Adjuvant Therapy Benefits for Patients With Human Epidermal Growth Factor Receptor 2-Positive T1aN0M0 Breast Cancer: A Systematic Review and Meta-Analysis.

IF 2.1 Q3 ONCOLOGY
World Journal of Oncology Pub Date : 2025-06-01 Epub Date: 2025-06-09 DOI:10.14740/wjon2578
Ezzeldin M Ibrahim, Ahmed A Refae, Ali M Bayer, Nouf Abdullah, Meteb E Al-Foheidi
{"title":"Adjuvant Therapy Benefits for Patients With Human Epidermal Growth Factor Receptor 2-Positive T1aN0M0 Breast Cancer: A Systematic Review and Meta-Analysis.","authors":"Ezzeldin M Ibrahim, Ahmed A Refae, Ali M Bayer, Nouf Abdullah, Meteb E Al-Foheidi","doi":"10.14740/wjon2578","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>While the prognosis for patients with human epidermal growth factor receptor 2 (HER2)-positive pT1a-bN0M0 breast cancer is generally favorable, the optimal approach to personalize adjuvant treatment for T1a tumors remains unclear, which prompted an impetus to conduct a systematic review and meta-analysis for the latter group.</p><p><strong>Methods: </strong>We examined the literature for studies that provided relevant data about HER2-positive T1a patients. Patient and disease characteristics, therapy details, and survival outcomes were extracted.</p><p><strong>Results: </strong>Thirteen studies with 2,089 patients were eligible; four were prospective and nine were retrospective. In the studies where patients did not receive chemotherapy or anti-HER2 therapy, the prognosis was generally favorable, with disease-free survival (DFS) and overall survival of approximately 92% to 99%. Studies comparing treated versus untreated patients showed a survival benefit that varied between 2% and 15%, favoring adjuvant therapy without reaching statistical significance. In the only included randomized trial where all patients received adjuvant paclitaxel and trastuzumab, 10% demonstrated 5-year invasive DFS events. A meta-analysis of four studies showed a nonsignificant survival advantage trend among treated patients. There was inconsistency about the prognostic role of the co-existing hormone receptor status.</p><p><strong>Conclusion: </strong>Patients with HER2-positive T1aN0 have a favorable prognosis; the benefit of adjuvant chemotherapy plus anti-HER2 varied and showed no convincing statistically significant benefit. The decision to offer adjuvant therapy should balance the expected benefits and risks. Prospective trials that include this population should be able to identify who should receive adjuvant therapy and determine the magnitude of benefit.</p>","PeriodicalId":46797,"journal":{"name":"World Journal of Oncology","volume":"16 3","pages":"276-285"},"PeriodicalIF":2.1000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12185127/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"World Journal of Oncology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14740/wjon2578","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/9 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: While the prognosis for patients with human epidermal growth factor receptor 2 (HER2)-positive pT1a-bN0M0 breast cancer is generally favorable, the optimal approach to personalize adjuvant treatment for T1a tumors remains unclear, which prompted an impetus to conduct a systematic review and meta-analysis for the latter group.

Methods: We examined the literature for studies that provided relevant data about HER2-positive T1a patients. Patient and disease characteristics, therapy details, and survival outcomes were extracted.

Results: Thirteen studies with 2,089 patients were eligible; four were prospective and nine were retrospective. In the studies where patients did not receive chemotherapy or anti-HER2 therapy, the prognosis was generally favorable, with disease-free survival (DFS) and overall survival of approximately 92% to 99%. Studies comparing treated versus untreated patients showed a survival benefit that varied between 2% and 15%, favoring adjuvant therapy without reaching statistical significance. In the only included randomized trial where all patients received adjuvant paclitaxel and trastuzumab, 10% demonstrated 5-year invasive DFS events. A meta-analysis of four studies showed a nonsignificant survival advantage trend among treated patients. There was inconsistency about the prognostic role of the co-existing hormone receptor status.

Conclusion: Patients with HER2-positive T1aN0 have a favorable prognosis; the benefit of adjuvant chemotherapy plus anti-HER2 varied and showed no convincing statistically significant benefit. The decision to offer adjuvant therapy should balance the expected benefits and risks. Prospective trials that include this population should be able to identify who should receive adjuvant therapy and determine the magnitude of benefit.

辅助治疗对人表皮生长因子受体2阳性T1aN0M0乳腺癌患者的益处:系统回顾和荟萃分析
背景:虽然人表皮生长因子受体2 (HER2)阳性pT1a-bN0M0乳腺癌患者的预后普遍良好,但T1a肿瘤个性化辅助治疗的最佳方法仍不清楚,这促使人们对后者进行系统回顾和荟萃分析。方法:我们查阅了提供her2阳性T1a患者相关数据的研究文献。提取患者和疾病特征、治疗细节和生存结果。结果:13项研究纳入2089例患者;4例为前瞻性研究,9例为回顾性研究。在患者未接受化疗或抗her2治疗的研究中,预后普遍良好,无病生存期(DFS)和总生存率约为92%至99%。比较治疗和未治疗患者的研究显示,生存获益在2%到15%之间变化,辅助治疗更有利,但没有达到统计学意义。在唯一纳入的随机试验中,所有患者接受辅助紫杉醇和曲妥珠单抗治疗,10%的患者出现5年侵袭性DFS事件。四项研究的荟萃分析显示,在接受治疗的患者中,生存优势趋势不显著。关于共存激素受体状态的预后作用存在不一致。结论:her2阳性T1aN0患者预后良好;辅助化疗加抗her2的益处各不相同,没有令人信服的统计学显著益处。提供辅助治疗的决定应该平衡预期的益处和风险。包括这一人群的前瞻性试验应该能够确定谁应该接受辅助治疗并确定获益的程度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
6.10
自引率
15.40%
发文量
37
期刊介绍: World Journal of Oncology, bimonthly, publishes original contributions describing basic research and clinical investigation of cancer, on the cellular, molecular, prevention, diagnosis, therapy and prognosis aspects. The submissions can be basic research or clinical investigation oriented. This journal welcomes those submissions focused on the clinical trials of new treatment modalities for cancer, and those submissions focused on molecular or cellular research of the oncology pathogenesis. Case reports submitted for consideration of publication should explore either a novel genomic event/description or a new safety signal from an oncolytic agent. The areas of interested manuscripts are these disciplines: tumor immunology and immunotherapy; cancer molecular pharmacology and chemotherapy; drug sensitivity and resistance; cancer epidemiology; clinical trials; cancer pathology; radiobiology and radiation oncology; solid tumor oncology; hematological malignancies; surgical oncology; pediatric oncology; molecular oncology and cancer genes; gene therapy; cancer endocrinology; cancer metastasis; prevention and diagnosis of cancer; other cancer related subjects. The types of manuscripts accepted are original article, review, editorial, short communication, case report, letter to the editor, book review.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信