Sequencing of therapies in relapsed follicular lymphoma
- PMID: 30504309
- PMCID: PMC6245973
- DOI: 10.1182/asheducation-2018.1.189
Sequencing of therapies in relapsed follicular lymphoma
Abstract
Follicular lymphoma (FL) is an incurable but treatable disease with vast treatment options. Despite the abundance of efficacious treatment modalities, there is no universally agreed upon standard approach to treatment, particularly in the relapsed/refractory setting. There is an increasing need for more robust and clinically available tools to risk-stratify patients and identify those likely to experience early relapse, which is currently recognized as the unmet need in FL. Additionally, the use of gene-expression profiling and next-generation sequencing techniques in recent years has led to a wealth of knowledge regarding the molecular drivers of lymphomagenesis. However, much of this knowledge is not currently available in the clinic to inform treatment decisions. Future studies are needed to generate clinically relevant predictive models adept at incorporating patient-specific and molecular features to inform management strategies along the entire disease continuum as treatment decisions should not be made in a vacuum with a one-size-fits-all approach. Sequencing of therapy in the management of relapsed FL should involve personalized decision-making for care plans that balance patient characteristics, preferences, and comorbidities with treatment-related factors such as efficacy, toxicity profile, and mechanisms of action to achieve a durable, quality remission.
© 2018 by The American Society of Hematology. All rights reserved.
Conflict of interest statement
Conflict-of-interest disclosure: C.R.F. has received research funding from Abbvie, Acerta, Celgene, Gilead, Genentech/Roche, Janssen Pharmaceutical, Millennium/Takeda, Pharmacyclics, TG Therapeutics, Burroughs Wellcome Fund, Eastern Cooperative Oncology Group, National Cancer Institute, and the V Foundation, and has consulted for Abbvie, Bayer, Denovo Biopharma, Gilead, OptumRx, Karyopharm, Pharmacyclics/Janssen, and Spectrum. J.P.L has consulted for Celgene, Juno, Bristol-Myers Squibb, Sutro, Gilead, Epizyme, Genentech/Roche, Pfizer, Bayer, Biotest, United Therapeutics, Karyopharm, ADC Therapeutics, MEI Pharma, AstraZeneca, and Novartis. L.J.N. has received honoraria from Celgene, Genentech, Gilead, Merck, Novartis, Spectrum, and TG Therapeutics.
References
-
- Solal-Céligny P, Roy P, Colombat P, et al. . Follicular Lymphoma International Prognostic Index. Blood. 2004;104(5):1258-1265. - PubMed
-
- Arcaini L, Merli M, Passamonti F, et al. . Validation of Follicular Lymphoma International Prognostic Index 2 (FLIPI2) score in an independent series of follicular lymphoma patients. Br J Haematol. 2010;149(3):455-457. - PubMed
-
- Pastore A, Jurinovic V, Kridel R, et al. . Integration of gene mutations in risk prognostication for patients receiving first-line immunochemotherapy for follicular lymphoma: a retrospective analysis of a prospective clinical trial and validation in a population-based registry. Lancet Oncol. 2015;16(9):1111-1122. - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
