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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04665882
Other study ID # ZNJC201935
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 11, 2020
Est. completion date December 31, 2027

Study information

Verified date December 2020
Source Wuhan University
Contact Qianqian Yuan, M.D.
Phone 13026322297
Email Yuanqq11@whu.edu.cn
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

It has been hypothesized that damaged arm lymphatic drainage is associated with the arm lymphedema after axillary lymph node dissection (ALND). However, the majority of breast cancer patients with complete ALND has not suffered from arm lymphedema, which appears to be due to the residual arm lymph nodes that has not been removed in the axillary dissection. With the compensation of the residual arm lymph flow above the level of axillary vein, the arm lymphatic drainage could keep balance and remain normal function. This arm lymphedema prediction model that included the protective factor, the proportion of arm lymph flow above the level of axillary vein, allows intraoperative intervention to be performed for the high-risk group. The arm lymphatics of these distinguished patients would be preserved to eliminate the occurrence of arm lymphedema in this study.


Recruitment information / eligibility

Status Recruiting
Enrollment 600
Est. completion date December 31, 2027
Est. primary completion date December 31, 2022
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Patients aged 18 years or older with T1-3 invasive breast cancer; - Clinically node-positive breast cancer, defined as positive on preoperative axillary palpation, ultrasound examination, and computed tomography scan with contrast; - Patients who underwent mastectomy with a positive sentinel lymph node (SLN); - Patients who underwent breast-conserving surgery containing more than two positive SLNs. Exclusion Criteria: - Neoadjuvant chemotherapy; - Previous history of breast cancer.

Study Design


Intervention

Procedure:
Axillary surgery based on lymphedema prediction nomogram
Based on the intraoperative lymphedema prediction nomogram, individualized treatment was recommended to breast cancer patients with different level of risk. For patients with low possibility of developing breast cancer related lymphedema, it was not necessary to preserve arm lymphatics. While the breast cancer patients who were performed mastectomy and ALND with 28 kg/m2 prepared to receive taxane-based chemotherapy, supraclavicular and infraclavicular radiotherapy, according to the established intraoperative nomogram, the proportion of the arm lymph flow above the axillary vein needed to exceed 52%. Otherwise, the arm lymphatics should be identified and preserved.

Locations

Country Name City State
China Zhongnan Hospital of Wuhan University Wuhan Hubei

Sponsors (1)

Lead Sponsor Collaborator
Wuhan University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of arm lymphedema A difference in volume between the arms < 10% was defined as lymphedema Up to 5 years
Primary Rate of locoregional recurrence Locoregional recurrence included local recurrence and regional recurrence. Local recurrence was defined as chest wall recurrence of breast cancer, and regional recurrence was defined as the axilla recurrence of breast cancer Up to 5 years
Primary Rate of distant metastasis Cancer cells from breast metastasized to other organs. Up to 5 years
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