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Histological type and marker expression of the primary tumour compared with its local recurrence after breast-conserving therapy for ductal carcinoma in situ

机译:乳腺导管原位癌保乳治疗后原发灶的组织学类型和标志物表达与局部复发的比较

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摘要

We have investigated primary ductal carcinomas in situ (DCIS) of the breast and their local recurrences after breast-conserving therapy (BCT) for histological characteristics and marker expression. Patients who were randomized in the EORTC trial 10853 (wide local excision versus excision plus radiotherapy) and who developed a local recurrence were identified. Histology was reviewed for 116 cases; oestrogen and progesterone receptor status, and HER2/ neu and p53 overexpression were assessed for 71 cases. Comparing the primary DCIS and the invasive or non-invasive recurrence, concordant histology was found in 62%, and identical marker expression in 63%. Although 11% of the recurrences developed at a distance from the primary DCIS, nearly all these showed the same histological and immunohistochemical profile. 5 patients developed well-differentiated DCIS or grade I invasive carcinoma after poorly differentiated DCIS. Although these recurrences occurred in the same quadrant as the primary DCIS, they may be considered as second primary tumours. Only 4 patients developed poorly differentiated DCIS or grade III invasive carcinoma after well differentiated DCIS. We conclude that in most cases the primary DCIS and its local recurrence are related histologically or by marker expression, suggesting that local recurrence usually reflects outgrowth of residual DCIS; progression of well differentiated DCIS towards poorly differentiated DCIS or grade III invasive carcinoma is a non-frequent event. © 2001 Cancer Research Campaign
机译:我们研究了乳腺癌的原位导管癌(DCIS)及其保乳治疗(BCT)后的局部复发的组织学特征和标志物表达。在EORTC试验10853(广泛的局部切除术与切除术加上放射治疗)中被随机分组​​并发生局部复发的患者被确定。组织学检查了116例。评估了71例患者的雌激素和孕激素受体状态以及HER2 / neu和p53过表达。比较原发性DCIS和有创或无创复发,发现组织学一致的占62%,标记表达相同的占63%。尽管11%的复发发生在距原发性DCIS较远的地方,但几乎所有这些都显示出相同的组织学和免疫组化特征。 5例DCIS分化不良后发展为高分化DCIS或I级浸润性癌。尽管这些复发与原发性DCIS发生在同一象限,但它们可被视为第二原发性肿瘤。高分化DCIS后仅4例患者发展为低分化DCIS或III级浸润癌。我们得出的结论是,在大多数情况下,原发性DCIS及其局部复发在组织学或标记表达方面相关,这表明局部复发通常反映了残留DCIS的生长。高分化DCIS向低分化DCIS或III级浸润性癌的进展是罕见的。 ©2001癌症研究运动

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