NCT04426136

Brief Summary

The incidence and mortality rates of breast cancer are still increasing in both developing and developed countries. The number of women ≥70 years who are affected by breast cancer (BC) worldwide is also on the increase. Based on the largest population and increasing aging, BC is also rapidly increasing among the elderly in China. According to the epidemiological profile data regarding BC in China, the second onset age peak of BC morbidity occurred after 70 years old and in 2020, the proportion of patients older than 65 is expected to exceed one-fifth and reach 27.0% by 2030. However, some controversies remain to be resolved due to the lack of high quality evidence. The tumor biological behavior, treatment choice and treatment tolerance among the elderly prominently differ from their young counterparts. Besides, they are rarely enrolled in large-scale randomized clinical trials or prospective cohort studies and the results are obtained mainly from retrospective studies. Also, frequent deviations from the standard guidelines lead to insufficient or excessive treatments, though the so-called standard guidelines are based on the clinicopathological characteristics and research findings among the younger BC patients. Studies focusing on the global population confirmed that the biological behavior of tumors among elderly patients was more favorable compared with younger patients but did not transform into survival benefits eventually. Numerous prospective, randomized trials have demonstrated that breast conserving surgery (BCS), consisting of segmental mastectomy and radiation treatment with or without axillary lymph node dissection (ALND), is equivalent to mastectomy in terms of overall survival (OS) and disease free survival (DFS) for patients with early stage breast carcinoma. Presentation of the ACOZOG-Z011 study results in 2011 resulted in a downward trend in the use of a completion axillary lymph node dissection in early breast cancer patients with 1-2 positive sentinel lymph nodes (SLN), treated with wide local excision (WLE) and whole breast irradiation. However, there is little evidence regarding the optimal axillary treatment in elderly breast cancer patients, since these patients are often excluded from clinical trials. We had done a retrospective study of breast cancer in the elderly, which demonstrated that those who with complex comorbidities receiving wide local excision merely were about 1.5 times more than those who without (71.2% vs 46.0%, p\<0.001). However, it is paradoxical that, on the one hand, the risk of dying from breast cancer may increase if patients do not receive the standard treatment; on the other hand, they could not live long enough to benefit or even suffer more from the standard treatment. The key is to figure out who they are. Given the high proportion of patients treated only with WLE, we believe that it is important to compare the effects of different surgical procedures on prognosis among the elderly BC patient in a prospective cohort study, to be more specific, comparing the WLE versus any other surgical procedures.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
300

participants targeted

Target at P75+ for all trials

Timeline
13mo left

Started Jun 2020

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress85%
Jun 2020Jun 2027

Study Start

First participant enrolled

June 1, 2020

Completed
2 days until next milestone

First Submitted

Initial submission to the registry

June 3, 2020

Completed
8 days until next milestone

First Posted

Study publicly available on registry

June 11, 2020

Completed
6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2026

Expected
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2027

Last Updated

June 11, 2020

Status Verified

June 1, 2020

Enrollment Period

6 years

First QC Date

June 3, 2020

Last Update Submit

June 8, 2020

Conditions

Keywords

elderlybreast cancerwide local excisionsurvival

Outcome Measures

Primary Outcomes (3)

  • disease free survival

    the time interval from surgery to disease recurrence or metastasis or considered as still alive at the observation deadline or missed during follow-up

    From date of surgery until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 72 months

  • overall survival

    the time interval from surgery to all cause death or considered as still alive at the observation deadline or missed during follow-up

    From date of surgery until the date of death from any cause, assessed up to 72 months

  • breast cancer-specific survival

    the time interval from surgery to breast cancer related death or considered as still alive at the observation deadline or missed during follow-up

    From date of surgery until the date of death from breast cancer related cause, assessed up to 72 months

Study Arms (2)

1. WLE group

patients in this group receiving WLE merely

2. other method group

patients in this group receiving any other surgical procedures except WLE

Eligibility Criteria

Age70 Years+
Sexfemale
Healthy VolunteersNo
Age GroupsOlder Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

We intend to enroll all patients who have been treated in the breast surgery department of our hospital and meet the inclusion criteria from the date of enrollment.

You may qualify if:

  • Clinical diagnosis of breast cancer
  • Received surgical treatment in this institution
  • Specific surgical method data available
  • Demographic and pathological data available
  • No clear evidence of distant metastasis
  • Agree to participate in the trial and receive long-term follow-up

You may not qualify if:

  • Being intolerant of surgical treatment
  • Distant metastases have been merged
  • Patients who had simultaneous bilateral breast cancer
  • Follow-up interval being less than 12 months except reaching endpoints of observation

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Breast Surgery,Peking Union Medical College Hospital

Beijing, Beijing Municipality, 100730, China

Location

MeSH Terms

Conditions

Breast Neoplasms

Condition Hierarchy (Ancestors)

Neoplasms by SiteNeoplasmsBreast DiseasesSkin DiseasesSkin and Connective Tissue Diseases

Central Study Contacts

Qiang Sun, Professor

CONTACT

Ying Zhong, Doctor

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
5 Years
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 3, 2020

First Posted

June 11, 2020

Study Start

June 1, 2020

Primary Completion (Estimated)

June 1, 2026

Study Completion (Estimated)

June 1, 2027

Last Updated

June 11, 2020

Record last verified: 2020-06

Locations