Evidence map›Paper›PMID 36860654›Full record

ArticleCancer research communications2023

Combination of a New Oral Demethylating Agent, OR2100, and Venetoclax for Treatment of Acute Myeloid Leukemia.

Kazuharu Kamachi, Hiroshi Ureshino, Tatsuro Watanabe, Nao Yoshida-Sakai, Yuki Fukuda-Kurahashi, Kazunori Kawasoe, Toshimi Hoshiko, Yuta Yamamoto, Yuki Kurahashi, Shinya Kimura

Open access · goldAbstract read
In one paragraph

Article in Cancer research communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
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 3 institutions in 1 country.

Kazuharu KamachiDepartment of Drug Discovery and Biomedical Sciences, Faculty of Medicine, Saga University, Saga, Japan.ORCID 0000-0002-7346-4864
Hiroshi UreshinoDepartment of Drug Discovery and Biomedical Sciences, Faculty of Medicine, Saga University, Saga, Japan.ORCID 0000-0002-5034-3699
Tatsuro WatanabeDepartment of Drug Discovery and Biomedical Sciences, Faculty of Medicine, Saga University, Saga, Japan.ORCID 0000-0002-4166-4781
Nao Yoshida-SakaiDepartment of Drug Discovery and Biomedical Sciences, Faculty of Medicine, Saga University, Saga, Japan.ORCID 0000-0001-8375-3662
Yuki Fukuda-KurahashiDepartment of Drug Discovery and Biomedical Sciences, Faculty of Medicine, Saga University, Saga, Japan.ORCID 0000-0002-5909-9303
Kazunori KawasoeDepartment of Drug Discovery and Biomedical Sciences, Faculty of Medicine, Saga University, Saga, Japan.ORCID 0000-0001-9476-3161
Toshimi HoshikoDivision of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.ORCID 0000-0001-9083-1200
Yuta YamamotoDepartment of Drug Discovery and Biomedical Sciences, Faculty of Medicine, Saga University, Saga, Japan.ORCID 0000-0001-5905-7843
Yuki KurahashiDepartment of Drug Discovery and Biomedical Sciences, Faculty of Medicine, Saga University, Saga, Japan.ORCID 0000-0001-6136-9037
Shinya KimuraDepartment of Drug Discovery and Biomedical Sciences, Faculty of Medicine, Saga University, Saga, Japan.ORCID 0000-0003-1717-6208
Saga University · JPMochida Pharmaceutical (Japan) · JPHiroshima University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The standard treatment for elderly patients with acute myeloid leukemia (AML) is venetoclax (Ven), a BCL-2-selective inhibitor, combined with hypomethylating agents (HMA) such as azacitidine or decitabine. This regimen results in low toxicity, high response rates, and potentially durable remission; however, because of low oral bioavailability, these conventional HMAs must be administered intravenously or subcutaneously. A combination of oral HMAs and Ven would provide a therapeutic advantage over parenteral administration of drugs and improve quality of life by reducing the number of hospital visits. Previously, we showed the promising oral bioavailability and antileukemia effects of a new HMA, OR2100 (OR21). Here, we investigated the efficacy and underlying mechanism of OR21 when used in combination with Ven to treat AML. OR21/Ven showed synergistic antileukemia effects Significance: The standard treatment for elderly patients with AML is Ven combined with HMAs. OR21, a new oral HMA plus Ven showed synergistic antileukemia effects

Indexed as

Antineoplastic AgentsLeukemia, Myeloid, AcuteAgedAnimalsAzacitidineBridged Bicyclo Compounds, HeterocyclicHumansMiceQuality of LifeSulfonamidesAntineoplastic AgentsAzacitidineBridged Bicyclo Compounds, HeterocyclicSulfonamidesvenetoclax

Identifiers

PMID36860654
PMCPMC9973401
OpenAlexW4319593868

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.