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Enrique M. Ocio

Researcher at University of Cantabria

Publications -  264
Citations -  9830

Enrique M. Ocio is an academic researcher from University of Cantabria. The author has contributed to research in topics: Multiple myeloma & Bortezomib. The author has an hindex of 52, co-authored 224 publications receiving 8113 citations. Previous affiliations of Enrique M. Ocio include Spanish National Research Council & Purdue University.

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Journal ArticleDOI

Panobinostat plus bortezomib and dexamethasone versus placebo plus bortezomib and dexamethasone in patients with relapsed or relapsed and refractory multiple myeloma: a multicentre, randomised, double-blind phase 3 trial

Jesús F. San-Miguel, +44 more
- 01 Oct 2014 - 
TL;DR: Panobinostat is a potent oral pan-deacetylase inhibitor that in preclinical studies has synergistic anti-myeloma activity when combined with bortezomib and dexamethasone and the proportion of patients achieving an overall response did not differ between treatment groups.
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Isatuximab plus pomalidomide and low-dose dexamethasone versus pomalidomide and low-dose dexamethasone in patients with relapsed and refractory multiple myeloma (ICARIA-MM): a randomised, multicentre, open-label, phase 3 study

Michel Attal, +111 more
- 07 Dec 2019 - 
TL;DR: The aim of this study was to determine the progression-free survival benefit of isatuximab plus pomalidomide and dexamethasone compared with pomidine and dexAMethas one in patients with relapsed and refractory multiple myeloma.
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The effect of mesenchymal stem cells on the viability, proliferation and differentiation of B-lymphocytes

TL;DR: The findings of this study indicate that mesenchymal stem cells promote survival and inhibit proliferation and maturation of B cells, and support a role of these cells in the immune response.
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International myeloma working group consensus recommendations on imaging in monoclonal plasma cell disorders

TL;DR: Recommendations on imaging within and outside of clinical trials will help standardise imaging for monoclonal plasma cell disorders worldwide to allow the comparison of results and the unification of treatment approaches for multiple myeloma.