Clinical and pathological features of ovarian cancer in women with germ-line mutations of BRCA1

被引:359
作者
Rubin, SC
Benjamin, I
Behbakht, K
Takahashi, H
Morgan, MA
LiVolsi, VA
Berchuck, A
Muto, MG
Garber, JE
Weber, BL
Lynch, HT
Boyd, J
机构
[1] UNIV PENN, MED CTR, DEPT LAB MED & PATHOL, DIV ANAT PATHOL, PHILADELPHIA, PA 19104 USA
[2] UNIV PENN, MED CTR, DIV HEMATOL & ONCOL, DEPT MED, PHILADELPHIA, PA 19104 USA
[3] BRIGHAM & WOMENS HOSP, DEPT OBSTET & GYNECOL, DIV GYNECOL ONCOL, BOSTON, MA 02115 USA
[4] DANA FARBER CANC INST, DIV CANC EPIDEMIOL & CONTROL, BOSTON, MA 02115 USA
[5] CREIGHTON UNIV, SCH MED, DEPT PREVENT MED & PUBL HLTH, OMAHA, NE USA
关键词
D O I
10.1056/NEJM199611073351901
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background We tested the hypothesis that ovarian cancers associated with germ-line mutations of BRCA1 have distinct clinical and pathological features as compared with sporadic ovarian cancers. Methods We reviewed clinical and pathological data on patients with primary epithelial ovarian cancer found to have germ-fine mutations of BRCA1. Survival among patients with advanced-stage cancer and such mutations was compared with that in control patients matched for age and stage, grade, and histologic subtype of the tumors. A combination of single-strand conformation and sequencing analyses was used to examine the 22 coding exons and intronic splice-donor and splice-acceptor regions of BRCA1 for mutations in pathological specimens. Alternatively, some patients were known to be obligate carriers of the mutant BRCA1 gene because of their parental relationships with documented mutant-gene carriers. Results We identified 53 patients with germ-line mutations of BRCA1. The average age at diagnosis was 48 years (range, 28 to 78). Histologic examination in 43 of the 53 patients showed serous adenocarcinoma. Thirty-seven tumors were of grade 3, 11 were of grade 2, 2 were of grade 1, and 3 were of low malignant potential. In 38 patients, the tumors were of stage III; 9 patients (including those with tumors of low malignant potential) had stage I disease, 5 had stage IV, and 1 had stage II. As of June 1996, with a median follow-up among survivors of 71 months from diagnosis, 20 patients had died of ovarian cancer, 27 had no evidence of the disease, 4 were alive with the disease, and 2 had died of other diseases. Actuarial median survival for the 43 patients with advanced-stage disease was 77 months, as compared with 29 months for the matched controls (P<0.001). Conclusions As compared with sporadic ovarian cancers, cancers associated with BRCA1 mutations appear to have a significantly more favorable clinical course. (C)1996, Massachusetts Medical Society.
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页码:1413 / 1416
页数:4
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共 21 条
  • [11] Cyclophosphamide and cisplatin compared with paclitaxel and cisplatin in patients with stage III and stage IV ovarian cancer
    McGuire, WP
    Hoskins, WJ
    Brady, MF
    Kucera, PR
    Partridge, EE
    Look, KY
    ClarkePearson, DL
    Davidson, M
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (01) : 1 - 6
  • [12] Merajver SD, 1995, CLIN CANCER RES, V1, P539
  • [13] A STRONG CANDIDATE FOR THE BREAST AND OVARIAN-CANCER SUSCEPTIBILITY GENE BRCA1
    MIKI, Y
    SWENSEN, J
    SHATTUCKEIDENS, D
    FUTREAL, PA
    HARSHMAN, K
    TAVTIGIAN, S
    LIU, QY
    COCHRAN, C
    BENNETT, LM
    DING, W
    BELL, R
    ROSENTHAL, J
    HUSSEY, C
    TRAN, T
    MCCLURE, M
    FRYE, C
    HATTIER, T
    PHELPS, R
    HAUGENSTRANO, A
    KATCHER, H
    YAKUMO, K
    GHOLAMI, Z
    SHAFFER, D
    STONE, S
    BAYER, S
    WRAY, C
    BOGDEN, R
    DAYANANTH, P
    WARD, J
    TONIN, P
    NAROD, S
    BRISTOW, PK
    NORRIS, FH
    HELVERING, L
    MORRISON, P
    ROSTECK, P
    LAI, M
    BARRETT, JC
    LEWIS, C
    NEUHAUSEN, S
    CANNONALBRIGHT, L
    GOLDGAR, D
    WISEMAN, R
    KAMB, A
    SKOLNICK, MH
    [J]. SCIENCE, 1994, 266 (5182) : 66 - 71
  • [14] MILLER BA, NIH PUBLICATION
  • [15] Ozols RF, 1992, PRINCIPLES PRACTICE, P731
  • [16] PIVER MS, 1993, CANCER-AM CANCER SOC, V71, P582
  • [17] BREAST-CANCER INCIDENCE, PENETRANCE AND SURVIVAL IN PROBABLE CARRIERS OF BRCA1 GENE MUTATION IN FAMILIES LINKED TO BRCA1 ON CHROMOSOME 17Q12-21
    PORTER, DE
    COHEN, BB
    WALLACE, MR
    SMYTH, E
    CHETTY, U
    DIXON, JM
    STEEL, CM
    CARTER, DC
    [J]. BRITISH JOURNAL OF SURGERY, 1994, 81 (10) : 1512 - 1515
  • [18] Better survival rates in patients with MLH1-associated hereditary colorectal cancer
    Sankila, R
    Aaltonen, LA
    Jarvinen, HJ
    Mecklin, JP
    [J]. GASTROENTEROLOGY, 1996, 110 (03) : 682 - 687
  • [19] STEICHENGERSDORF E, 1994, AM J HUM GENET, V55, P870
  • [20] TAKAHASHI H, 1995, CANCER RES, V55, P2998