Evidence map›Paper›PMID 31248056›Full record

ArticleCancers2019

Elevated Lactate Dehydrogenase Has Prognostic Relevance in Treatment-Naïve Patients Affected by Chronic Lymphocytic Leukemia with Trisomy 12.

Francesco Autore, Paolo Strati, Idanna Innocenti, Francesco Corrente, Livio Trentin, Agostino Cortelezzi, Carlo Visco, Marta Coscia, Antonio Cuneo, Alessandro Gozzetti and 20 more

Abstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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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

30 authors.

Francesco AutoreInstitute of Hematology, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Roma, Italy. francesco_autore@yahoo.it.
Paolo StratiDepartments of Leukemia, MD Anderson Cancer Centre, 77030 Houston, USA. PStrati@mdanderson.org.
Idanna InnocentiInstitute of Hematology, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Roma, Italy. idanna.innocenti@yahoo.it.
Francesco CorrenteInstitute of Hematology, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Roma, Italy. correns@hotmail.it.
Livio TrentinHematology and Clinical Immunology Unit, Department of Medicine, Università di Padova, 35122 Padova, Italy. livio.trentin@unipd.it.
Agostino CortelezziHematology Unit, IRCCS Ca' Granda Policlinico-Università degli Studi, 55031 Milano, Italy. mchiarat@libero.it.
Carlo ViscoDivision of Hematology, Ospedale San Bortolo di Vicenza, 36100 Vicenza, Italy. carlovisco@hotmail.com.
Marta CosciaDepartment of Molecular Biotechnology and Health Sciences, University of Torino, 10126 Torino, Italy. marta.coscia@unito.it.
Antonio CuneoHematology section, Department of Medical Sciences, Azienda Ospedaliero Universitaria Arcispedale S. Anna, 44124 Ferrara, Italy. a.cuneo@unife.it.
Alessandro GozzettiHematology Unit, Azienda Ospedaliera Universitaria Senese, 53100 Siena, Italy. gozzetti@unisi.it.
Francesca Romana MauroHematology division, Policlinico Umberto I, Università Sapienza, 00161 Roma, Italy. mauro@bce.uniroma1.it.
Anna Maria FrustaciDepartment of Hematology, Ospedale Niguarda, 20162 Milano, Italy. annamaria.frustaci@ospedaleniguarda.it.
Massimo GentileBiothecnology Research Unit, Azienda Ospedaliera di Cosenza, 87100 Cosenza, Italy. massim.gentile@tiscali.it.
Fortunato MorabitoBiothecnology Research Unit, Azienda Ospedaliera di Cosenza, 87100 Cosenza, Italy. fortunato_morabito@tiscali.it.
Stefano MolicaDepartment of Hematology-Oncology, Ospedale Pugliese-Ciacco, 88100 Catanzaro, Italy. smolica@libero.it.
Paolo FalcucciDivision of Hematology, Ospedale Belcolle, 01100 Viterbo, Italy. falcuccipaolo@gmail.com.
Giovanni D'ArenaHematology and Stem cell Transplantation Unit, IRCCS Centro di Riferimento Oncologico della Basilicata, 85028 Rionero in Vulture, Italy. giovannidarena@libero.it.
Roberta MurruHematology and Stem Cell Transplantation Unit, Ospedale A. Businco, 09121 Cagliari, Italy. roberta.murru@tiscali.it.
Donatella VincelliDepartment of Hematology, Azienda Ospedaliera Bianchi-Melacrino-Morelli, 89124 Reggio Calabria, Italy. donatella.vincelli@gmail.com.
Dimitar G EfremovMolecular Hematology, International Centre for Genetic Engineering and Biotechnology, 34149 Trieste, Italy. dimitar.efremov@icgeb.org.
Antonietta FerrettiHematology division, Policlinico Umberto I, Università Sapienza, 00161 Roma, Italy. ferretti@bce.uniroma1.it.
Gian Matteo RigolinHematology section, Department of Medical Sciences, Azienda Ospedaliero Universitaria Arcispedale S. Anna, 44124 Ferrara, Italy. rglgmt@unife.it.
Candida VitaleDepartment of Molecular Biotechnology and Health Sciences, University of Torino, 10126 Torino, Italy. cvitale@unito.it.
Maria Chiara TisiDivision of Hematology, Ospedale San Bortolo di Vicenza, 36100 Vicenza, Italy. mchiarat@libero.it.
Gianluigi RedaHematology Unit, IRCCS Ca' Granda Policlinico-Università degli Studi, 55031 Milano, Italy. gianluigi.reda@policlinico.mi.it.
Andrea VisentinHematology and Clinical Immunology Unit, Department of Medicine, Università di Padova, 35122 Padova, Italy. andrea.visentin@sanita.padova.it.
Simona SicaInstitute of Hematology, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Roma, Italy. simona.sica@unicatt.it.
Robin FoàHematology division, Policlinico Umberto I, Università Sapienza, 00161 Roma, Italy. rfoa@bce.uniroma1.it.
Alessandra FerrajoliDepartments of Leukemia, MD Anderson Cancer Centre, 77030 Houston, USA. aferrajo@mdanderson.org.
Luca LaurentiInstitute of Hematology, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Roma, Italy. luca.laurenti@unicatt.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic Lymphocytic Leukemia (CLL) patients with +12 have been reported to have specific clinical and biologic features. We performed an analysis of the association between demographic; clinical; laboratory; biologic features and outcome in CLL patients with +12 to identify parameters predictive of disease progression; time to treatment; and survival. The study included 487 treatment-naive CLL patients with +12 from 15 academic centers; diagnosed between January 2000 and July 2016; and 816 treatment-naïve patients with absence of Fluorescence In Situ Hybridization (FISH) abnormalities. A cohort of 250 patients with +12 CLL followed at a single US institution was used for external validation. In patients with +12; parameters associated with worse prognosis in the multivariate model were high Lactate DeHydrogenase (LDH) and β-2-microglobulin and unmutated immunoglobulin heavy-chain variable region gene (IGHV). CLL patients with +12 and high LDH levels showed a shorter Progression-Free-Survival (PFS) (30 months vs. 65 months; p < 0.001), Treatment-Free-Survival (TFS) (33 months vs. 69 months; p < 0.001), Overall Survival (OS) (131 months vs. 181 months; p < 0.001) and greater CLL-related mortality (29% vs. 11% at 10 years; p < 0.001) when compared with +12 CLL patients with normal LDH levels. The same differences were observed in the validation cohort. These data suggest that serum LDH levels can predict PFS; TFS; OS and CLL-specific survival in CLL patients with +12.

Indexed as

CLLLDHprognosistrisomy 12

Identifiers

PMID31248056
PMCPMC6678692

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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.