Evidence map›Paper›PMID 28892084›Full record

ArticleBone marrow transplantation2017

Validation of the revised IPSS at transplant in patients with myelodysplastic syndrome/transformed acute myelogenous leukemia receiving allogeneic stem cell transplantation: a retrospective analysis of the EBMT chronic malignancies working party.

C Scheid, L de Wreede, A van Biezen, C Koenecke, G Göhring, L Volin, J Maertens, J Finke, J Passweg, D Beelen and 18 more

Abstract readValidation Study
In one paragraph

Article in Bone marrow transplantation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Allogeneic transplantation for advanced acute leukemia.Hematology. American Society of Hematology. Education Program · 2022
    Article
  5. Room for Improvement: A 20-Year Single Center Experience with Allogeneic Stem Cell Transplantation for Myelodysplastic Syndromes.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2022
    Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. 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

28 authors.

C ScheidDepartment of Medicine, University of Cologne, Cologne, Germany.
L de WreedeDepartment of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, The Netherlands.
A van BiezenDepartment of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, The Netherlands.
C KoeneckeDepartment of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
G GöhringInstitute of Cell and Molecular Pathology, Hannover Medical School, Hannover, Germany.
L VolinStem Cell Transplantation Unit, HUCH Comprehensive Cancer Center, Helsinki, Finland.
J MaertensDepartment of Hematology, University Hospital Gasthuisberg, Leuven, Belgium.
J FinkeDepartment of Medicine-Hematology, Oncology, University of Freiburg, Freiburg, Germany.
J PasswegHematology, University Hospital, Basel, Switzerland.
D BeelenDepartment of Bone Marrow Transplantation, University Hospital, Essen, Germany.
J J CornelissenErasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands.
M Itälä-RemesTD7 (Stem Cell Transplant Unit), Turku University Hospital, Turku, Finland.
P ChevallierDepartment D'Hematologie, CHU Nantes, Nantes, France.
N RussellNottingham University, Nottingham, UK.
E PetersenDepartment of Haematology, University Medical Centre, Utrecht, The Netherlands.
N MilpiedCHU Bordeaux, Hôpital Haut-leveque, Pessac, France.
C Richard EspigaServicio de Hematología-Hemoterapia, Hospital U. Marqués de Valdecilla, Santander, Spain.
A PeniketCancer and Haematology Centre, Churchill Hospital, Oxford, UK.
J SierraHematology Department, Hospital Santa Creu i Sant Pau, Barcelona, Spain.
G MuftiDepartment of Haematological Medicine, GKT School of Medicine, London, UK.
C CrawleyDepartment of Haematology, Addenbrookes Hospital, Cambridge, UK.
J H VeelkenBMT Centre Leiden, Leiden University Hospital, Leiden, The Netherlands.
P LjungmanDepartment of Hematology, Karolinska University Hospital, Stockholm, Sweden.
J Y CahnHématologie Clinique, Hopital A. Michallon, Grenoble, France.
E P AlessandrinoClinica Ematologica, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
T de WitteDepartment of Hematology, Radboud University-Nijmegen Medical Centre, Nijmegen, The Netherlands.
M RobinDepartment of Hematology-BMT, Hopital St. Louis, Paris, France.
N KrögerDepartment of Stem cell Transplantation, University Hospital Eppendorf, Hamburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The International Prognostic Scoring System has been revised (IPSS-R) to predict prognosis of patients with myelodysplastic syndromes at diagnosis. To validate the use of the IPSS-R assessed before transplant rather than at diagnosis we performed a retrospective analysis of the EBMT database. A total of 579 patients had sufficient information available to calculate IPSS-R at transplant. Median overall survival (OS) from transplant was significantly different according to IPSS-R: very low 23.6 months, low 55.0 months, intermediate 19.7 months, high 13.5 months, very high 7.8 months (P<0.001). In a multivariate Cox model the following parameters were significant risk factors for OS: IPSS-R, graft source, age and prior treatment. Median relapse free survival also showed significant differences according to IPSS-R: very low: 23.6 months, low: 24.8 months, intermediate 10.6 months, high 7.9 months, very high 5.5 months (P<0.001). Multivariate risk factors for relapse-free survival (RFS) were: IPSS-R, reduced intensity conditioning, graft source and prior treatment. A trend for an increased relapse incidence was noted for very high risk IPSS-R. We conclude that the IPSS-R at transplant is a useful prognostic score for predicting OS and RFS after transplantation, capturing both disease evolution and response to prior treatment before transplant.

Indexed as

PrognosisAdolescentAdultAgedAged, 80 and overDatabases, FactualDisease-Free SurvivalFemaleHematopoietic Stem Cell TransplantationHumansLeukemia, Myeloid, AcuteMaleMiddle AgedMyelodysplastic SyndromesRetrospective StudiesRisk Factors

Identifiers

PMID28892084
PMCPMC5671928

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Registered trials

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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.