Evidence map›Paper›PMID 36467792›Full record

ArticleEJHaem2022

Selinexor-based regimens in patients with multiple myeloma after prior anti-B-cell maturation antigen treatment.

Muhamed Baljevic, Cristina Gasparetto, Gary J Schiller, Sascha A Tuchman, Natalie S Callander, Suzanne Lentzsch, Jorge Monge, Rami Kotb, Nizar J Bahlis, Darrell White and 16 more

Open access · diamondAbstract read
In one paragraph

Article in EJHaem, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.4field-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

16 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
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  7. Review
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  10. Options at the time of relapse after anti-BCMA therapy.Hematology. American Society of Hematology. Education Program · 2023
    Article
  11. Observational
  12. Review
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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

26 authors at 20 institutions in 2 countries.

Muhamed BaljevicVanderbilt-Ingram Cancer Center Vanderbilt University Medical Center Nashville Tennessee USA.ORCID https://orcid.org/0000-0002-0630-8458
Cristina GasparettoDuke Cancer Institute Duke University Durham North Carolina USA.
Gary J SchillerHematological Malignancy/Stem Cell Transplant Program University of California - Los Angeles David Geffen School of Medicine Los Angeles California USA.
Sascha A TuchmanDepartment of Medicine Division of Hematology The University of North Carolina at Chapel Hill Chapel Hill North Carolina USA.
Natalie S CallanderDivision of Hematology/Oncology, Department of Medicine University of Wisconsin-Madison School of Medicine and Public Health Madison Wisconsin USA.
Suzanne LentzschColumbia University Medical Center New York New York USA.
Jorge MongeWeill Cornell Medicine New York New York USA.
Rami KotbMedical Oncology and Hematology CancerCare Manitoba Winnipeg Manitoba Canada.
Nizar J BahlisArnie Charbonneau Cancer Research Institute University of Calgary Calgary Alberta Canada.ORCID https://orcid.org/0000-0001-7353-7034
Darrell WhiteDepartment of Medicine/Division of Hematology Dalhousie University Halifax Nova Scotia Canada.
Christine I ChenPrincess Margaret Cancer Centre Toronto Ontario Canada.
Heather J SutherlandDivision of Hematology Vancouver General Hospital Vancouver British Columbia Canada.
Sumit MadanBanner MD Anderson Cancer Center Gilbert Arizona USA.
Richard LeBlancMaisonneuve-Rosemont Hospital University of Montreal Montreal Québec Canada.
Michael SebagDivision of Hematology McGill University Health Centre Montreal Québec Canada.
Christopher P VennerCross Cancer Institute University of Alberta Edmonton Alberta Canada.
William I BensingerCenter for Blood Disorders and Stem Cell Transplantation Swedish Cancer Institute Seattle Washington USA.
Noa BiranJohn Theurer Cancer Center, Hackensack Meridian Health Hackensack University Medical Center Hackensack New Jersey USA.ORCID https://orcid.org/0000-0003-0693-4202
Andrew DeCastroKaryopharm Therapeutics Inc. Newton Massachusetts USA.
Dane R Van DomelenKaryopharm Therapeutics Inc. Newton Massachusetts USA.
Chris ZhangKaryopharm Therapeutics Inc. Newton Massachusetts USA.
Jatin J ShahKaryopharm Therapeutics Inc. Newton Massachusetts USA.
Sharon ShachamKaryopharm Therapeutics Inc. Newton Massachusetts USA.
Michael G KauffmanKaryopharm Therapeutics Inc. Newton Massachusetts USA.
Ohad S BenturKaryopharm Therapeutics Inc. Newton Massachusetts USA.
Brea LipeWilmot Cancer Institute University of Rochester Medical Center Rochester New York USA.
Karyopharm Therapeutics (United States) · USBanner MD Anderson Cancer CenterCancerCare Manitoba · CAColumbia University Irving Medical Center · USCornell University · USDalhousie University · CADuke University · USHackensack University Medical Center · USHôpital Maisonneuve-Rosemont · CAMcGill University Health Centre · CAPrincess Margaret Cancer Centre · CASwedish Medical Center · USUniversity of Alberta · CAUniversity of Calgary · CAUniversity of California, Los Angeles · USUniversity of North Carolina at Chapel Hill · USUniversity of Rochester Medical Center · USUniversity of Wisconsin–Madison · USVancouver General Hospital · CAVanderbilt University Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a lack of consensus on therapy sequencing in previously treated multiple myeloma, particularly after anti-B-cell maturation antigen (BCMA) therapy. Earlier reports on selinexor (X) regimens demonstrated considerable efficacy in early treatment, and after anti-BCMA-targeted chimeric antigen receptor-T cell therapy. Here, we present data from 11 heavily pretreated patients who predominantly received BCMA-antibody-drug conjugate therapy. We observe that X-containing regimens are potent and achieve durable responses with numerically higher overall response and clinical benefit rates, as well as median progression free survival compared to patients' prior anti-BCMA therapies, despite being used later in the treatment course. In an area of evolving unmet need, these data reaffirm the efficacy of X-based regimens following broader anti-BCMA therapy.

Indexed as

anti‐BCMAmultiple myelomaselinexor

Identifiers

PMID36467792
PMCPMC9713049
OpenAlexW4298143191

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.