Overall Survival and Clinical Characteristics of BRCA-Associated Cholangiocarcinoma: A Multicenter Retrospective Study

被引:97
作者
Golan, Talia [1 ,3 ]
Raitses-Gurevich, Maria [1 ]
Kelley, Robin K. [4 ]
Bocobo, Andrea G. [4 ]
Borgida, Ayelet [5 ]
Shroff, Rachna T. [6 ]
Holter, Spring [5 ]
Gallinger, Steven [5 ]
Ahn, Daniel H. [7 ]
Aderka, Dan [1 ,3 ]
Apurva, Jain [6 ]
Bekaii-Saab, Tanois [7 ]
Friedman, Eitan [2 ,3 ]
Javle, Milind [6 ]
机构
[1] Sheba Med Ctr, Inst Human Genet, Dept Oncol, Tel Hashomer, Israel
[2] Sheba Med Ctr, Inst Human Genet, Oncogenet Unit, Tel Hashomer, Israel
[3] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
[4] Univ Calif San Francisco, Med Ctr, San Francisco, CA 94143 USA
[5] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON, Canada
[6] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[7] Mayo Clin, Phoenix, AZ USA
关键词
Cholangiocarcinoma; BRCA-associated; Germline; somatic; PARPi; DNA-REPAIR DEFECT; BILIARY-TRACT; INTRAHEPATIC CHOLANGIOCARCINOMA; OVARIAN-CANCER; MUTANT-CELLS; BREAST; RISK; MUTATIONS; MORTALITY; VARIANTS;
D O I
10.1634/theoncologist.2016-0415
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Biliary tract malignancies, in particular cholangiocarcinomas (CCA), are rare tumors that carry a poor prognosis. BRCA2 mutation carriers have an increased risk of developing CCA with a reported relative risk of similar to 5 according to the Breast Cancer Linkage Consortium. In addition to this risk, there are potential therapeutic implications in those harboring somatic and/or germline (GL) BRCA mutations. Therefore, it is important to define the clinical characteristics of GL/somatic BRCA1/2 variants in CCA patients. Materials and Methods. We performed a multicenter retrospective analysis of CCA patients diagnosed between January 2000 and December 2013 with GL or somatic variants in BRCA1/2 genes detected by GL mutations testing and/or by tumor next generation sequencing. Cases were identified from clinical databases at participating institutions. Data including demographics, clinical history, surgical procedures, and systemic chemotherapy or radiation were extracted from patients' records. Results. Overall, 18 cases were identified: 5 carriers of GL BRCA1/2 mutations (4 BRCA2; 1 BRCA1) and 13 harboring somatic variations (7 BRCA1; 6 BRCA2). Mean age at diagnosis was 60, SD610 years (range 36-75 years), with male and female prevalence rates of 61.2% and 38.8%, respectively. Stage at diagnosis was I (n = 4), II (n = 3), III (n = 3), and IV (n = 8). Six patients had extrahepatic CCA and the rest intrahepatic CCA. Thirteen patients received platinumbased therapy and four were treated with poly ADP ribose polymerase inhibitors, of whom one experienced sustained disease response with a progression-free survival of 42.6 months. Median overall survival from diagnosis for patients with stage I/II in this study was 40.3 months (95% confidence interval [CI], 6.73-108.15) and with stages III/IV was 25 months (95% CI, 15.23-40.57). Conclusion. BRCA-associated CCA is uncommon. This multicenter retrospective study provides a thorough clinical analysis of a BRCA-associated CCA cohort, which can serve as a benchmark for future development and design of expanded analyses and clinical trials.
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页码:804 / 810
页数:7
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