Evidence map›Paper›PMID 26758422›Full record

Trial reportLeukemia & lymphoma2016

A phase II study of belinostat (PXD101) in relapsed and refractory aggressive B-cell lymphomas: SWOG S0520.

Soham D Puvvada, Hongli Li, Lisa M Rimsza, Steven H Bernstein, Richard I Fisher, Michael LeBlanc, Monika Schmelz, Betty Glinsmann-Gibson, Thomas P Miller, Anne-Marie Maddox and 3 more

Open access · greenAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Leukemia & lymphoma, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Advances in targeted therapy for malignant lymphoma.Signal transduction and targeted therapy · 2020
    Review
  14. Review
  15. Recent Update of HDAC Inhibitors in Lymphoma.Frontiers in cell and developmental biology · 2020
    Review
  16. Emerging epigenetic-modulating therapies in lymphoma.Nature reviews. Clinical oncology · 2019
    Review
  17. Review
  18. Review
  19. Article
  20. Diffuse large B-cell lymphoma: R-CHOP failure-what to do?Hematology. American Society of Hematology. Education Program · 2016
    Review
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

13 authors at 7 institutions in 1 country.

Soham D Puvvadaa University of Arizona Cancer Center , Tucson , AZ , USA ;
Hongli Lib SWOG Statistical Center , Seattle , WA , USA ;
Lisa M Rimszac Department of Pathology , University of Arizona , Tucson , AZ , USA ;
Steven H Bernsteind Wilmot Cancer Center , University of Rochester , Rochester , NY , USA ;
Richard I Fishere Fox Chase Cancer Center - Temple Health , Philadelphia , PA , USA ;
Michael LeBlancb SWOG Statistical Center , Seattle , WA , USA ;
Monika Schmelzc Department of Pathology , University of Arizona , Tucson , AZ , USA ;
Betty Glinsmann-Gibsonc Department of Pathology , University of Arizona , Tucson , AZ , USA ;
Thomas P Millera University of Arizona Cancer Center , Tucson , AZ , USA ;
Anne-Marie Maddoxf University of Arkansas for Medical Sciences , Little Rock , AK , USA ;
Jonathan W Friedbergd Wilmot Cancer Center , University of Rochester , Rochester , NY , USA ;
Sonali M Smithg Department of Medicine, University of Chicago , Chicago , IL , USA.
Daniel O Perskya University of Arizona Cancer Center , Tucson , AZ , USA ;
University of Arizona · USUniversity of Arizona Cancer CenterCancer Research And Biostatistics · USUniversity of Rochester · USTemple University Health System · USUniversity of Arkansas for Medical Sciences · USUniversity of Chicago · US

Funding

SWOG Network Group Operations Center of the NCTNU10CA180888 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI PRIMO N. LARA · 2014 to 2026
$152.1M
WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Margaret von Mehren · 1985 to 2026
$138.8M
SWOG Statistics & Data Management Center complex - extension supplement for GY06U10CA180819 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Michael L. LeBlanc · 2014 to 2026
$115.2M
Heartland Cancer Research NCORPUG1CA189830 · NCI · DECATUR MEMORIAL HOSPITAL · PI Bryan A. Faller · 2014 to 2026
$40.9M
Southeast Clinical Oncology Research Consortium, Inc. (SCOR)UG1CA189858 · NCI · SOUTHEAST CLINICAL ONCOL RES CONSORTIUM · PI Judith O Hopkins, William J Irvin · 2014 to 2026
$38.8M
The Pacific Cancer Research Consortium (PCRC), an NCORP Community SiteUG1CA189953 · NCI · SWEDISH MEDICAL CENTER, FIRST HILL · PI Alison Katherine Conlin, Charles Drescher · 2014 to 2026
$27.4M
Gulf South Minority/Underserved Clinical Trials Network (Gulf South M/U CTN)UG1CA189854 · NCI · LSU HEALTH SCIENCES CENTER · PI AUGUSTO C. OCHOA · 2014 to 2026
$27.1M
Montana Cancer Consortium NCORPUG1CA189872 · NCI · MONTANA CANCER CONSORTIUM · PI Jeffrey Warren Allen, John M. Schallenkamp · 2014 to 2026
$11.0M
Dayton Clinical Oncology ProgramUG1CA189957 · NCI · DAYTON CLINICAL ONCOLOGY PROGRAM · PI Howard M Gross · 2014 to 2026
$10.7M
Bay Area Tumor Institute NCORPUG1CA189817 · NCI · BAY AREA TUMOR INSTITUTE · PI BAILEY, LISA (NMN) · 2014 to 2023
$7.7M
NCI NIH HHS P30 CA006927NCI NIH HHS U10 CA180819NCI NIH HHS U10 CA180888NCI NIH HHS UG1 CA189817NCI NIH HHS UG1 CA189830NCI NIH HHS UG1 CA189854NCI NIH HHS UG1 CA189858NCI NIH HHS UG1 CA189872NCI NIH HHS UG1 CA189953NCI NIH HHS UG1 CA189957
6 · The paper itself

Abstract

Recent advances in diffuse large B-cell lymphomas (DLBCL) have underscored the importance of tumor microenvironment in escaping host anti-tumor responses. One mechanism is loss of major histocompatibility Class II antigens (MHCII) associated with decreased tumor infiltrating T lymphocytes (TIL) and poor survival. Transcription of MHCII is controlled by CIITA which in turn is regulated by histone acetylation. In this study, we hypothesized that HDAC inhibition with belinostat increases MHCII, CIITA expression, TIL and improves patient outcomes. Primary objective was evaluation of toxicity and response. Twenty-two patients were enrolled for the study. Belinostat was well tolerated with mild toxicity. Two partial responses were observed at 5, 13 months after registration for an overall response rate (ORR) (95% CI) of 10.5% (1.3-33.1%), and three patients had stable disease for 4.7, 42.3+, and 68.4 + months with minimum 3-year follow-up. Included correlative studies support the hypothesis and serve as the basis for SWOG S0806 combining vorinostat with R-CHOP.

Indexed as

AgedAged, 80 and overAntineoplastic AgentsBiomarkersDrug Resistance, NeoplasmFemaleHistone Deacetylase InhibitorsHLA-DR AntigensHumansHydroxamic AcidsLymphoma, Large B-Cell, DiffuseMaleMiddle AgedNeoplasm StagingRecurrenceRetreatmentAntineoplastic AgentsbelinostatBiomarkersHistone Deacetylase InhibitorsHLA-DR AntigensHydroxamic AcidsSulfonamidesCIITADLBCLHDAC inhibitionMHC Class II expressionnon-Hodgkin lymphomaSWOG

Identifiers

PMID26758422
PMCPMC5140034
OpenAlexW2280483683

What OpenQuestion holds

Textmetadata
LicenceTDM
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.