Homologous recombination deficiency in newly diagnosed FIGO stage III/IV high-grade epithelial ovarian cancer: a multi-national observational study

被引:11
|
作者
Morgan, Robert D. [1 ,2 ]
Clamp, Andrew R. [1 ,2 ]
Barnes, Bethany M. [2 ]
Timms, Kirsten [3 ]
Schlecht, Helene [4 ]
Yarram-Smith, Laura [5 ]
Wallis, Yvonne [6 ]
Valganon-Petrizan, Mikel [7 ]
MacMahon, Suzanne [7 ]
White, Rhian [8 ]
Morgan, Sian [8 ]
McKenna, Sarah [9 ]
Hudson, Emma [10 ]
Tookman, Laura [11 ]
George, Angela [12 ,13 ]
Manchanda, Ranjit [14 ,15 ,16 ]
Sundar, Sudha S. [17 ,18 ]
Nicum, Shibani [19 ,20 ]
Brenton, James D. [21 ,22 ]
Kristeleit, Rebecca S. [23 ]
Banerjee, Susana [12 ,13 ]
McNeish, Iain A. [11 ,24 ]
Ledermann, Jonathan A. [19 ,20 ]
Taylor, Stephen S. [2 ]
Evans, D. Gareth R. [25 ,26 ]
Jayson, Gordon C. [1 ,2 ]
机构
[1] Christie NHS Fdn Trust, Manchester, Lancs, England
[2] Univ Manchester, Sch Med Sci, Div Canc Sci, Fac Biol, Manchester, Lancs, England
[3] Myriad Genet Inc, Salt Lake City, UT USA
[4] Manchester Univ NHS Fdn Trust, North West Genom Lab Hub, Manchester, Lancs, England
[5] North Bristol NHS Trust, South West Genom Lab Hub, Bristol, Avon, England
[6] Birmingham Womens & Childrens NHS Fdn Trust, Cent & South Genom Lab Hub, Birmingham, W Midlands, England
[7] Royal Marsden Hosp NHS Fdn Trust, North Thames Genom Lab Hub, Surrey, England
[8] Univ Hosp Wales, Inst Med Genet, All Wales Genom Lab, Cardiff, Wales
[9] Belfast Hlth & Social Care Trust, Belfast, Antrim, North Ireland
[10] Velindre Univ NHS Trust, Cardiff, Wales
[11] Imperial Coll Healthcare NHS Trust, London, England
[12] Royal Marsden NHS Fdn Trust, London, England
[13] Inst Canc Res, London, England
[14] Barts Hlth NHS Trust, London, England
[15] London Sch Hyg & Trop Med, Fac Publ Hlth & Policy, Dept Hlth Serv Res, London, England
[16] Queen Marys Univ London, Wolfson Inst Populat Hlth, London, England
[17] Sandwell & West Birmingham Hosp NHS Trust, Birmingham, W Midlands, England
[18] Univ Birmingham, Inst Canc & Genom Sci, Birmingham, W Midlands, England
[19] Univ Coll London Hosp NHS Fdn Trust, London, England
[20] UCL Canc Inst, London, England
[21] Cambridge Univ Hosp NHS Fdn Trust, Cambridge, England
[22] Univ Cambridge, CRUK Cambridge Inst, Cambridge, England
[23] Guys & St Thomas NHS Fdn Trust, London, England
[24] Imperial Coll London, Dept Surg & Canc, Ovarian Canc Action Res Ctr, London, England
[25] Manchester Univ NHS Fdn Trust, Manchester, Lancs, England
[26] Univ Manchester, Fac Biol Med & Hlth, Sch Biol Sci, Div Evolut Infect & Genom0, Manchester, Lancs, England
关键词
BRCA1; Protein; BRCA2; Homologous recombination; Ovarian Cancer; NIRAPARIB MAINTENANCE THERAPY; OLAPARIB PLUS BEVACIZUMAB; DOUBLE-BLIND; NEOADJUVANT CHEMOTHERAPY; SURVIVAL; TRIAL;
D O I
10.1136/ijgc-2022-004211
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ObjectiveOlaparib plus bevacizumab maintenance therapy improves survival outcomes in women with newly diagnosed, advanced, high-grade ovarian cancer with a deficiency in homologous recombination. We report data from the first year of routine homologous recombination deficiency testing in the National Health Service (NHS) in England, Wales, and Northern Ireland between April 2021 and April 2022. MethodsThe Myriad myChoice companion diagnostic was used to test DNA extracted from formalin-fixed, paraffin-embedded tumor tissue in women with newly diagnosed International Federation of Gynecology and Obstetrics (FIGO) stage III/IV high-grade epithelial ovarian, fallopian tube, or primary peritoneal cancer. Tumors with homologous recombination deficiency were those with a BRCA1/2 mutation and/or a Genomic Instability Score (GIS) >= 42. Testing was coordinated by the NHS Genomic Laboratory Hub network. ResultsThe myChoice assay was performed on 2829 tumors. Of these, 2474 (87%) and 2178 (77%) successfully underwent BRCA1/2 and GIS testing, respectively. All complete and partial assay failures occurred due to low tumor cellularity and/or low tumor DNA yield. 385 tumors (16%) contained a BRCA1/2 mutation and 814 (37%) had a GIS >= 42. Tumors with a GIS >= 42 were more likely to be BRCA1/2 wild-type (n=510) than BRCA1/2 mutant (n=304). The distribution of GIS was bimodal, with BRCA1/2 mutant tumors having a higher mean score than BRCA1/2 wild-type tumors (61 vs 33, respectively, chi(2) test p<0.0001). ConclusionThis is the largest real-world evaluation of homologous recombination deficiency testing in newly diagnosed FIGO stage III/IV high-grade epithelial ovarian, fallopian tube, or primary peritoneal cancer. It is important to select tumor tissue with adequate tumor content and quality to reduce the risk of assay failure. The rapid uptake of testing across England, Wales, and Northern Ireland demonstrates the power of centralized NHS funding, center specialization, and the NHS Genomic Laboratory Hub network.
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收藏
页码:1253 / 1259
页数:7
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