Evidence map›Paper›PMID 38892379›Full record

ReviewInternational journal of molecular sciences2024

Current Novel Targeted Therapeutic Strategies in Multiple Myeloma.

Cindy Hsin-Ti Lin, Muhammad Junaid Tariq, Fauzia Ullah, Aishwarya Sannareddy, Farhan Khalid, Hasan Abbas, Abbas Bader, Christy Samaras, Jason Valent, Jack Khouri and 3 more

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
–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

19 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  5. Identification of exhausted CD8Translational cancer research · 2026
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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

13 authors.

Cindy Hsin-Ti LinDepartment of Internal Medicine, Case Western Reserve University, MetroHealth Campus, Cleveland, OH 44109, USA.
Muhammad Junaid TariqDepartment of Hematology-Oncology, Roswell Park Comprehensive Cancer Center, Buffalo, NY 14203, USA.
Fauzia UllahDepartment of Hematology-Oncology, Cleveland Clinic, Taussig Cancer Institute, Cleveland, OH 44195, USA.ORCID 0000-0003-1991-1202
Aishwarya SannareddyDepartment of Hematology-Oncology, UT Southwestern, Dallas, TX 75235, USA.ORCID 0009-0000-4779-6905
Farhan KhalidDepartment of Internal Medicine, Monmouth Medical Center, Long Branch, NJ 07740, USA.
Hasan AbbasMedical College of Wisconsin, Milwaukee, WI 53226, USA.
Abbas BaderSchool of Medicine, University of Missouri-Kansas City, Kansas City, MO 64110, USA.
Christy SamarasDepartment of Hematology-Oncology, Cleveland Clinic, Taussig Cancer Institute, Cleveland, OH 44195, USA.
Jason ValentDepartment of Hematology-Oncology, Cleveland Clinic, Taussig Cancer Institute, Cleveland, OH 44195, USA.
Jack KhouriDepartment of Hematology-Oncology, Cleveland Clinic, Taussig Cancer Institute, Cleveland, OH 44195, USA.ORCID 0000-0002-2473-6528
Faiz AnwerDepartment of Hematology-Oncology, Cleveland Clinic, Taussig Cancer Institute, Cleveland, OH 44195, USA.ORCID 0000-0001-6914-7439
Shahzad RazaDepartment of Hematology-Oncology, Cleveland Clinic, Taussig Cancer Institute, Cleveland, OH 44195, USA.ORCID 0000-0002-2739-2265
Danai DimaDepartment of Hematology-Oncology, Cleveland Clinic, Taussig Cancer Institute, Cleveland, OH 44195, USA.ORCID 0000-0002-3587-7975

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is a hematologic malignancy caused by the clonal expansion of immunoglobulin-producing plasma cells in the bone marrow and/or extramedullary sites. Common manifestations of MM include anemia, renal dysfunction, infection, bone pain, hypercalcemia, and fatigue. Despite numerous recent advancements in the MM treatment paradigm, current therapies demonstrate limited long-term effectiveness and eventual disease relapse remains exceedingly common. Myeloma cells often develop drug resistance through clonal evolution and alterations of cellular signaling pathways. Therefore, continued research of new targets in MM is crucial to circumvent cumulative drug resistance, overcome treatment-limiting toxicities, and improve outcomes in this incurable disease. This article provides a comprehensive overview of the landscape of novel treatments and emerging therapies for MM grouped by molecular target. Molecular targets outlined include BCMA, GPRC5D, FcRH5, CD38, SLAMF7, BCL-2, kinesin spindle protein, protein disulfide isomerase 1, peptidylprolyl isomerase A, Sec61 translocon, and cyclin-dependent kinase 6. Immunomodulatory drugs, NK cell therapy, and proteolysis-targeting chimera are described as well.

Indexed as

Molecular Targeted TherapyMultiple MyelomaAnimalsAntineoplastic AgentsHumansAntineoplastic Agentsimmunotherapymultiple myelomatargeted therapy

Identifiers

PMID38892379
PMCPMC11172591

What OpenQuestion holds

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Registered trials

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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.