Abstract
BACKGROUND: In the era of novel agents such as lenalidomide and bortezomib, risk stratification by chromosomal abnormalities may enable a more rational selection of therapeutic approaches in patients with multiple myeloma (MM). METHODS: The authors analyzed the prognostic value of deletion del(13q14), del(17p13), +1q21, translocation t(4;14), t(11;14), and t(14;16) by fluorescence in situ hybridization (FISH) in a series of 92 patients with recurrent MM who were treated with lenalidomide and dexamethasone (len/dex) at the study center. RESULTS: Patients carrying del(13q14) or t(14;16) were found to have a shorter median time to disease progression (TTP) of 5.1 months (vs 14.4 months; P =.009) and 2.0 months (vs 10.5 months; P
Author supplied keywords
Cite
CITATION STYLE
Klein, U., Jauch, A., Hielscher, T., Hillengass, J., Raab, M. S., Seckinger, A., … Neben, K. (2011). Chromosomal aberrations +1q21 and del(17p13) predict survival in patients with recurrent multiple myeloma treated with lenalidomide and dexamethasone. Cancer, 117(10), 2136–2144. https://doi.org/10.1002/cncr.25775
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.