Abstract PO5-18-10: Omission of SLNB in triple-negative and HER2-positive breast cancer patients with radiologic and pathologic complete response in the breast after NAST: a single-arm, prospective surgical trial (EUBREAST-01 trial, GBG 104)

IF 2.9 Q2 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
T. Reimer, B. Gerber, Thorsten Kuehn, Nikola Bangemann, A. Kleine-Tebbe, A. Stefek, Ulrike Doerste, Carolin Hammerle, Oliver Hoffmann, Alexander Hein, Isabel Rubio, F. Peintinger, K. Mehta, S. Loibl, E. Botteri, Oreste D Gentilini
{"title":"Abstract PO5-18-10: Omission of SLNB in triple-negative and HER2-positive breast cancer patients with radiologic and pathologic complete response in the breast after NAST: a single-arm, prospective surgical trial (EUBREAST-01 trial, GBG 104)","authors":"T. Reimer, B. Gerber, Thorsten Kuehn, Nikola Bangemann, A. Kleine-Tebbe, A. Stefek, Ulrike Doerste, Carolin Hammerle, Oliver Hoffmann, Alexander Hein, Isabel Rubio, F. Peintinger, K. Mehta, S. Loibl, E. Botteri, Oreste D Gentilini","doi":"10.1158/1538-7445.sabcs23-po5-18-10","DOIUrl":null,"url":null,"abstract":"\n Background: Currently, axillary surgery for breast cancer is considered a staging procedure that does not seem to influence breast cancer mortality since the risk of developing metastasis depends mainly on the biological behavior of the primary (seed-and-soil model). Based on this, postsurgical therapy should be considered based on biological tumor characteristics. Retrospective data of cancer registry trials showed a strong correlation between breast pathologic complete response (pCR) and nodal pCR depending on intrinsic subtypes. Improvements in systemic treatments for breast cancer have increased the rates of pCR in patients receiving neoadjuvant systemic therapy (NAST), offering the opportunity to decrease, and perhaps eliminate, surgery in patients who have a pCR. Trial design: The EUBREAST network designed a clinical trial (NCT04101851) in which only patients with the highest likelihood of having a pCR after NAST (triple-negative or HER2-positive breast cancer) will be included, and type of surgery will be defined according to the response to NAST rather than on the classical T and N status at presentation. In the ongoing trial, axillary surgery will be eliminated (no axillary sentinel lymph node biopsy [SLNB]) for initially clinical node-negative (cN0) patients with radiologic complete remission (rCR) and a breast pCR (ypT0/ypTis) as determined in the lumpectomy specimen. The trial design is a multicenter single-arm study with a limited number of patients (N=440 as the screening population with an expected 80% pCR-rate) which might give practice-changing results in a short period, sparing the time and the costs of a randomized comparison. Patients will be recruited in European countries (Austria, Germany, Italy, and Spain) over 48 months. Inclusion criteria: -Written informed consent -Histologically confirmed unilateral primary invasive carcinoma of the breast (core biopsy). Multifocal or multicentric tumors are allowed if breast-conserving surgery (BCS) is planned. -Age at diagnosis at least 18 years -imaging techniques with estimated tumor stage between cT1-T3 before NAST -triple-negative (TNBC) or HER2-positive invasive breast cancer -TNBC is defined by: ER-negative (< 10% positive cells in IHC) and PgR-negative (< 10% positive cells in IHC), HER2-negative -clinically and sonographically tumor-free axilla before core biopsy (cN0/iN0) -in cases with cN0 and iN+, a negative core biopsy or fine-needle aspiration biopsy of the sonographically suspected lymph node is required -no evidence for distant metastasis (M0) -standard NAST with rCR -planned BCS with postoperative external whole-breast irradiation (conventional fractionation or hypofractionation) Primary objective: 3-year rate of axillary recurrence-free survival (ARFS) after BCS Statistics: The calculated total case number for per-protocol analysis is N=350, and the expected total number of screened patients is N=440. The assumption for acceptable 3-year ARFS ≥98.5% in the experimental arm is based on previous study findings. Timelines: -First patient in: January 2021 -Last patient in: December 2024 -Primary outcome analysis: Q1/2027 Current accrual: In June 2023, 255 patients were recruited; the majority of them in Germany. Contact: Prof. Dr. Toralf Reimer (eubreast-01@kliniksued-rostock.de), study chair Dr. Oreste D. Gentilini (gentilini.oreste@hsr.it), study co-chair Funding by Else Kroener-Fresenius Foundation, German Society of Senology, University of Rostock (Germany), and San Raffaele Hospital (Milan, Italy).\n Citation Format: Toralf Reimer, Bernd Gerber, Thorsten Kuehn, Nikola Bangemann, Anke Kleine-Tebbe, Andrea Stefek, Ulrike Doerste, Carolin Hammerle, Oliver Hoffmann, Alexander Hein, Isabel Rubio, Florentia Peintinger, Keyur Mehta, Sibylle Loibl, Edoardo Botteri, Oreste Gentilini. Omission of SLNB in triple-negative and HER2-positive breast cancer patients with radiologic and pathologic complete response in the breast after NAST: a single-arm, prospective surgical trial (EUBREAST-01 trial, GBG 104) [abstract]. In: Proceedings of the 2023 San Antonio Breast Cancer Symposium; 2023 Dec 5-9; San Antonio, TX. 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引用次数: 0

