已入深夜,您辛苦了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!祝你早点完成任务,早点休息,好梦!

AB023. 11. Axillary complete pathological response to neo-adjuvant chemotherapy in breast cancer, can we predict it?

作者
Ghassan Elamin,D Sapre,Wajiha Tehniyat,Ali Jahan,Mahmoud Dakka
出处
期刊:Mesentery and peritoneum [AME Publishing Company]
卷期号:3: AB023-AB023
标识
DOI:10.21037/map.2019.ab023
摘要

Background: The recommended surgical procedure for the involved lymph nodes (LNs) in breast cancer is axillary nodes dissection (AND), even after pathological complete response (PCR) to neo-adjuvant chemotherapy (NACT). Many trials are studying the benefit of re-staging the axilla post NACT with targeted nodes dissection (TAD) with the assumption that they can represent the whole axillary response, and if they show PCR then those patients can avoid the potentially morbid AND. The TAD technique is showing promising results but still there are significant false negative rates (FNR). In this study our aim is to identify common imaging and/or histopathology characteristics in patients who showed PCR in the axilla. This subgroup if found with predictable axillary PCR can be a target for TAD in future studies with possibly less FNR. Methods: Retrospective data collected from all patients with axillary metastasis underwent NACT in our institution between 2009 and 2017. Pre and post-surgery imaging and final histopathology characteristics were compared to the axillary response to NACT. Analysis done using R. Citation: R Core Team (in 2018). Results: We found statistically significant association between PCR in the axilla and HER2+ cancers (P=0.012), absent lympho-vascular invasion (LVI) (P<0.001), and complete main tumour response to NACT (P<0.001). Relation of axillary response to ER, PR, and MRI were statistically insignificant (P=0.120, 0.249, and 0.310). Conclusions: It is possible to find a subgroup with predictable PCR showing common characteristics like LVI negative, HER2 positive, and main tumour PCR. Findings can help in further prospective studies.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
斯文棒球发布了新的文献求助20
刚刚
1秒前
3秒前
SF完成签到,获得积分20
3秒前
情怀的应助被Nature采纳,获得10
4秒前
王王发布了新的文献求助10
5秒前
5秒前
5秒前
5秒前
领导范儿的应助被jiayu采纳,获得10
6秒前
chen发布了新的文献求助10
6秒前
杳杳完成签到 ,获得积分10
8秒前
8秒前
玻璃杯完成签到 ,获得积分10
8秒前
11秒前
12秒前
Zhang完成签到 ,获得积分10
12秒前
SciGPT的应助被雪山大地采纳,获得10
12秒前
13秒前
14秒前
14秒前
绵绵发布了新的文献求助10
14秒前
15秒前
SF关注了科研通微信公众号
15秒前
上官若男的应助被陈博士采纳,获得10
15秒前
巴音布鲁克完成签到 ,获得积分10
16秒前
16秒前
16秒前
17秒前
不晓得先生完成签到,获得积分10
17秒前
19秒前
行走发布了新的文献求助10
20秒前
Aurinse发布了新的文献求助10
21秒前
21秒前
22秒前
23秒前
科研小白白完成签到,获得积分10
24秒前
24秒前
26秒前
27秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Rosenblum, Global Change Biology 800
自動車の空力技術 800
Using Projective Methods with Children 600
Organizational Behavior 510
Management and the Arts 510
Issues in Task-Based Language Teaching 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 化学工程 工程类 有机化学 物理 复合材料 生物化学 内科学 细胞生物学 基因 遗传学 免疫学 冶金 光电子学 癌症研究
热门帖子
关注 科研通微信公众号,转发送积分 7784985
求助须知:如何正确求助?哪些是违规求助? 9324183
关于积分的说明 20397380
捐赠科研通 7373627
什么是DOI,文献DOI怎么找? 3321217
关于科研通互助平台的介绍 2469095
邀请新用户注册赠送积分活动 2337507