Clinicopathological characteristics and survival results of patients with ultralow risk breast cancer.

Características clínico-patológicas y supervivencia de pacientes con cáncer de mama de riesgo muy bajo.
Breast cancer Cribado mamográfico Cáncer de mama Enfermedad indolente Indolent disease Riesgo muy bajo Screening mammography Supervivencia Survival Ultralow threshold

Journal

Medicina clinica
ISSN: 1578-8989
Titre abrégé: Med Clin (Barc)
Pays: Spain
ID NLM: 0376377

Informations de publication

Date de publication:
28 10 2022
Historique:
received: 03 09 2021
revised: 24 11 2021
accepted: 25 11 2021
pubmed: 20 2 2022
medline: 19 10 2022
entrez: 19 2 2022
Statut: ppublish

Résumé

To identify subgroups with good progress over an extended period, we used diagnostic screening, tumour palpability, tumour phenotype, and node involvement. We identified patients with good progress by means of a descriptive, observational and retrospective study. Of 746 patients diagnosed with node-negative breast cancer between 2001 and 2015: 110 (14.75%) had non-palpable screening-diagnosed tumours; 88 (80%) were endocrine-sensitive, 10 (9.10%) were triple-negative and 11 (10%) were HER2. Only 3 patients developed metastases, and there were 4 deaths: 2 from breast cancer and 2 from other causes. The distant recurrence-free interval (DRFI) was 95.60%: 100% in 34 endocrine-sensitive histological grade 1 (equivalent to luminal A) tumours, and 94.40% (95% CI 86.76-102.04) in 54 grade 2-3 (luminal B) tumours. In triple-negative and HER2 cases, it was 100%. In tumours <1 cm it was 100%, and >1 cm it was 95.50% (95% CI 79.42-100.98). Patients with non-palpable tumours detected by mammogram screening have ultralow risk. The good progress in the luminal A, triple-negative, HER2, and less than 1 cm subgroups may explain the efficacy of the treatment but it also makes them candidates to de-escalation of their treatment.

Sections du résumé

BACKGROUND AND OBJECTIVE
To identify subgroups with good progress over an extended period, we used diagnostic screening, tumour palpability, tumour phenotype, and node involvement.
PATIENTS AND METHODS
We identified patients with good progress by means of a descriptive, observational and retrospective study.
RESULTS
Of 746 patients diagnosed with node-negative breast cancer between 2001 and 2015: 110 (14.75%) had non-palpable screening-diagnosed tumours; 88 (80%) were endocrine-sensitive, 10 (9.10%) were triple-negative and 11 (10%) were HER2. Only 3 patients developed metastases, and there were 4 deaths: 2 from breast cancer and 2 from other causes. The distant recurrence-free interval (DRFI) was 95.60%: 100% in 34 endocrine-sensitive histological grade 1 (equivalent to luminal A) tumours, and 94.40% (95% CI 86.76-102.04) in 54 grade 2-3 (luminal B) tumours. In triple-negative and HER2 cases, it was 100%. In tumours <1 cm it was 100%, and >1 cm it was 95.50% (95% CI 79.42-100.98).
CONCLUSIONS
Patients with non-palpable tumours detected by mammogram screening have ultralow risk. The good progress in the luminal A, triple-negative, HER2, and less than 1 cm subgroups may explain the efficacy of the treatment but it also makes them candidates to de-escalation of their treatment.

Identifiants

pubmed: 35181168
pii: S0025-7753(21)00715-6
doi: 10.1016/j.medcli.2021.11.008
pii:
doi:

Substances chimiques

Receptor, ErbB-2 EC 2.7.10.1

Types de publication

Journal Article

Langues

eng spa

Sous-ensembles de citation

IM

Pagination

351-358

Informations de copyright

Copyright © 2022 Elsevier España, S.L.U. All rights reserved.

Auteurs

José M Baena-Cañada (JM)

Servicio de Oncología Médica. Hospital Universitario Puerta del Mar, Cádiz, España; Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Cádiz, España. Electronic address: josem.baena.sspa@juntadeandalucia.es.

Salvador Gámez-Casado (S)

Servicio de Oncología Médica. Hospital Universitario Puerta del Mar, Cádiz, España; Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Cádiz, España.

Lourdes Rodríguez-Pérez (L)

Servicio de Oncología Médica. Hospital Universitario Puerta del Mar, Cádiz, España; Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Cádiz, España.

Cristina Bandera-López (C)

Servicio de Oncología Médica. Hospital Universitario Virgen de la Victoria, Málaga, España; Instituto de Investigación Biomédica de Málaga (IBIMA), Málaga, España.

Andrés Mesas-Ruiz (A)

Servicio de Oncología Médica. Hospital Universitario Virgen de la Victoria, Málaga, España; Instituto de Investigación Biomédica de Málaga (IBIMA), Málaga, España.

Alicia Campini-Bermejo (A)

Servicio de Oncología Médica. Hospital Universitario Puerta del Mar, Cádiz, España; Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Cádiz, España.

Marta Bernal-Gómez (M)

Servicio de Oncología Médica. Hospital Universitario Puerta del Mar, Cádiz, España; Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Cádiz, España.

Manuel Zalabardo-Aguilar (M)

Servicio de Oncología Médica. Hospital Universitario Virgen de la Victoria, Málaga, España; Instituto de Investigación Biomédica de Málaga (IBIMA), Málaga, España.

Julio Calvete-Candenas (J)

Servicio de Oncología Médica. Hospital Universitario Puerta del Mar, Cádiz, España; Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Cádiz, España.

Gala Martínez-Bernal (G)

Servicio de Oncología Médica. Hospital Universitario Puerta del Mar, Cádiz, España; Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Cádiz, España.

Alicia Quílez-Cutillas (A)

Servicio de Oncología Médica. Hospital Universitario Puerta del Mar, Cádiz, España; Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Cádiz, España.

Lidia Atienza-Cuevas (L)

Unidad de Patología. Hospital Universitario Puerta del Mar, Cádiz, España; Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Cádiz, España.

Marcial García-Rojo (M)

Unidad de Patología. Hospital Universitario Puerta del Mar, Cádiz, España; Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Cádiz, España.

Encarnación Benítez-Rodríguez (E)

Registro Provincial del Cáncer, Cádiz, España; Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Cádiz, España.

Bella Pajares-Hachero (B)

Servicio de Oncología Médica. Hospital Universitario Virgen de la Victoria, Málaga, España; Instituto de Investigación Biomédica de Málaga (IBIMA), Málaga, España.

María José Bermejo-Pérez (MJ)

Servicio de Oncología Médica. Hospital Universitario Virgen de la Victoria, Málaga, España; Instituto de Investigación Biomédica de Málaga (IBIMA), Málaga, España.

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Classifications MeSH