Determining cell-of-origin subtypes of diffuse large B-cell lymphoma using gene expression in formalin-fixed paraffin-embedded tissue.

By David Steven Scott, G. Wright, P. Williams, C. Lih, W. Walsh, E. Jaffe, Andreas Rosenwald, E. Campo, Wing C. Chan, J. Connors and 14 more. Blood, 2014

705 citations recorded by the source corpus.

Subfields: Immunology, Oncology, Pathology and Forensic Medicine

View Paper: https://www.semanticscholar.org/paper/a19f39c01672af8a3e2f40e1687f50812d07eeda

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Citations in the corpus

Diffuse large B-cell lymphoma (DLBCL): ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. (2012, methodology): “Newer methods, based on evaluation of a limited set of genes, have been validated in comparison with standard gene expression, and are now used in the setting of clinical trials [9, 10].”
Molecular profiling for precision cancer therapies (2020, background): “Examples include additional subgroups of diffuse large B cell lymphoma and also a prognostic prediction of disease recurrence in breast cancer [113, 114].”
Phase I First-in-Human Study of Venetoclax in Patients With Relapsed or Refractory Non-Hodgkin Lymphoma. (2017, background): “and MCL cell lines, as well as in a t(14;18)carrying xenograft model.”
Axicabtagene Ciloleucel CAR T-Cell Therapy in Refractory Large B-Cell Lymphoma (2017, neutral): “(%) ≥Three prior lines of therapy 49 (64) 21 (88) 70 (69) History of primary refractory disease** 23 (30) 3 (12) 26 (26) History of resistance to two consecutive lines 39 (51) 15 (62) 54 (53) Table 1.”
The 2016 revision of the World Health Organization classification of lymphoid neoplasms. (2016, neutral): “63-66 These methods are still not accessible to most laboratories but may represent a promising alternative to the current IHC-based algorithms.”