Evidence map›Paper›PMID 40454396›Full record

ArticleBlood neoplasia2024

Devimistat plus chemotherapy vs chemotherapy alone for older relapsed or refractory patients with AML: results of the ARMADA trial.

Timothy S Pardee, Bayard L Powell, Richard A Larson, Joseph Maly, Michael Keng, Matthew Foster, Eun-Ji Choi, Heinz Sill, Thomas Cluzeau, Deepa Jeyakumar and 14 more

Abstract read
In one paragraph

Article in Blood neoplasia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. 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

24 authors.

Timothy S PardeeSection on Hematology and Oncology, Comprehensive Cancer Center of Atrium Health Wake Forest Baptist, Winston-Salem, NC.
Bayard L PowellSection on Hematology and Oncology, Comprehensive Cancer Center of Atrium Health Wake Forest Baptist, Winston-Salem, NC.
Richard A LarsonMedicine-Hematology/Oncology, University of Chicago, Chicago, IL.
Joseph MalyDepartment of Hematologic Malignancies and Cellular Therapy, Norton Cancer Institute, Louisville, KY.
Michael KengDivision of Hematology and Oncology, Department of Medicine, University of Virginia, Charlottesville, VA.
Matthew FosterLineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC.
Eun-Ji ChoiHematology Section, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Heinz SillDivision of Hematology, Medical University of Graz, Graz, Austria.
Thomas CluzeauUniversité Cote d'Azur, CHU de Nice, Service d'hématologie, Nice, France.
Deepa JeyakumarDivision of Hematology/Oncology, Department of Medicine, Chao Family Comprehensive Cancer Center, University of California Irvine Health, Orange, CA.
Olga FrankfurtRobert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL.
Prapti PatelHarold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX.
Michael SchusterStony Brook University Hospital Cancer Center, Stony Brook, NY.
Elisabeth KollerOeGK Hanusch-Krankenhaus Vienna, Austria.
Regis CostelloHematology and Cellular Therapy Department, Conception University Hospital, Marseille, France.
Uwe PlatzbeckerMedical Clinic and Policlinic 1, Hematology, Cellular Therapy and Hemostaseology, University of Leipzig Medical Center, Leipzig, Germany.
Pau MontesinosHematology Department, Hospital Universitari i Politècnic, La Fe, València, Spain.
Susana VivesICO Badalona-Hospital Germans Trias i Pujol, Badalona, Spain.
Aziz NazhaDepartment of Medical Oncology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA.
Rachel CookOHSU Knight Cancer Institute, Portland, OR.
Carlos Vigil-GonzalesUniversity of Iowa, Iowa City, IA.
Sylvain ChantepieInstitut d'Hématologie de Basse Normandie, CHU Caen, Caen, France.
Sanjeev LutherCornerstone Pharmaceuticals, Cranbury, NJ.
Jorge CortesGeorgia Cancer Center, Augusta University, Augusta, GA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is an aggressive cancer of the myeloid lineage. Outcomes in older patients are poor, with high rates of resistant and relapsed disease. Devimistat is a lipoic acid analog that inhibits mitochondrial metabolism. Devimistat combined with high-dose cytarabine and mitoxantrone resulted in promising phase 1 and 2 response rates especially in older patients. Therefore, the phase 3 ARMADA 2000 trial was conducted in patients aged ≥50 years with relapsed or refractory AML. The study randomized patients between devimistat combined with high-dose cytarabine and mitoxantrone (CHAM) or 1 of 3 control treatment regimens without devimistat: high-dose cytarabine and mitoxantrone; mitoxantrone, etoposide, and cytarabine; or fludarabine, cytarabine, and filgrastim. Overall, 265 patients consented to participate from 56 sites across 11 countries, and 200 patients were randomized, 98 patients to the devimistat arm and 102 patients to the control arm. The safety profile was consistent with high-dose cytarabine-based salvage regimens. There were 18 (9%) deaths on study (11 on CHAM and 7 on control). The study failed to meet its primary end point, with a complete remission (CR) rate of 20.4% in the devimistat arm compared with 21.6% in the control arm (

Identifiers

PMID40454396
PMCPMC12082102

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.