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Clinical Significance of Supraclavicular Lymph Node Dissection for Breast Cancer

Primary Purpose

Breast Cancer Stage III

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
supraclavicular lymph node dissection
supraclavicular area radiotherapy
Sponsored by
Xinhong Wu
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Cancer Stage III focused on measuring breast cancer, supraclavicular lymph node, dissection, radiotherpy, prognosis

Eligibility Criteria

undefined - 75 Years (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Ability to understand the study procedures and contents, and willingness to voluntarily sign the written informed consent form;
  2. Age≤75 years old, female;
  3. Histologically confirmed breast cancer;
  4. Histologically or cytologically confirmed ipsilateral supraclavicular lymph node metastasis;
  5. cT0-T3;
  6. low and moderate risk for anesthesia

Exclusion Criteria:

  1. Absolute and relative contraindication for surgery or radiation;
  2. existing distant metastasis before surgery;
  3. non-invasive breast cancer;
  4. with contralateral breast cancer;
  5. Previous history of breast cancer or other malignancies;
  6. ECOG≥2;
  7. inflammatory breast cancer;
  8. pregnancy;
  9. any serious complications which caused patients not suitable to participate this study

Sites / Locations

  • Wu XinhongRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

supraclavicular lymph node dissection and raidiotherapy

supraclavicular area radiotherapy

Arm Description

breast cancer patients with supraclavicular lymph node metastasis receive supraclavicular lymph node dissection and supraclavicular area radiotherapy

breast cancer patients with supraclavicular lymph node metastasis receive supraclavicular area radiotherapy

Outcomes

Primary Outcome Measures

Disease free survival
Disease free survival for 3 years and 5 years, which means the rate of patients without local recurrence and distant metastasis in the whole patients at the same group will be calculated with Kaplan Meier survival curves.

Secondary Outcome Measures

Occurring rate of complications
Occurring rate of complications including the occurring rate of infection, hemorrhage, limb lymphedema, time in hospital, brachial plexopahy, radiation induced lung injury in each group were recorded in patients' medical record.
Overall survival
Overall survival for 3 years and 5 years, which means the rate of patients alive in the whole patients at the same group will be calculated with kaplan meier survival curves.
Life quality score
Life quality score was evaluated by European Organization of Research and treatment of Cancer-Questionnaire of Life Quality-C30 Version 3 (EORTC-QLQ-C30 V3), which conduct a series of questions about the patients' physical condition, activity of daily life, adverse reaction and mood condition. The range in the questionnaire for the score is from 1 to 4, in which 1 stands for having no discomfort and 4 stands for having great discomfort.
Recurrence free survival
Recurrence free survival for 3 years and 5 years, which means the rate of patients without local recurrence in the whole patients at the same group will be calculated with Kaplan Meier survival curves.

Full Information

First Posted
October 14, 2018
Last Updated
August 30, 2023
Sponsor
Xinhong Wu
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1. Study Identification

Unique Protocol Identification Number
NCT03716245
Brief Title
Clinical Significance of Supraclavicular Lymph Node Dissection for Breast Cancer
Official Title
A Multicenter, Randomised, Open-label Prospective Clinical Trial to Evaluate the Clinical Significance of Supraclavicular Lymph Node Dissection for Breast Cancer Patients With Ipsilateral Supraclavicular Lymph Node Metastasis
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 27, 2019 (Actual)
Primary Completion Date
August 17, 2023 (Actual)
Study Completion Date
September 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Xinhong Wu

