MYC gene rearrangements are associated with a poor prognosis in diffuse large B-cell lymphoma patients treated with R-CHOP chemotherapy.
By K. Savage, N. Johnson, S. Ben-Neriah, J. Connors, L. Sehn, Pedro Farinha, D. Horsman, R. Gascoyne. Blood, 2009
659 citations recorded by the source corpus.
Subfields: Neurology, Oncology, Pathology and Forensic Medicine
View Paper: https://www.semanticscholar.org/paper/2f9d7e0309244515db4e8692d6c057ae94cbe6f8
How researchers see this paper
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- George W. Wright
- N. Johnson
- Elaine S. Jaffe
- E. Campo
- G. Lenz
- H. Tilly
- Andreas Rosenwald
- K. Savage
Citations in the corpus
- An enhanced International Prognostic Index (NCCN-IPI) for patients with diffuse large B-cell lymphoma treated in the rituximab era. (2014, background): “For example, CNS involvement carries a poor prognosis and has been associated with MYC translocations, itself a marker of high-risk disease.(28) Limitations of the current study are principally those typically associated with observational studies using large health care databases.”
- Diffuse large B-cell lymphoma (DLBCL): ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. (2012, background): “However, the prognostic significance of these rearrangements remains controversial and optimal clinical management is not established [14–16].”
- Concurrent expression of MYC and BCL2 in diffuse large B-cell lymphoma treated with rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone. (2012, methodology): “FISH Translocations involving BCL2 and MYC were identified by interphase FISH in FFPE tissue in tissue microarrays from both data sets using commercial dual-color break-apart probes from Abbott Molecular (Abbott Park, IL) according to previously described methods.(14) Patient cases with break-apart ”