The Sweden Cancerome Analysis Network - Breast (SCAN-B) Initiative: a large-scale multicenter infrastructure towards implementation of breast cancer genomic analyses in the clinical routine

被引:148
作者
Saal, Lao H. [1 ,2 ,3 ]
Vallon-Christersson, Johan [1 ,2 ,3 ]
Hakkinen, Jari [1 ,2 ,3 ]
Hegardt, Cecilia [1 ,2 ,3 ]
Grabau, Dorthe [4 ]
Winter, Christof [1 ,2 ]
Brueffer, Christian [1 ,2 ]
Tang, Man-Hung Eric [1 ,2 ]
Reutersward, Christel [1 ,2 ,5 ]
Schulz, Ralph [1 ,2 ,5 ]
Karlsson, Anna [1 ,2 ,5 ]
Ehinger, Anna [1 ,2 ,6 ]
Malina, Janne [7 ]
Manjer, Jonas [8 ,9 ]
Malmberg, Martin [10 ]
Larsson, Christer [2 ,11 ]
Ryden, Lisa [2 ,12 ,13 ]
Loman, Niklas [1 ,2 ,10 ]
Borg, Ake [1 ,2 ,5 ]
机构
[1] Lund Univ, Dept Clin Sci, Div Oncol & Pathol, SE-22381 Lund, Sweden
[2] Lund Univ, Ctr Canc, SE-22381 Lund, Sweden
[3] Lund Univ, CREATE, Hlth Strateg Ctr Translat Canc Res, SE-22381 Lund, Sweden
[4] Skane Univ Hosp, Dept Pathol, SE-22185 Lund, Sweden
[5] Lund Univ, SCIBLU Genom, Dept Clin Sci, SE-22381 Lund, Sweden
[6] Blekinge Cty Hosp, Dept Pathol & Cytol, SE-37185 Karlskrona, Sweden
[7] Skane Univ Hosp, Dept Pathol, SE-20502 Malmo, Sweden
[8] Lund Univ, Dept Surg, SE-20502 Malmo, Sweden
[9] Skane Univ Hosp, SE-20502 Malmo, Sweden
[10] Skane Univ Hosp, Dept Oncol, SE-22185 Lund, Sweden
[11] Lund Univ, Dept Lab Med, Div Mol Pathol, SE-22185 Lund, Sweden
[12] Lund Univ, Dept Surg, SE-22185 Lund, Sweden
[13] Skane Univ Hosp, SE-22185 Lund, Sweden
基金
瑞典研究理事会;
关键词
MICROARRAY PLATFORMS; MOLECULAR PORTRAITS; SEQUENCING DATA; GENE; EXPRESSION; SIGNATURE; CARCINOMA; SUBTYPES; SURVIVAL; TUMORS;
D O I
10.1186/s13073-015-0131-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: Breast cancer exhibits significant molecular, pathological, and clinical heterogeneity. Current clinicopathological evaluation is imperfect for predicting outcome, which results in overtreatment for many patients, and for others, leads to death from recurrent disease. Therefore, additional criteria are needed to better personalize care and maximize treatment effectiveness and survival. Methods: To address these challenges, the Sweden Cancerome Analysis Network - Breast (SCAN-B) consortium was initiated in 2010 as a multicenter prospective study with longsighted aims to analyze breast cancers with next-generation genomic technologies for translational research in a population-based manner and integrated with healthcare; decipher fundamental tumor biology from these analyses; utilize genomic data to develop and validate new clinically-actionable biomarker assays; and establish real-time clinical implementation of molecular diagnostic, prognostic, and predictive tests. In the first phase, we focus on molecular profiling by next-generation RNA-sequencing on the Illumina platform. Results: In the first 3 years from 30 August 2010 through 31 August 2013, we have consented and enrolled 3,979 patients with primary breast cancer at the seven hospital sites in South Sweden, representing approximately 85% of eligible patients in the catchment area. Preoperative blood samples have been collected for 3,942 (99%) patients and primary tumor specimens collected for 2,929 (74%) patients. Herein we describe the study infrastructure and protocols and present initial proof of concept results from prospective RNA sequencing including tumor molecular subtyping and detection of driver gene mutations. Prospective patient enrollment is ongoing. Conclusions: We demonstrate that large-scale population-based collection and RNA-sequencing analysis of breast cancer is feasible. The SCAN-B Initiative should significantly reduce the time to discovery, validation, and clinical implementation of novel molecular diagnostic and predictive tests. We welcome the participation of additional comprehensive cancer treatment centers.
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页数:12
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