Evidence map›Paper›PMID 39103678›Full record

ArticleLeukemia2024

Transfusion independence after lenalidomide discontinuation in patients with del(5q) myelodysplastic neoplasm: a HARMONY Alliance study.

Elena Crisà, Elvira Mora, Ulrich Germing, Cecile Bally, Maria Diez Campelo, Mikko Myllymäki, Martin Jädersten, Rami Komrokji, Uwe Platzbecker, Detlef Haase and 34 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Leukemia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Trial
  2. Review
  3. 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

44 authors.

Elena Crisà *Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy. elena.crisa@ircc.it.ORCID 0000-0003-1912-0574
Elvira MoraHospital Universitario y Politécnico La Fe, Instituto de Investigación Sanitaria La Fe, Valencia, Spain.
Ulrich GermingDepartment of Hematology, Oncology and Clinical Immunology, Universitätsklinik Düsseldorf, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
Cecile BallyHématologie clinique, hôpital Necker. Assistance publique hôpitaux de Paris (APHP), Paris, France.
Maria Diez CampeloHematology, Institute for Biomedical Research of Salamanca (IBSAL), University Hospital of Salamanca, Salamanca, Spain.
Mikko MyllymäkiHematology Research Unit Helsinki, University of Helsinki and Helsinki University Hospital Comprehensive Cancer Center, Helsinki, Finland.
Martin JäderstenDepartment of Hematology M64 Karolinska University Hospital, Stockholm, Sweden.
Rami KomrokjiMalignant Hematology Department, Moffitt Cancer Center, Tampa, FL, USA.ORCID 0000-0002-1876-5269
Uwe PlatzbeckerDepartment of Hematology, Cellular Therapy,Hemostaseology and Infectiology, University Hospital Leipzig, Leipzig, Germany.ORCID 0000-0003-1863-3239
Detlef HaaseClinics of Hematology and Medical Oncology, University Medical Center Göttingen, Göttingen, Germany.
Wolf-Karsten HofmannDepartment of Hematology and Oncology, University Hospital Mannheim, Heidelberg University, Heidelberg, Germany.
Najla H Al AliMalignant Hematology Department, Moffitt Cancer Center, Tampa, FL, USA.
Daniela BarracoFondazione Sindromi Mielodisplastiche FISiM-ETS, Bologna, Italy.
Juan José BargayHematology Department. Hospital Son Llatzer, Mallorca, Spain.
Teresa BernalHematology Department. Hospital Central de Asturias, Oviedo, Spain.
Felix López CadenasHematology Department. Hospital Clinico Universitario de Salamanca, Salamanca, Spain.
Anna CalvisiFondazione Sindromi Mielodisplastiche FISiM-ETS, Bologna, Italy.
Isabella CapodannoFondazione Sindromi Mielodisplastiche FISiM-ETS, Bologna, Italy.
Marco CerranoHematology-University Hospital Città della Salute e della Scienza, Turin, Italy.ORCID 0000-0003-1666-3100
Rosanna CianciaFondazione Sindromi Mielodisplastiche FISiM-ETS, Bologna, Italy.
Monica CrugnolaFondazione Sindromi Mielodisplastiche FISiM-ETS, Bologna, Italy.
Andrea KündgenDepartment of Hematology, Oncology and Clinical Immunology, Universitätsklinik Düsseldorf, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
Carlo FinelliFondazione Sindromi Mielodisplastiche FISiM-ETS, Bologna, Italy.ORCID 0000-0001-9372-1197
Claudio FozzaFondazione Sindromi Mielodisplastiche FISiM-ETS, Bologna, Italy.
Chiara FrairiaFondazione Sindromi Mielodisplastiche FISiM-ETS, Bologna, Italy.
Ebeling FrejaDepartment of Medicine, Helsinki University Central Hospital, Helsinki, Finland.
Christina GansterClinics of Hematology and Medical Oncology, University Medical Center Göttingen, Göttingen, Germany.ORCID 0000-0002-7566-5985
Anne Sophie KubaschDepartment of Hematology, Cellular Therapy,Hemostaseology and Infectiology, University Hospital Leipzig, Leipzig, Germany.ORCID 0000-0002-0747-4941
Maria Jose JimenezHematology Department. Hospital Gemans Trias i Pujol, Badalona, Spain.ORCID 0000-0002-5469-5237
Roberto LatagliataUnità Operativa Complessa (UOC) Ematologia, Ospedale Belcolle, Viterbo and Division of Cellular Biotechnology and Hematology, Sapienza University, Rome, Italy.
Francisca Hernandez MohedoHematology Department. Hopital Unversitario Virgen de las Nieves, Granada, Spain.
Antonieta MoleroHematology Department. Hospital Universitario Vall D'Hebron, Barcelona, Spain.
Miriam Vara PampliegaHematology Department. Hospital de Cruces, Barakaldo, Spain.
Clara Aparicio PerezHematology Department. Hospital Universitario Reina Sofia, Cordoba, Spain.ORCID 0009-0007-9283-6188
Giuseppe PietrantuonoFondazione Sindromi Mielodisplastiche FISiM-ETS, Bologna, Italy.
Antonella PoloniFondazione Sindromi Mielodisplastiche FISiM-ETS, Bologna, Italy.ORCID 0000-0002-4221-4125
Helena PomaresHematology Department. ICO Duran i Reynals, L'Hospitalet de LLobregat, LLobregat, Spain.
Valle RecasensValle Recasens. Hematology Department. Hospital Miguel Servent, Zaragoza, Spain.ORCID 0000-0001-5129-8597
Axel RüferDivision of Hematology, Luzerner Kantonsspital-in association with University Luzern, Luzern, Switzerland.
Alessio SignoriDepartment of Health Sciences - Section of Biostatistics University of Genoa, Genova, Italy.
Eva Hellstrom-LindbergHematology Research Unit Helsinki, University of Helsinki and Helsinki University Hospital Comprehensive Cancer Center, Helsinki, Finland.ORCID 0000-0002-7839-3743
Pierre FenauxService d'Hématologie Séniors, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris, Paris, France.
Guillermo SanzHematology, Institute for Biomedical Research of Salamanca (IBSAL), University Hospital of Salamanca, Salamanca, Spain.ORCID 0000-0002-2767-8191
Valeria Santini *Fondazione Sindromi Mielodisplastiche FISiM-ETS, Bologna, Italy. valeria.santini@unifi.it.ORCID 0000-0002-5439-2172

