Evidence map›Paper›PMID 31346132›Full record

ReviewThe oncologist2019

Follicular Lymphoma: Recent and Emerging Therapies, Treatment Strategies, and Remaining Unmet Needs.

Matthew J Matasar, Stefano Luminari, Paul M Barr, Stefan K Barta, Alexey V Danilov, Brian T Hill, Tycel J Phillips, Mats Jerkeman, Massimo Magagnoli, Loretta J Nastoupil and 2 more

Open access · bronzeAbstract readReview
In one paragraph

Review in The oncologist, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
4.9field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 2 syntheses or guidelines pooled it, 57 citations in OpenAlex.

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  7. A Phase II Study ofPharmaceuticals (Basel, Switzerland) · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 12 institutions in 4 countries.

Matthew J MatasarMemorial Sloan Kettering Cancer Center and New York Presbyterian, New York New York, USA matasarm@mskcc.org.ORCID 0000-0002-4581-3721
Stefano LuminariHematology Unit, Azienda Unità Sanitaria Locale-IRCCS, Reggio Emilia, Italy.
Paul M BarrUniversity of Rochester Medical Center, Rochester, New York, USA.
Stefan K BartaUniversity of Pennsylvania, Philadelphia, Pennsylvania, USA.
Alexey V DanilovOregon Health and Science University, Portland, Oregon, USA.
Brian T HillCleveland Clinic Taussig Cancer Institute, Cleveland, Ohio, USA.
Tycel J PhillipsRogel Cancer Center, Ann Arbor, Michigan, USA.
Mats JerkemanSkane University Hospital, Lund, Sweden.
Massimo MagagnoliHumanitas Cancer Center, Humanitas Research Hospital, Rozzano, Milan, Italy.
Loretta J NastoupilMD Anderson Cancer Center, Houston, Texas, USA.
Daniel O PerskyUniversity of Arizona Cancer Center, Tucson, Arizona, USA.
Jessica OkosunBarts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Cleveland Clinic · USIRCCS Humanitas Research Hospital · ITMemorial Sloan Kettering Cancer Center · USOregon Health & Science University · USQueen Mary University of London · GBSkåne University Hospital · SEThe University of Texas MD Anderson Cancer Center · USU-M Rogel Cancer Center · USUniversity of Arizona · USUniversity of Modena and Reggio Emilia · ITUniversity of Pennsylvania · USUniversity of Rochester Medical Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

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.

Indexed as

AnimalsAntineoplastic AgentsCombined Modality TherapyHumansImmunotherapyLymphoma, FollicularNeeds AssessmentPrognosisAntineoplastic AgentsAntineoplastic agentsFollicular lymphomaNeoplasmsNon‐Hodgkin lymphoma

Identifiers

PMID31346132
PMCPMC6853118
OpenAlexW2963067169

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.