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多导管加速部分乳腺照射的临床结局及放疗相关毒性的系统评价

A systematic review of clinical outcomes and radiotherapy-associated toxicity in multicatheter accelerated partial breast irradiation.

作者信息

Lv Yang, He Lin, Wang Chao, Zhang Lijiu, Zhang Biyuan, Song Yuhua

机构信息

Department of Oncology, The PLA Navy Anqing Hospital, Anqing, Anhui Province.

Breast Center B ward, The Affiliated Hospital of Qingdao University, Qingdao, Shandong Province.

出版信息

Medicine (Baltimore). 2019 Feb;98(6):e14407. doi: 10.1097/MD.0000000000014407.

DOI:10.1097/MD.0000000000014407
PMID:30732191
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6380720/
Abstract

BACKGROUND

To integrate relevant clinical data of multicatheter accelerated partial breast irradiation (mAPBI) for reaching a comprehensive conclusion.

METHODS

We did 3 meta-analyses for clinical outcomes including 1740 women from 4 articles, for acute radiotherapy (RT)-associated toxicity including 1255 patients from 5 articles, and for late RT-related toxicity involving 1565 patients from 9 papers. Clinical outcomes analyses were stratified by molecular subtypes, lymph nodes status, receptor status, and human epidermal growth factor receptor 2 (HER2) status.

RESULTS

For the Luminal A/B phenotypes, the disease relapse and failure in survival significantly decreased when compared with triple negative (TN)/HER2-amplified subtypes (P < .00001). The 5-year regional nodal recurrence (RNR), 5-year distant metastasis-free survival (DMFS) and 5-year disease free-survival (DFS) of TN patients were significantly superior to HER2-overexpression patients (P < .00001). The 5-year cause-specific survival (CSS), 5-year DMFS and 5-year overall survival (OS) in women with lymph nodes-negative were significantly improved versus patients with lymph nodes-positive (P = .0001). Conversely, the positive status of HER2 compared with negative one significantly increased the rate of local recurrence (LR) (P = .02). For acute toxicity, the morbidity of dermatitis was significantly higher than hematoma and implant infection (P = .01, P < .0001, respectively). For late toxicity, the occurrences of fibrosis (32%) and telangiectasia (14%) were significantly higher than other complications (P < .0001).

CONCLUSION

HER2-enriched subtype compared with other subtypes has significantly increased disease relapse and failure in survival. HER2-positive status is positively associated with an increased incidence of LR. Dermatitis is the most common acute RT-related toxicity and fibrosis is the first rife late RT-related toxicity.

摘要

背景

整合多导管加速部分乳腺照射(mAPBI)的相关临床数据以得出全面结论。

方法

我们针对临床结局进行了3项荟萃分析,其中4篇文章纳入了1740名女性;针对急性放疗(RT)相关毒性进行了3项荟萃分析,5篇文章纳入了1255名患者;针对晚期RT相关毒性进行了3项荟萃分析,9篇论文纳入了1565名患者。临床结局分析按分子亚型、淋巴结状态、受体状态和人表皮生长因子受体2(HER2)状态进行分层。

结果

对于Luminal A/B表型,与三阴性(TN)/HER2扩增亚型相比,疾病复发和生存失败显著降低(P<0.00001)。TN患者的5年区域淋巴结复发(RNR)、5年无远处转移生存期(DMFS)和5年无病生存期(DFS)显著优于HER2过表达患者(P<0.00001)。淋巴结阴性女性的5年特定病因生存期(CSS)、5年DMFS和5年总生存期(OS)与淋巴结阳性患者相比显著改善(P=0.0001)。相反,HER2阳性状态与阴性状态相比,局部复发(LR)率显著增加(P=0.02)。对于急性毒性,皮炎的发病率显著高于血肿和植入物感染(分别为P=0.01,P<0.0001)。对于晚期毒性,纤维化(32%)和毛细血管扩张(14%)的发生率显著高于其他并发症(P<0.0001)。

结论

与其他亚型相比,HER2富集亚型的疾病复发和生存失败显著增加。HER2阳性状态与LR发生率增加呈正相关。皮炎是最常见的急性RT相关毒性,纤维化是最常见的晚期RT相关毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f6/6380720/62937be71334/medi-98-e14407-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f6/6380720/245a5e16da14/medi-98-e14407-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f6/6380720/ff162e1b2573/medi-98-e14407-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f6/6380720/b3f4d57e085c/medi-98-e14407-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f6/6380720/1946e291529b/medi-98-e14407-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f6/6380720/62937be71334/medi-98-e14407-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f6/6380720/245a5e16da14/medi-98-e14407-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f6/6380720/ff162e1b2573/medi-98-e14407-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f6/6380720/b3f4d57e085c/medi-98-e14407-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f6/6380720/1946e291529b/medi-98-e14407-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f6/6380720/62937be71334/medi-98-e14407-g005.jpg

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