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lenalidomide (LEN) can induce red blood cell-transfusion independence (RBC-TI) in 60-70% of del(5q) myelodysplastic neoplasm (MDS) patients. Current recommendation is to continue LEN in responding patients until failure or progression, with likelihood of toxicity and a high cost for healthcare systems. This HARMONY Alliance study investigated the outcome of MDS del(5q) patients who discontinued LEN while RBC-transfusion independent. We enrolled 118 patients with IPSS-R low-intermediate risk. Seventy patients (59%) discontinued LEN for intolerance, 38 (32%) per their physician decision, nine (8%) per their own decision and one (1%) for unknown reasons. After a median follow-up of 49 months from discontinuation, 50/118 patients lost RBC-TI and 22/30 who underwent cytogenetic re-evaluation lost complete cytogenetic response. The median RBC-TI duration was 56 months. In multivariate analysis, RBC-TI duration after LEN discontinuation correlated with low transfusion burden before LEN therapy, treatment ≥ 12 LEN cycles, younger age and higher Hb level at LEN withdrawal. Forty-eight patients were re-treated with LEN for loss of response and 28 achieved again RBC-TI. These data show that stopping LEN therapy in MDS del(5q) patients who reached RBC-TI allows prolonged maintenance of TI in a large subset of patients.

Indexed as

Chromosome DeletionChromosomes, Human, Pair 5LenalidomideMyelodysplastic SyndromesThalidomideAdultAgedAged, 80 and overBlood TransfusionErythrocyte TransfusionFemaleFollow-Up StudiesHumansMaleMiddle AgedLenalidomideThalidomide

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