Evidence map›Paper›PMID 38938528›Full record

ArticleMedicine international

Biomarker‑driven phase Ib clinical trial of OPB‑111077 in acute myeloid leukemia.

Joaquín Martínez-López, Pau Montesinos, Nieves López-Muñoz, Rosa Ayala, Pilar Martínez-Sánchez, Julian Gorrochategui, José Luis Rojas-Rudilla, Daniel Primo, Juan-Miguel Bergua-Burgues, María Calbacho and 10 more

Abstract read
In one paragraph

Article in Medicine international. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

20 authors.

Joaquín Martínez-LópezDepartment of Hematology, 12 de Octubre Hospital, Instituto de Investigación Hospital 12 de Octubre (i+12), Complutense University, H12O-CNIO Clinical Research Unit, CIBERONC, 28041 Madrid, Spain.
Pau MontesinosDepartment of Hematology and Hemotherapy, La Fe University and Polytechnic Hospital, 46026 Valencia, Spain.
Nieves López-MuñozDepartment of Hematology, 12 de Octubre Hospital, 28041 Madrid, Spain.
Rosa AyalaDepartment of Hematology, 12 de Octubre Hospital, 28041 Madrid, Spain.
Pilar Martínez-SánchezDepartment of Hematology, 12 de Octubre Hospital, 28041 Madrid, Spain.
Julian GorrochateguiBioinformatics, Vivia Biotech, 28760 Madrid, Spain.
José Luis Rojas-RudillaBioinformatics, Vivia Biotech, 28760 Madrid, Spain.
Daniel PrimoVP Science, Vivia Biotech, 28760 Madrid, Spain.
Juan-Miguel Bergua-BurguesDepartment of Hematology, San Pedro de Alcántara Hospital, 10003 Cáceres, Spain.
María CalbachoDepartment of Hematology, 12 de Octubre Hospital, 28041 Madrid, Spain.
Evelyn Acuña-CruzDepartment of Hematology and Hemotherapy, La Fe University and Polytechnic Hospital, 46026 Valencia, Spain.
José Antonio Pérez-SimónDepartment of Hematology, Virgen del Rocio University Hospital, Institute of Biomedicine of Sevilla (IBIS/CSIC, CIBERONC), University of Sevilla, 41013 Sevilla, Spain.
Adolfo De La FuenteDepartment of Hematology, MD Anderson Cancer Center, 28033 Madrid, Spain.
Jaime Pérez De OteyzaDepartment of Hematology, HM Sanchinarro University Hospital, School of Medicine, University CEU San Pablo, 28050 Madrid, Spain.
Rebeca Rodriguez-VeigaDepartment of Hematology and Hemotherapy, La Fe University and Polytechnic Hospital, 46026 Valencia, Spain.
José Sánchez PinaDepartment of Hematology, 12 de Octubre Hospital, 28041 Madrid, Spain.
Blanca BoludaDepartment of Hematology and Hemotherapy, La Fe University and Polytechnic Hospital, 46026 Valencia, Spain.
Isabel CanoDepartment of Hematology and Hemotherapy, La Fe University and Polytechnic Hospital, 46026 Valencia, Spain.
María Liz Paciello CoronelDepartment of Hematology, 12 de Octubre Hospital, 28041 Madrid, Spain.
Juan BallesterosVivia Biotech, 28760 Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

OPB-111077 is a novel, highly specific oral signal transducer and activator of transcription 3 inhibitor that has exhibited good efficacy against solid and blood cancers, including acute myeloid leukemia (AML), in preclinical models. In the present study, a phase 1b, two-stage, 3+3 dose-escalation clinical trial [dose level (DL)1 of 200 mg/day and DL2 of 250 mg/day on a once daily dose schedule in 28-day cycles] was conducted to assess the maximum tolerated dose (MTD), safety profile and the preliminary antitumor activity of OPB-111077 in patients with high-risk AML. A preliminary preclinical analysis evaluated the anti-proliferative activity of OPB-111077 in 19 patients with AML with a Vivia Biotech

Indexed as

ex vivo sensitivity testmaximum tolerated doseOPB-111077relapsed/refractory acute myeloid leukemiaSTAT3

Identifiers

PMID38938528
PMCPMC11208994

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Registered trials

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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.