Evidence map›Paper›PMID 32951163›Full record

ArticleInternational journal of hematology2021

Phase 1 dose escalation trial of volasertib in combination with decitabine in patients with acute myeloid leukemia.

Jorge Cortes, Nikolai Podoltsev, Hagop Kantarjian, Gautam Borthakur, Amer M Zeidan, Maximilian Stahl, Tillmann Taube, Nora Fagan, Sushmita Rajeswari, Geoffrey L Uy

Abstract readClinical Trial, Phase I
PubMed Publisher
In one paragraph

Article in International journal of hematology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. PLK1 inhibition impairs erythroid differentiation.Frontiers in cell and developmental biology · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. 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

10 authors at 5 institutions in 2 countries.

Jorge CortesDepartment of Leukemia, Anderson Cancer Center, University of Texas, 1515 Holcombe Blvd, Houston, TX, 77030, USA. jcortes@mdanderson.org.
Nikolai PodoltsevDepartment of Internal Medicine, Hematology Section, Yale University School of Medicine, New Haven, CT, USA.
Hagop KantarjianDepartment of Leukemia, Anderson Cancer Center, University of Texas, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Gautam BorthakurDepartment of Leukemia, Anderson Cancer Center, University of Texas, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Amer M ZeidanDepartment of Internal Medicine, Hematology Section, Yale University School of Medicine, New Haven, CT, USA.
Maximilian StahlDepartment of Internal Medicine, Hematology Section, Yale University School of Medicine, New Haven, CT, USA.
Tillmann TaubeBoehringer Ingelheim International GmbH, Biberach, Germany.
Nora FaganBoehringer Ingelheim Pharmaceuticals, Inc, Ridgefield, CT, USA.
Sushmita RajeswariBoehringer Ingelheim Pharmaceuticals, Inc, Ridgefield, CT, USA.
Geoffrey L UyDivision of Oncology, Washington University School of Medicine, St. Louis, MO, USA.
The University of Texas MD Anderson Cancer Center · USYale University · USBoehringer Ingelheim (United States) · USBoehringer Ingelheim (Germany) · DEWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polo-like kinase 1 (PLK1) regulates mitotic checkpoints and cell division. PLK1 overexpression is reported in numerous cancers, including acute myeloid leukemia (AML), and is associated with poor prognosis. Volasertib is a selective, potent cell-cycle kinase inhibitor that targets PLK to induce mitotic arrest and apoptosis. This phase 1 trial investigated the maximum tolerated dose (MTD), safety, pharmacokinetics, and anti-leukemic activity of volasertib in combination with decitabine in AML patients aged ≥ 65 years. Thirteen patients were treated with escalating volasertib doses (3 + 3 design; 300 mg, 350 mg, and 400 mg) plus standard-dose decitabine. Dose-limiting toxicity was reported in one patient in cycle 1; the MTD of volasertib in combination with decitabine was determined as 400 mg. The most common treatment-emergent adverse events were febrile neutropenia, pneumonia, and decreased appetite. Objective response rate was 23%. The combination was well tolerated, and the adverse event profile was in line with previous findings.

Indexed as

Cell Cycle ProteinsGene ExpressionProtein Serine-Threonine KinasesProto-Oncogene ProteinsAgedAntineoplastic Combined Chemotherapy ProtocolsDecitabineDose-Response Relationship, DrugFebrile NeutropeniaFeeding and Eating DisordersFemaleHumansLeukemia, Myeloid, AcuteMaleMolecular Targeted TherapyPolo-Like Kinase 1BI 6727Cell Cycle ProteinsDecitabinePolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsPteridinesAMLDecitabinePhase 1PLK1Volasertib

Identifiers

PMID32951163
OpenAlexW3087629880

What OpenQuestion holds

Textmetadata
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.