Evidence map›Paper›PMID 32108228›Full record

Trial reportBlood2020

A prospective phase 2 trial of daratumumab in patients with previously treated systemic light-chain amyloidosis.

Murielle Roussel, Giampaolo Merlini, Sylvie Chevret, Bertrand Arnulf, Anne Marie Stoppa, Aurore Perrot, Giovanni Palladini, Lionel Karlin, Bruno Royer, Antoine Huart and 10 more

Registry-linked trialOpen access · bronzeAbstract readClinical Trial, Phase IIMulticenter Study
PubMed Publisher
In one paragraph

Trial report in Blood, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02816476 (A Multicentre Open Label Phase II Study of Daratumumab in AL Amyloidosis Patients Not in VGPR or Better), which is not on this map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
8.2field-weighted citation impact, top 2% 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.

NCT02816476 phase2completednot on this map

A Multicentre Open Label Phase II Study of Daratumumab in AL Amyloidosis Patients Not in VGPR or Better

TypeinterventionalSponsorUniversity Hospital, LimogesRan2016 to 2020Enrolled40ConditionsAmyloidosisArmsDaratumumab
3 · Its place in the literature

Who cites it

59 citing papers in PubMed, 126 citations in OpenAlex.

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  17. World journal of clinical cases · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 14 institutions in 2 countries.

Murielle RousselHématologie Clinique, IUC Oncopole, Toulouse, France.
Giampaolo MerliniAmyloidosis Research and Treatment Center, Foundation Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo, Pavia, Italy.
Sylvie ChevretU1153 Centre de Recherche en Épidémiologie et Statistiques (CRESS), Equipe de Recherche en Biostatistiques et Epidémiologie Clinique (ECSTRRA).
Bertrand ArnulfService d'Immuno-Hématologie Clinique, Hôpital Saint Louis, Assistance Publique-Hôpitaux de Paris (AP-HP), Université de Paris, Paris, France.
Anne Marie StoppaService d'Hématologie, Institut Paoli Calmette, Marseille, France.
Aurore PerrotService d'Hématologie Clinique, Centre Hospitalier Universitaire (CHU) Nancy, Nancy, France.
Giovanni PalladiniAmyloidosis Research and Treatment Center, Foundation Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo, Pavia, Italy.
Lionel KarlinService d'Hématologie, Hôpital Sud, CHU Lyon, Lyon, France.
Bruno RoyerService d'Immuno-Hématologie Clinique, Hôpital Saint Louis, Assistance Publique-Hôpitaux de Paris (AP-HP), Université de Paris, Paris, France.
Antoine HuartService Néphrologie et Transplantation d'Organes, Hôpital Rangueil, CHU Toulouse, Toulouse, France.
Margaret MacroInstitut d'Hématologie de Basse-Normandie, CHU Caen, Caen, France.
Pierre MorelService Hématologie Clinique et Thérapies Cellulaires, CHU Amiens, Amiens, France.
Laurent FrenzelService d'Hématologie Adultes Hôpital Necker, AP-HP Paris, Paris, France.
Cyrille TouzeauService d'Hématologie, CHU Nantes, Nantes, France.
Eileen BoyleService des Maladies du Sang, Centre Hospitalier Régional Universitaire (CHRU) Lille, Lille, France.
Véronique DorvauxService d'Hématologie, CH Metz, France.
Fabien Le BrasUnité Hémopathies Lymphoïdes, Hôpital Henri-Mondor, AP-HP Créteil, Créteil, France.
David LavergneCentre de Référence pour l'Amylose AL et autres Maladies de Dépôts d'Immunoglobulines Monoclonales and.
Frank BridouxCentre de Référence pour l'Amylose AL et autres Maladies de Dépôts d'Immunoglobulines Monoclonales and.
Arnaud JaccardCentre de Référence pour l'Amylose AL et autres Maladies de Dépôts d'Immunoglobulines Monoclonales and.
Centre Hospitalier Universitaire de Limoges · FRUniversité Paris Cité · FRUniversity of Pavia · ITCentre de Recherche Épidémiologie et Statistique · FRCentre Hospitalier Régional et Universitaire de Nancy · FRCentre Hospitalier Universitaire de Caen Normandie · FRCentre Hospitalier Universitaire de Lille · FRCentre Hospitalier Universitaire de Nantes · FRHôpital Necker-Enfants Malades · FRHôpital Nord · FRHôpital Rangueil · FRInserm · FRInstitut Paoli-Calmettes · FRInstitut universitaire du cancer de Toulouse Oncopole · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Daratumumab is a human monoclonal antibody targeting CD38, an antigen uniformly expressed by plasma cells in multiple myeloma and light-chain amyloidosis (AL). We report the results of a prospective multicenter phase 2 study of daratumumab monotherapy in AL (NCT02816476). Forty previously treated AL patients with a difference between involved and uninvolved free light chains (dFLC) >50 mg/L were included in 15 centers between September of 2016 and April of 2018. Patients received 6 28-day cycles of IV daratumumab, every week for cycles 1 and 2 and every 2 weeks for cycles 3 through 6. Median age was 69 years (range, 45-83). Twenty-six patients had ≥2 organs involved, with heart in 24 and kidney in 26. Median time from diagnosis to enrollment was 23 months (interquartile range, 4-122), with a median of 3 prior therapies (range, 1-5). At data cutoff (September of 2019), all patients discontinued therapy; 33 received the planned 6 cycles. Overall, 22 patients had hematological response, and 19 patients (47.5%) achieved very good partial response (dFLC <40 mg/L) or better. Median time to hematological response was 1 week. Patients with no response after 4 doses were unlikely to respond further. Renal and cardiac responses occurred in 8 and 7 patients, respectively. Daratumumab was well tolerated, with no unexpected adverse events. With a median follow-up of 26 months, the 2-year overall survival rate was 74% (95% confidence interval, 62-81). Daratumumab monotherapy is associated with deep and rapid hematological responses in previously treated AL patients, with a good safety profile. Further studies of daratumumab in combination regimens are warranted.

Indexed as

AgedAntibodies, MonoclonalBiomarkersCombined Modality TherapyFemaleHumansImmunoglobulin Light-chain AmyloidosisMaleMiddle AgedPrognosisRetreatmentSeverity of Illness IndexTreatment OutcomeAntibodies, MonoclonalBiomarkersdaratumumab

Identifiers

PMID32108228
OpenAlexW3006893827

What OpenQuestion holds

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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.