Evidence map›Paper›PMID 35608822›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2022

Selinexor Combined with Ibrutinib Demonstrates Tolerability and Safety in Advanced B-Cell Malignancies: A Phase I Study.

Deborah M Stephens, Ying Huang, Amy S Ruppert, Janek S Walker, Daniel Canfield, Casey B Cempre, Qiang Fu, Sharyn Baker, Boyu Hu, Harsh Shah and 8 more

Registry-linked trialOpen access · bronzeAbstract readClinical Trial, Phase I
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02303392 (A Dose Escalation Study of Selinexor), which is not on this map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
3.5field-weighted citation impact, top 6% 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.

NCT02303392 phase1completednot on this map

A Dose Escalation Study of Selinexor (KPT-330), a Selective Inhibitor of Nuclear Export, and Ibrutinib, a Bruton's Tyrosine Kinase Inhibitor, in Patients With Relapsed and Refractory Chronic Lymphocytic Leukemia or Aggressive Non-Hodgkin Lymphoma

TypeinterventionalSponsorJennifer WoyachRan2015 to 2022Enrolled34ConditionsProlymphocytic Leukemia, Recurrent Adult Diffuse Large Cell Lymphoma, Recurrent Mantle Cell Lymphoma, Recurrent Small Lymphocytic LymphomaArmsSelinexor, Ibrutinib, Pharmacological Study, Laboratory Biomarker Analysis
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 2 syntheses or guidelines pooled it, 26 citations in OpenAlex.

  1. Pooled it
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  6. Modulation of anti-tumour immunity by XPO1 inhibitors.Exploration of targeted anti-tumor therapy · 2025
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  13. Nuclear transport proteins: structure, function, and disease relevance.Signal transduction and targeted therapy · 2023
    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

18 authors at 2 institutions in 1 country.

Deborah M StephensUniversity of Utah, Salt Lake City, Utah.ORCID 0000-0001-9188-5008
Ying HuangOhio State University, Columbus, Ohio.ORCID 0000-0001-9910-1212
Amy S RuppertOhio State University, Columbus, Ohio.
Janek S WalkerOhio State University, Columbus, Ohio.ORCID 0000-0002-2049-1527
Daniel CanfieldOhio State University, Columbus, Ohio.
Casey B CempreOhio State University, Columbus, Ohio.
Qiang FuOhio State University, Columbus, Ohio.
Sharyn BakerOhio State University, Columbus, Ohio.ORCID 0000-0003-3062-3252
Boyu HuUniversity of Utah, Salt Lake City, Utah.ORCID 0000-0001-9848-9497
Harsh ShahUniversity of Utah, Salt Lake City, Utah.
Renee VadeboncoeurUniversity of Utah, Salt Lake City, Utah.
Kerry A RogersOhio State University, Columbus, Ohio.ORCID 0000-0001-5748-7874
Seema BhatOhio State University, Columbus, Ohio.ORCID 0000-0001-7844-0856
Samantha M JaglowskiOhio State University, Columbus, Ohio.ORCID 0000-0002-4335-2554
Hank LockmanOhio State University, Columbus, Ohio.
Rosa LapalombellaOhio State University, Columbus, Ohio.
John C ByrdOhio State University, Columbus, Ohio.
Jennifer A WoyachOhio State University, Columbus, Ohio.
Ohio University · USUniversity of Utah · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
Targeted Therapy for LeukemiaR35CA197734 · NCI · UNIVERSITY OF CINCINNATI · PI BYRD, JOHN C. · 2015 to 2021
$6.6M
The Chesapeake-Ohio Pharmacokinetics Core for The ETCTNU24CA247648 · NCI · JOHNS HOPKINS UNIVERSITY · PI Jan Hendrik Beumer, Mitch A Phelps · 2020 to 2026
$3.6M
Dual targeting of XPO1 and BTK in B cell malignanciesR01CA192928 · NCI · OHIO STATE UNIVERSITY · PI BYRD, JOHN C., LAPALOMBELLA, ROSA · 2015 to 2019
$2.3M
NRSA Training CoreTL1TR002735 · NCATS · OHIO STATE UNIVERSITY · PI BUMGARDNER, GINNY L, KIRSCHNER, LAWRENCE S · 2018 to 2022
$1.3M
Novel Strategies to Eliminate Resistance to B-cell Receptor Inhibitor Therapy in Lymphoid MalignanciesK23CA212271 · NCI · UNIVERSITY OF UTAH · PI STEPHENS, DEBORAH · 2016 to 2020
$902k
NCATS NIH HHS TL1 TR002735NCI NIH HHS F31 CA261139NCI NIH HHS K23 CA212271NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA192928NCI NIH HHS R35 CA197734NCI NIH HHS U24 CA247648
6 · The paper itself

Abstract

purposeDual blockade of Bruton's tyrosine kinase with ibrutinib and selinexor has potential to deepen responses for patients with chronic lymphocytic leukemia (CLL) and non-Hodgkin lymphoma (NHL). PATIENTS AND

methodsIn this phase I study (clinicaltrials.gov: NCT02303392), adult patients with CLL/NHL, relapsed/refractory to ≥1 prior therapy were enrolled. Patients received weekly oral selinexor and daily oral ibrutinib in 28-day cycles until progression or intolerance. Primary objective was to determine MTD.

resultsIncluded patients had CLL (n = 16) or NHL (n = 18; 9 Richter transformation, 6 diffuse large B-cell lymphoma, and 3 mantle cell lymphoma). Median prior therapies were 4 (range = 1-14) and 59% previously received ibrutinib. The established MTD was 40 mg of selinexor (days 1, 8, 15) and 420 mg daily ibrutinib. Common nonhematologic adverse events were fatigue (56%), nausea (53%), anorexia (41%), and diarrhea (41%) and were mostly low grade. Overall response rate was 32%. An additional 47% achieved stable disease (SD), some prolonged (up to 36 months). Median progression-free survival for patients with CLL and NHL was 8.9 [95% confidence interval (CI), 3.9-16.1] and 2.7 (95% CI, 0.7-5.4) months, respectively. For patients with CLL who did not receive prior ibrutinib, only 20% (1/5) progressed. Estimated 2-year overall survival was 73.7% (95% CI, 44.1-89.2) and 27.8% (95% CI, 10.1-48.9) for patients with CLL and NHL, respectively.

conclusionsThe selinexor and ibrutinib combination has demonstrated tolerability in patients with relapsed/refractory CLL/NHL. Responses were durable. Notable responses were seen in patients with CLL with minimal prior therapy. Future study of this combination will focus on efforts to deepen remissions in patients with CLL receiving ibrutinib therapy.

Indexed as

Leukemia, Lymphocytic, Chronic, B-CellLymphoma, Large B-Cell, DiffuseLymphoma, Non-HodgkinAdenineAdultHumansHydrazinesPiperidinesPyrazolesPyrimidinesTriazolesAdenineHydrazinesibrutinibPiperidinesPyrazolesPyrimidinesselinexorTriazoles

Identifiers

PMID35608822
PMCPMC9364840
OpenAlexW4281385652

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.