Date | No. patients | Patient series | Publication |
---|---|---|---|
1-Jan-2006 | 351 | Newly diagnosed patients with MM treated with 2 cycles of high-dose melphalan and autologous stem cell transplantation [8]. | Shaughnessy JD Jr, Barlogie B. “Using genomics to identify high-risk Myeloma after autologous stem cell transplantation”. Biol Blood Marrow Transplant 2006; 12 (1 Suppl 1):77–80. |
25-May-2006 | 414 | Newly diagnosed patients treated with high-dose melphalan-based tandem transplants [9]. | Zhan et al. “The molecular classification of multiple myeloma”. Blood 2006; 108(6):2020–2028. |
14-Nov-2006 | 532 | Newly diagnosed patients with multiple myeloma (MM) treated on 2 separate protocols [6]. | Shaughnessy et al. “A validated gene expression model of high-risk multiple myeloma is defined by deregulated expression of genes mapping to chromosome 1”. Blood 2007; 109:2276–84. |
9-May-2007 | 220 | Newly diagnosed patients treated with TT2 [10]. | Shaughnessy et al. “Testing standard and genetic parameters in 220 patients with multiple Myeloma with complete data sets: superiority of molecular genetics”. Br J Haematol 2007; 137:530–536. |
22-Jun-2007 | 303 | Newly diagnosed patients with myeloma treated with Total therapy 3 (incorporating bortezomib into a melphalan-based tandem transplant regimen) [11]. | Barlogie et al. “Incorporating bortezomib into upfront treatment for multiple myeloma: early results of total therapy 3”. Br J Haemotol 2007; 138:176-185 |
7-Sep-2007 | 71 | Newly diagnosed multiple myeloma patients treated with high-dose melphalan and stem cell transplant [12]. | Chng et al. “Translocation t(4;14) retains prognostic significance even in the setting of high-risk molecular signature”. Leukemia 2008; 22:459–61. |
1-Dec-2007 | 326 | Newly diagnosed patients with myeloma received a tandem autotransplant regimen [13]. | Haessler et al. “Benefit of complete response in multiple myeloma limited to high-risk subgroup identified by gene expression profiling”. Clin Cancer Res. 2007; 13(23):7073-7079 |
15-Jan-2008 | 156 | Relapsed myeloma patients enrolled in the APEX phase 3 clinical trial that compared single-agent bortezomib (B) to high-dose dexamethasone (HD) [14]. | Zhan et al. “High-risk myeloma: a gene expression based risk-stratification model for newly diagnosed multiple myeloma treated with high-dose therapy is predictive of outcome in relapsed disease treated with single-agent bortezomib or high-dose dexamethasone.” Blood 2008; 111(2):968–969. |
30-Jun-2008 | 250 | Two hundred fifty patients with myeloma at diagnosis with at least 500,000 available bone marrow CD138+ plasma cells [15]. | Decaux etl al. Prediction of Survival in Multiple Myeloma Based on Gene Expression Profiles Reveals Cell Cycle and Chromosomal Instability Signatures in High-Risk Patients and Hyperdiploid Signatures in Low-Risk Patients: A Study of the Intergroupe Francophone du Myélome JCO October 10, 2008:4798–4805; |
29-Mar-2009 | 290 | Untreated myeloma patients with cytogenetic abnormalities (CA) present in randomly sampled (RS) or focal lesion (FL) bone marrow sites [16]. | Zhou et al. “Cytogenetic abnormalities in multiple myeloma: poor prognosis is linked to concomitant detection in random and focal lesion bone marrow samples and associated with high-risk gene expression profile”. Br J Haematol 2009; 145(5):637-641 |
25-Jun-2009 | 120 | Myeloma patients previously enrolled in tandem transplantation trial Total Therapy 2 [7]. | Nair et al. “Gene expression profiling of plasma cells at myeloma relapse from tandem transplantation trial Total Therapy 2 predicts subsequent survival”. Blood 2009; 113:6572–5. |
14-Mar-2010 | 258 | Newly diagnosed patients with multiple myeloma entered into the MRC Myeloma IX study [17]. | Dickens et al. Homozygous Deletion Mapping in Myeloma Samples Identifies Genes and an Expression Signature Relevant to Pathogenesis and Outcome. Clin Cancer Res March 15, 2010 16:1856–1864; |
12-Apr-2010 | 52 | Patients newly diagnosed with MM [18]. | Zhou et al. “High-risk myeloma is associated with global elevation of MiRNAs and overexpression of EIF2C2/AGO2”. Proc Natl Acad Sci USA 2010; 107(17): 7904-790 |
30-Sep-2010 | 757 | Previously untreated patients undergoing high-dose chemotherapy [19]. | Hose et al. “Proliferation is a central independent prognostic factor and target for personalized and risk adapted treatment in multiple myeloma”. Haematologica 2011; 96(1):87–95. |
20-Aug-2010 | 275 | Newly diagnosed patients with symptomatic or progressive myeloma [20]. | van Rhee et al. Total Therapy 3 for multiple myeloma: prognostic implications of cumulative dosing and premature discontinuation of VTD maintenance components, bortezomib, thalidomide, and dexamethasone, relevant to all phases of therapy. Blood 2010 116:1220–1227; |
7-Oct-2010 | 320 | Newly diagnosed patients with MM (Dutch-Belgian Cooperative Trial Group for Hemato-Oncology [21]. | Broyl et al. Gene expression profiling for molecular classification of multiple myeloma in newly diagnosed patients. Blood 2010 116:2543–2553; |
22-Aug-2011 | 45 | Patients with myeloma receiving initial therapy with lenalidomide and dexamethasone [22]. | Kumar et al. “Impact of gene expression profiling-based risk stratification in patients with myeloma receiving initial therapy with lenalidomide and dexamethasone”. Blood 2011; 118(16): 4359–4362. |