Evidence map›Paper›PMID 37601856›Full record

ReviewEJHaem2023

Selinexor: Targeting a novel pathway in multiple myeloma.

Clifton C Mo, Andrew J Yee, Shonali Midha, Monique A Hartley-Brown, Omar Nadeem, Elizabeth K O'Donnell, Giada Bianchi, Adam S Sperling, Jacob P Laubach, Paul G Richardson

Open access · diamondAbstract readReview
In one paragraph

Review in EJHaem, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Clifton C MoDepartment of Medical Oncology Dana-Farber Cancer Institute Jerome Lipper Center for Multiple Myeloma Research Harvard Medical School Boston Massachusetts USA.
Andrew J YeeMassachusetts General Cancer Center Harvard Medical School Boston Massachusetts USA.ORCID https://orcid.org/0000-0003-3623-7491
Shonali MidhaDepartment of Medical Oncology Dana-Farber Cancer Institute Jerome Lipper Center for Multiple Myeloma Research Harvard Medical School Boston Massachusetts USA.ORCID https://orcid.org/0000-0003-4948-5507
Monique A Hartley-BrownDepartment of Medical Oncology Dana-Farber Cancer Institute Jerome Lipper Center for Multiple Myeloma Research Harvard Medical School Boston Massachusetts USA.ORCID https://orcid.org/0000-0001-7277-0061
Omar NadeemDepartment of Medical Oncology Dana-Farber Cancer Institute Jerome Lipper Center for Multiple Myeloma Research Harvard Medical School Boston Massachusetts USA.
Elizabeth K O'DonnellDepartment of Medical Oncology Dana-Farber Cancer Institute Jerome Lipper Center for Multiple Myeloma Research Harvard Medical School Boston Massachusetts USA.
Giada BianchiDepartment of Medical Oncology Dana-Farber Cancer Institute Jerome Lipper Center for Multiple Myeloma Research Harvard Medical School Boston Massachusetts USA.
Adam S SperlingDepartment of Medical Oncology Dana-Farber Cancer Institute Jerome Lipper Center for Multiple Myeloma Research Harvard Medical School Boston Massachusetts USA.ORCID https://orcid.org/0000-0002-9369-4413
Jacob P LaubachDepartment of Medical Oncology Dana-Farber Cancer Institute Jerome Lipper Center for Multiple Myeloma Research Harvard Medical School Boston Massachusetts USA.
Paul G RichardsonDepartment of Medical Oncology Dana-Farber Cancer Institute Jerome Lipper Center for Multiple Myeloma Research Harvard Medical School Boston Massachusetts USA.ORCID https://orcid.org/0000-0002-7426-8865
Brigham and Women's Hospital · USDana-Farber Cancer Institute · USHarvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Selinexor is an orally bioavailable selective inhibitor of nuclear export compound that inhibits exportin-1 (XPO1), a novel therapeutic target that is overexpressed in multiple myeloma (MM) and is responsible for the transport of ∼220 nuclear proteins to the cytoplasm, including tumour suppressor proteins. Inhibition of this process has demonstrated substantial antimyeloma activity in preclinical studies, both alone and in combination with established MM therapeutics. Based on a clinical trial programme encompassing multiple combination regimens, selinexor-based therapy has been approved for the treatment of relapsed/refractory MM (RRMM), with selinexor-dexamethasone approved in the later-relapse setting for penta-refractory patients and selinexor-bortezomib-dexamethasone approved for patients who have received ≥1 prior therapy. Here, we provide a comprehensive review of the clinical data on selinexor-based regimens, including recent updates from the 2022 American Society of Hematology annual meeting, and summarise ongoing studies of this novel targeted agent in newly diagnosed MM and RRMM.

Indexed as

multiple myelomanuclear exportrefractoryrelapsedselective inhibitor of nuclear exporttargeted therapyXPO1

Identifiers

PMID37601856
PMCPMC10435704
OpenAlexW4376956687

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.