Chirurgia (Bucur). 2021 Dec;116(5 Suppl):S5-S6.
The introduction of mammographic screening in the early 1980's was associated, in the three following decades, with a dramatic increase in the detection of ductal carcinoma in situ (DCIS), pathology rarely detected before, on surgical specimen, at the periphery of an invasive cancer (1,2,3). It is estimated that in the United States the incidence of DCIS, each year, varies between 18 to 25% of the total number of newly diagnosed breast cancers (4,5). Ductal carcinoma in situ belongs, genetically and pathomorphologically, to a heterogenous group of preinvasive neoplastic lesions characterized by clonal proliferation of malignant cells limited to the lumen of breast ducts. It has not a known natural history and its phenotypical spectrum is wide, varying from a slowly evolving disease to a fast growing one, invading the surrounding stroma and even metastasizing to distant sites (6). In the absence of reliable prognostic markers, most of patients are submitted to invasive treatments consisting mainly in surgery, alone or associated with radiation and endocrine therapy (7). Molecular subtyping has improved the understanding of breast cancer biology and its possibilities for evolution and have provided the tools to design a more personalized treatment (8). In the absence of reliable molecular markers clinical management of patients with DCIS is based on patient's option and tumor characteristics. Based on the knowledge of today, DCIS could be used to exemplify the notions of overdiagnosis and overtreatment. The final goal of the treatment of DCIS is to prevent invasive breast cancer recurrence. Mortality rate associated with DCIS is very low, being estimated at 1-2 % at 10 years, while patients with DCIS treated by wide local excision with or without radiation may have a local recurrence rate of 5 to 30% and half of these present as an invasive cancer. Today's clinicians are not able to predict the risk of progression for a DCIS diagnosed by biopsy, but neither the risk of local recurrence, as an invasive cancer, of DCIS treated by conservative surgery with or without radiation (9). Progression to invasive cancer is difficult to be predicted as the disease is highly heterogenous. Because of these uncertainties, it is highly important to carefully inform the patient and engage her in the treatment decision process (10). There is a trend for de-escalation of treatment for DCIS. A study comparing two groups of patients with pure DCIS was conducted: one with standard care and the other under active surveillance (11). The main outcome was the probability to die from breast cancer at 10 years after the diagnosis. The mortality risk from breast cancer is higher for younger women, than the older ones, under active surveillance. Women over the age of 70 years, have many comorbidities that could induce the risk of dying, regardless of DCIS treatment decision. This study suggested that active surveillance could be a reasonable option for certain category of patients. This attitude is not without risks. A patient with DCIS on core needle biopsy could hide an invasive cancer in 25% of cases (12). Today, there are four randomized control trials of active surveillance offered to patients with low-grade DCIS: LORD (LOw Risk DCIS), COMET (Comparison of Operative to Monitoring and Endocrine Therapy), LORIS (LOw RISk DCIS) and LORETTA (10,13-16). Non-surgical approaches are of two types: active surveillance alone or associated with hormone therapy. There are some differences between the trials. While in LORD and LORIS trials the study arms are represented by active surveillance only, hormone therapy is an option in COMET trial and mandatory in the single arm trial LORETTA. The aim of these studies is to examine the safety and the effectiveness of active surveillance compared with surgical management for low-risk DCIS. The results of these trials are awaited with great interest. Patients with ductal carcinoma in situ need special counseling. To talk about "a good" cancer or even no cancer and to recommend as treatment a mastectomy is highly confusing. The language used by all members of the team must be unitary, removing the anxiety and helping patients to make the best decision. This special issue is a great opportunity to have the opinions of highly respected international specialists in the field for a comprehensive review of DCIS of the breast.
乳腺 X 线筛查于 20 世纪 80 年代初引入,此后的 30 年中,导管原位癌(DCIS)的检出率显著增加,这是一种在手术标本的浸润性癌周围很少发现的病理学表现(1,2,3)。据估计,在美国,每年 DCIS 的发病率在新诊断乳腺癌总数的 18%至 25%之间(4,5)。导管原位癌在遗传和病理形态上属于一组异质性的前浸润性肿瘤病变,其特征为恶性细胞的克隆性增殖局限于乳腺导管的管腔。它没有已知的自然病史,其表型谱很广,从缓慢进展的疾病到快速生长的疾病不等,可侵犯周围基质,甚至转移到远处部位(6)。由于缺乏可靠的预后标志物,大多数患者接受的是主要包括手术的侵袭性治疗,单独或联合放疗和内分泌治疗(7)。分子亚型分析提高了对乳腺癌生物学及其进化可能性的认识,并为设计更个性化的治疗提供了工具(8)。在缺乏可靠的分子标志物的情况下,DCIS 患者的临床管理基于患者的选择和肿瘤特征。基于目前的知识,DCIS 可以用来举例说明过度诊断和过度治疗的概念。DCIS 治疗的最终目标是预防浸润性乳腺癌的复发。DCIS 相关死亡率非常低,估计在 10 年内为 1%至 2%,而接受广泛局部切除联合或不联合放疗的 DCIS 患者局部复发率为 5%至 30%,其中一半为浸润性癌。目前的临床医生无法预测通过活检诊断的 DCIS 的进展风险,但也无法预测接受保乳手术联合或不联合放疗的 DCIS 的局部复发风险(9)。由于疾病高度异质性,进展为浸润性癌的风险难以预测。由于存在这些不确定性,因此仔细告知患者并让其参与治疗决策过程非常重要(10)。对于 DCIS 的治疗有一个降低强度的趋势。一项比较两组单纯 DCIS 患者的研究:一组接受标准治疗,另一组接受主动监测(11)。主要结果是诊断后 10 年死于乳腺癌的概率。在主动监测组中,年轻女性的乳腺癌死亡率高于老年女性。70 岁以上的女性有许多合并症,可能会导致她们死于任何原因,而不仅仅是 DCIS 治疗决策。这项研究表明,对于某些特定类型的患者,主动监测可能是一种合理的选择。这种态度并非没有风险。在核心针活检中有 DCIS 的患者在 25%的情况下可能隐藏有浸润性癌(12)。目前,有四项针对低级别 DCIS 的主动监测的随机对照试验:LOD(低风险 DCIS)、COMET(比较手术与监测和内分泌治疗)、LORIS(低风险 DCIS)和 LORETTA(10,13-16)。非手术方法有两种类型:单独主动监测或联合激素治疗。这些试验之间存在一些差异。在 LORD 和 LORIS 试验中,研究臂仅代表主动监测,而在 COMET 试验中激素治疗是一种选择,在单臂试验 LORETTA 中则是强制性的。这些研究的目的是检查与手术治疗相比,主动监测对低危 DCIS 的安全性和有效性。人们对这些试验的结果非常感兴趣。导管原位癌患者需要特别咨询。谈论“一种好的”癌症,甚至没有癌症,并建议进行乳房切除术,这是非常令人困惑的。团队的所有成员都必须使用统一的语言,消除焦虑,帮助患者做出最佳决策。本期特刊为大家提供了一个极好的机会,邀请了该领域备受尊敬的国际专家,对乳腺导管原位癌进行全面回顾。