Evidence map›Paper›PMID 37731147›Full record

ArticleAnnals of hematology2024

A real-life study of daratumumab-bortezomib-dexamethasone (D-VD) in lenalidomide exposed/refractory multiple myeloma patients: a report from the Triveneto Myeloma Working Group.

Gregorio Barilà, Francesca Maria Quaglia, Anna Furlan, Norbert Pescosta, Angela Bonalumi, Chiara Marcon, Anna Pascarella, Martina Tinelli, Elena De March, Albana Lico and 14 more

Open access · hybridAbstract read
In one paragraph

Article in Annals of hematology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Observational
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

24 authors at 9 institutions in 1 country.

Gregorio BarilàHematology Unit, San Bortolo Hospital, Vicenza, Italy.
Francesca Maria QuagliaHematology Unit, Azienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.
Anna FurlanHematology Unit, Santa Maria di Ca' Foncello Hospital, Treviso, Italy.
Norbert PescostaEmatologia e Centro TMO, Ospedale Centrale Bolzano, Bozen, Italy.
Angela BonalumiHematology Unit, Azienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.
Chiara MarconHematology and Transplant Center Unit, Udine University Hospital, DAME, University of Udine, Udine, Italy.
Anna PascarellaHematology Unit, Ospedale dell'Angelo, Mestre-Venezia, Italy.
Martina TinelliHematology Unit, Azienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.
Elena De MarchDepartment of Medicine, Section of Hematology, Belluno Hospital, Belluno, Italy.
Albana LicoHematology Unit, San Bortolo Hospital, Vicenza, Italy.
Roberto SartoriDepartment of Clinical and Experimental Oncology, Onco-hematology Unit, Veneto Institute of Oncology, IOV-IRCCS, Castelfranco Veneto (TV), Italy.
Cristina ClissaHematology Unit, Azienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.
Giovanni De SabbataStruttura Complessa Ematologia, Azienda Sanitaria Universitaria Giuliano Isontina, Trieste, Italy.
Davide NappiEmatologia e Centro TMO, Ospedale Centrale Bolzano, Bozen, Italy.
Marika PorrazzoStruttura Complessa Ematologia, Azienda Sanitaria Universitaria Giuliano Isontina, Trieste, Italy.
Roberta De MarchiDepartment of Clinical and Experimental Oncology, Onco-hematology Unit, Veneto Institute of Oncology, IOV-IRCCS, Castelfranco Veneto (TV), Italy.
Laura PavanDepartment of Medicine (DIMED), Hematology and Clinical Immunology section, Padova University School of Medicine, Via Giustiniani 2, 35128, Padua, Italy.
Alberto TosettoHematology Unit, San Bortolo Hospital, Vicenza, Italy.
Filippo GherlinzoniHematology Unit, Santa Maria di Ca' Foncello Hospital, Treviso, Italy.
Mauro KramperaHematology Unit, Azienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.
Renato BassanHematology Unit, Ospedale dell'Angelo, Mestre-Venezia, Italy.
Francesca PatriarcaHematology and Transplant Center Unit, Udine University Hospital, DAME, University of Udine, Udine, Italy.
Gianpietro SemenzatoDepartment of Medicine (DIMED), Hematology and Clinical Immunology section, Padova University School of Medicine, Via Giustiniani 2, 35128, Padua, Italy.
Renato ZambelloDepartment of Medicine (DIMED), Hematology and Clinical Immunology section, Padova University School of Medicine, Via Giustiniani 2, 35128, Padua, Italy. r.zambello@unipd.it.
Azienda Ospedaliera Universitaria Integrata Verona · ITOspedale San Bortolo · ITUniversity of Padua · ITAzienda Sanitaria Universitaria Integrata di Trieste · ITCa' Foncello Hospital · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITOspedale dell' Angelo · ITOspedale di Bolzano · ITUniversity of Udine · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Treatment of lenalidomide refractory (Len-R) multiple myeloma (MM) patients still represents an unmet clinical need. In the last years, daratumumab-bortezomib-dexamethasone (D-VD) combination was extensively used in this setting, even though only a small fraction of Len-R patients was included in the pivotal trial. This real-life study aimed to evaluate the efficacy and safety of the D-VD regimen in a cohort that exclusively enrolled Len exposed or refractory MM patients. The study cohort included 57 patients affected by relapsed/refractory MM. All patients were previously exposed to Len, with 77.2% being refractory. The overall response rate (ORR) was 79.6% with 43% of cases obtaining at least a very good partial response (VGPR). The D-VD regimen showed a favorable safety profile, with low frequency of grade 3-4 adverse events, except for thrombocytopenia observed in 21.4% of patients. With a median follow-up of 13 months, median progression-free survival (PFS) was 17 months. No significant PFS differences were observed according to age, ISS, LDH levels, type of relapse, and high-risk FISH. Len exposed patients displayed a PFS advantage as compared to Len refractory patients (29 vs 16 months, p = 0.2876). Similarly, patients treated after Len maintenance showed a better outcome as compared to patients who had received a full-dose Len treatment (23 vs 13 months, p = 0.1728). In conclusion, our real-world data on D-VD combination showed remarkable efficacy in Len-R patients, placing this regimen as one of the standards of care to be properly taken into account in this MM setting.

Indexed as

Multiple MyelomaAntibodies, MonoclonalAntineoplastic Combined Chemotherapy ProtocolsBortezomibDexamethasoneHumansLenalidomideNeoplasm Recurrence, LocalAntibodies, MonoclonalBortezomibdaratumumabDexamethasoneLenalidomideD-VDLenalidomide refractorinessMultiple myelomaReal-life

Identifiers

PMID37731147
PMCPMC10761376
OpenAlexW4386884355

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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.