The value of completion axillary treatment in sentinel node positive breast cancer patients undergoing a mastectomy: a Dutch randomized controlled multicentre trial (BOOG 2013-07) ...

Abstract Background Trials failed to demonstrate additional value of completion axillary lymph node dissection in case of limited sentinel lymph node metastases in breast cancer patients undergoing breast conserving therapy. It has been suggested that the low regional recurrence rates in these trials might partially be ascribed to accidental irradiation of part of the axilla by whole breast radiation therapy, which precludes extrapolation of results to mastectomy patients. The aim of the randomized controlled BOOG 2013–07 trial is therefore to investigate whether completion axillary treatment... Mehr ...

Verfasser: L. Van Roozendaal
J. De Wilt
T. Van Dalen
J. Van Der Hage
L. Strobbe
L. Boersma
S. Linn
M. Lobbes
P. Poortmans
V. Tjan-Heijnen
K. Van De Vijver
J. De Vries
A. Westenberg
A. Kessels
M. Smidt
Dokumenttyp: Datenquelle
Erscheinungsdatum: 2015
Verlag/Hrsg.: Figshare
Schlagwörter: Medicine / Cell Biology / Immunology / FOS: Clinical medicine / Cancer / Science Policy
Sprache: unknown
Permalink: https://search.fid-benelux.de/Record/base-28983605
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : https://dx.doi.org/10.6084/m9.figshare.c.3640430

Abstract Background Trials failed to demonstrate additional value of completion axillary lymph node dissection in case of limited sentinel lymph node metastases in breast cancer patients undergoing breast conserving therapy. It has been suggested that the low regional recurrence rates in these trials might partially be ascribed to accidental irradiation of part of the axilla by whole breast radiation therapy, which precludes extrapolation of results to mastectomy patients. The aim of the randomized controlled BOOG 2013–07 trial is therefore to investigate whether completion axillary treatment can be safely omitted in sentinel lymph node positive breast cancer patients treated with mastectomy. Design This study is designed as a non-inferiority randomized controlled multicentre trial. Women aged 18 years or older diagnosed with unilateral invasive clinically T1-2 N0 breast cancer who are treated with mastectomy, and who have a maximum of three axillary sentinel lymph nodes containing micro- and/or ...