| Literature DB >> 27986882 |
Lisa Rimsza1, Yuri Fedoriw2, Louis M Staudt2, Ari Melnick2, Randy Gascoyne2, Michael Crump2, Lawrence Baizer2, Kai Fu2, Eric Hsi2, John W C Chan2, Lisa McShane2, John P Leonard2, Brad S Kahl2, Richard F Little2, Jonathan W Friedberg2, Lale Kostakoglu2.
Abstract
Lymphoid malignancies are a heterogeneous group of tumors that have distinctive clinical and biological behaviors. The increasing prevalence of disease reflects both treatment advances and the fact that some of these tumors are indolent. The ability to determine treatment needs at diagnosis remains problematic for some of the tumors, such as in follicular lymphomas. Major clinical advances will likely depend on precision oncology that will enable identification of specific disease entities, prognostic determination at diagnosis, and identification of precise therapeutic targets and essential pathways. However, refinement in diagnostic evaluation is an evolving science. The ability to determine prognosis at diagnosis is variable, and for many of the lymphoid malignancies prognosis can only be made after initial treatment. Clinical trials that aim to evaluate specific features of these diseases are required in order to advance clinical practice that meaningfully addresses this important public health challenge. Herein, we describe the process and general recommendation from the National Cancer Institute (NCI) clinical trials planning meeting in November 2014 to address clinical trial design and biomarker proposals in the context of NCI-supported lymphoma clinical trials in the National Clinical Trials Network. Published by Oxford University Press 2016. This work is written by US Government employees and is in the public domain in the US.Entities:
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Year: 2016 PMID: 27986882 PMCID: PMC6080362 DOI: 10.1093/jnci/djw250
Source DB: PubMed Journal: J Natl Cancer Inst ISSN: 0027-8874 Impact factor: 13.506