Evidence map›Paper›PMID 22369572›Full record

ArticleLeukemia & lymphoma2012

Variations of the ataxia telangiectasia mutated gene in patients with chronic lymphocytic leukemia lack substantial impact on progression-free survival and overall survival: a Cancer and Leukemia Group B study.

Gerard Lozanski, Amy S Ruppert, Nyla A Heerema, Arletta Lozanski, David M Lucas, Amber Gordon, John G Gribben, Vicki A Morrison, Kanti M Rai, Guido Marcucci and 2 more

Abstract read
In one paragraph

Article in Leukemia & lymphoma, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Trial
  2. Article
  3. Rare GermlineJournal of clinical oncology : official journal of the American Society of Clinical Oncology · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
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 5 institutions in 2 countries.

Gerard LozanskiDepartment of Pathology, The Ohio State University, Columbus, OH 43210, USA.
Amy S Ruppert
Nyla A Heerema
Arletta Lozanski
David M Lucas
Amber Gordon
John G Gribben
Vicki A Morrison
Kanti M Rai
Guido Marcucci
Richard A Larson
John C Byrd
The Ohio State University · USLong Island Jewish Medical Center · USQueen Mary University of London · GBUniversity of Chicago · USUniversity of Minnesota · US

Funding

CANCER AND LEUKEMIA GROUP B MINORITY SATELLITE SUPPLEMENU10CA031946 · NCI · UNIVERSITY OF CHICAGO · PI BERTAGNOLLI, MONICA M · 1985 to 2013
$158.4M
Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
CANCER &LEUKEMIA GROUP B STATISTICAL CENTERU10CA033601 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI SARGENT, DANIEL J. · 1985 to 2013
$69.4M
SPORE Leukemia Tissue BankP50CA140158 · NCI · OHIO STATE UNIVERSITY · PI BLOOMFIELD, CLARA D · 2009 to 2013
$11.2M
Molecular Markers: Response to Chemo-immunotherapy in CLR21CA101332 · NCI · OHIO STATE UNIVERSITY · PI BYRD, JOHN C · 2004 to 2005
$564k
NCI NIH HHS CA31946NCI NIH HHS CA33601NCI NIH HHS P30 CA016058NCI NIH HHS P50 CA140158NCI NIH HHS R21 CA101332NCI NIH HHS U10 CA031946NCI NIH HHS U10 CA033601
6 · The paper itself

Abstract

The impact of mutation of the ATM (ataxia telangiectasia mutated) gene in chronic lymphocytic leukemia (CLL) treatment outcome has not been examined. We studied ATM mutations in 73 patients treated with fludarabine and rituximab. ATM gene mutation analysis was performed using temperature gradient capillary electrophoresis. The impact of detected variants on overall survival (OS) and progression-free survival (PFS) was tested with proportional hazards models. None of the 73 patients demonstrated truncating ATM mutations; 17 (23%, 95% confidence interval 14-35%) had non-silent variants (ATM-NSVs), including 13 known ATM polymorphisms and four missense variants. ATM-NSVs were not significantly associated with any baseline characteristics including immunoglobulin heavy chain variable gene (IGVH) status. In multivariable models, no significant differences in complete response (p =0.70), PFS (p =0.59) or OS (p =0.13) were observed. Our data indicate that truncating ATM mutations are rare in patients with CLL. Furthermore, in this dataset, these non-silent variants had limited impact on PFS and OS.

Indexed as

MutationAdultAgedAged, 80 and overAntibodies, Monoclonal, Murine-DerivedAntineoplastic Combined Chemotherapy ProtocolsAtaxia Telangiectasia Mutated ProteinsCell Cycle ProteinsDisease-Free SurvivalDNA-Binding ProteinsDNA Mutational AnalysisFemaleHumansImmunoglobulin Heavy ChainsImmunoglobulin Variable RegionKaplan-Meier EstimateAntibodies, Monoclonal, Murine-DerivedAtaxia Telangiectasia Mutated ProteinsATM protein, humanCell Cycle ProteinsDNA-Binding ProteinsfludarabineImmunoglobulin Heavy ChainsImmunoglobulin Variable RegionProtein Serine-Threonine KinasesRituximabTumor Suppressor ProteinsVidarabine

Identifiers

PMID22369572
PMCPMC3724930
OpenAlexW2112212299

What OpenQuestion holds

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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.