Evidence map›Paper›PMID 33322499›Full record

ReviewCells2020

Novel Insights in Anti-CD38 Therapy Based on CD38-Receptor Expression and Function: The Multiple Myeloma Model.

Beatrice Anna Zannetti, Angelo Corso Faini, Evita Massari, Massimo Geuna, Enrico Maffini, Giovanni Poletti, Claudio Cerchione, Giovanni Martinelli, Fabio Malavasi, Francesco Lanza

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

7 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Review
  3. Multi-targeted immunotherapeutics to treat B cell malignancies.Journal of controlled release : official journal of the Controlled Release Society · 2023
    Review
  4. CD38 Mediates Lung Fibrosis by Promoting Alveolar Epithelial Cell Aging.American journal of respiratory and critical care medicine · 2022
    Article
  5. Novel immunotherapies in multiple myeloma.International journal of hematology · 2022
    Review
  6. Review
  7. 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

10 authors at 4 institutions in 1 country.

Beatrice Anna ZannettiHematology Unit and Romagna Transplant Network, Ravenna Hospital, 48121 Ravenna, Italy.
Angelo Corso FainiDepartment of Medical Science, University of Torino and Fondazione Ricerca Molinette, 10129 Torino, Italy.
Evita MassariFlow Cytometry Unit, Laboratory Service, 47522 Pievesestina, Italy.ORCID 0000-0002-2502-7395
Massimo GeunaLaboratorio di Immunopatologia, A.O. Ordine Mauriziano, 10129 Torino, Italy.ORCID 0000-0002-6475-5547
Enrico MaffiniHematology Unit and Romagna Transplant Network, Ravenna Hospital, 48121 Ravenna, Italy.
Giovanni PolettiFlow Cytometry Unit, Laboratory Service, 47522 Pievesestina, Italy.
Claudio CerchioneIRST/IRCCS, Cancer Center, 47014 Meldola, Italy.
Giovanni MartinelliIRST/IRCCS, Cancer Center, 47014 Meldola, Italy.ORCID 0000-0002-1025-4210
Fabio MalavasiDepartment of Medical Science, University of Torino and Fondazione Ricerca Molinette, 10129 Torino, Italy.
Francesco LanzaHematology Unit and Romagna Transplant Network, Ravenna Hospital, 48121 Ravenna, Italy.ORCID 0000-0002-5189-7167
Azienda Unità Sanitaria Locale Della Romagna · ITFondazione Ricerca Molinette · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITA. O. Ordine Mauriziano di Torino · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is a hematological disease characterized by the proliferation and accumulation of malignant plasmacells (PCs) in the bone marrow (BM). Despite widespread use of high-dose chemotherapy in combination with autologous stem cell transplantation (ASCT) and the introduction of novel agents (immunomodulatory drugs, IMiDs, and proteasome inhibitors, PIs), the prognosis of MM patients is still poor. CD38 is a multifunctional cell-surface glycoprotein with receptor and ectoenzymatic activities. The very high and homogeneous expression of CD38 on myeloma PCs makes it an attractive target for novel therapeutic strategies. Several anti-CD38 monoclonal antibodies have been, or are being, developed for the treatment of MM, including daratumumab and isatuximab. Here we provide an in-depth look atCD38 biology, the role of CD38 in MM progression and its complex interactions with the BM microenvironment, the importance of anti-CD38 monoclonal antibodies, and the main mechanisms of antibody resistance. We then review a number of multiparametric flow cytometry techniques exploiting CD38 antigen expression on PCs to diagnose and monitor the response to treatment in MM patients.

Indexed as

ADP-ribosyl Cyclase 1Antibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntibody-Dependent Cell CytotoxicityHumansMultiple MyelomaTumor MicroenvironmentADP-ribosyl Cyclase 1Antibodies, MonoclonalAntibodies, Monoclonal, Humanizeddaratumumabisatuximabanti-CD38 monoclonal antibodiesbone marrow microenvironmentCD38CD38 antigen expression in various tissuesmultiple myelomaplasmacells

Identifiers

PMID33322499
PMCPMC7764337
OpenAlexW3112000154

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.