Evidence map›Paper›PMID 39432172›Full record

ReviewCurrent treatment options in oncology2024

Acquired Bortezomib Resistance in Multiple Myeloma: From Mechanisms to Strategy.

Fangfang Li, Jing Liu, Yunfeng Fu

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current treatment options in oncology, 2024. 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
–field-weighted citation impact
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.

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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

3 authors.

Fangfang LiDepartment of Hematology, The Third Xiangya Hospital, Central South University, Changsha, 410013, China.ORCID https://orcid.org/0009-0007-2372-3251
Jing LiuDepartment of Hematology, The Third Xiangya Hospital, Central South University, Changsha, 410013, China.ORCID https://orcid.org/0000-0001-9245-316X
Yunfeng FuDepartment of Blood Transfusion, The Third Xiangya Hospital of Central South University, Changsha, 410013, China. fuyunfeng@csu.edu.cn.ORCID https://orcid.org/0000-0002-1319-4938

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

opinion statementMultiple myeloma (MM) is a heterogeneous plasma cell tumor with a survival period of several months to over ten years. Despite the development of various new drugs, MM is still incurable and recurs repeatedly. Bortezomib, a landmark event in the history of MM treatment, has dramatically improved the prognosis of patients with MM. Although proteasome inhibitors (PIs) represented by bortezomib, have greatly prolonged MM survival, unfortunately, almost all MM will develop bortezomib resistance, leading to relapse with a shorter survival. It has been reported that both the tumor microenvironment and myeloma cells drive bortezomib resistance. Multiple treatment methods have been attempted to overcome bortezomib resistance, but unfortunately, there has been no breakthrough. It is believed that the key resistance mechanism has not yet been discovered. A deeper understanding of the mechanism of bortezomib resistance and strategies to overcome it can help identify key resistance mechanisms and further improve the prognosis of MM.

Indexed as

Antineoplastic AgentsBortezomibDrug Resistance, NeoplasmMultiple MyelomaAntineoplastic Combined Chemotherapy ProtocolsHumansPrognosisProteasome InhibitorsTumor MicroenvironmentAntineoplastic AgentsBortezomibProteasome InhibitorsBortezomibDrug resistanceMechanismsMultiple myelomaStrategy

Identifiers

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.