Evidence map›Paper›PMID 34680358›Full record

ReviewCancers2021

Novel Non-Immunologic Agents for Relapsed and Refractory Multiple Myeloma: A Review Article.

Arthur Bobin, Cécile Gruchet, Stéphanie Guidez, Hélène Gardeney, Laly Nsiala Makunza, Mathilde Vonfeld, Anthony Lévy, Laura Cailly, Florence Sabirou, Thomas Systchenko and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
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

12 authors.

Arthur BobinDepartment of Hematology, CIC 1402, University Hospital, 86000 Poitiers, France.ORCID 0000-0002-8416-391X
Cécile GruchetDepartment of Hematology, CIC 1402, University Hospital, 86000 Poitiers, France.
Stéphanie GuidezDepartment of Hematology, CIC 1402, University Hospital, 86000 Poitiers, France.
Hélène GardeneyDepartment of Hematology, CIC 1402, University Hospital, 86000 Poitiers, France.
Laly Nsiala MakunzaDepartment of Hematology, CIC 1402, University Hospital, 86000 Poitiers, France.
Mathilde VonfeldDepartment of Hematology, CIC 1402, University Hospital, 86000 Poitiers, France.
Anthony LévyDepartment of Hematology, CIC 1402, University Hospital, 86000 Poitiers, France.
Laura CaillyDepartment of Hematology, CIC 1402, University Hospital, 86000 Poitiers, France.
Florence SabirouDepartment of Hematology, CIC 1402, University Hospital, 86000 Poitiers, France.
Thomas SystchenkoDepartment of Hematology, CIC 1402, University Hospital, 86000 Poitiers, France.
Niels MoyaDepartment of Hematology, CIC 1402, University Hospital, 86000 Poitiers, France.
Xavier LeleuDepartment of Hematology, CIC 1402, University Hospital, 86000 Poitiers, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Novel treatments are needed to address the lack of options for patients with relapsed or refractory multiple myeloma. Even though immunotherapy-based treatments have revolutionized the field in recent years, offering new opportunities for patients, there is still no curative therapy. Thus, non-immunologic agents, which have proven effective for decades, are still central to the treatment of multiple myeloma, especially for advanced disease. Building on their efficacy in myeloma, the development of proteasome inhibitors and immunomodulatory drugs has been pursued, and has led to the emergence of a novel generation of agents (e.g., carfilzomib, ixazomib, pomalidomide). The use of alkylating agents is decreasing in most treatment regimens, but melflufen, a peptide-conjugated alkylator with a completely new mechanism of action, offers interesting opportunities. Moreover, with the identification of novel targets, new drug classes have entered the myeloma armamentarium, such as XPO1 inhibitors (selinexor), HDAC inhibitors (panobinostat), and anti-BCL-2 agents (venetoclax). New pathways are still being explored, especially the possibility of a mutation-driven strategy, as biomarkers and targeted treatments are increasing. Though multiple myeloma is still considered incurable, the treatment options are expanding and are progressively becoming more diverse, largely because of the continuous development of non-immunologic agents.

Indexed as

anti BCL-2anti MCL-1HDAC inhibitorsIMiDsmultiple myelomanon-immunologic agentspeptide–drug conjugatesproteasome inhibitorsrelapsed or refractoryXPO1 inhibitors

Identifiers

PMID34680358
PMCPMC8534104
OpenAlexW3207931776

What OpenQuestion holds

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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.