Evidence map›Paper›PMID 25425691›Full record

Trial reportHaematologica2015

Low non-relapse mortality and long-term preserved quality of life in older patients undergoing matched related donor allogeneic stem cell transplantation: a prospective multicenter phase II trial.

Didier Blaise, Raynier Devillier, Anne-Gaëlle Lecoroller-Sorriano, Jean-Marie Boher, Agnès Boyer-Chammard, Reza Tabrizi, Patrice Chevallier, Nathalie Fegueux, Anne Sirvent, Mauricette Michallet and 9 more

Open access · goldAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Haematologica, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.1field-weighted citation impact, top 12% 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.

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

17 citing papers in PubMed, 33 citations in OpenAlex.

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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

19 authors at 10 institutions in 2 countries.

Didier BlaiseHematology Department, Transplantation Unit, Paoli Calmettes Institute, Marseille Centre de Recherche sur le Cancer de Marseille (CRCM), Inserm U 1068, Marseille Aix-Marseille University, Marseille blaised@ipc.unicancer.fr.
Raynier DevillierHematology Department, Transplantation Unit, Paoli Calmettes Institute, Marseille Centre de Recherche sur le Cancer de Marseille (CRCM), Inserm U 1068, Marseille Aix-Marseille University, Marseille.
Anne-Gaëlle Lecoroller-SorrianoMixed Research Unit 912, Institute of Research and Development, National Institute of Health and Medical Research, Paoli Calmettes Institute, Aix-Marseille University, Marseille.
Jean-Marie BoherClinical Trial Office and Biostatistics Unit, Paoli Calmettes Institute, Marseille.
Agnès Boyer-ChammardClinical Trial Office and Biostatistics Unit, Paoli Calmettes Institute, Marseille.
Reza TabriziHematology Department, Haut-Leveque Hospital and Bordeaux University Hospital Center, Pessac.
Patrice ChevallierHematology Department, University Hospital Center, Nantes.
Nathalie FegueuxHematology Department, University Hospital Center, Montpellier.
Anne SirventHematology Department, University Hospital Center, Montpellier.
Mauricette MichalletHematology Department, University Hospital Center, Lyon.
Jacques-Olivier BayHematology Department, University Hospital Center, Clermont-Ferrand.
Sabine FürstHematology Department, Transplantation Unit, Paoli Calmettes Institute, Marseille.
Jean El-CheikhHematology Department, Transplantation Unit, Paoli Calmettes Institute, Marseille.
Laure VincentHematology Department, University Hospital Center, Montpellier.
Thierry GuillaumeHematology Department, University Hospital Center, Nantes.
Caroline RegnyHematology Department, University Hospital Center, Grenoble.
Noël MilpiedHematology Department, Haut-Leveque Hospital and Bordeaux University Hospital Center, Pessac.
Luca CastagnaHematology Department, Transplantation Unit, Paoli Calmettes Institute, Marseille.
Mohamad MohtyHematology Department, University Hospital Center, Nantes CRNCA, UMR 892 INSERM - 6299 CNRS, and Université de Nantes, Faculté de Médecine, Nantes, France Hematology and Cellular Therapy Unit, AP-HP, Université Paris 6, Hôpital Saint Antoine, Paris, France.
Institut Paoli-Calmettes · FRCentre Hospitalier Universitaire de Montpellier · FRCentre Hospitalier Universitaire de Nantes · FRHôpital Sainte-Marguerite · FRCentre Hospitalier Universitaire de Bordeaux · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRCentre Hospitalier Universitaire de Grenoble · FRHôpital Cardiologique du Haut-Lévêque · FRHôpital Lyon Sud · FRInstitut de Recherche pour le Développement · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allogeneic transplantation is a challenge in patients of advanced age because of a high risk of non-relapse mortality and potential long-lasting impairment of health-related quality of life. The development of reduced-intensity conditioning regimens has allowed the use of allogeneic transplantation in this population, but the optimal regimen remains undefined. We conducted a multicenter phase II trial evaluating the safety and efficacy of a reduced-intensity conditioning regimen combining fludarabine, intravenous busulfan, and rabbit antithymocyte globulins in patients older than 55 years of age transplanted from matched-related donor. In addition, health-related quality of life was prospectively measured. Seventy-five patients with a median age of 60 years (range 55-70) were analyzed. Grade III-IV acute and extensive chronic graft-versus-host diseases were found in 3% and 27% of patients, respectively. The day 100 and 1-year non-relapse mortality incidences were 1% and 9%, respectively. The cumulative incidences of relapse, progression-free survival and overall survival at two years were 36%, 51% and 67%, respectively, with a median follow up of 49 months. Global health-related quality of life, physical functioning, emotional functioning, and social functioning were not impaired compared to baseline for more than 75% of the patients (75%, 81.4%, 82.3%, and 75%, respectively). Thirty-four of the 46 (74%) progression-free patients at one year were living without persistent extensive chronic graft-versus-host disease. We conclude that the reduced-intensity conditioning regimen combining fludarabine, intravenous busulfan, and rabbit antithymocyte globulins is well tolerated in patients older than 55 years with low non-relapse mortality and long-term preserved quality of life.

Indexed as

Quality of LifeAgedFemaleFollow-Up StudiesGraft vs Host DiseaseHematologic NeoplasmsHematopoietic Stem Cell TransplantationHumansMaleMiddle AgedNeoplasm StagingPrognosisProspective StudiesSurvival RateTransplantation ConditioningTransplantation, Homologous

Identifiers

PMID25425691
PMCPMC4803127
OpenAlexW2136483341

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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.