Should positive sentinel node cases have a further axillary dissection

B. Cady
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引用次数: 2

Abstract

The treatment of lymph node metastasis in human cancers has been a source of controversy for many years. Several contemporary randomized trials indicate no survival advantage to performing axillary dissection in contrast to merely observing the axilla after invasive breast cancer. This assumption is confirmed since survival advantages cannot be demonstrated when comparing greater or lesser lymph node dissections or dissection vs. observation of regional lymph nodes in melanoma and breast cancer and all other epithelial cancers. Many recent studies indicate that axillary metastases, when they do occur in this era of mammographic screening and small invasive cancers, demonstrate metastases in the axillary sentinel nodes only in from 20% to almost 100% depending on primary cancer size. For instance, in T1a and T1b cancers, 50–100% of lymph node metastases, infrequently discovered, are contained entirely within the sentinel nodes. In T2 cancers, this proportion is roughly 25–50%, and in T3 cancers it ranges from 20% to 40%. A number of recent articles have demonstrated no difference in survival and very little nodal recurrence when patients with positive sentinel nodes are not followed by axillary dissection although the axillary disease tends to be less advanced in observed compared to treated patients with axillary dissection. Nevertheless, basic principles have been reconfirmed in these reports. grow in other metastatic sites; this has been demonstrated clinically in clinical trials previously mentioned. Therefore, there is no benefit in performing subsequent axillary dissections even when the sentinel node biopsy is positive, because of: (1) very low risk ( (cid:1) 2%) of recurrent clinical nodal metastases, (2) the lack of impact on disease specific or overall survival, (3) most lymph node metastases are limited to the sentinel nodes, and (4) lymph node metastases are only indicators not governors of the distant metastases. The American College of Surgeons Oncology Group (ACOSOG) Z-11 Trial was designed to specifically address this point, but unfor-tunately was closed early because of poor accrual; nevertheless, 900 patients were enrolled and will be analyzed over time to address this point. https://www.cambridge.org/core.
前哨淋巴结阳性病例是否需要进一步腋窝清扫
多年来,人类癌症中淋巴结转移的治疗一直是争议的来源。几项当代随机试验表明,与浸润性乳腺癌后仅仅观察腋窝相比,进行腋窝解剖没有生存优势。这一假设得到了证实,因为在黑色素瘤、乳腺癌和所有其他上皮性癌症中,当比较较大或较小的淋巴结清扫或清扫与观察区域淋巴结时,无法证明生存优势。最近的许多研究表明,在乳房x线摄影筛查和小型侵袭性癌症的时代,腋窝转移确实发生,但根据原发肿瘤的大小,腋窝前哨淋巴结的转移率仅为20%至几乎100%。例如,在T1a和T1b癌症中,50-100%的淋巴结转移,很少被发现,完全包含在前哨淋巴结内。在T2癌症中,这一比例约为25-50%,而在T3癌症中,这一比例在20%至40%之间。最近的一些文章表明,当前哨淋巴结阳性的患者不进行腋窝清扫时,生存率和淋巴结复发率没有差异,尽管与接受腋窝清扫治疗的患者相比,观察到的腋窝疾病往往不那么晚期。然而,这些报告再次确认了基本原则。在其他转移部位生长;这已经在前面提到的临床试验中得到证实。因此,即使前哨淋巴结活检呈阳性,后续进行腋窝清扫也没有好处,因为:(1)复发临床淋巴结转移的风险非常低((cid:1) 2%),(2)对疾病特异性或总体生存缺乏影响,(3)大多数淋巴结转移仅限于前哨淋巴结,(4)淋巴结转移只是指示物,而不是远处转移的控制因子。美国外科医师学会肿瘤组(ACOSOG) Z-11试验旨在专门解决这一问题,但不幸的是,由于累积不良而提前结束;然而,900名患者被纳入,并将随着时间的推移进行分析,以解决这一问题。https://www.cambridge.org/core。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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