Evidence map›Paper›PMID 38199608›Full record

ArticleJournal for immunotherapy of cancer2024

Endothelial Activation and Stress Index (EASIX) to predict mortality after allogeneic stem cell transplantation: a prospective study.

Olaf Penack, Thomas Luft, Christophe Peczynski, Axel Benner, Simona Sica, Mutlu Arat, Maija Itäla-Remes, Lucia López Corral, Nicolaas P M Schaap, Michal Karas and 12 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Journal for immunotherapy of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
13.6field-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.

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

37 citing papers in PubMed, 30 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

22 authors at 18 institutions in 13 countries.

Olaf PenackDepartment for Haematology, Oncology and Tumorimmunology, Charité Universitätsmedizin Berlin, Berlin, Germany olaf.penack@charite.de.ORCID 0000-0003-4876-802X
Thomas LuftMedicine V, University Hospital Heidelberg, Heidelberg, Germany.
Christophe PeczynskiEBMT Transplant Complications Working Party, Paris, France.
Axel BennerGerman Cancer Research Centre, Heidelberg, Germany.
Simona SicaIstituto di Ematologia, Universita Cattolica S. Cuore, Rome, Italy.
Mutlu AratFlorence Nightingale Hospital, Hematopoietic SCT Unit, Demiroglu Bilim University Istanbul, Istanbul, Turkey.
Maija Itäla-RemesTurku University Hospital FI, Turku, Finland.
Lucia López CorralDepartment for Haematology, Hospital Clinico San Carlos, Salamanca, Spain.
Nicolaas P M SchaapDepartment of Hematology, Radboudumc, Nijmegen, The Netherlands.
Michal KarasHospital Dept. of Hematology/Oncology, Charles University, Pilsen, Czech Republic.
Ludek RaidaOlomouc University Social Health Institute, Olomouc, Czech Republic.
Thomas SchroederDept. of Hematology and Stem Cell Transplantation, University Hospital Essen, Essen, Germany.
Peter DregerMedicine V, University Hospital Heidelberg, Heidelberg, Germany.
Elisabetta MetafuniIstituto di Ematologia, Universita Cattolica S. Cuore, Rome, Italy.
Tulay OzcelikFlorence Nightingale Hospital, Hematopoietic SCT Unit, Demiroglu Bilim University Istanbul, Istanbul, Turkey.
Brenda M SandmaierUniversity of Washington, Seattle, Washington, USA.
Lambros KordelasDept. of Hematology and Stem Cell Transplantation, University Hospital Essen, Essen, Germany.
Ivan MoiseevEBMT Transplant Complications Working Party, Paris, France.
Hélène SchoemansEBMT Transplant Complications Working Party, Paris, France.
Christian KoeneckeHematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
Grzegorz W BasakEBMT Transplant Complications Working Party, Paris, France.
Zinaida PericEBMT Transplant Complications Working Party, Paris, France.
Essen University Hospital · DEHeidelberg University · DEIstanbul Bilim University · TRUniversità Cattolica del Sacro Cuore · ITCharité - Universitätsmedizin Berlin · DECharles University · CZEuropean Society for Blood and Marrow Transplantation · FRFirst Pavlov State Medical University of St. Petersburg · RUGerman Cancer Research Center · DEHospital Clínico San Carlos · ESMedical University of Warsaw · PLMedizinische Hochschule Hannover · DERadboud University Nijmegen · NLSorbonne Université · FRTurku University Hospital · FIUniversity Hospital Olomouc · CZUniversity of Rijeka · HRUniversity of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe previously reported that the "Endothelial Activation and Stress Index" (EASIX; ((creatinine×lactate dehydrogenase)÷thrombocytes)) measured before start of conditioning predicts mortality after allogeneic hematopoietic stem cell transplantation (alloSCT) when used as continuous score. For broad clinical implementation, a prospectively validated EASIX-pre cut-off is needed that defines a high-risk cohort and is easy to use.

methodIn the current study, we first performed a retrospective cohort analysis in n=2022 alloSCT recipients and identified an optimal cut-off for predicting non-relapse mortality (NRM) as EASIX-pre=3. For cut-off validation, we conducted a multicenter prospective study with inclusion of n=317 first alloSCTs from peripheral blood stem cell in adult patients with acute leukemia, lymphoma or myelodysplastic syndrome/myeloproliferative neoplasms in the European Society for Blood and Marrow Transplantation network.

resultsTwenty-three % (n=74) of alloSCT recipients had EASIX-pre ≥3 taken before conditioning. NRM at 2 years was 31.1% in the high EASIX group versus 11.5% in the low EASIX group (p<0.001). Patients with high EASIX-pre also had worse 2 years overall survival (51.6% vs 70.9%; p=0.002). We were able to validate the cut-off and found that EASIX ≥3 was associated with more than twofold increased risk for NRM in multivariate analysis (HR=2.18, 95% CI 1.2 to 3.94; p=0.01). No statistically significant difference could be observed for the incidence of relapse.

conclusionsThe results of this study provide a prospectively validated standard laboratory biomarker index to estimate the transplant-related mortality risk after alloSCT. EASIX ≥3 taken before conditioning identifies a population of alloSCT recipients who have a more than twofold increased risk of treatment-related mortality.

Indexed as

Hematopoietic Stem Cell TransplantationAdultBlood PlateletsCreatinineHumansProspective StudiesRetrospective StudiesCreatinineHematologic NeoplasmsImmunotherapyInflammation

Identifiers

PMID38199608
PMCPMC10806535
OpenAlexW4390700812

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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.