Evidence map›Paper›PMID 34192312›Full record

ArticleBlood2022

Remission, treatment failure, and relapse in pediatric ALL: an international consensus of the Ponte-di-Legno Consortium.

Swantje Buchmann, Martin Schrappe, Andre Baruchel, Andrea Biondi, Michael Borowitz, Myriam Campbell, Gunnar Cario, Giovanni Cazzaniga, Gabriele Escherich, Christine J Harrison and 16 more

Registry-linked trialOpen access · bronzeAbstract readConsensus Statement
In one paragraph

Article in Blood, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07476729 (International Study for Treatment of Childhood Relapsed Precursor B-Cell ALL 2020 A Randomized Phase III Study Conducted by the Resistant Disease Committee of the International BFM Study Group), which is not on this map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
9.0field-weighted citation impact, top 2% 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.

NCT07476729 phase3not yet recruitingnot on this mapstarted 2026, after this paper: background citation

International Study for Treatment of Childhood Relapsed Precursor B-Cell ALL 2020 A Randomized Phase III Study Conducted by the Resistant Disease Committee of the International BFM Study Group

TypeinterventionalSponsorCharite University, Berlin, GermanyRan2026 to 2033Enrolled750ConditionsB-Cell Acute Lymphoblastic LeukaemiaArmsInotuzumab ozogamicin (INO), Blinatumomab
3 · Its place in the literature

Who cites it

51 citing papers in PubMed, 72 citations in OpenAlex.

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  12. A Survival Analysis of Pediatric Acute Lymphoblastic Leukemia in Morocco.Asian Pacific journal of cancer prevention : APJCP · 2025
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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

26 authors at 20 institutions in 15 countries.

