Evidence map›Paper›PMID 34271963›Full record

Trial reportJournal of hematology & oncology2021

Survival among patients with relapsed/refractory diffuse large B cell lymphoma treated with single-agent selinexor in the SADAL study.

Marie Maerevoet, Josee M Zijlstra, George Follows, Rene-Olivier Casasnovas, J S P Vermaat, Nagesh Kalakonda, Andre Goy, Sylvain Choquet, Eric Van Den Neste, Brian Hill and 24 more

Registry-linked trialOpen access · goldAbstract readClinical TrialLetter
In one paragraph

Trial report in Journal of hematology & oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02227251 (A Phase 2b Open-label Study of Selinexor), which is not on this map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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.

NCT02227251 phase2active not recruitingnot on this map

A Phase 2b Open-label Study of Selinexor (KPT-330) in Patients With Relapsed/Refractory Diffuse Large B-Cell Lymphoma (DLBCL)

TypeinterventionalSponsorKaryopharm Therapeutics IncRan2014 to 2026Enrolled244ConditionsDiffuse Large B-cell LymphomaArmsSelinexor
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
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

34 authors at 20 institutions in 15 countries.

Marie MaerevoetService Hématologie, Institut Jules Bordet, 1000, Brussels, Belgium. marie.maerevoet@bordet.be.ORCID 0000-0002-5413-0164
Josee M ZijlstraAmsterdam UMC, Vrije Universiteit, Cancer Center, Amsterdam, Netherlands.
George FollowsAddenbrooke's Hospital, Cambridge, UK.
Rene-Olivier CasasnovasHématologie Clinique and INSERM 1231, CHU Dijon, Dijon, France.
J S P VermaatLUMC, Leiden, Netherlands.
Nagesh KalakondaUniversity of Liverpool, Liverpool, UK.
Andre GoyHackensack University Medical Center, Hackensack, USA.
Sylvain ChoquetHôpital Pitié Salpêtrière, Paris, France.
Eric Van Den NesteCliniques Universitaires Saint-Luc, Brussels, Belgium.
Brian HillCleveland Clinic, Cleveland, USA.
Catherine ThieblemontAPHP, Hemato-oncology, Saint-Louis Hospital, Paris, France.
Federica CavalloUniversity of Torino, Turin, Italy.
Fatima De la CruzHospital Universitario Virgen del Rocio, Sevilla, Spain.
John KuruvillaPrincess Margaret Cancer Centre, Toronto, Canada.
Nada HamadSt. Vincent's Hospital Sydney, Darlinghurst, Australia.
Ulrich JaegerMedical University of Vienna, Vienna, Austria.
Paolo CaimiUH Seidman Cancer Center, Cleveland, USA.
Ronit GurionRabin MC, Petah Tiqwa, Israel.
Krzysztof WarzochaInstytut Hematologii I Transfuzjologii, Warsaw, Poland.
Sameer BakhshiDr. B. R. A. Institute Rotary Cancer Hospital, New Delhi, India.
Juan-Manuel SanchoHospital Universitari Germans Trias I Pujol, Barcelona, Spain.
Michael SchusterStony Brook University Hospital Cancer Center, Stony Brook, USA.
Miklos EgyedTeaching Hospital Mór Kaposi, Kaposvár, Hungary.
Fritz OffnerUZ Gent, Gent, Belgium.
Theodoros P VassilakopoulosLaikon General Hospital, National and Kapodistrian University of Athens, Athens, Greece.
Priyanka SamalInstitute of Medical Sciences and SUM Hospital, Bhubaneswar, Odisha, India.
Matthew KuSt.Vincent's Hospital Melbourne, Fitzroy, Australia.
Xiwen MaKaryopharm Therapeutics, Newton, USA.
Kelly CoronaKaryopharm Therapeutics, Newton, USA.
Kamal ChamounKaryopharm Therapeutics, Newton, USA.
Jatin ShahKaryopharm Therapeutics, Newton, USA.
Sharon ShachamKaryopharm Therapeutics, Newton, USA.
Michael G KauffmanKaryopharm Therapeutics, Newton, USA.
Miguel CanalesHospital Universitario La Paz, Madrid, Spain.
Karyopharm Therapeutics (United States) · USAddenbrooke's Hospital · GBAmsterdam University Medical Centers · NLCleveland Clinic · USCliniques Universitaires Saint-Luc · BEDélégation Paris 7 · FRDR. B.R.A. Institute Rotary Cancer Hospital · INGhent University Hospital · BEHackensack University Medical Center · USHospital Universitari Germans Trias i Pujol · ESHospital Universitario La Paz · ESHospital Universitario Virgen del Rocío · ESInserm · FRInstitute of Medical Sciences and Sum Hospital · INInstitut Jules Bordet · BEInstytut Hematologii i Transfuzjologi · PLMedical University of Vienna · ATNational and Kapodistrian University of Athens · GRPrincess Margaret Cancer Centre · CASomogy Megyei Kaposi Mór Oktató Kórház · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with RR DLBCL who have received ≥ 2 lines of therapy have limited treatment options and an expected overall survival (OS) of < 6 months. The SADAL study evaluated single-agent oral selinexor in patients with RR DLBCL and demonstrated an overall response rate (ORR) of 29.1% with median duration of response (DOR) of 9.3 months. The analyses described here evaluated a number of subpopulations in order to understand how response correlates with survival outcomes in order to identify patients who could most optimally benefit from selinexor treatment. Median age was 67 years; 44.8% of patients were ≥ 70 years of age. The median OS was 9.0 months (95% CI 6.2, 13.7) at a median follow-up of 14.8 months. The median OS was not reached in patients with a CR or PR, while patients who did not respond have a median OS of 4.9 months (p < 0.0001). Patients < 70 years had an OS of 11.1 months compared with 7.8 months in patients ≥ 70 years. Among patients with or without prior ASCT, the median OS was 10.9 and 7.8 months, respectively. Among patients with disease refractory to the most recent DLBCL treatment regimen, the median OS was 7.0 months compared with 11.1 months for disease not refractory to the most recent treatment. In a patient population in which survival is expected to be < 6 months, treatment with single-agent oral selinexor was associated with a median survival of 9 months. Increased median OS observed in patients responding to selinexor was consistent across subgroups regardless of age, prior ASCT therapy, or refractory status. Randomized studies of selinexor in combination with a variety of other anti-DLBCL agents are planned. This trial was registered at ClinicalTrials.gov (NCT02227251) on August 28, 2014. https://clinicaltrials.gov/ct2/show/NCT02227251 .

Indexed as

AgedAge FactorsHumansHydrazinesLymphoma, Large B-Cell, DiffuseNeoplasm Recurrence, LocalSurvival AnalysisTreatment OutcomeTriazolesHydrazinesselinexorTriazolesDLBCLExportin-1SelinexorSINE compounds

Identifiers

PMID34271963
PMCPMC8283921
OpenAlexW3178156199

What OpenQuestion holds

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LicenceCC BY
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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.