Skip to main content
OpenTrials
Completed

NCT Number: NCT03669705

No Axillary Surgery for Early Breast Cancer.

After breast cancer (BC) screening was introduced for all Swedish women in 1989-90 the number of early invasive BC, clin N0 rose dramatically. For these BC it was known that only 10 % or less was N+ after axillary dissection and the morbidity for axillary surgery was substantial. Omitting axillary dissection in a randomized trial was ruled out because of anticipated few events. A national cohort was decided for invasive unifocal BC, histological grade 1 or 2, T=max 10mm, free margins, clin node neg. No axillary dissection should be undertaken. This was before the Sentinel Node era. Adjuvant treatment could be given according to regional guidelines for early breast cancer. Not uniform concerning postoperative radiotherapy and antihormonal treatment. Follow-up was clinical the first 5 years with mammography and then by hospital records and national Death register. Primary aim: Number of axillary recurrence and BC specific survival.

Completed

Looking for future studies?

Notify Me

Key information

Sex eligibility

Female

Study type

Observational

About this study

After national breast cancer screening was introduced in Sweden in 1989-90 the number of early invasive BC, clin N0 rose dramatically. Only 10 % or less of these was N+ after axillary dissection with a substantial morbidity after the axillary intervention. Omitting axillary dissection in a randomized trial was ruled out because of anticipated few events. A national cohort was decided for invasive unifocal BC, Screening or clinical diagnosis were eligible, only histological grade 1 or 2, T=max 10mm, free margins , clinical node negative. No axillary dissection should be undertaken, only radical removal of the breast cancer. (Note; This was before the Sentinel Node era). Adjuvant treatment could be given according to regional guidelines for early breast cancer as no regular national guidelines existed then concerning postoperative radiotherapy and antihormonal treatment. Chemotherapy was not recommended to this type of breast cancer. Follow-up was done by the treating surgeon the first 5 years including mammography. Then hospital records including mammography and reports from Pathology and Oncology and Death register were followed at intervals 5, 10 and 15 years. Primary aim: Number of axillary recurrence and distant metastases/ BC specific survival. Correlation to adjuvant therapy. Inclusion started in 1997 and ended in 2002. 1584 patients were included. If the axillary recurrence rate was more than 1% per year the first five years the inclusion should be stopped.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Invasive breast cancer, unifocal
  • T=max 10mm
  • Clinical node negative and clinical M0
  • Histological grade 1 or 2
  • Both screening / clinical detected accepted
  • Radical operation = free margins in breast specimen
  • Partial mastectomy and mastectomy accepted
  • Fit to understand inclusion criteria

Exclusion criteria

  • Previous breast cancer diagnosis, including carcinoma in situ
  • Previous ipsilateral axillary dissection
  • Non radical operation = no free margins
  • Multifocal cancer
  • Previous treatment for other cancer.
  • Unable to understand information (informed consent)
  • Bilateral breast cancer at diagnosis

Treatment and study plan

Omitting axillary surgery in early breast cancer

Procedure

Before the Sentinel Node era all invasive breast cancer was recommended to have axillary dissection but after the introduction of national breast cancer screening this guideline statement was challenged by this national Swedish cohort.

Primary outcomes

  1. Axillary recurrence

    Time frame: at 15 years

    Time to axillary node recurrence

Secondary outcomes

  1. Breast cancer specific survival (BCSS)

    Time frame: at 15 years

    Breast cancer specific survival

  2. Breast cancer specific survival according to given adjuvant treatment

    Time frame: at 15 years

    BCSS for patients given postop radiotherapy to the breast or no radiotherapy

Sponsors and collaborators

Lead sponsor

Lund University

Other

Collaborators

  • Swedish Breast Cancer Group

Registry information

Official study title

Prospective Cohort Study With no Axillary Surgery for Breast Cancer T</= 10 mm

Important dates

Study start
1997
Primary completion
2002
Study completion
2017
First posted
Sep 13, 2018
Registry last updated
Sep 13, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.