False-negative rate in the extended prospective TATTOO trial evaluating targeted axillary dissection by carbon tattooing in clinically node-positive breast cancer patients receiving neoadjuvant systemic therapy.


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:
Jun 2022
Historique:
received: 04 02 2022
accepted: 27 03 2022
pubmed: 23 4 2022
medline: 20 5 2022
entrez: 22 4 2022
Statut: ppublish

Résumé

In clinically node-positive breast cancer patients receiving neoadjuvant systemic therapy (NST), nodal metastases can be initially marked and then removed during surgical axillary staging. Marking methods vary significantly in terms of feasibility and cost. The purpose of the extended TATTOO trial was to report on the false-negative rate (FNR) of the low-cost method carbon tattooing. The international prospective single-arm TATTOO trial included clinically node-positive breast cancer patients planned for NST from November 2017 to January 2021. For the present analysis, patients who received both the targeted procedure with or without an additional sentinel lymph node (SLN) biopsy and a completion axillary lymph node dissection (ALND) were selected. Primary endpoint was the FNR. Out of 172 included patients, 149 had undergone a completion ALND. The detection rate for the tattooed node was 94.6% (141 out of 149). SLN biopsy was attempted in 132 out of 149 patients with a detection rate of 91.7% (121 out of 132). SLN and tattooed node were identical in 58 out of 121 individuals (47.9%). The combined procedure, i.e. targeted axillary dissection (TAD) was successful in 147 of 149 cases (98.7%). Four out of 65 patients with a clinically node-negative status after NST had a negative TAD but metastases on ALND, corresponding to a FNR of 6.2%. All false-negative TAD procedures were performed in the first 2 years of the trial (2018-2019, p = 0.022). Carbon tattooing is a feasible marking method for TAD with a high detection rate and an acceptably low FNR. The TATTOO trial was preregistered as prospective trial before initiation at the University of Rostock, Germany (DRKS00013169).

Identifiants

pubmed: 35451733
doi: 10.1007/s10549-022-06588-2
pii: 10.1007/s10549-022-06588-2
pmc: PMC9114094
doi:

Substances chimiques

Carbon 7440-44-0

Banques de données

DRKS
['DRKS00013169']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

589-595

Informations de copyright

© 2022. The Author(s).

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Auteurs

Jana de Boniface (J)

Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden. jana.de-boniface@ki.se.
Department of Surgery, Breast Centre, Capio St. Göran's Hospital, Mariebergsporten 2, 11219, Stockholm, Sweden. jana.de-boniface@ki.se.

Jan Frisell (J)

Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Department of Breast, Endocrine and Sarcoma Surgery, Karolinska University Hospital, Stockholm, Sweden.

Thorsten Kühn (T)

Department of Obstetrics and Gynecology, Klinikum Esslingen, Esslingen, Germany.

Ingrid Wiklander-Bråkenhielm (I)

Department of Radiology, Capio St. Göran's Hospital, Stockholm, Sweden.

Karin Dembrower (K)

Department of Radiology, Capio St. Göran's Hospital, Stockholm, Sweden.
Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.

Per Nyman (P)

Department of Surgery, Skaraborg Hospital, Lidköping, Sweden.

Athanasios Zouzos (A)

Department of Mammography, Karolinska University Hospital, Stockholm, Sweden.
Department of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.

Bernd Gerber (B)

Department of Obstetrics and Gynecology, University of Rostock, Rostock, Germany.

Toralf Reimer (T)

Department of Obstetrics and Gynecology, University of Rostock, Rostock, Germany.

Steffi Hartmann (S)

Department of Obstetrics and Gynecology, University of Rostock, Rostock, Germany.

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