Evidence map›Paper›PMID 30626425›Full record

Trial reportJournal of hematology & oncology2019

Prognostic or predictive value of circulating cytokines and angiogenic factors for initial treatment of multiple myeloma in the GIMEMA MM0305 randomized controlled trial.

Ilaria Saltarella, Fortunato Morabito, Nicola Giuliani, Carolina Terragna, Paola Omedè, Antonio Palumbo, Sara Bringhen, Lorenzo De Paoli, Enrica Martino, Alessandra Larocca and 19 more

Registry-linked trialAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of hematology & oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01063179 (A PHASE III, MULTI-CENTER, RANDOMIZED OPEN LABEL STUDY OF VELCADE, MELPHALAN, PREDNISONE AND THALIDOMIDE), which is not on this map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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.

NCT01063179 phase3completednot on this map

A PHASE III, MULTI-CENTER, RANDOMIZED OPEN LABEL STUDY OF VELCADE, MELPHALAN, PREDNISONE AND THALIDOMIDE (V-MPT) Versus VELCADE, MELPHALAN, PREDNISONE (V-MP) IN ELDERLY UNTREATED MULTIPLE MYELOMA PATIENTS

TypeinterventionalSponsorFondazione EMN Italy OnlusRan2006 to 2014Enrolled511ConditionsMultiple MyelomaArmsBortezomib, Melphalan, Prednisone, Thalidomide, Bortezomib, Melphalan, Prednisone
3 · Its place in the literature

Who cites it

26 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. [Latest Findings on the Mechanism of the Interaction Between Multiple Myeloma Cells and Bone Marrow Microenvironment].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2023
    Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
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  19. Review
  20. Review
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

29 authors.

Ilaria SaltarellaDepartment of Biomedical Science and Human Oncology, University of Bari "Aldo Moro" Medical School, Bari, Italy.
Fortunato MorabitoBiothecnology Research Unit, Aprigliano, Cosenza, Italy.
Nicola GiulianiDepartment of Clinical and Experimental Medicine, Myeloma Unit, University of Parma, Parma, Italy.
Carolina Terragna"Seràgnoli" Institute of Hematology, Department of Experimental, Diagnostic and Specialty Medicine (DIMES), Bologna University School of Medicine, Bologna, Italy.
Paola OmedèDivision of Hematology, University of Torino, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino, Turin, Italy.
Antonio PalumboDivision of Hematology, University of Torino, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino, Turin, Italy.
Sara BringhenDivision of Hematology, University of Torino, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino, Turin, Italy.
Lorenzo De PaoliUniversità degli Studi del Piemonte Orientale, Novara, Italy.
Enrica MartinoDivision of Hematology, AOU "Policlinico-Vittorio Emanuele", Catania, Italy.
Alessandra LaroccaDivision of Hematology, University of Torino, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino, Turin, Italy.
Massimo OffidaniHematology Unit A.O.U. Ospedali Riuniti, Ancona, Italy.
Francesca PatriarcaDAME, University of Udine, Udine, Italy.
Chiara NozzoliCellular Therapies and Transfusion Medicine Unit, AOU Careggi, Florence, Italy.
Tommasina GuglielmelliA.O. San Luigi, Gonzaga, Orbassano, Turin, Italy.
Giulia BenevoloSC Hematology AO Città della Salute e della Scienza, Turin, Italy.
Vincenzo CalleaDivisione di Ematologia, Ospedali Riuniti, Reggio di Calabria, Italy.
Luca BaldiniHematology Unit, Fondazione IRCCS, Cà Granda, OM Policlinico, DIPO, University of Milan, Milan, Italy.
Mariella GrassoA.O. S. Croce e Carle, Cuneo, Italy.
Giovanna LeonardiDepartment of Oncology and Hematology AOU, Hematology Unit, Modena, Italy.
Manuela RizzoUniversity Tor Vergata, Rome, Italy.
Antonietta Pia FalconeIRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy.
Daniela GottardiA.O.U. S. Giovanni Battista A.O. Mauriziano-Umberto I, Turin, Italy.
Vittorio MontefuscoIRCCS Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy.
Pellegrino MustoIRCCS Centro di Riferimento Oncologico della Basilicata, Rionero in Vulture, Italy.
Maria Teresa PetrucciHematology, Department of Cellular Biotechnologies and Hematology, Sapienza University of Rome, Rome, Italy.
Franco DammaccoDepartment of Biomedical Science and Human Oncology, University of Bari "Aldo Moro" Medical School, Bari, Italy.
Mario BoccadoroDivision of Hematology, University of Torino, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino, Turin, Italy.
Angelo VaccaDepartment of Biomedical Science and Human Oncology, University of Bari "Aldo Moro" Medical School, Bari, Italy.
Roberto RiaDepartment of Biomedical Science and Human Oncology, University of Bari "Aldo Moro" Medical School, Bari, Italy. roberto.ria@uniba.it.ORCID 0000-0002-1515-0090

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSeveral new drugs are approved for treatment of patients with multiple myeloma (MM), but no validated biomarkers are available for the prediction of a clinical outcome. We aimed to establish whether pretreatment blood and bone marrow plasma concentrations of major cytokines and angiogenic factors (CAFs) of patients from a phase 3 trial of a MM treatment could have a prognostic and predictive value in terms of response to therapy and progression-free and overall survival and whether these patients could be stratified for their prognosis.

methodsBlood and bone marrow plasma levels of Ang-2, FGF-2, HGF, VEGF, PDGF-β, IL-8, TNF-α, TIMP-1, and TIMP-2 were determined at diagnosis in MM patients enrolled in the GIMEMA MM0305 randomized controlled trial by an enzyme-linked immunosorbent assay (ELISA). These levels were correlated both reciprocally and with the type of therapy and patients' characteristics and with a group of non-MM patients as controls.

resultsNo significant differences were detected between the blood and bone marrow plasma levels of angiogenic cytokines. A cutoff for each CAF was established. The therapeutic response of patients with blood plasma levels of CAFs lower than the cutoff was better than the response of those with higher levels in terms of percentage of responding patients and quality of response.

conclusionFGF-2, HGF, VEGF, and PDGF-β plasma levels at diagnosis have predictive significance for response to treatment. The stratification of patients based on the levels of CAFs at diagnosis and their variations after therapy is useful to characterize different risk groups concerning outcome and response to therapy.

trial registrationClinical trial information can be found at the following link: NCT01063179.

Indexed as

AgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsBecaplerminBiomarkers, TumorBone MarrowFemaleFibroblast Growth Factor 2Follow-Up StudiesHepatocyte Growth FactorHumansLogistic ModelsMaleMiddle AgedMultiple MyelomaPrognosisBecaplerminBiomarkers, TumorFibroblast Growth Factor 2Hepatocyte Growth FactorHGF protein, humanVascular Endothelial Growth Factor AVEGFA protein, humanAngiogenic factorsMultiple myelomaOverall survivalProgression-free survivalResponse rate

Identifiers

PMID30626425
PMCPMC6327520

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Registered trials

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.