Evidence map›Paper›PMID 39911057›Full record

ArticleFuture oncology (London, England)2025

Selinexor plus ruxolitinib in JAK inhibitor treatment-naïve myelofibrosis: SENTRY Phase 3 study design.

John Mascarenhas, Keri Maher, Raajit Rampal, Prithviraj Bose, Nikolai Podoltsev, Junshik Hong, Yi Chai, Steve Kye, Michael Method, Claire Harrison and 1 more

Registry-linked trialAbstract readClinical Trial Protocol
In one paragraph

Article in Future oncology (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04562389 (A Phase 1/3 Study to Evaluate Efficacy and Safety of Selinexor, a Selective Inhibitor of Nuclear Export, in Combination With Ruxolitinib in Treatment-naïve Patients With Myelofibrosis), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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.

NCT04562389 phase3active not recruitingnot on this map

A Phase 1/3 Study to Evaluate Efficacy and Safety of Selinexor, a Selective Inhibitor of Nuclear Export, in Combination With Ruxolitinib in Treatment-naïve Patients With Myelofibrosis

TypeinterventionalSponsorKaryopharm Therapeutics IncRan2021 to 2028Enrolled353ConditionsMyelofibrosisArmsSelinexor, Placebo, Ruxolitinib
3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Selinexor Plus Ruxolitinib in Janus Kinase Inhibitor-Naïve Myelofibrosis: Phase III SENTRY Trial.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026
    Trial
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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

11 authors.

John MascarenhasInternal Medicine Department, Icahn School of Medicine at Mount Sinai (ISMMS), New York, NY, USA.
Keri MaherOncology Department, VCU Medical Center, Richmond, VA, USA.
Raajit RampalOncology Department, Memorial Sloan and Kettering Center, New York, NY, USA.
Prithviraj BoseDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, USA.
Nikolai PodoltsevDepartment of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.
Junshik HongHemato Oncology, Seoul National University, Seoul, South Korea.
Yi ChaiDepartment of Research, Karyopharm Therapeutics, Newton, MA, USA.
Steve KyeDepartment of Research, Karyopharm Therapeutics, Newton, MA, USA.
Michael MethodDepartment of Research, Karyopharm Therapeutics, Newton, MA, USA.
Claire HarrisonDepartment of Internal Medicine, Guy's and St Thomas' NHS Foundation Trust, London, UK.
SENTRY investigators

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Selinexor is an investigational, selective oral XPO1 inhibitor that may inhibit myelofibrosis (MF)-relevant JAK/STAT and non-JAK/STAT pathways with potential synergy with ruxolitinib. SENTRY (XPORT-MF-034; NCT04562389) is a Phase 1/3 study evaluating safety and efficacy of selinexor plus ruxolitinib for treatment of patients with JAK inhibitor (JAKi) treatment-naïve MF. The Phase 1 open label portion of the study included a 3 + 3 dose escalation and dose expansion, with no dose limiting toxicities observed. Described here is the Phase 3 randomized, double-blind, placebo-controlled study designed to evaluate selinexor+ruxolitinib versus placebo+ruxolitinib in patients with JAKi treatment-naïve MF. Approximately 350 patients will be enrolled. Primary endpoints will evaluate spleen volume reduction ≥ 35% and absolute mean change in total symptom score from baseline to week 24.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsHydrazinesJanus Kinase InhibitorsPrimary MyelofibrosisPyrazolesTriazolesAdultClinical Trials, Phase III as TopicDouble-Blind MethodFemaleHumansMaleMiddle AgedNitrilesPyrimidinesRandomized Controlled Trials as TopicHydrazinesJanus Kinase InhibitorsNitrilesPyrazolesPyrimidinesruxolitinibselinexorTriazolesClinical trialsmyelofibrosisphase 3ruxolitinibselinexor

Identifiers

PMID39911057
PMCPMC11916360

What OpenQuestion holds

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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.