Evidence map›Paper›PMID 42056024›Full record

ArticleBritish journal of haematology2026

Prospective implementation of the HCT frailty scale in adults with lymphoproliferative syndromes candidates for autologous haematopoietic stem cell transplantation: Results from a multicentre GETH-TC study.

Javier Cornago, Mónica Baile, Marina Acera, Laura Fox, María Del Mar Pérez-Artigas, Ana Santamaría, María Del Carmen Quintela, Andrés Sánchez-Salinas, Joaquina M Salmerón, Verónica Illana and 21 more

Abstract readMulticenter Study
In one paragraph

Article in British journal of haematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

31 authors.

Javier CornagoHospital Universitario Fundación Jiménez Díaz, Instituto Investigación Sanitaria FJD, Madrid, Spain.ORCID https://orcid.org/0000-0002-0737-4211
Mónica BaileComplejo Asistencial Universitario de Salamanca/IBSAL, Salamanca, Spain.
Marina AceraComplejo Asistencial Universitario de Salamanca/IBSAL, Salamanca, Spain.
Laura FoxHospital Universitari Vall d'Hebron, Barcelona, Spain.
María Del Mar Pérez-ArtigasHospital Universitari Vall d'Hebron, Barcelona, Spain.
Ana SantamaríaHospital Álvaro Cunqueiro, Vigo, Pontevedra, Spain.
María Del Carmen QuintelaHospital Álvaro Cunqueiro, Vigo, Pontevedra, Spain.
Andrés Sánchez-SalinasH.C.U. Virgen de la Arrixaca, Murcia, Spain.
Joaquina M SalmerónH.C.U. Virgen de la Arrixaca, Murcia, Spain.
Verónica IllanaHospital Universitario de la Princesa, Madrid, Spain.
Zahra Abdallahi-LefdilHospital Universitario de la Princesa, Madrid, Spain.
Laura PardoHospital Universitario Fundación Jiménez Díaz, Instituto Investigación Sanitaria FJD, Madrid, Spain.
Laura SolánHospital Universitario Fundación Jiménez Díaz, Instituto Investigación Sanitaria FJD, Madrid, Spain.
José Luis López-LorenzoHospital Universitario Fundación Jiménez Díaz, Instituto Investigación Sanitaria FJD, Madrid, Spain.
Sara Fernández-LuisHospital Universitario Marqués de Valdecilla, Santander, Spain.
Leddy Patricia VegaHospital Universitario Marqués de Valdecilla, Santander, Spain.
Sara VillarClínica Universidad de Navarra, Pamplona, Spain.ORCID https://orcid.org/0000-0002-4761-6692
Patricia Beorlegui-MurilloClínica Universidad de Navarra, Pamplona, Spain.
Mónica MolinaHospital Clínic de Barcelona, Barcelona, Spain.
Albert EsquirolHospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Isabel IzquierdoHospital Miguel Servet, Zaragoza, Spain.ORCID https://orcid.org/0000-0002-3599-4901
Julia RibesInstitut Català d'Oncologia-Hospital Duran i Reynals, L'Hospitalet del Llobregat, Barcelona, Spain.
Alberto MussettiInstitut Català d'Oncologia-Hospital Duran i Reynals, L'Hospitalet del Llobregat, Barcelona, Spain.
Esperanza LavillaHospital Universitario Lucus Augusti, Lugo, Spain.
Olga AldaHospital Universitario de Alicante, Alicante, Spain.
Javier López-MarínHospital Universitario de Alicante, Alicante, Spain.
Leyre BentoHospital Universitario Son Espases, Palma de Mallorca, Spain.
Silvia FilaferroGrupo Español de Trasplante de Progenitores Hematopoyéticos y Terapia Celular, Spain.
Pascual BalsalobreGrupo Español de Trasplante de Progenitores Hematopoyéticos y Terapia Celular, Spain.
Anna SuredaInstitut Català d'Oncologia-Hospital Duran i Reynals, L'Hospitalet del Llobregat, Barcelona, Spain.
María Queralt SalasHospital Clínic de Barcelona, Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This prospective study evaluated the incidence and dynamics of frailty in 156 adults with lymphoproliferative syndromes undergoing autologous haematopoietic stem cell transplantation (HSCT). Frailty was assessed using the haematopoietic cell transplantation (HCT) frailty scale in patients from 15 Spanish institutions at initial consultation, transplant admission and day +100. Quality of life (QoL) was measured using the EuroQoL. At first consultation, 45 patients (28.8%) were classified as fit, 93 (59.6%) as pre-frail and 18 (11.6%) as frail. Frailty was more frequent among older patients, those with Karnofsky performance status (KPS) below 90%, and abnormal Mini-Cog scores (<3). Rates of relapse, death, readmission and median hospital stay were similar across frailty groups. However, frail patients reported significantly worse QoL. One-year non-relapse mortality was higher in frail patients than in pre-frail and fit patients, although differences were not statistically significant (p = 0.19). At day +100, 33.6% of patients were fit, 57.9% pre-frail and 8.5% frail, demonstrating significant transitions in frailty over time (p = 0.001). Moreover, frail patients showed lower relapse-free [53.3% (17.7-79.6) vs. 85.3% (68.3-93.6), p = 0.05] and overall survival [77.8% (36.5-93.9) vs. 100%, p = 0.16], and worse perceived QoL than fit ones. Overall, frailty was dynamic and clinically relevant, supporting routine assessment and targeted interventions to mitigate adverse outcomes.

Indexed as

FrailtyHematopoietic Stem Cell TransplantationLymphoproliferative DisordersAdultAgedFemaleHumansMaleMiddle AgedProspective StudiesQuality of LifeTransplantation, Autologousautologous haematopoietic stem cell transplantationdynamic assessmentfrailtylymphoproliferative syndromequality of life

Identifiers

PMID42056024
PMCPMC13340484

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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.