Multiple myeloma future or investigational therapies: Difference between revisions
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*Lymphoma-like polychemotherapy regimen "Dexa-BEAM" (including [[dexamethasone]], [[carmustine]], [[cytarabine]], [[etoposide]] and [[melphalan]]) in treating advanced and extramedullary multiple myeloma has been studied by Rasche L etal. It showed improved survival, when used as a bridge to [[stem cell transplantation]].<ref name="Rasche-2014">{{Cite journal | last1 = Rasche | first1 = L. | last2 = Strifler | first2 = S. | last3 = Duell | first3 = J. | last4 = Rosenwald | first4 = A. | last5 = Buck | first5 = A. | last6 = Maeder | first6 = U. | last7 = Einsele | first7 = H. | last8 = Knop | first8 = S. | title = The lymphoma-like polychemotherapy regimen Dexa-BEAM in advanced and extramedullary multiple myeloma. | journal = Ann Hematol | volume = | issue = | pages = | month = Feb | year = 2014 | doi = 10.1007/s00277-014-2023-2 | PMID = 24526137 }}</ref> | *Lymphoma-like polychemotherapy regimen "Dexa-BEAM" (including [[dexamethasone]], [[carmustine]], [[cytarabine]], [[etoposide]] and [[melphalan]]) in treating advanced and extramedullary multiple myeloma has been studied by Rasche L etal. It showed improved survival, when used as a bridge to [[stem cell transplantation]].<ref name="Rasche-2014">{{Cite journal | last1 = Rasche | first1 = L. | last2 = Strifler | first2 = S. | last3 = Duell | first3 = J. | last4 = Rosenwald | first4 = A. | last5 = Buck | first5 = A. | last6 = Maeder | first6 = U. | last7 = Einsele | first7 = H. | last8 = Knop | first8 = S. | title = The lymphoma-like polychemotherapy regimen Dexa-BEAM in advanced and extramedullary multiple myeloma. | journal = Ann Hematol | volume = | issue = | pages = | month = Feb | year = 2014 | doi = 10.1007/s00277-014-2023-2 | PMID = 24526137 }}</ref> | ||
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Vidit Bhargava, M.B.B.S [2]
- Lymphoma-like polychemotherapy regimen "Dexa-BEAM" (including dexamethasone, carmustine, cytarabine, etoposide and melphalan) in treating advanced and extramedullary multiple myeloma has been studied by Rasche L etal. It showed improved survival, when used as a bridge to stem cell transplantation.[1]
- Carfilzomib is a new proteasome inhibitor that selectively and irreversibly binds to its target, resulting in sustained inhibition. It thus has a better response as compared to bortezomib along with a favorable safety profile. Clinical trials have been approved and under process to study the effects of the drug. The prospect of its combination with several other agents such as immunomodulators, alkylating agents, glucocorticoids, histone deacetylase inhibitors and kinesin spindle protein inhibitors also holds promise.[2]
- Eda etal is studying a novel Bruton's tyrosine kinase inhibitor CC-292 in combination with the proteasome inhibitor carfilzomib and its rols as anti-multiple myeloma combiantion therpay.[3]
References
- ↑ Rasche, L.; Strifler, S.; Duell, J.; Rosenwald, A.; Buck, A.; Maeder, U.; Einsele, H.; Knop, S. (2014). "The lymphoma-like polychemotherapy regimen Dexa-BEAM in advanced and extramedullary multiple myeloma". Ann Hematol. doi:10.1007/s00277-014-2023-2. PMID 24526137. Unknown parameter
|month=ignored (help) - ↑ Moreau, P. (2014). "The emerging role of carfilzomib combination therapy in the management of multiple myeloma". Expert Rev Hematol. doi:10.1586/17474086.2014.873699. PMID 24521249. Unknown parameter
|month=ignored (help) - ↑ Eda, H.; Santo, L.; Cirstea, DD.; Yee, A.; Scullen, TA.; Nemani, N.; Mishima, Y.; Waterman, PR.; Arastu-Kapur, S. (2014). "A novel Bruton's tyrosine kinase inhibitor CC-292 in combination with the proteasome inhibitor carfilzomib impacts the bone microenvironment in a multiple myeloma model with resultant anti-myeloma activity". Leukemia. doi:10.1038/leu.2014.69. PMID 24518207. Unknown parameter
|month=ignored (help)