Skip to content

Axillary Lymph Node Dissection Versus no Dissection in Breast Cancer With Positive Sentinel Lymph Node

A Prospective Randomized Multicenter Phase III Study of Axillary Lymph Node Dissection Versus no Dissection in Breast Cancer With Positive Sentinel Lymph Node--the Validation of Z0011 in China

Status
Withdrawn
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01796444
Acronym
Z0011-China
Enrollment
0
Registered
2013-02-21
Start date
2013-01-31
Completion date
2026-06-30
Last updated
2018-04-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

Breast Cancer, Sentinel Lymph Node Biopsy, Axillary Lymph Node Dissection

Brief summary

The recently randomized trial (ASCOG Z0011) support that among patients with limited sentinel lymph node (SLN) metastatic breast cancer treated with breast conservation and systemic therapy, the use of sentinel lymph node biopsy (SLNB) alone compared with axillary lymph node dissection (ALND) did not result in inferior survival. These patients, therefore, are unlikely to benefit from further surgery that results in a longer period of hospitalization, higher costs and higher postoperative morbidity. This result has been written in the 2012 National Comprehensive Cancer Network Clinical Practice Guidelines. However, Limitations of Z0011, such as failure to achieve target accrual and possible randomization imbalance favoring the SLNB-alone group, must be considered. In the other hand, further testing in different country are needed. The investigators design and begin a prospective randomized multicenter phase III study of ALND vs. no ALND in breast Cancer with positive SLN--the validation of Z0011 in China.

Detailed description

OBJECTIVES: To determine the effects of complete axillary lymph node dissection (ALND) on survival of patients with sentinel lymph node (SLN) metastasis of breast cancer. OUTLINE: This is a randomized multicenter study. Before randomization, all women were stratified according to age (≤50 years, \>50 years), tumor size(≤2cm, \>2cm) and research center. All the patients underwent lumpectomy and sentinel lymph node biopsy (SLNB). Eligible women were randomly assigned to ALND or no ALND Active Comparator: Patients undergo axillary lymph node dissection involving removal of at least level I and II nodes. Experimental: No surgery of axillary lymph node in this arm. All the patients were to receive whole-breast opposing tangential-field radiation therapy. The use of adjuvant systemic therapy was determined by the treating physician according to the recently NCCN. Patients are followed up every 4 months for the first 2 years, every 6 months from the third year to the fifth year, and then annually for a total of 10 years.

Interventions

PROCEDURESentinel Lymph Node Biopsy

Sentinel lymph nodes are identified with the combining use of intraoperative gamma detector and/or blue dye.

PROCEDUREIntraoperative Pathological Examination

touch imprint cytology and/or frozen section and/or OSNA

Axillary lymph node dissection involving removal of at least level I and II nodes.

PROCEDUREPathological Evaluation

H&E and IHC

Adjuvant systemic therapy was determined by the treating physician according to the recently NCCN.

RADIATIONRadiation Therapy

Whole-breast opposing tangential-field radiation therapy.

Sponsors

Shandong Cancer Hospital and Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Female; * Patient aged 18 years and above; * Patient with histological proven invasive breast cancer; * Clinical T1-T2 disease with no distant metastasis; * Patient with clinical N0 status; * Patient for whom conservative surgery with sentinel lymph node (SLN) technique is feasible from the start in terms of carcinologic; * Patient with positive SLNs 1\ 2; * Signed consent to participate.

Exclusion criteria

* History of neoadjuvant chemotherapy or hormone therapy; * History of breast cancer (ipsilateral, i.e. recurrence, or contralateral breast); * History of any other invasive cancer; * Initial metastatic disease known; * Pregnant women or lactating women; * Impossibility to undergo medical examinations of the study for geographical, social or psychological reasons.

Design outcomes

Primary

MeasureTime frameDescription
Disease Free SurvivalTime to relapse or progression up to 10 yearsTime from randomization to relapse or death.

Secondary

MeasureTime frameDescription
Overall SurvivalTime to death up to 10 yearsTime from randomization to date of death.
Axillary Recurrence RateTime to local relapse up to 10 yearsEstimate the incidence of axillary recurrence after surgery followed by axillary dissection or after surgery alone.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026