Evidence map›Paper›PMID 34406850›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2021

Personalized Prediction Model to Risk Stratify Patients With Myelodysplastic Syndromes.

Aziz Nazha, Rami Komrokji, Manja Meggendorfer, Xuefei Jia, Nathan Radakovich, Jacob Shreve, C Beau Hilton, Yasunubo Nagata, Betty K Hamilton, Sudipto Mukherjee and 17 more

Abstract read
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

90 citing papers in PubMed, 1 synthesis or guideline pooled it.

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30 more citing papers are in PubMed but not listed here.

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

27 authors.

Aziz NazhaLeukemia Program, Department of Hematology and Medical Oncology, Cleveland Clinic, Cleveland, OH.ORCID 0000-0002-6695-7994
Rami KomrokjiDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.ORCID 0000-0002-1876-5269
Manja MeggendorferMLL Munich Leukemia Laboratory, Munich, Germany.
Xuefei JiaDepartment of Quantitative Health Sciences, Cleveland Clinic, Cleveland, OH.
Nathan RadakovichLerner College of Medicine, Case Western Reserve University, Cleveland, OH.ORCID 0000-0001-5712-1952
Jacob ShreveLeukemia Program, Department of Hematology and Medical Oncology, Cleveland Clinic, Cleveland, OH.ORCID 0000-0003-4897-6961
C Beau HiltonLerner College of Medicine, Case Western Reserve University, Cleveland, OH.ORCID 0000-0002-1363-7452
Yasunubo NagataDepartment of Translational Hematology and Oncology Research, Cleveland Clinic, Cleveland, OH.
Betty K HamiltonLeukemia Program, Department of Hematology and Medical Oncology, Cleveland Clinic, Cleveland, OH.
Sudipto MukherjeeLeukemia Program, Department of Hematology and Medical Oncology, Cleveland Clinic, Cleveland, OH.
Najla Al AliDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.
Wencke WalterMLL Munich Leukemia Laboratory, Munich, Germany.ORCID 0000-0002-5083-9838
Stephan HutterMLL Munich Leukemia Laboratory, Munich, Germany.
Eric PadronDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.ORCID 0000-0002-4707-7916
David SallmanDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL.ORCID 0000-0003-0504-8233
Teodora KuzmanovicDepartment of Translational Hematology and Oncology Research, Cleveland Clinic, Cleveland, OH.
Cassandra KerrDepartment of Translational Hematology and Oncology Research, Cleveland Clinic, Cleveland, OH.
Vera AdemaDepartment of Translational Hematology and Oncology Research, Cleveland Clinic, Cleveland, OH.ORCID 0000-0001-6051-4378
David P SteensmaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA.ORCID 0000-0001-5130-9284
Amy DezernSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD.
Gail RobozDivision of Hematology and Oncology, New York Presbyterian Hospital-Weill Cornell Medical College, New York, NY.ORCID 0000-0002-0384-3658
Guillermo Garcia-ManeroDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.ORCID 0000-0002-3631-2482
Harry ErbaSWOG Cooperative Group, Houston, TX.ORCID 0000-0003-1093-2189
Claudia HaferlachMLL Munich Leukemia Laboratory, Munich, Germany.
Jaroslaw P MaciejewskiDepartment of Translational Hematology and Oncology Research, Cleveland Clinic, Cleveland, OH.
Torsten HaferlachMLL Munich Leukemia Laboratory, Munich, Germany.
Mikkael A SekeresSylvester Comprehensive Cancer Center, University of Miami, Miami, FL.ORCID 0000-0003-2009-6524

Funding

SWOG Network Group Operations Center of the NCTNU10CA180888 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI PRIMO N. LARA · 2014 to 2026
$152.1M
TRANSLATIONAL RESEARCH ONCOLOGY TRAINING GRANTK12CA076917 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI GERSON, STANTON L. · 1997 to 2022
$14.2M
NCI NIH HHS K12 CA076917NCI NIH HHS U10 CA180888
6 · The paper itself

Abstract

purposePatients with myelodysplastic syndromes (MDS) have a survival that can range from months to decades. Prognostic systems that incorporate advanced analytics of clinical, pathologic, and molecular data have the potential to more accurately and dynamically predict survival in patients receiving various therapies.

methodsA total of 1,471 MDS patients with comprehensively annotated clinical and molecular data were included in a training cohort and analyzed using machine learning techniques. A random survival algorithm was used to build a prognostic model, which was then validated in external cohorts. The accuracy of the proposed model, compared with other established models, was assessed using a concordance (c)index.

resultsThe median age for the training cohort was 71 years. Commonly mutated genes included

conclusionA personalized prediction model on the basis of clinical and genomic data outperformed established prognostic models in MDS. The new model was dynamic, predicting survival and leukemia transformation probabilities at different time points that are unique for a given patient, and can upstage and downstage patients into more appropriate risk categories.

Indexed as

AlgorithmsModels, StatisticalMutationAdultAgedAged, 80 and overBiomarkers, TumorCell Transformation, NeoplasticClinical Trials, Phase II as TopicDisease ProgressionFemaleFollow-Up StudiesGenomicsHematopoietic Stem Cell TransplantationHumansMaleBiomarkers, Tumor

Identifiers

PMID34406850
PMCPMC8601291

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.