Evidence map›Paper›PMID 40289118›Full record

ArticleBMC cancer2025

Autologous stem cell transplantation for adults with Philadelphia-negative acute lymphoblastic leukemia in first complete remission. A study by the Acute Leukemia Working Party of the EBMT.

Ryszard Swoboda, Myriam Labopin, Sebastian Giebel, Johan Maertens, Elena Parovichnikova, Jurjen Versluis, Jiri Pavlu, Anna Kopinska, Saveria Capria, Ludek Raida and 12 more

Abstract read
In one paragraph

Article in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Review
  2. 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

22 authors.

Ryszard SwobodaDepartment of Bone Marrow Transplantation and Onco-Hematology, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch, Str. Wybrzeze Armii Krajowej 15, Gliwice, 44-101, Poland. ryszard.swoboda@gliwice.nio.gov.pl.
Myriam LabopinDepartment of Hematology and Cellular Therapy, National Institute of Health and Medical Research Unit UMR-S 938, Sorbonne University and St Anthony Scientific Research Center, Public Assistance Hospital of Paris, St Anthony Hospital, Paris, France.
Sebastian GiebelDepartment of Bone Marrow Transplantation and Onco-Hematology, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice Branch, Str. Wybrzeze Armii Krajowej 15, Gliwice, 44-101, Poland.
Johan MaertensDepartment of Hematology, University Hospital Gasthuisberg, Leuven, Belgium.
Elena ParovichnikovaNational Research Center for Hematology, Bone Marrow Transplantation, Moscow, Russian Federation.
Jurjen VersluisDepartment of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Jiri PavluDepartment of Haematology, Imperial College, Hammersmith Hospital, London, UK.
Anna KopinskaDepartment of Hematology and Bone Marrow Transplantation, Medical University of Silesia, Katowice, Poland.
Saveria CapriaUniv. La Sapienza, Dip. Biotecnologie Cellulari ed Ematologia, Rome, Italy.
Ludek RaidaDepartment of Haemato-Oncology, Olomouc University Hospital and Faculty of Medicine and Dentistry, Palacký University, Olomouc, Czech Republic.
Alessandro RambaldiDepartment of Oncology and Hematology, University of Milan and Azienda Socio-Sanitaria Territoriale Papa Giovanni XXIII, Milan, Italy.
Denis CaillotHopital d'Enfants, CHU de Dijon, Service Hematologie Adultes, Dijon, France.
Frantisek FolberDepartment of Internal Medicine, Hematology and Oncology, Masaryk University Hospital Brno, Brno, Czech Republic.
David NachbaurDepartment of Internal Medicine V (Hematology and Medical Oncology), Medical University of Innsbruck, Anichstrasse 35, Innsbruck, A- 6020, Austria.
Mustafa OzturkGATA BMT Center, Gülhane Military Medical Academy, Ankara, Turkey.
Mahmoud AljurfKing Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.
Marie Thérèse RubioDepartment of Hematology, CHU Brabois, Nancy, France.
Norbert Claude GorinDepartment of Hematology, Hôpital Saint-Antoine, Paris, France.
Francesco LanzaHematology Unit, University Hospital and Romagna Transplant Network, Ravenna, University of Bologna, Bologna, Italy.
Arnon NaglerDivision of Hematology, Sheba Medical Center, Tel Hashomer, Israel.
Mohamad MohtyDepartment of Hematology and Cellular Therapy, National Institute of Health and Medical Research Unit UMR-S 938, Sorbonne University and St Anthony Scientific Research Center, Public Assistance Hospital of Paris, St Anthony Hospital, Paris, France.
Fabio CiceriOspedale San Raffaele s.r.l., Haematology and BMT, Milano, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe role of autologous hematopoietic stem cell transplantation (AHSCT) in adults with Philadelphia chromosome-negative acute lymphoblastic leukemia (Ph-ALL) remains controversial. The aim of this retrospective study was to analyze results of AHSCT and to identify prognostic factors.

methodsOverall, 700 patients transplanted in first complete remission between the years 1999-2020 were included. Median patient age was 31.9 years (68% male). B-cell precursor ALL (BCP-ALL) and T-cell precursor ALL (TCP-ALL) was diagnosed in 35% and 65%, respectively. Among 190 patients with available data, negative minimal residual disease (MRD) status was reported in 167 (88%) cases.

resultsThe probabilities of overall survival (OS) and leukemia-free survival (LFS) at 2 years were 67% and 56%; relapse incidence (RI) and non-relapse mortality (NRM) were 39% and 5%, respectively. TCP-ALL was associated with lower RI (41% vs. 56%, p=0.001), higher LFS (52% vs. 38%, p=0.002) and OS (58% vs 45%, p=0.001) at 5 years when compared to BCP-ALL. In the multivariate analysis, TCP-ALL and longer interval from diagnosis do AHSCT were associated with reduced risk of relapse (HR 0.7, p=0.006 and HR=0.95, p=0.018), better LFS (HR=0.76, p=0.02 and HR=0.95, p=0.01) and OS (HR=0.75, p=0.024 and HR=0.94, p=0.013, respectively). Increasing patient age was associated with higher NRM (HR=1.49, p<0.0001), worse LFS (HR=1.1, p=0.01) and OS (HR=1.17, p=0.0001).

conclusionsAutologous hematopoietic stem cell transplantation is relatively safe option of late treatment intensification in adults with Ph- ALL. It may be a valuable option especially in patients with TCP-ALL, however it should be proved in prospective clinical trials.

Indexed as

Hematopoietic Stem Cell TransplantationPrecursor Cell Lymphoblastic Leukemia-LymphomaAdolescentAdultFemaleHumansMaleMiddle AgedNeoplasm, ResidualPhiladelphia ChromosomePrognosisRemission InductionRetrospective StudiesTransplantation, AutologousYoung AdultAutologous stem cell transplantationComplete remissionPhiladelphia negative acute lymphoblastic leukemia

Identifiers

PMID40289118
PMCPMC12036279

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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.