Outcome of BRCA1- compared with BRCA2-associated ovarian cancer: a nationwide study in the Netherlands

被引:17
|
作者
Vencken, P. M. L. H. [1 ]
Reitsma, W. [2 ]
Kriege, M. [3 ]
Mourits, M. J. E. [2 ]
de Bock, G. H. [4 ]
de Hullu, J. A. [5 ]
van Altena, A. M. [5 ]
Gaarenstroom, K. N. [6 ]
Vasen, H. F. A. [7 ]
Adank, M. A. [8 ]
Schmidt, M. K. [9 ]
van Beurden, M. [10 ]
Zweemer, R. P. [11 ]
Rijcken, F. [12 ]
Slangen, B. F. M. [13 ]
Burger, C. W. [1 ]
Seynaeve, C.
机构
[1] Erasmus Univ, Med Ctr, Dept Obstet & Gynecol, Div Gynecol Oncol, NL-3075 EA Rotterdam, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Obstet & Gynecol, Div Gynecol Oncol, Groningen, Netherlands
[3] Erasmus Univ, Med Ctr, Daniel den Hoed Canc Ctr, Dept Med Oncol,Family Canc Clin, NL-3075 EA Rotterdam, Netherlands
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen, Netherlands
[5] Univ Med Ctr St Radboud Nijmegen, Dept Obstet & Gynecol, Div Gynecol Oncol, Nijmegen, Netherlands
[6] Leiden Univ, Med Ctr, Dept Obstet & Gynecol, Div Gynecol Oncol, Leiden, Netherlands
[7] Netherlands Fdn Detect Hereditary Tumours, Leiden, Netherlands
[8] Vrije Univ Amsterdam, Med Ctr, Dept Clin Genet, Amsterdam, Netherlands
[9] NKI AVL, Div Psychosocial Res & Epidemiol, Div Mol Pathol, Amsterdam, Netherlands
[10] NKI AVL, Dept Gynecol Oncol, Amsterdam, Netherlands
[11] Univ Med Ctr Utrecht, Div Woman & Baby, Dept Gynecol Oncol, Utrecht, Netherlands
[12] Amsterdam Med Ctr, Dept Obstet & Gynecol, Div Gynecol Oncol, Amsterdam, Netherlands
[13] Maastricht Univ, Med Ctr, Dept Obstet & Gynecol, Div Gynecol Oncol, Maastricht, Netherlands
关键词
BRCA1; BRCA2; chemotherapy; ovarian cancer; response; survival; DOUBLE-STRAND BREAKS; MUTATION CARRIERS; FAMILY-HISTORY; SURVIVAL; WOMEN; TUMORS; CHEMOSENSITIVITY; METAANALYSIS; ASSOCIATION; CARCINOMA;
D O I
10.1093/annonc/mdt068
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recent studies suggested an improved overall survival (OS) for BRCA2- versus BRCA1-associated epithelial ovarian cancer (EOC), whereas the impact of chemotherapy is not yet clear. In a nationwide cohort, we examined the results of primary treatment, progression-free survival (PFS), treatment-free interval (TFI), and OS of BRCA1 versus BRCA2 EOC patients. Two hundred and forty-five BRCA1- and 99 BRCA2-associated EOC patients were identified through all Dutch university hospitals. Analyses were carried out with the Pearson's Chi-square test, Kaplan-Meier, and Cox regression methods. BRCA1 patients were younger at EOC diagnosis than BRCA2 patients (51 versus 55 years; P < 0.001), without differences regarding histology, tumor grade, and International Federation of Gynecology and Obstetrics (FIGO) stage. Complete response rates after primary treatment, including chemotherapy, did not differ between BRCA1 (86%) and BRCA2 patients (90%). BRCA1 versus BRCA2 patients had a shorter PFS (median 2.2 versus 3.9 years, respectively; P = 0.006), TFI (median 1.7 versus 2.8 years; P = 0.009), and OS (median 6.0 versus 9.7 years; P = 0.04). Differences could not be explained by age at diagnosis, FIGO stage or type of treatment. PFS and OS were substantially longer in BRCA2- than in BRCA1-associated EOC patients. While response rates after primary treatment were similarly high in both groups, TFI, as surrogate for chemosensitivity, was significantly longer in BRCA2 patients.
引用
收藏
页码:2036 / 2042
页数:7
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