Evidence map›Paper›PMID 30793108›Full record

ReviewHematology, transfusion and cell therapy

New proteasome inhibitors in the treatment of multiple myeloma.

Vania Tietsche de Moraes Hungria, Edvan de Queiroz Crusoé, Rosane Isabel Bittencourt, Angelo Maiolino, Roberto José Pessoa Magalhães, Jairo do Nascimento Sobrinho, Jorge Vaz Pinto, Ricardo Coutinho Fortes, Eloisa de Sá Moreira, Paula Yurie Tanaka

Open access · diamondAbstract readReview
In one paragraph

Review in Hematology, transfusion and cell therapy. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 33 citations in OpenAlex.

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  17. Emerging Strategies Targeting Catabolic Muscle Stress Relief.International journal of molecular sciences · 2020
    Review
  18. The role of deubiquitinating enzymes in cancer drug resistance.Cancer chemotherapy and pharmacology · 2020
    Review
  19. 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 7 institutions in 1 country.

Vania Tietsche de Moraes HungriaFaculdade de Ciências Médicas da Santa Casa de São Paulo, São Paulo, SP, Brazil. Electronic address: hungria@dialdata.com.br.
Edvan de Queiroz CrusoéUniversidade Federal da Bahia, Hospital Universitário Professor Edgar Santos, Serviço de Hematologia, Salvador, BA, Brazil.
Rosane Isabel BittencourtHospital de Clínicas de Porto Alegre, Serviço de Hematologia, Porto Alegre, RS, Brazil.
Angelo MaiolinoUniversidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Roberto José Pessoa MagalhãesUniversidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Jairo do Nascimento SobrinhoHospital Israelita Albert Einstein, São Paulo, SP, Brazil.
Jorge Vaz PintoUniversidade Católica de Brasília, Brasília, DF, Brazil.
Ricardo Coutinho FortesEvidências - Kantar Health, São Paulo, SP, Brazil.
Eloisa de Sá MoreiraEvidências - Kantar Health, São Paulo, SP, Brazil.
Paula Yurie TanakaTakeda Pharma, São Paulo, SP, Brazil.
Kantar Health (Brazil) · BRUniversidade Federal do Rio de Janeiro · BRFaculdade de Ciências Médicas da Santa Casa de São Paulo · BRHospital de Clínicas de Porto Alegre · BRHospital Israelita Albert Einstein · BRUniversidade Católica de Brasília · BRUniversidade Federal da Bahia · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The treatment of patients with relapsed and/or refractory multiple myeloma has improved considerably in the last 15 years, after the introduction of proteasome inhibitors and immunomodulatory drugs. The first clinical trials with new proteasome inhibitors have produced exciting results, particularly those comparing triplet regimens with standard doublet regimens, with a gain in progression-free survival accompanied by an acceptable safety profile and either similar or better health-related quality of life. New proteasome inhibitors hold the potential to fill unmet needs in multiple myeloma management regarding improvement of clinical outcomes, including delayed progression of disease in high-risk patients. This review summarizes the main pharmacological properties and clinical outcomes of these agents, and discusses their potential to change the whole multiple myeloma therapeutic landscape.

Indexed as

BortezomibCarfilzomibIxazomibMultiple myelomaProteasome inhibitors

Identifiers

PMID30793108
PMCPMC6371737
OpenAlexW2895810624

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.