Evidence map›Paper›PMID 25441108›Full record

Trial reportClinical lymphoma, myeloma & leukemia2015

A phase I/II study of the Janus kinase (JAK)1 and 2 inhibitor ruxolitinib in patients with relapsed or refractory acute myeloid leukemia.

Naveen Pemmaraju, Hagop Kantarjian, Tapan Kadia, Jorge Cortes, Gautam Borthakur, Kate Newberry, Guillermo Garcia-Manero, Farhad Ravandi, Elias Jabbour, Sara Dellasala and 2 more

Open access · greenAbstract readClinical Trial, Phase IClinical Trial, Phase II
In one paragraph

Trial report in Clinical lymphoma, myeloma & leukemia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

43 citing papers in PubMed, 77 citations in OpenAlex.

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  17. Proteomics: Concepts and applications in human medicine.World journal of biological chemistry · 2021
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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

12 authors at 1 institution in 1 country.

Naveen PemmarajuDepartment of Leukemia, The University of Texas, M.D. Anderson Cancer Center, Houston, TX.
Hagop KantarjianDepartment of Leukemia, The University of Texas, M.D. Anderson Cancer Center, Houston, TX.
Tapan KadiaDepartment of Leukemia, The University of Texas, M.D. Anderson Cancer Center, Houston, TX.
Jorge CortesDepartment of Leukemia, The University of Texas, M.D. Anderson Cancer Center, Houston, TX.
Gautam BorthakurDepartment of Leukemia, The University of Texas, M.D. Anderson Cancer Center, Houston, TX.
Kate NewberryDepartment of Leukemia, The University of Texas, M.D. Anderson Cancer Center, Houston, TX.
Guillermo Garcia-ManeroDepartment of Leukemia, The University of Texas, M.D. Anderson Cancer Center, Houston, TX.
Farhad RavandiDepartment of Leukemia, The University of Texas, M.D. Anderson Cancer Center, Houston, TX.
Elias JabbourDepartment of Leukemia, The University of Texas, M.D. Anderson Cancer Center, Houston, TX.
Sara DellasalaDepartment of Leukemia, The University of Texas, M.D. Anderson Cancer Center, Houston, TX.
Sherry PierceDepartment of Leukemia, The University of Texas, M.D. Anderson Cancer Center, Houston, TX.
Srdan VerstovsekDepartment of Leukemia, The University of Texas, M.D. Anderson Cancer Center, Houston, TX. Electronic address: sverstov@mdanderson.org.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Transgenic Mouse and Biobank CoreP01CA095616 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DEPINHO, RONALD ANTHONY · 2003 to 2012
$20.3M
NCI NIH HHS CA016672NCI NIH HHS P01 CA095616NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

backgroundRuxolitinib is a potent and specific JAK1/JAK2 inhibitor recently approved for the treatment of myelofibrosis. PATIENTS AND

methodsWe conducted a single-center phase I/II clinical study testing 3 dose levels (50 mg b.i.d. [n = 4], 100 mg b.i.d. [n = 5], and 200 mg b.i.d. [n = 18]). We enrolled 27 patients older than 14 years with relapsed or refractory acute myeloid leukemia (n = 26) or acute lymphoid leukemia (n = 1).

resultsThe median age was 66 (range, 25-88) years. Thirteen patients were evaluable for dose-limiting toxicities. The most common Grade 3 or 4 nonhematologic event was infection (n = 26 events; most frequently pneumonia; 15 of 26; 58%). One patient with multiple relapses after 7 lines of therapy had a CRp at a ruxolitinib dose of 200 mg b.i.d.

conclusionIn this cohort of heavily pretreated patients with relapsed or refractory acute leukemias, ruxolitinib was overall reasonably well tolerated, with 1 patient achieving CRp.

Indexed as

AdultAgedAged, 80 and overAntineoplastic AgentsBone MarrowChromosome AberrationsHumansJanus Kinase 1Janus Kinase 2Leukemia, Myeloid, AcuteMiddle AgedMutationNitrilesProtein Kinase InhibitorsPyrazolesPyrimidinesAntineoplastic AgentsJanus Kinase 1Janus Kinase 2NitrilesProtein Kinase InhibitorsPyrazolesPyrimidinesruxolitinibAcute myelogenous leukemiaClinical studyJAK2V617 mutationJanus kinase inhibitorMyelofibrosisRuxolitinib

Identifiers

PMID25441108
PMCPMC4344906
OpenAlexW2047154875

What OpenQuestion holds

Textmetadata
LicenceTDM
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.