TP53-associated early breast cancer: new observations from a large cohort.


Journal

Journal of the National Cancer Institute
ISSN: 1460-2105
Titre abrégé: J Natl Cancer Inst
Pays: United States
ID NLM: 7503089

Informations de publication

Date de publication:
03 Apr 2024
Historique:
received: 14 02 2024
revised: 19 03 2024
accepted: 21 03 2024
medline: 4 4 2024
pubmed: 4 4 2024
entrez: 3 4 2024
Statut: aheadofprint

Résumé

A large well-annotated recent international cohort of Li-Fraumeni (LFS) patients with early-stage breast cancer (BC) was examined for shared features. This multicentre cohort study included females with a germline TP53 pathogenic or likely pathogenic variant and nonmetastatic BC diagnosed between 2002-2022. Clinical and genetic data were obtained from institutional registries and clinical charts. Descriptive statistics were utilized to summarize proportions and differences were assessed by Chi square or Wilcoxon rank sum tests. Metachronous contralateral breast cancer (CBC) risk, radiation-induced sarcoma risk, and recurrence-free survival (RFS) were analyzed by Kaplan-Meier methodology. Among 227 females who met study criteria, the median age of first BC diagnosis was 37 years (range 21-71), 11.9% presented with bilateral synchronous BC and 18.1% had ductal carcinoma in situ (DCIS) only. In total, 166 (73.1%) underwent mastectomies including 67 bilateral mastectomies as first BC surgery. Among those with retained breast tissue, CBC rate was 25.3% at 5-years. Among 186 invasive tumors, 72.1% were stages I-II, 48.9% node-negative, and the most common subtypes were HR+/HER2- (40.9%) and HR+/HER2 + (34.4%). At a median follow-up of 69.9 months (IQR 32.6-125.9), invasive HR+/HER2- disease had the highest recurrence risk among the subtypes (5-year RFS 61.1%, p = .0012). Among those who received radiation therapy (n = 79), the 5-year radiation-induced sarcoma rate was 4.8%. We observed high rates of DCIS, HR+ and HER2+ breast cancers, with a worse outcome in the HR+/HER2- luminal tumors despite appropriate treatment. Confirmation of these findings in further studies could have implications for BC care in LFS.

Sections du résumé

BACKGROUND BACKGROUND
A large well-annotated recent international cohort of Li-Fraumeni (LFS) patients with early-stage breast cancer (BC) was examined for shared features.
METHODS METHODS
This multicentre cohort study included females with a germline TP53 pathogenic or likely pathogenic variant and nonmetastatic BC diagnosed between 2002-2022. Clinical and genetic data were obtained from institutional registries and clinical charts. Descriptive statistics were utilized to summarize proportions and differences were assessed by Chi square or Wilcoxon rank sum tests. Metachronous contralateral breast cancer (CBC) risk, radiation-induced sarcoma risk, and recurrence-free survival (RFS) were analyzed by Kaplan-Meier methodology.
RESULTS RESULTS
Among 227 females who met study criteria, the median age of first BC diagnosis was 37 years (range 21-71), 11.9% presented with bilateral synchronous BC and 18.1% had ductal carcinoma in situ (DCIS) only. In total, 166 (73.1%) underwent mastectomies including 67 bilateral mastectomies as first BC surgery. Among those with retained breast tissue, CBC rate was 25.3% at 5-years. Among 186 invasive tumors, 72.1% were stages I-II, 48.9% node-negative, and the most common subtypes were HR+/HER2- (40.9%) and HR+/HER2 + (34.4%). At a median follow-up of 69.9 months (IQR 32.6-125.9), invasive HR+/HER2- disease had the highest recurrence risk among the subtypes (5-year RFS 61.1%, p = .0012). Among those who received radiation therapy (n = 79), the 5-year radiation-induced sarcoma rate was 4.8%.
CONCLUSION CONCLUSIONS
We observed high rates of DCIS, HR+ and HER2+ breast cancers, with a worse outcome in the HR+/HER2- luminal tumors despite appropriate treatment. Confirmation of these findings in further studies could have implications for BC care in LFS.

Identifiants

pubmed: 38569880
pii: 7639984
doi: 10.1093/jnci/djae074
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Renata L Sandoval (RL)

Medical Oncology Center, Hospital Sírio-Libanês, Brasília, DF, Brazil.
Division of Cancer Genetics and Prevention, Dana-Farber Cancer Institute, Boston, MA, USA.

Michele Bottosso (M)

Department of Surgery, Oncology and Gastroenterology, University of Padua, Italy.
Medical Oncology Department, Gustave Roussy Cancer Campus, INERM U981, Université Paris Saclay, France.

Li Tianyu (L)

Department of Data Science, Dana-Farber Cancer Institute, Boston, MA, USA.

Natalia Polidorio (N)

Breast Surgery Department, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Brittany L Bychkovsky (BL)

Division of Cancer Genetics and Prevention, Dana-Farber Cancer Institute, Boston, MA, USA.
Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Breast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, MA.
Harvard Medical School, Boston, MA, USA.

Benjamin Verret (B)

Medical Oncology Department, Gustave Roussy Cancer Campus, INERM U981, Université Paris Saclay, France.

Alessandra Gennari (A)

Department of Translational Medicine, University of Piemonte Orientale, Novara, Italy.

Sophie Cahill (S)

Division of Cancer Genetics and Prevention, Dana-Farber Cancer Institute, Boston, MA, USA.

Maria Isabel Achatz (MI)

Medical Oncology Center, Hospital Sírio-Libanês, São Paulo, SP, Brazil.

Olivier Caron (O)

Medical Oncology Department, Institut Gustave Roussy, Villejuif, F-94805, France.

Marion Imbert-Bouteille (M)

Oncology Department, Institut of Cancer of Montpellier, Montpellier, France.

Catherine Noguès (C)

Cancer Risk Management Department, Clinical Oncogenetics, Institut Paoli-Calmettes, Marseille, France.
Aix Marseille Université, INSERM, IRD, SESSTIM, Marseille, France.

Kara N Mawell (KN)

Department of Medicine, Abramson Cancer Center, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.

Cristina Fortuno (C)

Population Health Program, QIMR Berghofer Medical Research Institute, Brisbane, Australia.

Amanda B Spurdle (AB)

Population Health Program, QIMR Berghofer Medical Research Institute, Brisbane, Australia.

Nabihah Tayob (N)

Department of Data Science, Dana-Farber Cancer Institute, Boston, MA, USA.
Harvard Medical School, Boston, MA, USA.

Fabrice Andre (F)

Medical Oncology Department, Gustave Roussy Cancer Campus, INERM U981, Université Paris Saclay, France.

Judy E Garber (JE)

Division of Cancer Genetics and Prevention, Dana-Farber Cancer Institute, Boston, MA, USA.
Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Breast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, MA.
Harvard Medical School, Boston, MA, USA.

Classifications MeSH