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DOI 10.1001/jamasurg.2026.1268

Медицинская библиотека · JAMA surgery · 2026

Sentinel Lymph Node Biopsy for Patients With cN1 HR+/HER2- Breast Cancer and Palpable Adenopathy: A Nonrandomized Clinical Trial.

Mamtani Anita, Pilewskie Melissa, Wilson Niamey, Chung Whang Heiwon, Barrio Andrea V, Bassin Leah, Capko Deborah, Choi Daniel X, Cody Hiram S, Downs-Canner Stephanie, El-Tamer Mahmoud, Gemignani Mary L, Heerdt Alexandra S, Kirstein Laurie, Lee Minna K, Mango Victoria L, Montagna Giacomo, Moo Tracy-Ann, Oxenberg Jacqueline, Plitas George, Sabel Michael, Sacchini Virgilio, Sclafani Lisa, Sevilimedu Varadan, Tadros Audree B, Van Zee Kimberly J, Morrow Monica

СтатьяКлиническое исследованиеМногоцентровое исследованиеПеревод в очереди

Аннотация

IMPORTANCE

Randomized trials established the safety of omitting axillary lymph node dissection (ALND) among patients with clinically node-negative breast cancer and less than 3 positive sentinel lymph nodes (+SLNs) having upfront surgery and adjuvant radiation. Patients with palpable mobile level I/II axillary adenopathy (cN1) were not eligible for these studies. Presently, more than 80% of patients with HR+/HER2- cN1 disease undergo ALND either at upfront surgery or after neoadjuvant therapy, despite evidence that 50% to 60% will have only 1 or 2 positive nodes.

OBJECTIVE

To determine upfront sentinel lymph node biopsy (SLNB) feasibility and evaluate ALND rate among patients with HR+/HER2- cN1 breast cancer selected with axillary ultrasound (AUS).

DESIGN, SETTING, AND

PARTICIPANTS

This nonrandomized clinical trial involved patients with cTx/cT1-2 cN1 HR+/HER2- breast cancer with 3 or fewer morphologically abnormal nodes on AUS at 4 centers. The trial began on April 20, 2021, and the database for this report was frozen on September 26, 2024.

INTERVENTIONS: Patients underwent upfront lumpectomy/mastectomy and SLNB, with single/dual-tracer mapping. ALND was indicated for 3 or more positive SLNs.

MAIN OUTCOMES AND MEASURES: The primary outcome was ALND rate. Secondary outcomes were frequency of palpable nodes being radioactive/blue and locoregional recurrence.

RESULTS

Among 78 enrolled patients, the median (IQR) age was 58 (49.0-66.5) years. Most tumors were cT1 (37 [47%]) or cT2 (40 [51%]), 56 patients (72%) had ductal histology, and 59 tumors (76%) were moderately differentiated. On AUS, 39 patients (50%) had 1 abnormal-appearing node, 33 (42%) had 2, and 6 (8%) had 3. Median (IQR) pathologic tumor size was 2.3 (1.6-3.3) cm, 50 patients (64%) had lymphovascular invasion, and 54 (69%) had extracapsular extension. SLNB was performed with dual tracer in 68 (87%), and 3 or more SLNs were retrieved in 75 (96%). The palpable diseased nodes were blue and/or radioactive in 107 of 161 instances (66.5%). Overall, 24 patients (31%) had 1 +SLN, 30 patients (38%) had 2 +SLNs, and 24 patients (31%) had 3 or more +SLNs. SLNB alone was performed in 59 patients (76%), while 19 (24%) had ALND; indicated ALND was deferred in 5 cases. Among those with 12 months or more follow-up (n = 68; median, 25 months), there have been no isolated axillary or locoregional recurrences.

CONCLUSIONS AND RELEVANCE: This study found that SLNB is feasible among patients with cN1 HR+/HER2- disease and that resection of palpable nodes is necessary to minimize false-negative rates. This approach affords the opportunity to omit ALND and minimize morbidity among patients with cN1 cancer and limited nodal burden.

TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT04854005.

Для цитирования: Mamtani Anita, Pilewskie Melissa, Wilson Niamey, Chung Whang Heiwon, Barrio Andrea V, Bassin Leah, Capko Deborah, Choi Daniel X, Cody Hiram S, Downs-Canner Stephanie, El-Tamer Mahmoud, Gemignani Mary L, Heerdt Alexandra S, Kirstein Laurie, Lee Minna K, Mango Victoria L, Montagna Giacomo, Moo Tracy-Ann, Oxenberg Jacqueline, Plitas George, Sabel Michael, Sacchini Virgilio, Sclafani Lisa, Sevilimedu Varadan, Tadros Audree B, Van Zee Kimberly J, Morrow Monica. Sentinel Lymph Node Biopsy for Patients With cN1 HR+/HER2- Breast Cancer and Palpable Adenopathy: A Nonrandomized Clinical Trial.. JAMA surgery. 2026. DOI: 10.1001/jamasurg.2026.1268.

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