Low risk of invasive lobular carcinoma of the breast in carriers of BRCA1 (hereditary breast and ovarian cancer) and TP53 (Li-Fraumeni syndrome) germline mutations.


Journal

The breast journal
ISSN: 1524-4741
Titre abrégé: Breast J
Pays: United States
ID NLM: 9505539

Informations de publication

Date de publication:
01 2019
Historique:
received: 11 10 2017
revised: 21 12 2017
accepted: 21 12 2017
pubmed: 11 11 2018
medline: 14 9 2019
entrez: 11 11 2018
Statut: ppublish

Résumé

Invasive lobular carcinoma (ILC) of the breast has epidemiological, molecular and clinical specificities, and should likely be considered a unique entity. As for genetic susceptibility, CDH1 germline mutations predispose exclusively to ILC. Data are however scarce regarding ILC in women with BRCA1/2 (Hereditary Breast and Ovarian Cancer) and TP53 (Li-Fraumeni syndrome) germline mutations. We included all breast cancers from female patients tested at our institute between 1992 and 2016 (n = 3469) for which pathology data were available. ILC proportion comparison according to mutational status was performed by a chi-squared test. The impact of susceptibility genes on ILC proportion was investigated by univariate logistic regression with wild-type patients as reference. There were 265 (7.64%) ILC: 2/342 (0.58%) in BRCA1 patients, 24/238 (10%) in BRCA2 patients, 1/57 (1.75%) in TP53 patients and 238/2832 (8.4%) in non-carriers. The majority of breast cancers in all groups were invasive ductal and ductal in situ carcinomas. The difference in ILC proportion was highly significant (P < 0.001). Compared to wild-type patients, BRCA1 was associated with a lower ILC proportion (OR 0.064 [95% CI 0.016;0.259], P < 0.0001). BRCA2 OR was 1.222 [95%CI 0.785;1.902] (P = 0.374), TP53 OR was 0.195 [95%CI 0.027;1.412] (P = 0.105). ILC are therefore underrepresented in BRCA1 and TP53 mutation carriers. Formal significance (P = 0.05) was not reached for TP53, but statistical power was only 38%. Based on ILC incidence in the general population, we make the hypothesis that BRCA1 and TP53 do not predispose to ILC, as the few occurrences of ILC in mutation carriers could be attributed to chance and not to germline mutations. Our observations will be useful to clinical cancer geneticists managing patients with ILC, as a BRCA1 or TP53 mutation in these patients would be unlikely. Genetic counseling should be adapted accordingly.

Sections du résumé

BACKGROUND
Invasive lobular carcinoma (ILC) of the breast has epidemiological, molecular and clinical specificities, and should likely be considered a unique entity. As for genetic susceptibility, CDH1 germline mutations predispose exclusively to ILC. Data are however scarce regarding ILC in women with BRCA1/2 (Hereditary Breast and Ovarian Cancer) and TP53 (Li-Fraumeni syndrome) germline mutations.
METHODS
We included all breast cancers from female patients tested at our institute between 1992 and 2016 (n = 3469) for which pathology data were available. ILC proportion comparison according to mutational status was performed by a chi-squared test. The impact of susceptibility genes on ILC proportion was investigated by univariate logistic regression with wild-type patients as reference.
RESULTS AND DISCUSSION
There were 265 (7.64%) ILC: 2/342 (0.58%) in BRCA1 patients, 24/238 (10%) in BRCA2 patients, 1/57 (1.75%) in TP53 patients and 238/2832 (8.4%) in non-carriers. The majority of breast cancers in all groups were invasive ductal and ductal in situ carcinomas. The difference in ILC proportion was highly significant (P < 0.001). Compared to wild-type patients, BRCA1 was associated with a lower ILC proportion (OR 0.064 [95% CI 0.016;0.259], P < 0.0001). BRCA2 OR was 1.222 [95%CI 0.785;1.902] (P = 0.374), TP53 OR was 0.195 [95%CI 0.027;1.412] (P = 0.105). ILC are therefore underrepresented in BRCA1 and TP53 mutation carriers. Formal significance (P = 0.05) was not reached for TP53, but statistical power was only 38%. Based on ILC incidence in the general population, we make the hypothesis that BRCA1 and TP53 do not predispose to ILC, as the few occurrences of ILC in mutation carriers could be attributed to chance and not to germline mutations. Our observations will be useful to clinical cancer geneticists managing patients with ILC, as a BRCA1 or TP53 mutation in these patients would be unlikely. Genetic counseling should be adapted accordingly.

Identifiants

pubmed: 30414230
doi: 10.1111/tbj.13154
doi:

Substances chimiques

BRCA1 Protein 0
BRCA1 protein, human 0
BRCA2 Protein 0
BRCA2 protein, human 0
TP53 protein, human 0
Tumor Suppressor Protein p53 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

16-19

Informations de copyright

© 2018 Wiley Periodicals, Inc.

Auteurs

Yoan Ditchi (Y)

Département de Médecine Oncologique, Gustave Roussy, Université Paris-Saclay, Villejuif, France.

Chloé Broudin (C)

Département de Médecine Oncologique, Gustave Roussy, Université Paris-Saclay, Villejuif, France.

Yolla El Dakdouki (Y)

Département de Médecine Oncologique, Gustave Roussy, Université Paris-Saclay, Villejuif, France.

Marie Muller (M)

Département de Médecine Oncologique, Gustave Roussy, Université Paris-Saclay, Villejuif, France.
Département de Médecine Oncologique, Institut de Cancérologie de Lorraine Alexis Vautrin, Vandœuvre-lès-Nancy, France.

Pernelle Lavaud (P)

Département de Médecine Oncologique, Gustave Roussy, Université Paris-Saclay, Villejuif, France.

Olivier Caron (O)

Département de Médecine Oncologique, Gustave Roussy, Université Paris-Saclay, Villejuif, France.

Donia Lejri (D)

Département de Médecine Oncologique, Gustave Roussy, Université Paris-Saclay, Villejuif, France.

Caroline Baynes (C)

Department of Oncology, Strangeways Research Laboratory, University of Cambridge, Cambridge, UK.

Marie-Christine Mathieu (MC)

Département de Biologie et Pathologie Médicales, Gustave Roussy, Université Paris-Saclay, Villejuif, France.

Julia Salleron (J)

Département de Biostatistiques, Institut de Cancérologie de Lorraine Alexis Vautrin, Vandœuvre-lès-Nancy, France.

Patrick R Benusiglio (PR)

Département de Médecine Oncologique, Gustave Roussy, Université Paris-Saclay, Villejuif, France.
Consultation d'Oncogénétique, UF d'Oncogénétique, Groupe Hospitalier Pitié-Salpêtrière APHP, Paris, France.

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Classifications MeSH