Report from the European Myeloma Network on interphase FISH in multiple myeloma and related disorders

被引:260
作者
Ross, Fiona M. [1 ]
Avet-Loiseau, Herve [2 ,3 ]
Ameye, Genevieve [4 ]
Gutierrez, Norma C. [5 ]
Liebisch, Peter [6 ]
O'Connor, Sheila [7 ]
Dalva, Klara [8 ]
Fabris, Sonia [9 ,10 ]
Testi, Adele M. [11 ]
Jarosova, Marie [12 ]
Hodkinson, Clare [13 ]
Collin, Anna [14 ]
Kerndrup, Gitte [15 ]
Kuglik, Petr [16 ]
Ladon, Dariusz [17 ]
Bernasconi, Paolo [18 ]
Maes, Brigitte [19 ]
Zemanova, Zuzana [20 ,21 ]
Michalova, Kyra [20 ,21 ]
Michau, Lucienne [22 ]
Neben, Kai [23 ]
Hermansen, N. Emil U. [24 ]
Rack, Katrina [25 ]
Rocci, Alberto [26 ]
Protheroe, Rebecca [1 ]
Chiecchio, Laura [1 ]
Poirel, Helene A. [4 ]
Sonneveld, Pieter [27 ]
Nyegaard, Mette [28 ]
Johnsen, Hans E. [28 ]
机构
[1] Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury, Wilts, England
[2] Univ Hosp, Dept Clin Hematol, Nantes, France
[3] Univ Hosp, Hematol Lab, Nantes, France
[4] Clin Univ St Luc, UCL, Ctr Human Genet, B-1200 Brussels, Belgium
[5] Univ Hosp Salamanca, Dept Hematol, Salamanca, Spain
[6] Univ Hosp Ulm, Dept Internal Med 3, Ulm, Germany
[7] St Jamess Inst Oncol, HMDS, Leeds, W Yorkshire, England
[8] Ankara Univ, Ibni Sina Hosp, Dept Hematol, TR-06100 Ankara, Turkey
[9] Univ Milan, Dept Med Sci, Milan, Italy
[10] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Milan, Italy
[11] Fdn IRCCS Ist Nazl Tumori Milano, Dept Diagnost Pathol & Lab Med, Milan, Italy
[12] Univ Hosp, Dept Hematooncol, Olomouc, Czech Republic
[13] Belfast HSC Trust, Belfast City Hosp, Haematooncol Lab, Dept Haematol, Belfast, Antrim, North Ireland
[14] Lund Univ, Skane Univ Hosp, Univ & Reg Labs, Dept Clin Genet, Lund, Sweden
[15] Vejle Hosp, Dept Clin Genet, Vejle, Denmark
[16] Masaryk Univ, Fac Med, Babak Res Inst, Lab Mol Cytogenet, Brno, Czech Republic
[17] Kings Coll London, Dept Haematol Med, London WC2R 2LS, England
[18] Fdn Policlin San Matteo IRCCS, Div Hematol, Pavia, Italy
[19] Virga Jesse Hosp, Clin Lab, Hasselt, Belgium
[20] Gen Teaching Hosp, Inst Clin Biochem & Lab Diagnost, Ctr Oncocytogenet, Prague, Czech Republic
[21] Charles Univ Prague, Fac Med 1, Prague, Czech Republic
[22] Catholic Univ Louvain, Ctr Human Genet, B-3000 Louvain, Belgium
[23] Univ Klinikum Heidelberg, Med Klin 5, Heidelberg, Germany
[24] Natl Hosp, Dept Haematol, Copenhagen, Denmark
[25] Ctr Human Genet, Inst Pathol & Genet, Gosselies, Belgium
[26] Univ Turin, Dept Hematol, San Giovanni Battista Hosp, Turin, Italy
[27] Erasmus MC, Dept Hematol, Rotterdam, Netherlands
[28] Aarhus Univ Hosp, Aalborg Hosp Sci & Innovat Ctr, Res Lab, Dept Haematol, DK-9000 Aalborg, Denmark
[29] Aalborg Hosp Sci & Innovat Ctr, European Myeloma Network, Aalborg, Denmark
来源
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2012年 / 97卷 / 08期
关键词
myeloma; cytogenetic; interphase FISH; recommendation; ADVERSE PROGNOSTIC-FACTOR; IN-SITU HYBRIDIZATION; UNDETERMINED SIGNIFICANCE; MONOCLONAL GAMMOPATHY; GENETIC EVENTS; TRANSLOCATIONS; ABNORMALITIES; DYSREGULATION;
D O I
10.3324/haematol.2011.056176
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The European Myeloma Network has organized two workshops on fluorescence in situ hybridization in multiple myeloma. The first aimed to identify specific indications and consensus technical approaches of current practice. A second workshop followed a quality control exercise in which 21 laboratories analyzed diagnostic cases of purified plasma cells for recurrent abnormalities. The summary report was discussed at the EHA Myeloma Scientific Working Group Meeting 2010. During the quality control exercise, there was acceptable agreement on more than 1,000 tests. The conclusions from the exercise were that the primary clinical applications for FISH analysis were for newly diagnosed cases of MM or frank relapse cases. A range of technical recommendations included: 1) material should be part of the first draw of the aspirate; 2) samples should be sent at suitable times to allow for the lengthy processing procedure; 3) most importantly, PCs must be purified or specifically identified; 4) positive cut-off levels should be relatively conservative: 10% for fusion or break-apart probes, 20% for numerical abnormalities; 5) informative probes should be combined to best effect; 6) in specialist laboratories, a single experienced analyst is considered adequate; 7) at least 100 PC should be scored; 8) essential abnormalities to test for are t(4;14), t(14;16) and 17p13 deletions; 9) suitable commercial probes should be available for clinically relevant abnormalities; 10) the clinical report should be expressed clearly and must state the percentage of PC involved and the method used for identification; 11) a retrospective European based FISH data bank linked to clinical data should be generated; and 12) prospective analysis should be centralized for upcoming trials based on the recommendations made. The European Myeloma Network aims to build on these recommendations to establish standards for a common European data base to define subgroups with prognostic significance.
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收藏
页码:1272 / 1277
页数:6
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