Evidence map›Paper›PMID 26864107›Full record

ReviewImmunological reviews2016

Monoclonal antibodies targeting CD38 in hematological malignancies and beyond.

Niels W C J van de Donk, Maarten L Janmaat, Tuna Mutis, Jeroen J Lammerts van Bueren, Tahamtan Ahmadi, A Kate Sasser, Henk M Lokhorst, Paul W H I Parren

2 registry-linked trialsOpen access · hybridAbstract readReview
In one paragraph

Review in Immunological reviews, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 195 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
195citing papers in PubMed, 2 pooled it
27.1field-weighted citation impact, top 1% 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.

NCT02751255 phase1 / phase2completednot on this map

A Phase 1 and Phase 2 Study of Daratumumab in Combination With All-trans Retinoic Acid in Relapsed/Refractory Multiple Myeloma

TypeinterventionalSponsorAmsterdam UMC, location VUmcRan2016 to 2022Enrolled60ConditionsMultiple MyelomaArmsall-trans retinoic acid (ATRA)
NCT05558319 phase3recruitingnot on this mapstarted 2022, after this paper: background citation

GEM21menos65. A Phase III Trial for NDMM Patients Who Are Candidates for ASCT Comparing Extended VRD Plus Early Rescue Intervention vs Isatuximab-VRD vs Isatuximab-V-Iberdomide-D

TypeinterventionalSponsorPETHEMA FoundationRan2022 to 2029Enrolled480ConditionsNewly Diagnosed Multiple MyelomaArmsBortezomib, Isatuximab, Iberdomide, Lenalidomide, Dexamethasone
3 · Its place in the literature

Who cites it

195 citing papers in PubMed, 2 syntheses or guidelines pooled it, 327 citations in OpenAlex.

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  6. Health-Related Quality of Life in Transplant-Ineligible Patients With Newly Diagnosed Multiple Myeloma: Findings From the Phase III MAIA Trial.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2021
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135 more citing papers are in PubMed but not listed here.

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

8 authors at 4 institutions in 3 countries.

Niels W C J van de DonkDepartment of Hematology, VU University Medical Center, Amsterdam, the Netherlands.
Maarten L JanmaatGenmab, Utrecht, the Netherlands.
Tuna MutisDepartment of Hematology, VU University Medical Center, Amsterdam, the Netherlands.
Jeroen J Lammerts van BuerenGenmab, Utrecht, the Netherlands.
Tahamtan AhmadiJanssen Research and Development, Spring House, PA, USA.
A Kate SasserJanssen Research and Development, Spring House, PA, USA.
Henk M LokhorstDepartment of Hematology, VU University Medical Center, Amsterdam, the Netherlands.
Paul W H I ParrenGenmab, Utrecht, the Netherlands.
Amsterdam UMC Location VUmc · NLGenmab (Netherlands) · NLJanssen (United States) · USLeiden University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD38 is a multifunctional cell surface protein that has receptor as well as enzyme functions. The protein is generally expressed at low levels on various hematological and solid tissues, while plasma cells express particularly high levels of CD38. The protein is also expressed in a subset of hematological tumors, and shows especially broad and high expression levels in plasma cell tumors such as multiple myeloma (MM). Together, this triggered the development of various therapeutic CD38 antibodies, including daratumumab, isatuximab, and MOR202. Daratumumab binds a unique CD38 epitope and showed strong anti-tumor activity in preclinical models. The antibody engages diverse mechanisms of action, including complement-dependent cytotoxicity, antibody-dependent cellular cytotoxicity, antibody-dependent cellular phagocytosis, programmed cell death, modulation of enzymatic activity, and immunomodulatory activity. CD38-targeting antibodies have a favorable toxicity profile in patients, and early clinical data show a marked activity in MM, while studies in other hematological malignancies are ongoing. Daratumumab has single agent activity and a limited toxicity profile, allowing favorable combination therapies with existing as well as emerging therapies, which are currently evaluated in the clinic. Finally, CD38 antibodies may have a role in the treatment of diseases beyond hematological malignancies, including solid tumors and antibody-mediated autoimmune diseases.

Indexed as

ADP-ribosyl Cyclase 1AnimalsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsClinical Studies as TopicCytotoxicity, ImmunologicDrug Evaluation, PreclinicalDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticHematologic NeoplasmsHumansImmunomodulationProtein BindingRecurrenceADP-ribosyl Cyclase 1Antibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic AgentsdaratumumabcancerCD38daratumumabisatuximabmultiple myelomatherapeutic antibody

Identifiers

PMID26864107
PMCPMC4755228
OpenAlexW2253038466

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.