NAB-Paclitaxel Improves Disease-Free Survival in Early Breast Cancer: GBG 69-GeparSepto.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
01 09 2019
Historique:
pubmed: 15 5 2019
medline: 11 6 2020
entrez: 15 5 2019
Statut: ppublish

Résumé

The GeparSepto trial demonstrated that weekly nanoparticle albumin-bound (NAB)-paclitaxel significantly improves the pathologic complete remission rate compared with weekly solvent-based (sb) paclitaxel followed by epirubicin plus cyclophosphamide as neoadjuvant treatment in patients with primary breast cancer (BC). Here, we report data on long-term outcomes. Patients with histologically confirmed primary BC were randomly assigned in a 1:1 ratio to 12 times weekly NAB-paclitaxel 150 mg/m A total of 1,206 patients started treatment, 606 with NAB-paclitaxel and 600 with sb-paclitaxel. After a median follow-up of 49.6 months (range, 0.5 to 64.0 months), 243 invasive disease-free survival (iDFS) events were reported (143 in the sb-paclitaxel and 100 in the NAB-paclitaxel arm). At 4 years, overall patients treated with NAB-paclitaxel had a significantly better iDFS compared with sb-paclitaxel (84.0% The significantly higher pathologic complete response rate with NAB-paclitaxel translated into a significantly improved iDFS in patients with early BC as compared with sb-paclitaxel. PSN improved much faster under NAB-paclitaxel 125 mg/m

Identifiants

pubmed: 31082269
doi: 10.1200/JCO.18.01842
doi:

Substances chimiques

130-nm albumin-bound paclitaxel 0
Albumins 0
Epirubicin 3Z8479ZZ5X
Cyclophosphamide 8N3DW7272P
Paclitaxel P88XT4IS4D

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2226-2234

Commentaires et corrections

Type : CommentIn

Auteurs

Michael Untch (M)

Helios Klinikum Berlin-Buch, Berlin, Germany.

Christian Jackisch (C)

Sana Klinikum, Offenbach, Germany.

Andreas Schneeweiss (A)

Nationales Centrum für Tumorerkrankungen, Heidelberg, Germany.

Sabine Schmatloch (S)

St Elisabeth Krankenhaus Kassel, Kassel, Germany.

Bahriye Aktas (B)

Klinik und Poliklinik für Frauenheilkunde Leipzig, Leipzig, Germany.

Carsten Denkert (C)

Charité-Universitätsmedizin Berlin, Berlin, Germany.

Christian Schem (C)

Universitätsklinikum Kiel, Kiel, Germany.

Hermann Wiebringhaus (H)

St Barbara-Klinik Hamm-Heessen, Hamm, Germany.

Sherko Kümmel (S)

Interdisziplinäres Brustzentrum an den Kliniken Essen-Mitte, Essen, Germany.

Mathias Warm (M)

Brustzentrum im Krankenhaus Köln-Holweide, Cologne, Germany.

Peter A Fasching (PA)

Universitätsklinikum Erlangen, Erlangen, Germany.

Marianne Just (M)

Onkologische Schwerpunktpraxis Bielefeld, Bielefeld, Germany.

Claus Hanusch (C)

Klinikum zum Roten Kreuz, Munich, Germany.

John Hackmann (J)

Marien Hospital Witten, Witten, Germany.

Jens-Uwe Blohmer (JU)

Klinik für Gynäkologie am Campus Charité Mitte, Berlin, Germany.

Kerstin Rhiem (K)

Uniklinik Köln, Cologne, Germany.

Wolfgang D Schmitt (WD)

Charité-Universitätsmedizin Berlin, Berlin, Germany.

Jenny Furlanetto (J)

German Breast Group, Neu-Isenburg, Germany.

Bernd Gerber (B)

Universitäts-Frauenklinik, Rostock, Germany.

Jens Huober (J)

Universitätsklinikum Ulm, Ulm, Germany.

Valentina Nekljudova (V)

German Breast Group, Neu-Isenburg, Germany.

Gunter von Minckwitz (G)

German Breast Group, Neu-Isenburg, Germany.

Sibylle Loibl (S)

German Breast Group, Neu-Isenburg, Germany.

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Classifications MeSH