Evidence map›Paper›PMID 40301145›Full record

Observational studyAnnals of hematology2025

Real-world data on the use of subcutaneous daratumumab plus bortezomib, thalidomide, and dexamethasone in transplant-eligible patients with newly diagnosed multiple myeloma.

Vania Hungria, Fernanda Lemos Moura, Abel Costa, Eduardo Flávio Oliveira Ribeiro, Paulo Soares, Juliana Souza Lima, Lisa Aquaroni Ricci, Celso Arrais-Rodrigues, Fabio Moore Nucci, Marinus de Moraes Lima and 7 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Annals of hematology, 2025. 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

17 authors.

Vania HungriaClinica São Germano, Rua Comendador Miguel Calfat 165, São Paulo, SP, 04537-080, Brazil. hungria@dialdata.com.br.
Fernanda Lemos MouraFundação Antonio Prudente - AC Camargo Cancer Center, São Paulo, SP, Brazil.
Abel CostaInstituto D'Or de Pesquisa e Ensino, São Paulo, SP, Brazil.
Eduardo Flávio Oliveira RibeiroHospital Santa Lúcia, Brasilia, Distrito Federal, Brazil.
Paulo SoaresInstituto D'Or de Pesquisa e Ensino, Brasilia, Distrito Federal, PE, Brazil.
Juliana Souza LimaInstituto de Hematologia e Oncologia Curitiba, Curitiba, PR, Brazil.
Lisa Aquaroni RicciInstituto de Oncologia de Sorocaba, Sorocaba, SP, Brazil.
Celso Arrais-RodriguesHospital Nove de Julho (DASA), São Paulo, SP, Brazil.
Fabio Moore NucciInstituto de Pesquisa e Ensino, Rio de Janeiro, RJ, Brazil.
Marinus de Moraes LimaInstituto D'Or de Pesquisa e Ensino, Recife, PE, Brazil.
Roberto Jose Pessoa de Magalhães FilhoComplexo Hospitalar de Niterói, Niterói, RJ, Brazil.
Amitabha BhaumikJohnson & Johnson, Titusville, NJ, USA.
Trilok ParekhJohnson & Johnson, Raritan, NJ, USA.
Fredrik BorgstenJohnson & Johnson, Raritan, NJ, USA.
Robin CarsonJohnson & Johnson, Spring House, PA, USA.
Damila C TrufelliJohnson & Johnson, São Paulo, SP, Brazil.
Edvan de Queiroz CrusoeInstituto D'Or de Pesquisa e Ensino, Hospital São Rafael, Salvador, BA, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Subcutaneous daratumumab in combination with bortezomib, thalidomide, and dexamethasone (D-VTd), is approved for transplant-eligible patients with newly diagnosed multiple myeloma (NDMM). However, additional real-world data are needed to assess the effectiveness and safety of D-VTd in routine clinical practice. We conducted a noninterventional, multicenter, observational study across hematology centers in Brazil to gather real-world data on D-VTd in patients with NDMM who were eligible for autologous stem cell transplant (ASCT). Eligible patients must have completed 1 or more cycle of D-VTd, on or before September 30, 2022, to be included. Data were collected retrospectively from the start of D-VTd to the study inclusion visit using patient medical records and prospectively thereafter using electronic case report forms. As of the data cutoff (August 8, 2023), 49 patients were included. By the end of consolidation, 91.7% of patients achieved an overall response (partial response or better) and 89.6% achieved very good partial response or better. Forty-five (91.8%) patients underwent stem cell mobilization with a median stem cell yield of 5.7 × 10

Indexed as

Antibodies, MonoclonalAntineoplastic Combined Chemotherapy ProtocolsHematopoietic Stem Cell TransplantationMultiple MyelomaAdultAgedBortezomibDexamethasoneFemaleHumansInjections, SubcutaneousMaleMiddle AgedRetrospective StudiesThalidomideAntibodies, MonoclonalBortezomibdaratumumabDexamethasoneThalidomideAutologous stem cell transplantDaratumumabMultiple myelomaReal-worldSubcutaneous

Identifiers

PMID40301145
PMCPMC12141371

What OpenQuestion holds

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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.