Evidence map›Paper›PMID 24879115›Full record

ArticleBlood cancer journal2014

The role of front-line anthracycline-containing chemotherapy regimens in peripheral T-cell lymphomas.

R Briski, A L Feldman, N G Bailey, M S Lim, K Ristow, T M Habermann, W R Macon, D J Inwards, J P Colgan, G S Nowakowski and 4 more

Open access · goldAbstract read
In one paragraph

Article in Blood cancer journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
5.1field-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

33 citing papers in PubMed, 67 citations in OpenAlex.

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  13. Gene Expression Signatures for the Accurate Diagnosis of Peripheral T-Cell Lymphoma Entities in the Routine Clinical Practice.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2022
    Article
  14. Genome-Wide miRNA Expression Profiling of Molecular Subgroups of Peripheral T-cell Lymphoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
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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

14 authors at 2 institutions in 1 country.

R BriskiDepartment of Internal Medicine, Division of Hematology and Oncology, University of Michigan, Ann Arbor, MI, USA.
A L FeldmanDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
N G BaileyDepartment of Pathology, University of Michigan, Ann Arbor, MI, USA.
M S LimDepartment of Pathology, University of Michigan, Ann Arbor, MI, USA.
K RistowDepartment of Internal Medicine, Division of Hematology, Mayo Clinic, Rochester, MN, USA.
T M HabermannDepartment of Internal Medicine, Division of Hematology, Mayo Clinic, Rochester, MN, USA.
W R MaconDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
D J InwardsDepartment of Internal Medicine, Division of Hematology, Mayo Clinic, Rochester, MN, USA.
J P ColganDepartment of Internal Medicine, Division of Hematology, Mayo Clinic, Rochester, MN, USA.
G S NowakowskiDepartment of Internal Medicine, Division of Hematology, Mayo Clinic, Rochester, MN, USA.
M S KaminskiDepartment of Internal Medicine, Division of Hematology and Oncology, University of Michigan, Ann Arbor, MI, USA.
T E WitzigDepartment of Internal Medicine, Division of Hematology, Mayo Clinic, Rochester, MN, USA.
S M AnsellDepartment of Internal Medicine, Division of Hematology, Mayo Clinic, Rochester, MN, USA.
R A WilcoxDepartment of Internal Medicine, Division of Hematology and Oncology, University of Michigan, Ann Arbor, MI, USA.
Mayo Clinic in Arizona · USUniversity of Michigan–Ann Arbor · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Felicity Enders · 1985 to 2026
$151.3M
The role of GATA-3 in T-cell lymphomasK08CA172215 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WILCOX, RYAN A · 2013 to 2017
$893k
NCI NIH HHS K08 CA172215NCI NIH HHS K08CA172215NCI NIH HHS P30 CA015083
6 · The paper itself

Abstract

Peripheral T-cell lymphomas (PTCLs) are a heterogenous group of aggressive non-Hodgkin's lymphomas that are incurable in the majority of patients with current therapies. Outcomes associated with anthracycline-based therapies are suboptimal, but remain the standard of care for most patients, even though the benefits of this approach remain uncertain. This study retrospectively examined outcomes in a cohort of North American PTCL patients treated with both anthracycline- and nonanthracycline-containing regimens. The incorporation of anthracycline-containing regimens was associated with improved progression-free survival (PFS) and overall survival (OS). Patients treated with nonanthracycline-containing regimens were more likely to have high-risk features and were less likely to undergo high-dose therapy and stem cell transplantation. However, anthracycline use remained an independent predictor of improved PFS and OS when adjusting for these confounding variables. Anthracycline-based regimens and consolidation with high-dose therapy and autologous stem cell transplantation in appropriately selected patients remains a viable option for patients unable to participate in a clinical trial. Long-term disease-free survival is not optimal, highlighting the need for an improved understanding of disease pathogenesis, and the development of novel therapeutic strategies.

Indexed as

AdolescentAdultAgedAged, 80 and overAnthracyclinesAntineoplastic Combined Chemotherapy ProtocolsCohort StudiesDisease-Free SurvivalFemaleHumansLymphoma, T-Cell, PeripheralMaleMiddle AgedRetrospective StudiesYoung AdultAnthracyclines

Identifiers

PMID24879115
PMCPMC4042304
OpenAlexW2026702457

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.