Evidence map›Paper›PMID 33026184›Full record

ArticlePediatric blood & cancer2021

Identification of prognostic factors in childhood T-cell acute lymphoblastic leukemia: Results from DFCI ALL Consortium Protocols 05-001 and 11-001.

Melissa A Burns, Andrew E Place, Kristen E Stevenson, Alejandro Gutiérrez, Suzanne Forrest, Yana Pikman, Lynda M Vrooman, Marian H Harris, Sarah K Hunt, Jane E O'Brien and 16 more

Erratum issued 2 registry-linked trialsOpen access · greenAbstract read
In one paragraph

Article in Pediatric blood & cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to 2 registered trials, which are not on this map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.7field-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.

NCT00165087 phase3terminatednot on this map

Treatment of Childhood Acute Lymphoblastic Leukemia

TypeinterventionalSponsorDana-Farber Cancer InstituteRan1996 to 2006Enrolled491ConditionsAcute Lymphoblastic LeukemiaArmsasparaginase (E. Coli), asparaginase (Erwina), dexrazoxane, doxorubicin, cranial radiation (once daily fractionation)
NCT01574274 phase2active not recruitingnot on this map

Randomized Study of Intravenous Calaspargase Pegol (SC-PEG Asparaginase) and Intravenous Oncaspar in Children and Adolescents With Acute Lymphoblastic Leukemia or Lymphoblastic Lymphoma

TypeinterventionalSponsorDana-Farber Cancer InstituteRan2012 to 2027Enrolled240ConditionsAcute Lymphoblastic Leukemia, Lymphoblastic LymphomaArmsSC-PEG, Oncaspar
3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 57 citations in OpenAlex.

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  17. [Clinical characteristics and prognosis of children with T-lineage acute lymphoblastic leukemia: a single-center study].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors at 15 institutions in 3 countries.

Melissa A BurnsDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0002-0953-766X
Andrew E PlaceDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0002-9604-4213
Kristen E StevensonDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Alejandro GutiérrezDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Suzanne ForrestDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Yana PikmanDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Lynda M VroomanDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Marian H HarrisDepartment of Pathology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
Sarah K HuntDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Jane E O'BrienDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Barbara L AsselinDepartment of Pediatrics, Golisano Children's Hospital, University of Rochester Medical Center, Rochester, New York.
Uma H AthaleDivision of Pediatric Hematology/Oncology, McMaster University, Hamilton, Ontario, Canada.ORCID 0000-0003-3236-6560
Luis A ClavellDivision of Pediatric Oncology, San Jorge Children's Hospital, San Juan, Puerto Rico.
Peter D ColeDivision of Pediatric Hematology/Oncology, Rutgers Cancer Institute of New Jersey, Rutgers; Robert Wood Johnson School of Medicine, New Brunswick, New Jersey.ORCID 0000-0002-3525-8015
Lisa M GennariniDivision of Pediatric Hematology/Oncology, Children's Hospital at Montefiore, Bronx, New York.
Justine M KahnDivision of Pediatric Hematology, Oncology, and Stem Cell Transplantation, Columbia University, New York, New York.ORCID 0000-0003-3330-6754
Kara M KellyDepartment of Pediatric Oncology, Roswell Park Comprehensive Cancer Center, University at Buffalo, Buffalo, New York.
Caroline LaverdiereDivision of Hematology and Oncology, Hospital Sainte-Justine, University of Montreal, Montreal, Quebec, Canada.
Jean-Marie LeclercDivision of Hematology and Oncology, Hospital Sainte-Justine, University of Montreal, Montreal, Quebec, Canada.
Bruno MichonDivision of Hematology-Oncology, Centre Hospitalier Universite de Quebec, Quebec City, Quebec, Canada.
Marshall A SchorinInova Fairfax Hospital for Children, Falls Church, Virginia.
Maria Luisa SulisPediatric Hematologic Malignancies Service, Department of Pediatric Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0003-2110-0193
Jennifer J G WelchDivision of Pediatric Hematology-Oncology, Hasbro Children's Hospital, Warren Alpert Medical School of Brown University, Providence, Rhode Island.ORCID 0000-0001-9117-4812
Donna S NeubergDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0003-2566-3145
Stephen E SallanDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Lewis B SilvermanDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Boston Children's Hospital · USHarvard University · USCentre Hospitalier Universitaire Sainte-Justine · CABrown University · USCentre hospitalier universitaire de Québec · CAChildren's Hospital at Montefiore · USInova Children's Hospital · USMcMaster University · CAMemorial Sloan Kettering Cancer Center · USNew York Stem Cell Foundation · USRoswell Park Comprehensive Cancer Center · USRutgers, The State University of New Jersey · USSan Juan City Hospital · PRSouthwestern Medical Center · USUniversity of Rochester Medical Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Zebrafish Screens for Genetic Modifiers and Human Application in T-ALLP01CA068484 · NCI · DANA-FARBER CANCER INSTITUTE · PI KUTOK, JEFFERY LORNE · 1995 to 2010
$31.9M
Discovery and targeting of apoptosis resistance mechanisms in high-risk T-ALLR01CA193651 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI GUTIERREZ, ALEJANDRO · 2015 to 2024
$4.4M
Targeting mitochondrial one carbon folate metabolism for novel T-cell acute lymphoblastic leukemia therapyK08CA222684 · NCI · DANA-FARBER CANCER INST · PI PIKMAN, YANA · 2018 to 2022
$886k
NCI NIH HHS 1R01CA193651NCI NIH HHS K08 CA222684NCI NIH HHS P01 CA068484NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA193651NIH HHS 5P01CA068484
6 · The paper itself

