TY - JOUR
T1 - Follicular Lymphoma
T2 - Recent and Emerging Therapies, Treatment Strategies, and Remaining Unmet Needs
AU - Matasar, Matthew J.
AU - Luminari, Stefano
AU - Barr, Paul M.
AU - Barta, Stefan K.
AU - Danilov, Alexey V.
AU - Hill, Brian T.
AU - Phillips, Tycel J.
AU - Jerkeman, Mats
AU - Magagnoli, Massimo
AU - Nastoupil, Loretta J.
AU - Persky, Daniel O.
AU - Okosun, Jessica
N1 - Funding Information:
This review article was written on behalf of LYMPHOMA CONNECT; for more information, please visit www.lymphomaconnect.info. LYMPHOMA CONNECT is supported by an Independent Educational Grant from Bayer. Bayer did not have a critical role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review and approval of the manuscript; or decision to submit the manuscript for publication.We thank Dr. Georg Lenz for his helpful comments in the preparation of this review. Medical writing assistance was provided by Tricia Newell, Ph.D., and Mark English, Ph.D., of COR2ED, Basel, Switzerland.
Publisher Copyright:
© 2019 The Authors. The Oncologist published by Wiley Periodicals, Inc. on behalf of AlphaMed Press.
PY - 2019/11/1
Y1 - 2019/11/1
N2 - Follicular lymphoma (FL) is a heterogeneous disease with varying prognosis owing to differences in clinical, laboratory, and disease parameters. Although generally considered incurable, prognosis for early- and advanced-stage disease has improved because of therapeutic advances, several of which have resulted from elucidation of the biologic and molecular basis of the disease. The choice of treatment for FL is highly dependent on patient and disease characteristics. Several tools are available for risk stratification, although limitations in their routine clinical use exist. For limited disease, treatment options include radiotherapy, rituximab monotherapy or combination regimens, and surveillance. Treatment of advanced disease is often determined by tumor burden, with surveillance or rituximab considered for low tumor burden and chemoimmunotherapy for high tumor burden disease. Treatment for relapsed or refractory disease is influenced by initial first-line therapy and the duration and quality of the response. Presently, there is no consensus for treatment of patients with early or multiply relapsed disease; however, numerous agents, combination regimens, and transplant options have demonstrated efficacy. Although the number of therapies available to treat FL has increased together with an improved understanding of the underlying biologic basis of disease, the best approach to select the most appropriate treatment strategy for an individual patient at a particular time continues to be elucidated. This review considers prognostication and the evolving treatment landscape of FL, including recent and emergent therapies as well as remaining unmet needs. Implications for Practice: In follicular lymphoma, a personalized approach to management based on disease biology, patient characteristics, and other factors continues to emerge. However, application of current management requires an understanding of the available therapeutic options for first-line treatment and knowledge of current development in therapies for previously untreated and for relapsed or refractory disease. Thus, this work reviews for clinicians the contemporary data in follicular lymphoma, from advances in characterizing disease biology to current treatments and emerging novel therapies.
AB - Follicular lymphoma (FL) is a heterogeneous disease with varying prognosis owing to differences in clinical, laboratory, and disease parameters. Although generally considered incurable, prognosis for early- and advanced-stage disease has improved because of therapeutic advances, several of which have resulted from elucidation of the biologic and molecular basis of the disease. The choice of treatment for FL is highly dependent on patient and disease characteristics. Several tools are available for risk stratification, although limitations in their routine clinical use exist. For limited disease, treatment options include radiotherapy, rituximab monotherapy or combination regimens, and surveillance. Treatment of advanced disease is often determined by tumor burden, with surveillance or rituximab considered for low tumor burden and chemoimmunotherapy for high tumor burden disease. Treatment for relapsed or refractory disease is influenced by initial first-line therapy and the duration and quality of the response. Presently, there is no consensus for treatment of patients with early or multiply relapsed disease; however, numerous agents, combination regimens, and transplant options have demonstrated efficacy. Although the number of therapies available to treat FL has increased together with an improved understanding of the underlying biologic basis of disease, the best approach to select the most appropriate treatment strategy for an individual patient at a particular time continues to be elucidated. This review considers prognostication and the evolving treatment landscape of FL, including recent and emergent therapies as well as remaining unmet needs. Implications for Practice: In follicular lymphoma, a personalized approach to management based on disease biology, patient characteristics, and other factors continues to emerge. However, application of current management requires an understanding of the available therapeutic options for first-line treatment and knowledge of current development in therapies for previously untreated and for relapsed or refractory disease. Thus, this work reviews for clinicians the contemporary data in follicular lymphoma, from advances in characterizing disease biology to current treatments and emerging novel therapies.
KW - Antineoplastic agents
KW - Follicular lymphoma
KW - Neoplasms
KW - Non-Hodgkin lymphoma
UR - http://www.scopus.com/inward/record.url?scp=85070288652&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85070288652&partnerID=8YFLogxK
U2 - 10.1634/theoncologist.2019-0138
DO - 10.1634/theoncologist.2019-0138
M3 - Article
C2 - 31346132
AN - SCOPUS:85070288652
SN - 1083-7159
VL - 24
SP - e1236-e1250
JO - Oncologist
JF - Oncologist
IS - 11
ER -