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Deletion 17p: a matter of size and number?

Sonja Zweegman, +1 more
- 04 Mar 2021 - 
- Vol. 137, Iss: 9, pp 1135-1136
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This article is published in Blood.The article was published on 2021-03-04 and is currently open access. It has received 1 citations till now.

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A pooled analysis of outcomes according to cytogenetic abnormalities in patients receiving ixazomib- vs placebo-based therapy for multiple myeloma

TL;DR: In this article , the authors evaluated 2247 multiple myeloma patients from the TOURMALINE-MM1/-MM2/-MM3/-MM4 trials to assess the PFS benefit of ixazomib plus lenalidomide-dexamethasone (Rd) vs placebo-Rd (TOURMALINE -MM3/MM4) in specific high-risk CAs.
References
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IMWG consensus on risk stratification in multiple myeloma

TL;DR: The International Myeloma Working Group proposes well-defined and easily applicable risk categories based on current available information and suggests the use of this set of prognostic factors as gold standards in all clinical trials and form the basis of subsequent development of more complex prognostic system or better prognostic Factors.
Journal ArticleDOI

A high-risk, Double-Hit, group of newly diagnosed myeloma identified by genomic analysis

TL;DR: In a genome-wide analysis of the largest set of molecular and clinical data established to date from NDMM, DNA drivers of aggressive clinical behavior are defined and Double-Hit patients have a dire prognosis despite modern therapies and should be considered for novel therapeutic approaches.
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Autologous haematopoietic stem-cell transplantation versus bortezomib-melphalan-prednisone, with or without bortezomib-lenalidomide-dexamethasone consolidation therapy, and lenalidomide maintenance for newly diagnosed multiple myeloma (EMN02/HO95): a multicentre, randomised, open-label, phase 3 study

Michele Cavo, +58 more
TL;DR: Progressive progression-free survival was significantly improved with autologous HSCT compared with VMP and bortezomib-melphalan-prednisone (VMP) as intensification therapy, and bORTezomIB-lenalidomide-dexamethasone (VRD) consolidation therapy with no consolidation.