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Breast cancer patients with ipsilateral supraclavicular lymph node metastasis are defined as Ⅲc stage (N3) according to the newly published 8th AJCC TNM staging system. No concret guide line was supported to such patients. It is still pending whether to exert supraclavicular lymph node dissection to breast cancer patients with ipsilateral supraclavicular lymph node metastasis. To evaluate the clinical significance and complication of supraclavicular lymph node dissection for breast cancer patients with ipsilateral supraclavicular lymph node metastasis, the investigators randomize patients into two groups, one group is supraclavicular lymph node dissection with radiotherapy group, the other group is radiotherapy group.
Detailed Description
Breast cancer is the most common cancer and the leading cause of deaths from cancer in women worldwide. Breast cancer patients with ipsilateral supraclavicular lymph node metastasis are defined as Ⅲc stage (N3) according to the newly published 8th AJCC TNM staging system. Clinical outcomes are similar for patients with ipsilateral supraclavicular lymph node metastases at first presentation and for patients with recurrent ipsilateral supraclavicular lymph node metastases. The survival rate was lower in patients with ipsilateral supraclavicular lymph node metastases than in patients with lower axillary or subclavian nodal involvement. No concrete guide line was supported to such patients. It is still pending whether to exert supraclavicular lymph node dissection to breast cancer patients with ipsilateral supraclavicular lymph node metastasis. Patients with ipsilateral supraclavicular lymph node metastases who were treated with surgery or radiotherapy and achieved good neck control were reported to achieve better survival than those for whom surgical treatment or irradiation did not result in good local control. Patients with ipsilateral supraclavicular lymph node metastases should be offered a combined modality approach, including systemic therapy, surgery, and radiotherapy. Furthermore, local treatment, usually including axillary and supraclavicular lymph node, either by surgical clearance or by radical radiotherapy, can prevent the tumor cells from drainage, might be play a more important role. However, the role of surgical removal of the supraclavicular nodes is uncertain compared with radical radiotherapy. To our knowledge, the available literature comparing these two local treatments of ipsilateral supraclavicular lymph node metastases is scarce. Furthermore, the studies comparing the outcome of dissection of supraclavicular lymph node combined with local radiotherapy and radiotherapy of supraclavicular lymph node is also rare. All the related reports up to date have mixed them up. To evaluate the clinical significance and complication of supraclavicular lymph node dissection for breast cancer patients with ipsilateral supraclavicular lymph node metastasis, we randomize patients into two groups, one group is supraclavicular lymph node dissection with radiotherapy group, the other group is radiotherapy group. Therefore, in addition to investigating the role of surgical removal of the supraclavicular nodes in Chinese patients, we also try to reveal the potential difference between these two treatments, hoping to bring more insight into clinical practice.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer Stage III
Keywords
breast cancer, supraclavicular lymph node, dissection, radiotherpy, prognosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
180 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
supraclavicular lymph node dissection and raidiotherapy
Arm Type
Experimental
Arm Description
breast cancer patients with supraclavicular lymph node metastasis receive supraclavicular lymph node dissection and supraclavicular area radiotherapy
Arm Title
supraclavicular area radiotherapy
Arm Type
Active Comparator
Arm Description
breast cancer patients with supraclavicular lymph node metastasis receive supraclavicular area radiotherapy
Intervention Type
Procedure
Intervention Name(s)
supraclavicular lymph node dissection
Intervention Description
people with supraclavicular lymph node metastasis before surgery should receive dissection of supraclavicular lymph node and the supraclavicular lymph node metastasis should be confirmed either by core needle biopsy or fine needle aspiration biopsy
Intervention Type
Radiation
Intervention Name(s)
supraclavicular area radiotherapy
Intervention Description
people with supraclavicular lymph node metastasis before surgery should receive radiotherapy of supraclavicular area and the supraclavicular lymph node metastasis should be confirmed either by core needle biopsy or fine needle aspiration biopsy
Primary Outcome Measure Information:
Title
Disease free survival
Description
Disease free survival for 3 years and 5 years, which means the rate of patients without local recurrence and distant metastasis in the whole patients at the same group will be calculated with Kaplan Meier survival curves.
Time Frame
3-5 years
Secondary Outcome Measure Information:
Title
Occurring rate of complications
Description
Occurring rate of complications including the occurring rate of infection, hemorrhage, limb lymphedema, time in hospital, brachial plexopahy, radiation induced lung injury in each group were recorded in patients' medical record.
Time Frame
3-5 years
Title
Overall survival
Description
Overall survival for 3 years and 5 years, which means the rate of patients alive in the whole patients at the same group will be calculated with kaplan meier survival curves.
Time Frame
3-5 years
Title
Life quality score
Description
Life quality score was evaluated by European Organization of Research and treatment of Cancer-Questionnaire of Life Quality-C30 Version 3 (EORTC-QLQ-C30 V3), which conduct a series of questions about the patients' physical condition, activity of daily life, adverse reaction and mood condition. The range in the questionnaire for the score is from 1 to 4, in which 1 stands for having no discomfort and 4 stands for having great discomfort.
Time Frame
3-5 years
Title
Recurrence free survival
Description
Recurrence free survival for 3 years and 5 years, which means the rate of patients without local recurrence in the whole patients at the same group will be calculated with Kaplan Meier survival curves.
Time Frame
3-5 years

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
female
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Ability to understand the study procedures and contents, and willingness to voluntarily sign the written informed consent form; Age≤75 years old, female; Histologically confirmed breast cancer; Histologically or cytologically confirmed ipsilateral supraclavicular lymph node metastasis; cT0-T3; low and moderate risk for anesthesia Exclusion Criteria: Absolute and relative contraindication for surgery or radiation; existing distant metastasis before surgery; non-invasive breast cancer; with contralateral breast cancer; Previous history of breast cancer or other malignancies; ECOG≥2; inflammatory breast cancer; pregnancy; any serious complications which caused patients not suitable to participate this study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xinhong Wu, Doctor
Phone
+8618602726300
Email
34053889@qq.com
First Name & Middle Initial & Last Name or Official Title & Degree
Hongmei Zheng, Doctor
Phone
+8618971624606
Email
18971624606@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xinhong Wu, Doctor
Organizational Affiliation
Hubei Cancer Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Wu Xinhong
City
Wuhan
State/Province
Hubei
ZIP/Postal Code
430079
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
xinhong wu, dotcor
Phone
+8618602726300
Email
34053889@qq.com
First Name & Middle Initial & Last Name & Degree
hongmei zheng, doctor
Phone
+8618971624606
Email
zhenghongmeicj@163.com

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Study Protocol Statistical Analysis Plan (SAP) Informed Consent Form (ICF) Clinical Study Report (CSR) Analytic Code

Learn more about this trial

Clinical Significance of Supraclavicular Lymph Node Dissection for Breast Cancer

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