Pathological Response in the Breast and Axillary Lymph Nodes after Neoadjuvant Systemic Treatment in Patients with Initially Node-Positive Breast Cancer Correlates with Disease Free Survival: An Exploratory Analysis of the GeparOcto Trial.

axillary surgery breast cancer lymph node neoadjuvant therapy pathological complete response prognosis

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
20 Jan 2022
Historique:
received: 01 12 2021
revised: 13 01 2022
accepted: 18 01 2022
entrez: 15 2 2022
pubmed: 16 2 2022
medline: 16 2 2022
Statut: epublish

Résumé

The conversion of initially histologically confirmed axillary lymph node-positive (pN+) to ypN0 after neoadjuvant systemic treatment (NAST) is an important prognostic factor in breast cancer (BC) patients and may influence surgical de-escalation strategies. We aimed to determine pCR rates in lymph nodes (pCR-LN), the breast (pCR-B), and both (tpCR) in women who present with pN+ BC, to assess predictors for response and the impact of pCR-LN, pCR-B, and tpCR on invasive disease-free survival (iDFS). Retrospective, exploratory analysis of 242 patients with pN+ at diagnosis from the multicentric, randomized GeparOcto trial. Of 242 patients with initially pN+ disease, 134 (55.4%) had a pCR-LN, and 109 (45.0%) a pCR-B. Of the 109 pCR-B patients, 9 (8.3%) patients had involved LN, and 100 (41.3%) patients had tpCR. Those with involved LN still had a bad prognosis. As expected, pCR-B and intrinsic subtypes (TNBC and HER2+) were identified as independent predictors of pCR-LN. pCR-LN (ypN0; hazard ratio 0.42; 95%, CI 0.23-0.75; In initially pN+ patients undergoing NAST, the conversion to ypN0 is of high prognostic value. Surgical axillary staging after NAST is still essential in these patients to offer tailored treatment.

Sections du résumé

BACKGROUND BACKGROUND
The conversion of initially histologically confirmed axillary lymph node-positive (pN+) to ypN0 after neoadjuvant systemic treatment (NAST) is an important prognostic factor in breast cancer (BC) patients and may influence surgical de-escalation strategies. We aimed to determine pCR rates in lymph nodes (pCR-LN), the breast (pCR-B), and both (tpCR) in women who present with pN+ BC, to assess predictors for response and the impact of pCR-LN, pCR-B, and tpCR on invasive disease-free survival (iDFS).
METHODS METHODS
Retrospective, exploratory analysis of 242 patients with pN+ at diagnosis from the multicentric, randomized GeparOcto trial.
RESULTS RESULTS
Of 242 patients with initially pN+ disease, 134 (55.4%) had a pCR-LN, and 109 (45.0%) a pCR-B. Of the 109 pCR-B patients, 9 (8.3%) patients had involved LN, and 100 (41.3%) patients had tpCR. Those with involved LN still had a bad prognosis. As expected, pCR-B and intrinsic subtypes (TNBC and HER2+) were identified as independent predictors of pCR-LN. pCR-LN (ypN0; hazard ratio 0.42; 95%, CI 0.23-0.75;
CONCLUSIONS CONCLUSIONS
In initially pN+ patients undergoing NAST, the conversion to ypN0 is of high prognostic value. Surgical axillary staging after NAST is still essential in these patients to offer tailored treatment.

Identifiants

pubmed: 35158789
pii: cancers14030521
doi: 10.3390/cancers14030521
pmc: PMC8833390
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Amgen
ID : n.a.
Organisme : Roche
ID : n.a.
Organisme : TEVA
ID : n.a.
Organisme : Vifor
ID : n.a.

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Auteurs

Bernd Gerber (B)

Department of Obstetrics and Gynecology, University of Rostock, Südring 81, 18059 Rostock, Germany.

Andreas Schneeweiss (A)

National Center for Tumor Diseases, Heidelberg University Hospital and German Cancer Research Center, Im Neuenheimer Feld 460, 69120 Heidelberg, Germany.

Volker Möbus (V)

Medical Clinic II, University Hospital Frankfurt, Theodor-Stern-Kai 7, 60590 Frankfurt, Germany.

Michael Golatta (M)

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

Hans Tesch (H)

Oncology Practice, Bethanien Hospital Frankfurt, Im Prüfling 17-19, 60389 Frankfurt, Germany.

David Krug (D)

Department of Radiotherapy, University Hospital Schleswig Holstein, Arnold-Heller-Straße 3, 24105 Kiel, Germany.

Claus Hanusch (C)

Department of Senology, Rotkreuz-Klinikum, Rotkreuzplatz 8, 80634 Munich, Germany.

Carsten Denkert (C)

Institute of Pathology, Philipps-University Marburg, Baldingerstraße, 35043 Marburg, Germany.

Kristina Lübbe (K)

Breast Center, Diakovere Henriettenstift, Schwemannstraße 17, 30559 Hannover, Germany.

Jörg Heil (J)

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

Jens Huober (J)

Department of Gynecology and Obstetrics, Ulm University Hospital, Albert-Einstein-Allee 23, 89081 Ulm, Germany.

Beyhan Ataseven (B)

Department of Obstetrics and Gynecology, University Hospital, Ludwig Maximilian University of Munich, 81377 Munich, Germany.
Department of Gynecology and Gynecologic Oncology, Kliniken Essen-Mitte, Henricistraße 92, 45136 Essen, Germany.

Peter Klare (P)

Oncologic Medical Care Center Krebsheilkunde, Möllendorffstraße 52, 10367 Berlin, Germany.

Markus Hahn (M)

Department for Women's Health, University of Tübingen, Calwerstraße 7, 72076 Tuebingen, Germany.

Michael Untch (M)

Department of Obstetrics and Gynecology, Helios Klinikum Berlin-Buch, Schwanebecker Chaussee 50, 13125 Berlin, Germany.

Karin Kast (K)

Center for Hereditary Breast and Ovarian Cancer, University Hospital of Cologne, Kerpener Straße 62, 50937 Cologne, Germany.

Christian Jackisch (C)

Department of Obstetrics and Gynecology, Sana Klinikum Offenbach GmbH, Starkenburgring 66, 63069 Offenbach, Germany.

Jörg Thomalla (J)

Praxisklinik für Hämatologie und Onkologie Koblenz, Neversstraße 5, 56068 Koblenz, Germany.

Fenja Seither (F)

German Breast Group, Martin Behaim Strasse 12, 63263 Neu-Isenburg, Germany.

Jens-Uwe Blohmer (JU)

Department of Gynecology with Breast Center Charité, Charitéplatz 1, 10117 Berlin, Germany.

Kerstin Rhiem (K)

Center for Hereditary Breast and Ovarian Cancer, Center for Integrated Oncology (CIO), Medical Faculty, University Hospital Cologne, Kerpener Straße 62, 50937 Cologne, Germany.

Peter A Fasching (PA)

Department of Obstetrics and Gynecology, University of Erlangen, Universitätsstraße 21/23, 91054 Erlangen, Germany.

Valentina Nekljudova (V)

German Breast Group, Martin Behaim Strasse 12, 63263 Neu-Isenburg, Germany.

Sibylle Loibl (S)

German Breast Group, Martin Behaim Strasse 12, 63263 Neu-Isenburg, Germany.

Thorsten Kühn (T)

Department of Gynecology, Klinikum Esslingen, Hirschlandstraße 97, 73730 Esslingen, Germany.

Classifications MeSH