Abstract

Background: Currently, axillary surgery for breast cancer is considered a staging procedure that does not seem to influence breast cancer mortality since the risk of developing metastasis depends mainly on the biological behavior of the primary (seed-and-soil model). Based on this, postsurgical therapy should be considered based on biological tumor characteristics. Retrospective data of cancer registry trials showed a strong correlation between breast pathologic complete response (pCR) and nodal pCR depending on intrinsic subtypes. Improvements in systemic treatments for breast cancer have increased the rates of pCR in patients receiving neoadjuvant systemic therapy (NAST), offering the opportunity to decrease, and perhaps eliminate, surgery in patients who have a pCR. Trial design: The EUBREAST network designed a clinical trial (NCT04101851) in which only patients with the highest likelihood of having a pCR after NAST (triple-negative or HER2-positive breast cancer) will be included, and type of surgery will be defined according to the response to NAST rather than on the classical T and N status at presentation. In the ongoing trial, axillary surgery will be eliminated (no axillary sentinel lymph node biopsy [SLNB]) for initially clinical node-negative (cN0) patients with radiologic complete remission (rCR) and a breast pCR (ypT0/ypTis) as determined in the lumpectomy specimen. The trial design is a multicenter single-arm study with a limited number of patients (N=440 as the screening population with an expected 80% pCR-rate) which might give practice-changing results in a short period, sparing the time and the costs of a randomized comparison. Patients will be recruited in European countries (Austria, Germany, Italy, and Spain) over 48 months. Inclusion criteria: -Written informed consent -Histologically confirmed unilateral primary invasive carcinoma of the breast (core biopsy). Multifocal or multicentric tumors are allowed if breast-conserving surgery (BCS) is planned. -Age at diagnosis at least 18 years -imaging techniques with estimated tumor stage between cT1-T3 before NAST -triple-negative (TNBC) or HER2-positive invasive breast cancer -TNBC is defined by: ER-negative (< 10% positive cells in IHC) and PgR-negative (< 10% positive cells in IHC), HER2-negative -clinically and sonographically tumor-free axilla before core biopsy (cN0/iN0) -in cases with cN0 and iN+, a negative core biopsy or fine-needle aspiration biopsy of the sonographically suspected lymph node is required -no evidence for distant metastasis (M0) -standard NAST with rCR -planned BCS with postoperative external whole-breast irradiation (conventional fractionation or hypofractionation) Primary objective: 3-year rate of axillary recurrence-free survival (ARFS) after BCS Statistics: The calculated total case number for per-protocol analysis is N=350, and the expected total number of screened patients is N=440. The assumption for acceptable 3-year ARFS ≥98.5% in the experimental arm is based on previous study findings. Timelines: -First patient in: January 2021 -Last patient in: December 2024 -Primary outcome analysis: Q1/2027 Current accrual: In June 2023, 255 patients were recruited; the majority of them in Germany. Contact: Prof. Dr. Toralf Reimer (eubreast-01@kliniksued-rostock.de), study chair Dr. Oreste D. Gentilini (gentilini.oreste@hsr.it), study co-chair Funding by Else Kroener-Fresenius Foundation, German Society of Senology, University of Rostock (Germany), and San Raffaele Hospital (Milan, Italy). Citation Format: Toralf Reimer, Bernd Gerber, Thorsten Kuehn, Nikola Bangemann, Anke Kleine-Tebbe, Andrea Stefek, Ulrike Doerste, Carolin Hammerle, Oliver Hoffmann, Alexander Hein, Isabel Rubio, Florentia Peintinger, Keyur Mehta, Sibylle Loibl, Edoardo Botteri, Oreste Gentilini. Omission of SLNB in triple-negative and HER2-positive breast cancer patients with radiologic and pathologic complete response in the breast after NAST: a single-arm, prospective surgical trial (EUBREAST-01 trial, GBG 104) [abstract]. In: Proceedings of the 2023 San Antonio Breast Cancer Symposium; 2023 Dec 5-9; San Antonio, TX. Philadelphia (PA): AACR; Cancer Res 2024;84(9 Suppl):Abstract nr PO5-18-10.
