Evidence map›Paper›PMID 31392600›Full record

ArticleInternational journal of hematology2019

Real-world data on the efficacy and safety of daratumumab treatment in Hungarian relapsed/refractory multiple myeloma patients.

Szilvia Lovas, Gergely Varga, Péter Farkas, Tamás Masszi, Nikolett Wohner, Ágnes Bereczki, Nóra Adamkovich, Zita Borbényi, Árpád Szomor, Hussain Alizadeh and 14 more

Abstract read
PubMed Publisher
In one paragraph

Article in International journal of hematology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Trial
  2. Article
  3. Observational
  4. Experience of Daratumumab in Relapsed/Refractory Multiple Myeloma: A Multicenter Study from TürkiyeTurkish journal of haematology : official journal of Turkish Society of Haematology · 2023
    Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. [The efficacy and safety of daratumumab in relapsed and refractory multiple myeloma].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2021
    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

24 authors.

Szilvia LovasDepartment of Hematology, Institute for Medicine, Faculty of Medicine, University of Debrecen, Nagyerdei krt. 98., 4032, Debrecen, Hungary.
Gergely Varga3rd Department of Internal Medicine, Semmelweis University, Budapest, Hungary.
Péter Farkas3rd Department of Internal Medicine, Semmelweis University, Budapest, Hungary.
Tamás Masszi3rd Department of Internal Medicine, Semmelweis University, Budapest, Hungary.
Nikolett Wohner3rd Department of Internal Medicine, Semmelweis University, Budapest, Hungary.
Ágnes Bereczki2nd Department of Internal Medicine and Cardiology Center, Faculty of Medicine, University of Szeged, Szeged, Hungary.
Nóra Adamkovich2nd Department of Internal Medicine and Cardiology Center, Faculty of Medicine, University of Szeged, Szeged, Hungary.
Zita Borbényi2nd Department of Internal Medicine and Cardiology Center, Faculty of Medicine, University of Szeged, Szeged, Hungary.
Árpád Szomor1st Department of Internal Medicine, University of Pécs, Pecs, Hungary.
Hussain Alizadeh1st Department of Internal Medicine, University of Pécs, Pecs, Hungary.
Erika SzaleczkyNational Institute of Oncology, Budapest, Hungary.
Krisztina WolfNational Institute of Oncology, Budapest, Hungary.
Tamás SchneiderNational Institute of Oncology, Budapest, Hungary.
Márk PlanderDepartment of Hematology, Markusovszky Teaching Hospital, Szombathely, Hungary.
Tamás SzendreiDepartment of Hematology, Markusovszky Teaching Hospital, Szombathely, Hungary.
Ottó CsacsovszkiDepartment of Hematology and Stem Cell Transplantation, South-Pest Central Hospital, National Institute for Hematology and Infectious Diseases, Budapest, Hungary.
Zoltán CsuklyDepartment of Hematology and Stem Cell Transplantation, South-Pest Central Hospital, National Institute for Hematology and Infectious Diseases, Budapest, Hungary.
Péter RajnicsDepartment of Hematology, Mór Kaposi Teaching Hospital, Kaposvár, Hungary.
Miklós EgyedDepartment of Hematology, Mór Kaposi Teaching Hospital, Kaposvár, Hungary.
Zsolt Nagy1st Department of Internal Medicine, Semmelweis University, Budapest, Hungary.
László RejtőDepartment of Hematology, Jósa András Teaching Hospital, Nyíregyháza, Hungary.
Árpád IllésDepartment of Hematology, Institute for Medicine, Faculty of Medicine, University of Debrecen, Nagyerdei krt. 98., 4032, Debrecen, Hungary.
Gábor MikalaDepartment of Hematology and Stem Cell Transplantation, South-Pest Central Hospital, National Institute for Hematology and Infectious Diseases, Budapest, Hungary.
László VáróczyDepartment of Hematology, Institute for Medicine, Faculty of Medicine, University of Debrecen, Nagyerdei krt. 98., 4032, Debrecen, Hungary. varoczy@internal.med.unideb.hu.ORCID http://orcid.org/0000-0002-2873-5581

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Daratumumab is a human anti-CD38 monoclonal antibody used in the treatment of refractory and relapsed multiple myeloma. We investigated the efficacy and safety of daratumumab therapy in a real-world setting. Ninety-nine Hungarian patients were included; 48 received monotherapy, while lenalidomide and bortezomib combinations were administered in 29 and 19 cases, respectively. Overall response rate was assessable in 88 patients, with 12 complete, 10 very good partial, 34 partial, and seven minor responses. At a median duration of follow-up of 18.6 months, median progression-free survival (PFS) among all patients was 17.0 months. These values were inferior in the bortezomib combination and monotherapy groups. Patients with early-stage disease (ISS1) had better survival results than those with stage 2 or 3 myeloma (p = 0.009). Heavily pretreated patients had inferior PFS compared to those with 1-3 therapies (p = 0.035). Patients with impaired renal function had PFS results comparable with those having no kidney involvement. There were 10 fatal infections, and the most frequent adverse events were mild infusion-associated reactions and hematologic toxicities. Our results confirm that daratumumab is an effective treatment option for relapsed/refractory MM with an acceptable safety profile in patients with normal and impaired renal function.

Indexed as

AdultAgedAntibodies, MonoclonalAntineoplastic AgentsBortezomibFemaleHumansHungaryLenalidomideMaleMiddle AgedMultiple MyelomaProgression-Free SurvivalSalvage TherapyTreatment OutcomeAntibodies, MonoclonalAntineoplastic AgentsBortezomibdaratumumabLenalidomideDaratumumabMultiple myelomaSurvivalToxicityTreatment response

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.