Swantje BuchmannDepartment of Pediatrics, University Medical Center Schleswig-Holstein, Kiel, Germany.
Martin SchrappeDepartment of Pediatrics, University Medical Center Schleswig-Holstein, Kiel, Germany.ORCID 0000-0003-0034-5845
Andre BaruchelPediatric Hematology-Immunology Department, University Hospital Robert Debré Assistance Publique-Hôpitaux de Paris (AP-HP), Université de Paris, Paris.ORCID 0000-0003-0120-6089
Andrea BiondiDepartment of Pediatrics and Tettamanti Research Center, Fondazione MBBM (Monza e Brianza per il Bambino e la sua Mamma)/Ospedale San Gerardo, University of Milano-Bicocca, Monza, Italy.ORCID 0000-0002-6757-6173
Michael BorowitzDepartment of Pediatrics and Pediatric Surgery, Hospital de Niños Roberto del Río, Facultad de Medicina, Universidad de Chile, Santiago, Chile.
Myriam CampbellChilean National Pediatric Oncology Group (PINDA), Santiago, Chile.
Gunnar CarioDepartment of Pediatrics, University Medical Center Schleswig-Holstein, Kiel, Germany.
Giovanni CazzanigaDepartment of Pediatrics and Tettamanti Research Center, Fondazione MBBM (Monza e Brianza per il Bambino e la sua Mamma)/Ospedale San Gerardo, University of Milano-Bicocca, Monza, Italy.ORCID 0000-0003-2955-4528
Gabriele EscherichClinic of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Christine J HarrisonTranslational and Clinical Research Institute, Newcastle University Centre for Cancer, Newcastle-upon-Tyne, United Kingdom.
Mats HeymanChildhood Cancer Research Unit, Karolinska Institutet-Astrid Lindgren's Children's Hospital, Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0001-7637-1949
Stephen P HungerDepartment of Pediatrics, Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Philadelphia, PA.ORCID 0000-0002-5492-3957
Csongor KissDepartment of Pediatric Hematology and Oncology, Institute of Pediatrics, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Hsi-Che LiuDivision of Pediatric Hematology-Oncology, MacKay Memorial Hospital-MacKay Children's Hospital, Taipei, Taiwan.ORCID 0000-0001-9721-167X
Franco LocatelliDepartment of Pediatric Hematology and Oncology, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Ospedale Pediatrico Bambino Gesù, Sapienza, Università di Roma, Rome, Italy.
Mignon L LohDepartment of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan.ORCID 0000-0003-4099-4700
Atsushi ManabeDepartment of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan.ORCID 0000-0002-6698-2348
Georg MannChildren's Cancer Research Institute-St Anna Children's Hospital, Department of Pediatrics, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-2258-0822
Rob PietersPrincess Maxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Ching-Hon PuiDepartment of Oncology, St Jude Children's Research Hospital, Memphis, TN.ORCID 0000-0003-0303-5658
Susana RivesPediatric Hematology and Oncology Department, Hospital Sant Joan de Déu de Barcelona-Institut de Recerca Sant Joan de Déu, Barcelona, Spain.ORCID 0000-0002-5658-1831
Kjeld SchmiegelowDepartment of Pediatrics and Adolescent Medicine, University Hospital Rigshospitalet-Institute of Clinical Medicine, Faculty of Medicine, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0002-0829-4993
Lewis B SilvermanDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA.
Jan StaryUniversity Hospital Motol-Second Faculty of Medicine, Charles University, Prague, Czech Republic.
Ajay VoraGreat Ormond Street Hospital, London, United Kingdom; and.
Patrick BrownJohns Hopkins Kimmel Cancer Center, Baltimore, MD.ORCID 0000-0002-8653-1069
University Hospital Schleswig-Holstein · DEHokkaido University · JPUniversity of Milano-Bicocca · ITBambino Gesù Children's Hospital · ITCharles University · CZChildren's Hospital of Philadelphia · USDana-Farber Cancer Institute · USGreat Ormond Street Hospital · GBHospital Roberto del Rio · CLHospital Sant Joan de Déu Barcelona · ESJohns Hopkins University · USKarolinska University Hospital · SEMackay Memorial Hospital · TWNewcastle University · GBPrincess Máxima Center · NLSt Anna Children's Hospital · ATSt. Jude Children's Research Hospital · USUniversität Hamburg · DEUniversité Paris Cité · FRUniversity of Copenhagen · DK

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
NCI NIH HHS P30 CA021765NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899
6 · The paper itself

Abstract

Comparison of treatment strategies in de novo pediatric acute lymphoblastic leukemia (ALL) requires standardized measures of efficacy. Key parameters that define disease-related events, including complete remission (CR), treatment failure (TF; not achieving CR), and relapse (loss of CR) require an updated consensus incorporating modern diagnostics. We collected the definitions of CR, TF, and relapse from recent and current pediatric clinical trials for the treatment of ALL, including the key components of response evaluation (timing, anatomic sites, detection methods, and thresholds) and found significant heterogeneity, most notably in the definition of TF. Representatives of the major international ALL clinical trial groups convened to establish consensus definitions. CR should be defined at a time point no earlier than at the end of induction and should include the reduction of blasts below a specific threshold in bone marrow and extramedullary sites, incorporating minimal residual disease (MRD) techniques for marrow evaluations. TF should be defined as failure to achieve CR by a prespecified time point in therapy. Relapse can only be defined in patients who have achieved CR and must include a specific threshold of leukemic cells in the bone marrow confirmed by MRD, the detection of central nervous system leukemia, or documentation of extramedullary disease. Definitions of TF and relapse should harmonize with eligibility criteria for clinical trials in relapsed/refractory ALL. These consensus definitions will enhance the ability to compare outcomes across pediatric ALL trials and facilitate development of future international collaborative trials.

Indexed as

Precursor Cell Lymphoblastic Leukemia-LymphomaChildHumansNeoplasm, ResidualPonsRecurrenceRemission InductionTreatment Failure

Identifiers

PMID34192312
PMCPMC8952186
OpenAlexW3175846973

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.