摘要 PO5-18-10:三阴性和HER2阳性乳腺癌患者在NAST术后乳腺放射学和病理学完全反应时不进行SLNB:单臂前瞻性手术试验(EUBREAST-01试验,GBG 104)
背景:目前,乳腺癌的腋窝手术被认为是一种分期手术,似乎不会影响乳腺癌的死亡率,因为发生转移的风险主要取决于原发肿瘤的生物学行为(种子-土壤模型)。因此,应根据肿瘤的生物学特征考虑术后治疗。癌症登记试验的回顾性数据显示,乳腺癌病理完全缓解(pCR)和结节完全缓解(pCR)之间有很强的相关性,这取决于内在亚型。乳腺癌全身治疗方法的改进提高了接受新辅助全身治疗(NAST)患者的 pCR 率,为获得 pCR 的患者减少甚至取消手术提供了机会。试验设计:EUBREAST网络设计了一项临床试验(NCT04101851),该试验只纳入接受新辅助系统治疗后最有可能获得pCR的患者(三阴性或HER2阳性乳腺癌),手术类型将根据患者对新辅助系统治疗的反应而非发病时的传统T和N状态来确定。在正在进行的试验中,对于最初临床结节阴性(cN0)、放射学完全缓解(rCR)且乳腺 pCR(ypT0/ypTis)由肿块切除术标本确定的患者,将取消腋窝手术(无腋窝前哨淋巴结活检 [SLNB])。试验设计为多中心单臂研究,患者人数有限(筛查人群为 440 人,预计 pCR 率为 80%),可能会在短期内产生改变实践的结果,从而节省随机对比的时间和成本。患者将在欧洲各国(奥地利、德国、意大利和西班牙)招募,为期 48 个月。纳入标准-经病理证实为单侧原发性浸润性乳腺癌(核心活检)。如果计划进行保乳手术(BCS),则允许多灶性或多中心性肿瘤。-确诊时年龄至少 18 岁 -在进行 NAST 之前,通过影像学技术估计肿瘤分期在 cT1-T3 之间 -三阴性(TNBC)或 HER2 阳性浸润性乳腺癌 -TNBC 的定义是:ER阴性(IHC中阳性细胞<10%)和PgR阴性(IHC中阳性细胞<10%),HER2阴性 - 核心活检前临床和声像图显示腋窝无肿瘤(cN0/iN0) - cN0和iN+的病例、在 cN0 和 iN+ 的病例中,需要进行阴性核心活检或声像图可疑淋巴结的细针穿刺活检 - 无远处转移证据(M0) - 带有 rCR 的标准 NAST - 计划 BCS,术后进行全乳房外部照射(常规分次或低分次) 主要目标:3 年腋窝复发率:BCS 后 3 年无腋窝复发生存率(ARFS) 统计:按方案分析计算出的病例总数为 N=350,预计筛选出的患者总数为 N=440。实验组可接受的 3 年无腋窝复发生存率(ARFS)≥98.5% 的假设是基于之前的研究结果。时间安排:-首例患者2021 年 1 月 -最后一名患者:2024 年 12 月2024 年 12 月 -主要结果分析:目前招募情况:2023 年 6 月,招募了 255 名患者,其中大部分在德国。联系方式:Prof:Toralf Reimer 博士教授(eubreast-01@kliniksued-rostock.de),研究主席 Oreste D. Gentilini 博士(gentilini.oreste@hsr.it),研究联合主席 资助方:Else Kroener-Fresenius 基金会、德国森学学会、罗斯托克大学(德国)和圣拉斐尔医院(意大利米兰)。引用格式:Toralf Reimer、Bernd Gerber、Thorsten Kuehn、Nikola Bangemann、Anke Kleine-Tebbe、Andrea Stefek、Ulrike Doerste、Carolin Hammerle、Oliver Hoffmann、Alexander Hein、Isabel Rubio、Florentia Peintinger、Keyur Mehta、Sibylle Loibl、Edoardo Botteri、Oreste Gentilini。三阴性和 HER2 阳性乳腺癌患者在 NAST 后乳腺放射学和病理学完全反应时省略 SLNB:单臂前瞻性手术试验(EUBREAST-01 试验,GBG 104)[摘要]。In:2023 年圣安东尼奥乳腺癌研讨会论文集;2023 年 12 月 5-9 日;德克萨斯州圣安东尼奥。费城(宾夕法尼亚州):AACR; Cancer Res 2024;84(9 Suppl):Abstract nr PO5-18-10。
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来源期刊
ACS Chemical Health & Safety
ACS Chemical Health & Safety PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
CiteScore
3.10
自引率
20.00%
发文量
63
期刊介绍: The Journal of Chemical Health and Safety focuses on news, information, and ideas relating to issues and advances in chemical health and safety. The Journal of Chemical Health and Safety covers up-to-the minute, in-depth views of safety issues ranging from OSHA and EPA regulations to the safe handling of hazardous waste, from the latest innovations in effective chemical hygiene practices to the courts'' most recent rulings on safety-related lawsuits. The Journal of Chemical Health and Safety presents real-world information that health, safety and environmental professionals and others responsible for the safety of their workplaces can put to use right away, identifying potential and developing safety concerns before they do real harm.
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