Correlation between outcome and extent of residual disease in the sentinel node after neoadjuvant chemotherapy in clinically fine-needle proven node-positive breast cancer patients.


Journal

European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology
ISSN: 1532-2157
Titre abrégé: Eur J Surg Oncol
Pays: England
ID NLM: 8504356

Informations de publication

Date de publication:
08 2021
Historique:
received: 01 03 2021
revised: 20 04 2021
accepted: 27 04 2021
pubmed: 12 5 2021
medline: 15 12 2021
entrez: 11 5 2021
Statut: ppublish

Résumé

Whether the extent of residual disease in the sentinel lymph node (SLN) after neoadjuvant chemotherapy (NAC) influences the prognosis in clinically node-positive breast cancer (BC) patients remains to be ascertained. One hundred and thirty-four consecutive cN+/BC-patients received NAC followed by SLN biopsy and axillary lymph node dissection. Cumulative incidence of overall (OS) and disease-free (DFS) survival, BC-related recurrences and death from BC were assessed using the Kaplan-Meier method both in the whole patient population and according to the SLN status. The log rank test was used for comparisons between groups. The SLN was identified in 123/134 (91.8%) patients and was positive in 98/123 (79.7%) patients. Sixty-five of them (66.3%) had other axillary nodes involved. SLN sensitivity and false-negative rate were 88.0% and 2.0%, Median follow-up was 10.2 years. Ten-year cumulative incidence of axillary, breast and distant recurrences, and death from BC were 6.5%, 11.9%, 33.4% and 31.3%, respectively. Ten-year OS and DFS were 67.3% and 55.9%. When stratified by SLN status, 10-year cumulative incidence of BC-related and loco-regional events, and death from BC were similar between disease-free SLN and micrometastatic SLN subgroups (28.9% vs 30.2%, p = 0.954; 21.6% vs 13.4%, p = 0.840; 12.9 vs 24.5%, p=0.494). Likewise, 10-year OS and DFS were comparable (80.0% vs 75.5%, p=0.975 and 68.0% vs 69.8, p=0.836). Both OS and DFS were lower in patients presenting a macrometastatic SLN (60.2% and 47.5%). Outcome of patients with micrometastatic SLN was similar to that of patients with disease-free SLN, which was more favorable as compared to that of patients with macrometastatic SLN.

Sections du résumé

BACKGROUND
Whether the extent of residual disease in the sentinel lymph node (SLN) after neoadjuvant chemotherapy (NAC) influences the prognosis in clinically node-positive breast cancer (BC) patients remains to be ascertained.
METHODS
One hundred and thirty-four consecutive cN+/BC-patients received NAC followed by SLN biopsy and axillary lymph node dissection. Cumulative incidence of overall (OS) and disease-free (DFS) survival, BC-related recurrences and death from BC were assessed using the Kaplan-Meier method both in the whole patient population and according to the SLN status. The log rank test was used for comparisons between groups.
RESULTS
The SLN was identified in 123/134 (91.8%) patients and was positive in 98/123 (79.7%) patients. Sixty-five of them (66.3%) had other axillary nodes involved. SLN sensitivity and false-negative rate were 88.0% and 2.0%, Median follow-up was 10.2 years. Ten-year cumulative incidence of axillary, breast and distant recurrences, and death from BC were 6.5%, 11.9%, 33.4% and 31.3%, respectively. Ten-year OS and DFS were 67.3% and 55.9%. When stratified by SLN status, 10-year cumulative incidence of BC-related and loco-regional events, and death from BC were similar between disease-free SLN and micrometastatic SLN subgroups (28.9% vs 30.2%, p = 0.954; 21.6% vs 13.4%, p = 0.840; 12.9 vs 24.5%, p=0.494). Likewise, 10-year OS and DFS were comparable (80.0% vs 75.5%, p=0.975 and 68.0% vs 69.8, p=0.836). Both OS and DFS were lower in patients presenting a macrometastatic SLN (60.2% and 47.5%).
CONCLUSION
Outcome of patients with micrometastatic SLN was similar to that of patients with disease-free SLN, which was more favorable as compared to that of patients with macrometastatic SLN.

Identifiants

pubmed: 33972144
pii: S0748-7983(21)00471-6
doi: 10.1016/j.ejso.2021.04.039
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1920-1927

Informations de copyright

Copyright © 2021. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of competing interest None of the authors declares conflicts of interest.

Auteurs

Giuseppe Canavese (G)

Breast Unit, Cancer Center, IRCCS Clinical Institute Humanitas, Rozzano (MI), Italy.

Corrado Tinterri (C)

Breast Unit, Cancer Center, IRCCS Clinical Institute Humanitas, Rozzano (MI), Italy.

Franca Carli (F)

Anatomia Patologica Ospedaliera, IRCCS Ospedale Policlinico San Martino, Genova, Italy.

Elsa Garrone (E)

Epidemiologia Clinica, IRCCS Ospedale Policlinico San Martino, Genova, Italy.

Stefano Spinaci (S)

Breast Unit, Ospedale Villa Scassi, Genova, Italy.

Angelica Della Valle (A)

Breast Unit, Cancer Center, IRCCS Clinical Institute Humanitas, Rozzano (MI), Italy.

Erika Barbieri (E)

Breast Unit, Cancer Center, IRCCS Clinical Institute Humanitas, Rozzano (MI), Italy.

Emilia Marrazzo (E)

Breast Unit, Cancer Center, IRCCS Clinical Institute Humanitas, Rozzano (MI), Italy.

Paolo Bruzzi (P)

Epidemiologia Clinica, IRCCS Ospedale Policlinico San Martino, Genova, Italy.

Beatrice Dozin (B)

Epidemiologia Clinica, IRCCS Ospedale Policlinico San Martino, Genova, Italy. Electronic address: beatrice.dozin@hsanmartino.it.

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