Germline and tumor BRCA1/2 pathogenic variants in Chinese triple-negative breast carcinomas

被引:8
作者
Ji, Gang [1 ,3 ,4 ]
Bao, Longlong [1 ,3 ,4 ]
Yao, Qianlan [1 ,3 ,4 ]
Zhang, Jing [1 ,3 ,4 ]
Zhu, Xiaoli [1 ,3 ,4 ]
Bai, Qianming [1 ,3 ,4 ]
Shao, Zhiming [2 ,3 ,4 ]
Yang, Wentao [1 ,3 ,4 ]
Zhou, Xiaoyan [1 ,3 ,4 ]
机构
[1] Fudan Univ, Dept Pathol, Shanghai Canc Ctr, Shanghai 200032, Peoples R China
[2] Fudan Univ, Dept Breast Surg, Shanghai Canc Ctr, Shanghai 200032, Peoples R China
[3] Fudan Univ, Shanghai Med Coll, Dept Oncol, Shanghai 200032, Peoples R China
[4] Fudan Univ, Inst Pathol, Shanghai 200032, Peoples R China
关键词
Triple-negative breast cancer (TNBC); BRCA1; 2; Somatic mutation; Large genomic rearrangement (LRG); CANCER SUSCEPTIBILITY GENE; MUTATIONS; OVARIAN; PREVALENCE; GUIDELINES; SPECTRUM;
D O I
10.1007/s00432-021-03696-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose BRCA1/2 screening for all triple-negative breast cancer (TNBC) patients younger than 60 years may still be an economic burden in China. Further evidences that include incidence and outcome of BRCA1/2 pathogenic variants (PV) screened based on younger age or family history (FH) are worth discussing for improving the cost-effectiveness of BRCA1/2 testing in Chinese TNBC. We aimed to investigate the prevalence of germline and tumor BRCA1/2 PV based on age screening in Chinese TNBC patients. Methods Paired blood and tumor DNA from 124 unselected Chinese TNBC patients with less than or equal to 55 years were collected and analyzed for BRCA1/2 PV. Clinicopathological characteristics including age at diagnosis, FH and follow-up data were collected for further analysis. Results The entire frequency of germline and tumor BRCA1/2 PV was 21.0 and 25%, respectively. Among them, 20 (16.1%) germline and 5 (4.0%) somatic BRCA1/2 single-nucleotide variant/insertion/deletions were found by NGS testing, 6 (4.8%) BRCA1 large genomic rearrangements were detected in blood DNA by MPLA. There was significant correlation between FH of HBOC and germline BRCA1/2 PVs among these patients. Patients with tumor BRCA1/2 PVs had significant improvements than non-carriers in PFS (p = 0.047). No significant impacts were found between various mutation status in OS outcomes. No significant differences were found between BRCA1 or BRCA2 and non-carriers in PFS or OS. Conclusion There is a high incidence of germline and tumor BRCA1/2 PVs in Chinese TNBC patients with less than or equal to 55 years old. Tumor BRCA1/2 PV carriers showed an improved survival outcome. Our results suggest that BRCA1/2 PVs testing addressed within each specific clinical scenario could be more cost-effective for patients.
引用
收藏
页码:2935 / 2944
页数:10
相关论文
共 26 条
[1]   Triple-negative breast cancer: challenges and opportunities of a heterogeneous disease [J].
Bianchini, Giampaolo ;
Balko, Justin M. ;
Mayer, Ingrid A. ;
Sanders, Melinda E. ;
Gianni, Luca .
NATURE REVIEWS CLINICAL ONCOLOGY, 2016, 13 (11) :674-690
[2]   Wise Management of Ovarian Cancer: On the Cutting Edge [J].
Boussios, Stergios ;
Mikropoulos, Christos ;
Samartzis, Eleftherios ;
Karihtala, Peeter ;
Moschetta, Michele ;
Sheriff, Matin ;
Karathanasi, Afroditi ;
Sadauskaite, Agne ;
Rassy, Elie ;
Pavlidis, Nicholas .
JOURNAL OF PERSONALIZED MEDICINE, 2020, 10 (02) :1-20
[3]   5th ESO-ESMO international consensus guidelines for advanced breast cancer (ABC 5) [J].
Cardoso, F. ;
Paluch-Shimon, S. ;
Senkus, E. ;
Curigliano, G. ;
Aapro, M. S. ;
Andre, F. ;
Barrios, C. H. ;
Bergh, J. ;
Bhattacharyya, G. S. ;
Biganzoli, L. ;
Boyle, F. ;
Cardoso, M-J ;
Carey, L. A. ;
Cortes, J. ;
El Saghir, N. S. ;
Elzayat, M. ;
Eniu, A. ;
Fallowfield, L. ;
Francis, P. A. ;
Gelmon, K. ;
Gligorov, J. ;
Haidinger, R. ;
Harbeck, N. ;
Hu, X. ;
Kaufman, B. ;
Kaur, R. ;
Kiely, B. E. ;
Kim, S-B ;
Lin, N. U. ;
Mertz, S. A. ;
Neciosup, S. ;
Offersen, B., V ;
Ohno, S. ;
Pagani, O. ;
Prat, A. ;
Penault-Llorca, F. ;
Rugo, H. S. ;
Sledge, G. W. ;
Thomssen, C. ;
Vorobiof, D. A. ;
Wiseman, T. ;
Xu, B. ;
Norton, L. ;
Costa, A. ;
Winer, E. P. .