Abstract

BACKGROUND/

objectivesWhile outcomes for pediatric T-cell acute lymphoblastic leukemia (T-ALL) are favorable, there are few widely accepted prognostic factors, limiting the ability to risk stratify therapy. DESIGN/

methodsDana-Farber Cancer Institute (DFCI) Protocols 05-001 and 11-001 enrolled pediatric patients with newly diagnosed B- or T-ALL from 2005 to 2011 and from 2012 to 2015, respectively. Protocol therapy was nearly identical for patients with T-ALL (N = 123), who were all initially assigned to the high-risk arm. End-induction minimal residual disease (MRD) was assessed by reverse transcription polymerase chain reaction (RT-PCR) or next-generation sequencing (NGS), but was not used to modify postinduction therapy. Early T-cell precursor (ETP) status was determined by flow cytometry. Cases with sufficient diagnostic DNA were retrospectively evaluated by targeted NGS of known genetic drivers of T-ALL, including Notch, PI3K, and Ras pathway genes.

resultsThe 5-year event-free survival (EFS) and overall survival (OS) for patients with T-ALL was 81% (95% CI, 73-87%) and 90% (95% CI, 83-94%), respectively. ETP phenotype was associated with failure to achieve complete remission, but not with inferior OS. Low end-induction MRD (<10

conclusionsTogether, our findings demonstrate that ETP phenotype, end-induction MRD, and PI3K pathway mutation status are prognostically relevant in pediatric T-ALL and should be considered for risk classification in future trials. DFCI Protocols 05-001 and 11-001 are registered at www.clinicaltrials.gov as NCT00165087 and NCT01574274, respectively.

Indexed as

AdolescentAdultAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorChildChild, PreschoolClinical Trials, Phase III as TopicFemaleFollow-Up StudiesHigh-Throughput Nucleotide SequencingHumansInfantMaleNeoplasm, ResidualPrecursor T-Cell Lymphoblastic Leukemia-LymphomaPrognosisBiomarkers, TumorALLclinical trialsminimal residual diseasemolecular diagnosis and therapypediatric oncologyT-ALL

Identifiers

PMID33026184
PMCPMC8369809
OpenAlexW3092226633

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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.