Which patients with sentinel node-positive breast cancer after breast conservation still receive completion axillary lymph node dissection in routine clinical practice?


Journal

Breast cancer research and treatment
ISSN: 1573-7217
Titre abrégé: Breast Cancer Res Treat
Pays: Netherlands
ID NLM: 8111104

Informations de publication

Date de publication:
Jan 2019
Historique:
received: 24 09 2018
accepted: 11 10 2018
pubmed: 14 10 2018
medline: 25 6 2019
entrez: 14 10 2018
Statut: ppublish

Résumé

In the American College of Surgeons Oncology Group (ACOSOG) Z0011 trial, patients with 1 or 2 tumour-involved sentinel lymph nodes (SLNs) gained no benefit from completion axillary lymph dissection (cALND). We examined implementation of evidence from this trial into routine clinical management. Data were included from patients diagnosed with primary breast cancer in German breast cancer units between 2008 and 2015 and analysed retrospectively from a prospective maintained database. Descriptive analyses assessed time-trend changes in axillary surgery. Factors associated with cALND in patients with 1 or 2 positive SLNs were identified using multivariable logistic regression analysis. Overall, 179 breast cancer units provided data for 188,909 patients, of whom 13,741 (7.3%) had pT1/2cN0M0 invasive breast cancer with 1 or 2 tumour-involved SLNs and underwent breast-conserving surgery and adjuvant radiotherapy. cALND use decreased from 94.6% in 2008 to 46.9% in 2015 (p < 0.001). In multivariable analyses, the following factors were associated with cALND: fewer removed SLNs; two tumour-affected SLNs; younger age; lower annual case volume per hospital; higher tumour grade and lymphovascular invasion. No statistically significant influence was detected for hormone receptor or HER2 status. In our cohort, 7.3% of patients with primary breast cancer met the ACOSOG Z0011 inclusion criteria and could potentially have been spared the morbidity of cALND. cALND tended to be performed in patients with a higher axillary tumour burden. This study shows a shift towards less extensive axillary surgery through rapid implementation of new clinical trial evidence into routine clinical practice.

Identifiants

pubmed: 30315437
doi: 10.1007/s10549-018-5009-2
pii: 10.1007/s10549-018-5009-2
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

429-438

Subventions

Organisme : Deutsche Krebshilfe
ID : 70112082

Auteurs

André Hennigs (A)

Department of Gynecology and Obstetrics, University of Heidelberg, Im Neuenheimer Feld 440, 69120, Heidelberg, Germany.

Melitta Köpke (M)

Department of Gynecology and Obstetrics, University of Heidelberg, Im Neuenheimer Feld 440, 69120, Heidelberg, Germany.

Manuel Feißt (M)

Institute of Medical Biometry and Informatics, University of Heidelberg, Heidelberg, Germany.

Fabian Riedel (F)

Department of Gynecology and Obstetrics, University of Heidelberg, Im Neuenheimer Feld 440, 69120, Heidelberg, Germany.

Mahdi Rezai (M)

European Breast Center, Luisen Hospital, Düsseldorf, Germany.

Ulrike Nitz (U)

Evangelical Hospital Johanniter Bethesda, Breast Center Niederrhein, Mönchengladbach, Germany.

Mareike Moderow (M)

West German Breast Center Ltd, Düsseldorf, Germany.

Michael Golatta (M)

Department of Gynecology and Obstetrics, University of Heidelberg, Im Neuenheimer Feld 440, 69120, Heidelberg, Germany.

Christof Sohn (C)

Department of Gynecology and Obstetrics, University of Heidelberg, Im Neuenheimer Feld 440, 69120, Heidelberg, Germany.

Andreas Schneeweiss (A)

National Center for Tumor Diseases, University of Heidelberg, Heidelberg, Germany.

Jörg Heil (J)

Department of Gynecology and Obstetrics, University of Heidelberg, Im Neuenheimer Feld 440, 69120, Heidelberg, Germany. joerg.heil@med.uni-heidelberg.de.

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