Journal of Clinical Oncology, Vol 16, 115-120, Copyright © 1998 by American Society of Clinical Oncology
Germ-line BRCA1 mutations in women with sporadic breast cancer: clinical correlations
E Garcia-Patino, B Gomendio, M Provencio, JM Silva, JM Garcia, P Espana and F Bonilla
Department of Medical Oncology, Clinical Puerta de Hierro, Madrid, Spain.
PURPOSE: Sporadic nonhereditary breast cancer is recognized as the most
common form of this malignancy. Presence of germ-line mutations in the
BRCA1 gene of these tumors is an infrequent event. We undertook the present
study to evaluate the prevalence of germ-line mutations in patients
diagnosed with sporadic breast cancer, and to delimit the clinical spectrum
of this subgroup of patients with germ-line mutations and their differences
with respect to patients with no evidence of BRCA1 gene mutations. METHODS:
We studied 105 patients diagnosed with breast cancer, selected from among
our living patients; those with carcinoma-in-situ and those with a definite
family history of breast or ovarian cancer were excluded. Genomic DNA,
obtained from peripheral- blood lymphocytes, was studied for BRCA1
mutations by polymerase chain reaction/single-strand conformation
polymorphism (PCR-SSCP) and direct DNA sequencing. Fourteen
clinicopathologic parameters were analyzed in each patient. RESULTS: Six
(5.7%) frameshift mutations that corresponded to truncating proteins and
three missense mutations, the functional meaning of which remains
speculative, were identified. The patients with germ-line mutations were
found to have a more advanced age at diagnosis, as well as a longer median
survival (51 months). CONCLUSION: Women with sporadic breast cancer of late
onset may display a significant incidence of germline BRCA1 mutations,
which occur at a rate not previously determined in this group of patients.
The presence of variations in the sequence of the BRCA1 gene could
influence the longer survival observed in these patients.
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