Evidence map›Paper›PMID 29296893›Full record

ArticleBlood advances2017

Early progression of disease as a predictor of survival in chronic lymphocytic leukemia.

Inhye E Ahn, Charles M Farber, Matthew S Davids, David L Grinblatt, Neil E Kay, Nicole Lamanna, Anthony Mato, Chadi Nabhan, Pavel Kiselev, Arlene S Swern and 4 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Blood advances, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01081015 (Connect™ CLL), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 26% 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.

NCT01081015 completednot on this map

Connect™ CLL: The Chronic Lymphocytic Leukemia Disease Registry

TypeobservationalSponsorCelgeneRan2010 to 2017Enrolled1,494ConditionsChronic Lymphocytic Leukemia
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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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 9 institutions in 1 country.

Inhye E AhnMedical Oncology Service, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Charles M FarberSummit Medical Group, MD Anderson Cancer Center, Morristown, NJ.
Matthew S DavidsDana-Farber Cancer Institute, Boston, MA.
David L GrinblattNorthShore University HealthSystem, Evanston, IL.
Neil E KayDivision of Hematology, Mayo Clinic, Rochester, MN.
Nicole LamannaLeukemia Service, Division of Hematology and Oncology, Department of Medicine, New York-Presbyterian/Columbia University Medical Center, New York, NY.
Anthony MatoCenter for Chronic Lymphocytic Leukemia, Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA.
Chadi NabhanCardinal Health, Dublin, OH.
Pavel KiselevCelgene Corporation, Summit, NJ.
Arlene S SwernCelgene Corporation, Summit, NJ.
E Dawn FlickCelgene Corporation, San Francisco, CA.
Kristen SullivanCelgene Corporation, Overland Park, KS.
Jeff P SharmanWillamette Valley Cancer Institute, US Oncology, Springfield, OR; and.
Christopher R FlowersWinship Cancer Institute, Emory University, Atlanta, GA.
Cardinal Health (United States) · USColumbia University Irving Medical Center · USDana-Farber Cancer Institute · USEmory University · USFox Chase Cancer Center · USMayo Clinic in Arizona · USNational Institutes of Health · USNorthShore University HealthSystem · USSummit Medical Group (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemoimmunotherapy for chronic lymphocytic leukemia (CLL) promotes clonal evolution of aggressive clones, which in some patients may lead to early progression of disease (POD). We studied the prognostic value of early POD in a cohort of patients with CLL enrolled between 2010 and 2014 in the Connect CLL Registry. Overall, 829 eligible patients receiving first-line therapy were categorized into 3 groups: early POD (progression <2 years after treatment initiation), late POD (progression ≥2 years after treatment initiation), and no POD as of 1 May 2017. Baseline demographics, treatment characteristics, and overall survival (OS) were analyzed. Logistic regression models identified independent predictors of early POD; Cox regression models were used to evaluate the risk of early POD. With a median follow-up of 48.8 months, 209 (25.2%), 162 (19.5%), and 458 (55.3%) patients had early, late, and no POD, respectively. Patients with early POD were older and had inferior response to similar first-line treatment regimens vs late and no POD groups (overall response rate: 53% vs 80% vs 84%). Patients with early POD were more likely to have unfavorable-risk cytogenetics (del[11q]/del[17p]) than patients with no POD (34% vs 20%;

Identifiers

PMID29296893
PMCPMC5729627
OpenAlexW2768375863

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.