ANNALS OF ONCOLOGY, 2020, 31 (12) :1623-1649
[4]   Inherited Mutations in 17 Breast Cancer Susceptibility Genes Among a Large Triple-Negative Breast Cancer Cohort Unselected for Family History of Breast Cancer [J].
Couch, Fergus J. ;
Hart, Steven N. ;
Sharma, Priyanka ;
Toland, Amanda Ewart ;
Wang, Xianshu ;
Miron, Penelope ;
Olson, Janet E. ;
Godwin, Andrew K. ;
Pankratz, V. Shane ;
Olswold, Curtis ;
Slettedahl, Seth ;
Hallberg, Emily ;
Guidugli, Lucia ;
Davila, Jaime I. ;
Beckmann, Matthias W. ;
Janni, Wolfgang ;
Rack, Brigitte ;
Ekici, Arif B. ;
Slamon, Dennis J. ;
Konstantopoulou, Irene ;
Fostira, Florentia ;
Vratimos, Athanassios ;
Fountzilas, George ;
Pelttari, Liisa M. ;
Tapper, William J. ;
Durcan, Lorraine ;
Cross, Simon S. ;
Pilarski, Robert ;
Shapiro, Charles L. ;
Klemp, Jennifer ;
Yao, Song ;
Garber, Judy ;
Cox, Angela ;
Brauch, Hiltrud ;
Ambrosone, Christine ;
Nevanlinna, Heli ;
Yannoukakos, Drakoulis ;
Slager, Susan L. ;
Vachon, Celine M. ;
Eccles, Diana M. ;
Fasching, Peter A. .
JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (04) :304-U154
[5]   NCCN: Continuing Education [J].
Daly, Mary B. ;
Pilarski, Robert ;
Yurgelun, Matthew B. ;
Berry, Michael P. ;
Buys, Saundra S. ;
Dickson, Patricia ;
Domchek, Susan M. ;
Elkhanany, Ahmed ;
Friedman, Susan ;
Garber, Judy E. ;
Goggins, Michael ;
Hutton, Mollie L. ;
Khan, Seema ;
Klein, Catherine ;
Kohlmann, Wendy ;
Kurian, Allison W. ;
Laronga, Christine ;
Litton, Jennifer K. ;
Mak, Julie S. ;
Menendez, Carolyn S. ;
Merajver, Sofia D. ;
Norquist, Barbara S. ;
Offit, Kenneth ;
Pal, Tuya ;
Pederson, Holly J. ;
Reiser, Gwen ;
Shannon, Kristen Mahoney ;
Visvanathan, Kala ;
Weitzel, Jeffrey N. ;
Wick, Myra J. ;
Wisinski, Kari B. ;
Dwyer, Mary A. ;
Darlow, Susan D. .
JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2020, 18 (04) :380-391
[6]   Molecular alterations in triple-negative breast cancer-the road to new treatment strategies [J].
Denkert, Carsten ;
Liedtke, Cornelia ;
Tutt, Andrew ;
von Minckwitz, Gunter .
LANCET, 2017, 389 (10087) :2430-2442
[7]   Incidence and Outcome of BRCA Mutations in Unselected Patients with Triple Receptor-Negative Breast Cancer [J].
Gonzalez-Angulo, Ana M. ;
Timms, Kirsten M. ;
Liu, Shuying ;
Chen, Huiqin ;
Litton, Jennifer K. ;
Potter, Jennifer ;
Lanchbury, Jerry S. ;
Stemke-Hale, Katherine ;
Hennessy, Bryan T. ;
Arun, Banu K. ;
Hortobagyi, Gabriel N. ;
Do, Kim-Anh ;
Mills, Gordon B. ;
Meric-Bernstam, Funda .
CLINICAL CANCER RESEARCH, 2011, 17 (05) :1082-1089
[8]   Multigene panel analysis identified germline mutations of DNA repair genes in breast and ovarian cancer [J].
Hirotsu, Yosuke ;
Nakagomi, Hiroshi ;
Sakamoto, Ikuko ;
Amemiya, Kenji ;
Oyama, Toshio ;
Mochizuki, Hitoshi ;
Omata, Masao .
MOLECULAR GENETICS & GENOMIC MEDICINE, 2015, 3 (05) :459-466
[9]   Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers [J].
Kuchenbaecker, Karoline B. ;
Hopper, John L. ;
Barnes, Daniel R. ;
Phillips, Kelly-Anne ;
Mooij, Thea M. ;
Roos-Blom, Marie-Jose ;
Jervis, Sarah ;
van Leeuwen, Flora E. ;
Milne, Roger L. ;
Andrieu, Nadine ;
Goldgar, David E. ;
Terry, Mary Beth ;
Rookus, Matti A. ;
Easton, Douglas F. ;
Antoniou, Antonis C. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2017, 317 (23) :2402-2416
[10]   The spectrum of BRCA mutations and characteristics of BRCA-associated breast cancers in China: Screening of 2,991 patients and 1,043 controls by next-generation sequencing [J].
Lang, Guan-Tian ;
Shi, Jin-Xiu ;
Hu, Xin ;
Zhang, Chen-Hui ;
Shan, Ling ;
Song, Chuan-Gui ;
Zhuang, Zhi-Gang ;
Cao, A-Yong ;
Ling, Hong ;
Yu, Ke-Da ;
Li, Shan ;
Sun, Meng-Hong ;
Zhou, Xiao-Yan ;
Huang, Wei ;
Shao, Zhi-Ming .
INTERNATIONAL JOURNAL OF CANCER, 2017, 141 (01) :129-142