Literature DB >> 15053073

Clinical features of familial ovarian cancer lacking mutations in BRCA1 or BRCA2.

J Menkiszak1, J Gronwald, B Górski, T Byrski, T Huzarski, A Jakubowska, M Foszczyńska-Kłoda, M Brzosko, J Fliciński, I Rzepka-Górska, S A Narod, J Lubiński.   

Abstract

PURPOSE OF INVESTIGATION: The purpose of the present study was to identify the clinical and pathologic features of ovarian cancers in patients who have a family history of breast or ovarian cancer but who do not have a mutation in the BRCA1 or BRCA2 gene.
METHODS: 303 patients with ovarian cancer were reviewed for clinical features and for cancer family histories. After the exclusion of 51 patients known to carry BRCA1 or BRCA2 mutations, 24 patients with familial cancer were compared with 228 patients with non-familial cancer.
RESULTS: Patients with familial cancer were more likely to have grade 2 tumors, Stage II disease and to present between ages 51 and 60 than were non-familial controls. Ten of 24 patients in the familial group presented between ages 51 and 60 with a grade 2 tumor compared to 3.0 expected (p = 0.001).
CONCLUSIONS: Families of women who present with grade 2 ovarian cancer between the ages of 51 and 60 may have an unidentified ovarian cancer susceptibility gene.

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Year:  2004        PMID: 15053073

Source DB:  PubMed          Journal:  Eur J Gynaecol Oncol        ISSN: 0392-2936            Impact factor:   0.196


  2 in total

1.  Hereditary breast and ovarian cancer.

Authors:  Jacek Gronwald; Tomasz Byrski; Tomasz Huzarski; Oleg Oszurek; Anna Janicka; Jolanta Szymanska-Pasternak; Bohdan Górski; Janusz Menkiszak; Izabella Rzepka-Górska; Jan Lubinski
Journal:  Hered Cancer Clin Pract       Date:  2008-06-15       Impact factor: 2.857

2.  BRCA1 and BRCA2 mutations in ovarian cancer patients from Belarus: update.

Authors:  Alena Savanevich; Olgierd Ashuryk; Cezary Cybulski; Jan Lubiński; Jacek Gronwald
Journal:  Hered Cancer Clin Pract       Date:  2021-01-21       Impact factor: 2.857

  2 in total

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