们定义了一个升级风险较低的亚组:活检未见单个细胞坏死,且 a)1 个 ADH 病灶切除≥50%,或 b)2-3 个病灶切除≥90%的女性。符合这些标准的病例升级率为 4.9%(95%CI:1.0-8.9%),而不符合低危定义的病例升级率为 21.4%(16.4-26.3%)。

结论

核心活检中 ADH 升级为癌症的低风险定义为无单个细胞坏死、ADH 病灶数量和影像学病变切除百分比。如果这些发现得到验证,符合低危标准的女性可能可以考虑预防治疗和监测,而无需手术切除。

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