Evidence map›Paper›PMID 31657981›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2019

Improved CNS Control of Childhood Acute Lymphoblastic Leukemia Without Cranial Irradiation: St Jude Total Therapy Study 16.

Sima Jeha, Deqing Pei, John Choi, Cheng Cheng, John T Sandlund, Elaine Coustan-Smith, Dario Campana, Hiroto Inaba, Jeffrey E Rubnitz, Raul C Ribeiro and 9 more

2 registry-linked trialsOpen access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 171 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
171citing papers in PubMed, 6 pooled it
28.2field-weighted citation impact, top 1% 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.

NCT06764238 phase2 / phase3recruitingnot on this mapstarted 2025, after this paper: background citation

Chinese Children's Cancer Group-2025 Protocol for Newly Diagnosed for Intermediate/High Risk Childhood B-cell ALL

TypeinterventionalSponsorInstitute of Hematology & Blood Diseases Hospital, ChinaRan2025 to 2031Enrolled1,800ConditionsAcute Lymphoblastic Leukemia ALL, Childhood Leukemia, Acute Lymphoblastic, B Cell Acute Lymphoblastic Leukemia (B-ALL)ArmsBlinatumomab (Group A), Venetoclax (nonRand Group), Blinatumomab (Group B)
NCT06882057 phase2 / phase3recruitingnot on this mapstarted 2025, after this paper: background citation

Chinese Children's Cancer Group-2025 Protocol for Newly Diagnosed Low Risk Childhood B-cell Acute Lymphoblastic Leukemia

TypeinterventionalSponsorInstitute of Hematology & Blood Diseases Hospital, ChinaRan2025 to 2033Enrolled3,000ConditionsAcute Lymphoblastic Leukemia ALL, Childhood Leukemia, Acute Lymphoblastic, B Cell Acute Lymphoblastic Leukemia (B-ALL)ArmsBlinatumomab, Reinduction-2 omission, Chemo-light Maintenance 2
3 · Its place in the literature

Who cites it

171 citing papers in PubMed, 6 syntheses or guidelines pooled it, 258 citations in OpenAlex.

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111 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

19 authors at 3 institutions in 2 countries.

Sima JehaSt Jude Children's Research Hospital, Memphis, TN.
Deqing PeiSt Jude Children's Research Hospital, Memphis, TN.
John ChoiSt Jude Children's Research Hospital, Memphis, TN.
Cheng ChengSt Jude Children's Research Hospital, Memphis, TN.
John T SandlundSt Jude Children's Research Hospital, Memphis, TN.
Elaine Coustan-SmithNational University of Singapore, Singapore.
Dario CampanaNational University of Singapore, Singapore.
Hiroto InabaSt Jude Children's Research Hospital, Memphis, TN.
Jeffrey E RubnitzSt Jude Children's Research Hospital, Memphis, TN.
Raul C RibeiroSt Jude Children's Research Hospital, Memphis, TN.
Tanja A GruberSt Jude Children's Research Hospital, Memphis, TN.
Susana C RaimondiSt Jude Children's Research Hospital, Memphis, TN.
Raja B KhanSt Jude Children's Research Hospital, Memphis, TN.
Jun J YangSt Jude Children's Research Hospital, Memphis, TN.
Charles G MullighanSt Jude Children's Research Hospital, Memphis, TN.
James R DowningSt Jude Children's Research Hospital, Memphis, TN.
William E EvansSt Jude Children's Research Hospital, Memphis, TN.
Mary V RellingSt Jude Children's Research Hospital, Memphis, TN.
Ching-Hon PuiSt Jude Children's Research Hospital, Memphis, TN.
University of Tennessee Health Science Center · USSt. Jude Children's Research Hospital · USNational University of Singapore · SG

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
CPML - Project 3: Genome-wide Studies of Adverse EffectsP50GM115279 · NIGMS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI LOH, MIGNON LEE-CHEUN, RELLING, MARY V · 2015 to 2019
$15.1M
Translating genomic discoveries to improved outcomes for high risk acute leukemiaR35CA197695 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Charles G Mullighan · 2017 to 2026
$11.4M
PHARMACOGENOMICS OF CHILDHOOD LEUKEMIA (ALL)R37CA036401 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI EVANS, WILLIAM E · 1987 to 2014
$9.7M
Pharmacogenomics of Childhood Leukemia ALLR01CA036401 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI EVANS, WILLIAM E · 1985 to 2019
$3.6M
ARID5B and disparities of childhood leukemiaU01CA176063 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI YANG, JUN J. · 2014 to 2018
$2.4M
Genetics-guided Individualization of Thiopurine TherapyR01GM118578 · NIGMS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI YANG, JUN J. · 2017 to 2020
$2.2M
NCI NIH HHS P30 CA021765NCI NIH HHS R01 CA036401NCI NIH HHS R35 CA197695NCI NIH HHS R37 CA036401NCI NIH HHS U01 CA176063NIGMS NIH HHS P50 GM115279NIGMS NIH HHS R01 GM118578
6 · The paper itself

Abstract

purposeDespite contemporary treatment, up to 10% of children with acute lymphoblastic leukemia still experience relapse. We evaluated whether a higher dosage of PEG-asparaginase and early intensification of triple intrathecal therapy would improve systemic and CNS control. PATIENTS AND

methodsBetween 2007 and 2017, 598 consecutive patients age 0 to 18 years received risk-directed chemotherapy without prophylactic cranial irradiation in the St Jude Total Therapy Study 16. Patients were randomly assigned to receive PEG-asparaginase 3,500 U/m

resultsThe 5-year event-free survival and overall survival rates for the 598 patients were 88.2% (95% CI, 84.9% to 91.5%) and 94.1% (95% CI, 91.7% to 96.5%), respectively. Cumulative risk of any-isolated or combined-CNS relapse was 1.5% (95% CI, 0.5% to 2.5%). Higher doses of PEG-asparaginase did not affect treatment outcome. T-cell phenotype was the only independent risk factor for any CNS relapse (hazard ratio, 5.15; 95% CI, 1.3 to 20.6;

conclusionHigher doses of PEG-asparaginase failed to improve outcome, but additional intrathecal therapy during early induction seemed to contribute to improved CNS control without excessive toxicity for high-risk patients.

Indexed as

AdolescentAntineoplastic Combined Chemotherapy ProtocolsAsparaginaseCentral Nervous System NeoplasmsChildChild, PreschoolCranial IrradiationCytarabineFemaleFollow-Up StudiesHumansInfantInfant, NewbornMaleMethotrexateNeoplasm Recurrence, LocalAsparaginaseCytarabineMethotrexatepegaspargasePolyethylene Glycols

Identifiers

PMID31657981
PMCPMC7351342
OpenAlexW2982248350

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.