From transplant to novel cellular therapies in multiple myeloma: European Myeloma Network guidelines and future perspectives
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61988987%3A17110%2F18%3AA1901VZ5" target="_blank" >RIV/61988987:17110/18:A1901VZ5 - isvavai.cz</a>
Alternative codes found
RIV/00843989:_____/18:E0107032
Result on the web
<a href="http://dx.doi.org/10.3324/haematol.2017.174573" target="_blank" >http://dx.doi.org/10.3324/haematol.2017.174573</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3324/haematol.2017.174573" target="_blank" >10.3324/haematol.2017.174573</a>
Alternative languages
Result language
angličtina
Original language name
From transplant to novel cellular therapies in multiple myeloma: European Myeloma Network guidelines and future perspectives
Original language description
Survival of myeloma patients has greatly improved with the use of autologous stem cell transplantation and novel agents, such as proteasome inhibitors, immunomodulatory drugs and monoclonal antibodies. Compared to bortezomib- and lenalidomide-based regimens alone, the addition of high-dose melphalan followed by autologous transplantation significantly improves progression-free survival, although an overall survival benefit was not observed in all trials. Moreover, follow up of recent trials is still too short to show any difference in survival. In the light of these findings, novel agent-based induction followed by autologous transplantation is considered the standard upfront treatment for eligible patients (level of evidence: 1A). Post-transplant consolidation and maintenance treatment can further improve patient outcome (1A). The availability of several novel agents has led to the development of multiple combination regimens such as salvage treatment options. In this context, the role of salvage autologous transplantation and allotransplant has not been extensively evaluated. In the case of prolonged remission after upfront autologous transplantation, another autologous transplantation at relapse can be considered (2B). Patients who experience early relapse and/or have high-risk features have a poor prognosis and may be considered as candidates for clinical trials that, in young and fit patients, may also include an allograft in combination with novel agents (2B). Ongoing studies are evaluating the role of novel cellular therapies, such as inclusion of antibody-based triplets and quadruplets, and chimeric antigen receptor-T cells. Despite encouraging preliminary results, longer follow up and larger patient numbers are needed before the clinical use of these novel therapies can be widely recommended.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30205 - Hematology
Result continuities
Project
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Continuities
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Others
Publication year
2018
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
HAEMATOLOGICA
ISSN
0390-6078
e-ISSN
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Volume of the periodical
103
Issue of the periodical within the volume
2
Country of publishing house
IT - ITALY
Number of pages
15
Pages from-to
197-211
UT code for WoS article
000423853800016
EID of the result in the Scopus database
2-s2.0-85041539082