ref

+ @nadeuGenomicEpigenomicInsights2020b, @pararajalingamCodingNoncodingDrivers2020 @zhangGenomicLandscapeMantle2014, @beaLandscapeSomaticMutations2013, @wuGeneticHeterogeneityPrimary2016, @freemanMolecularDeterminantsOutcomes2022

+@article{freemanMolecularDeterminantsOutcomes2022,

+ title = {Molecular Determinants of Outcomes in Relapsed or Refractory Mantle Cell Lymphoma Treated with Ibrutinib or Temsirolimus in the {{MCL3001}} ({{RAY}}) Trial},

+ author = {Freeman, Ciara L. and Pararajalingam, Prasath and Jin, Ling and Balasubramanian, Sriram and Jiang, Aixiang and Xu, Wendan and Grau, Michael and Zapukhlyak, Myroslav and Boyle, Merrill and Hodkinson, Brendan and Schaffer, Michael and Enny, Christopher and Deshpande, Sanjay and Sun, Steven and Vermeulen, Jessica and Morin, Ryan D. and Scott, David W. and Lenz, Georg},

+ date = {2022-10},

+ journaltitle = {Leukemia},

+ shortjournal = {Leukemia},

+ volume = {36},

+ number = {10},

+ eprint = {35963941},

+ eprinttype = {pmid},

+ pages = {2479--2487},

+ issn = {1476-5551},

+ doi = {10.1038/s41375-022-01658-2},

+ abstract = {Mantle cell lymphoma (MCL) is a rare, incurable lymphoma subtype characterized by heterogeneous outcomes. To better understand the clinical behavior and response to treatment, predictive biomarkers are needed. Using residual archived material from patients enrolled in the MCL3001 (RAY) study, we performed detailed analyses of gene expression and targeted genetic sequencing. This phase III clinical trial randomized patients with relapsed or refractory MCL to treatment with either ibrutinib or temsirolimus. We confirmed the prognostic capability of the gene expression proliferation assay MCL35 in this cohort treated with novel agents; it outperformed the simplified MCL International Prognostic Index in discriminating patients with different outcomes. Regardless of treatment arm, our data demonstrated that this assay captures the risk conferred by known biological factors, including increased MYC expression, blastoid morphology, aberrations of TP53, and truncated CCND1 3' untranslated region. We showed the negative impact of BIRC3 mutations/deletions on outcomes in this cohort and identified that deletion of chromosome 8p23.3 also negatively impacts survival. Restricted to patients with deletions/alterations in TP53, ibrutinib appeared to abrogate the deleterious impact on outcome. These data illustrate the potential to perform a molecular analysis of predictive biomarkers on routine patient samples that can meaningfully inform clinical practice.},

+ langid = {english},

+ keywords = {3' Untranslated Regions,Adenine,Adult,Biological Factors,Humans,Lymphoma Mantle-Cell,Neoplasm Recurrence Local,Piperidines,Pyrazoles,Pyrimidines,Sirolimus}

+}

+