Evidence map›Paper›PMID 42007254›Full record

Trial reportBlood neoplasia2026

Results of a phase 1 trial testing ruxolitinib plus venetoclax in patients with relapsed/refractory acute myeloid leukemia.

Uma Borate, Cristina E Tognon, Yazan F Madanat, Shikha Misra, Andy Kaempf, Prapti A Patel, Kara L Davis, Junwei Sun, Lucille Stuani, Eric D Eisenmann and 27 more

Abstract readClinical Trial
In one paragraph

Trial report in Blood neoplasia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

37 authors.

Uma BorateDepartment of Internal Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, OH.
Cristina E TognonDivision of Oncological Sciences, Department of Medicine, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Yazan F MadanatDepartment of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, TX.
Shikha MisraCenter for Hematologic Malignancies, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Andy KaempfBiostatistics Shared Resource, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Prapti A PatelDepartment of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, TX.
Kara L DavisDivision of Hematology, Oncology and Stem Cell Transplant and Regenerative Medicine, Department of Pediatrics, Stanford University, Stanford, CA.
Junwei SunDepartment of Statistics, Stanford University, Stanford, CA.
Lucille StuaniDivision of Hematology, Oncology and Stem Cell Transplant and Regenerative Medicine, Department of Pediatrics, Stanford University, Stanford, CA.
Eric D EisenmannDivision of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, OH.
Christopher A EideDivision of Hematology and Medical Oncology, Department of Medicine, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Stephen E KurtzDivision of Oncological Sciences, Department of Medicine, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Kevin Watanabe-SmithDivision of Oncological Sciences, Department of Medicine, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Kara JohnsonDivision of Hematology and Medical Oncology, Department of Medicine, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Astraea JagerDivision of Hematology, Oncology and Stem Cell Transplant and Regenerative Medicine, Department of Pediatrics, Stanford University, Stanford, CA.
Stein-Erik GullaksenDepartment of Biomedical Data Sciences, Stanford University, Stanford, CA.
Bridget RobinsonDepartment of Biomedical Engineering, School of Medicine, Oregon Health & Science University, Portland, OR.
Tania VuDepartment of Biomedical Engineering, School of Medicine, Oregon Health & Science University, Portland, OR.
Sylvia K PlevritisCentre of Cancer Biomarkers, Department of Clinical Science, University of Bergen, Bergen, Norway.
Sharyn D BakerDivision of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, OH.
Jessica MinnierBiostatistics Shared Resource, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Peter ClementCenter for Hematologic Malignancies, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Sammantha AvaylonDivision of Hematology and Medical Oncology, Department of Medicine, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Madison HayesCenter for Hematologic Malignancies, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Laura F NewellDivision of Hematology and Medical Oncology, Department of Medicine, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Arpita P GandhiDivision of Hematology and Medical Oncology, Department of Medicine, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Jessica LeonardDivision of Hematology and Medical Oncology, Department of Medicine, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Brandon Hayes-LattinDivision of Hematology and Medical Oncology, Department of Medicine, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Sumithira VasuDepartment of Internal Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, OH.
Rachel J CookDivision of Hematology and Medical Oncology, Department of Medicine, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Gabrielle MeyersDivision of Hematology and Medical Oncology, Department of Medicine, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Richard T MaziarzDivision of Hematology and Medical Oncology, Department of Medicine, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Elie TraerDivision of Hematology and Medical Oncology, Department of Medicine, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Ronan SwordsDivision of Hematology and Medical Oncology, Department of Medicine, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Jeffrey W TynerDepartment of Cell, Developmental and Cancer Biology, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Brian J DrukerDivision of Hematology and Medical Oncology, Department of Medicine, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.
Jennifer N SaultzDivision of Hematology and Medical Oncology, Department of Medicine, Knight Cancer Institute, Oregon Health & Science University, Portland, OR.

Funding

Tumor Intrinsic and Microenvironmental Mechanisms Driving Drug Combination Efficacy and Resistance in AMLU54CA224019 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI BRIAN J DRUKER · 2017 to 2026
$13.9M
Proteogenomic characterization of early and late resistance mechanisms in acute myeloid leukemiaU01CA271412 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI BRIAN J DRUKER, Paul D Piehowski · 2022 to 2026
$5.8M
Mechanisms of venetoclax combination activity in acute myeloid leukemiaR01CA262758 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Stephen E Kurtz, Jeffrey Wallace Tyner · 2021 to 2026
$2.1M
NCI NIH HHS R01 CA262758NCI NIH HHS U01 CA271412NCI NIH HHS U54 CA224019
6 · The paper itself

Abstract

Functional small-molecule screening of primary acute myeloid leukemia (AML) samples identified ex vivo synergy between the JAK1/2 inhibitor, ruxolitinib (Rux), and venetoclax (Ven) in newly diagnosed and relapsed/refractory (R/R) AML. This motivated a phase 1 multicenter trial to evaluate Rux + Ven in 30 patients with R/R AML. Patients had median age of 69 years and were heavily pretreated (40% with ≥3 previous lines, 43% with previous Ven failure). Rux (30 mg twice daily) and Ven (400 mg once daily) were well tolerated without dose-limiting toxicities. Median duration of therapy was 55 days. Over 2 cycles of Rux + Ven, clinical response rate was 20% and composite complete remission (CR) rate was 10%. Median survival was 3.7 months, with 23% alive at 1 year. There were 2 exceptional responders, including a patient who remained in CR/CR with incomplete hematologic recovery for nearly 4 years after hypomethylating agent + Ven failure. CD56 expression on blasts was significantly associated with lack of clinical response (odds ratio, 0.09;

Identifiers

PMID42007254
PMCPMC13087466

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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.