Clinical trial · Interventional
Surgery to Remove Sentinel Lymph Nodes With or Without Removing Lymph Nodes in the Armpit in Treating Women With Breast Cancer
A Randomized, Phase III Clinical Trial to Compare Sentinel Node Resection to Conventional Axillary Dissection in Clinically Node-Negative Breast Cancer Patients
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
RATIONALE: Removing the sentinel lymph nodes and examining them under a microscope may help plan more effective surgery for breast cancer. It is not yet known if surgery to remove the sentinel lymph nodes is more effective with or without removal of the lymph nodes in the armpit in treating breast cancer. PURPOSE: Randomized phase III trial to compare the effectiveness of surgery to remove the sentinel lymph nodes with or without removal of lymph nodes in the armpit in treating women who have breast cancer.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| conventional surgery | Procedure | — | UNRESOLVED |
| Sentinel node resection followed by node examination | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Arm I: Conventional axillary dissection
- description
- Sentinel node resection immediately followed by axillary dissection
- interventionNames
- Procedure: conventional surgery
- type
- EXPERIMENTAL
- label
- Arm II: Sentinel node resection followed by node examination
- description
- Sentinel node resection followed by node examination then axillary dissection if positive sentinel node.
- interventionNames
- Procedure: Sentinel node resection followed by node examination
Primary outcomes (6)
- measure
- Morbidity - Number of Participants With Residual Shoulder Abduction Deficit
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
DISEASE CHARACTERISTICS: * Resectable invasive adenocarcinoma of the breast, confirmed by 1 of the following: * Histologically confirmed by core or open biopsy * Confirmed by fine needle aspiration cytology AND positive clinical breast examination and ultrasound or mammography * Clinically negative lymph nodes * No positive ipsilateral axillary lymph nodes * No prior removal of ipsilateral axillary lymph nodes * No suspicious palpable nodes in the contralateral axilla or palpable supraclavicular or infraclavicular nodes, unless proven nonmalignant by biopsy * No ulceration, erythema, infiltration of the skin or underlying chest wall (complete fixation), peau d'orange, or skin edema of any magnitude * Tethering or dimpling of the skin or nipple inversion allowed * No bilateral malignancy or mass in the opposite breast that is suspicious for malignancy, unless proven nonmalignant by biopsy * No diffuse tumors or multiple malignant tumors in different quadrants of the breast * No other prior breast malignancy except lobular carcinoma in situ * No prior or concurrent breast implants * Hormone receptor status: * Not specified PATIENT CHARACTERISTICS: Age: * 18 years and older Sex: * Female Menopausal status: * Not specified Performance status: * Not specified Life expectancy: * At least 10 years (excluding diagnosis of cancer) Hematopoietic: * Not specified Hepatic: * No hepatic systemic disease Renal: * No renal systemic disease Cardiovascular: * No cardiovascular systemic disease Other: * No prior malignancy within past 5 years except: * Effectively treated squamous cell or basal cell skin cancer * Surgically treated carcinoma in situ of the cervix * Surgically treated lobular carcinoma in situ of the ipsilateral or contralateral breast * No concurrent psychiatric or addictive disorder PRIOR CONCURRENT THERAPY: Biologic therapy: * No prior immunotherapy for this cancer Chemotherapy: * No prior chemotherapy for this cancer, including neoadjuvant chemotherapy Endocrine therapy: * No prior hormonal therapy for this cancer Radiotherapy: * No prior radiotherapy for this cancer Surgery: * See Disease Characteristics * No prior breast reduction surgery * Prior excisional biopsy or lumpectomy allowed
References
Publications (11)
- BACKGROUNDLand SR, Ritter MW, Costantino JP, Julian TB, Cronin WM, Haile SR, Wolmark N, Ganz PA. Compliance with patient-reported outcomes in multicenter clinical trials: methodologic and practical approaches. J Clin Oncol. 2007 Nov 10;25(32):5113-20. doi: 10.1200/JCO.2007.12.1749. PMID 17991930
- RESULTWeaver DL, Le UP, Dupuis SL, Weaver KA, Harlow SP, Ashikaga T, Krag DN. Metastasis detection in sentinel lymph nodes: comparison of a limited widely spaced (NSABP protocol B-32) and a comprehensive narrowly spaced paraffin block sectioning strategy. Am J Surg Pathol. 2009 Nov;33(11):1583-9. doi: 10.1097/PAS.0b013e3181b274e7. PMID 19730364
- RESULTLand SR, Kopec JA, Lee M, et al.: Quality of life in breast cancer patients receiving sentinel-node (SN) biopsy alone or with axillary dissection (AD): results from NSABP protocol B-32. [Abstract] J Clin Oncol 26 (Suppl 15): A-9533, 2008.
- RESULTJulian TB, Anderson SJ, Fourchotte V, et al.: Is completion axillary dissection always required after a positive sentinel node biopsy? NSABP B-32. [Abstract] Breast Cancer Res Treat 106 (1): A-51, S15, 2007.
- RESULTJulian TB, Anderson SJ, Fourchotte V, et al.: Is intraoperative cytology of sentinel nodes useful and predictive for non-sentinel axillary nodes? NSABP B-32. [Abstract] Breast Cancer Res Treat 106 (1): A-3001, 2007.
- RESULTKrag DN, Anderson SJ, Julian TB, Brown AM, Harlow SP, Ashikaga T, Weaver DL, Miller BJ, Jalovec LM, Frazier TG, Noyes RD, Robidoux A, Scarth HM, Mammolito DM, McCready DR, Mamounas EP, Costantino JP, Wolmark N; National Surgical Adjuvant Breast and Bowel Project. Technical outcomes of sentinel-lymph-node resection and conventional axillary-lymph-node dissection in patients with clinically node-negative breast cancer: results from the NSABP B-32 randomised phase III trial. Lancet Oncol. 2007 Oct;8(10):881-8. doi: 10.1016/S1470-2045(07)70278-4. PMID 17851130
- RESULTJulian B, Fourchotte V, Anderson S, et al.: Predictive factors that identify patients not requiring a sentinel node biopsy: continued analysis of the NSABP B-32 sentinel node trial. [Abstract] Breast Cancer Res Treat 100 (Suppl 1): A-2003, S80-1, 2006.