Evidence map›Paper›PMID 18094935›Full record

ArticleInvestigational new drugs2008

Phase I study of a novel pro-apoptotic drug R-etodolac in patients with B-cell chronic lymphocytic leukemia.

Markus Jensen, Andreas Engert, Florian Weissinger, Wolfgang Knauf, Eva Kimby, Christopher Poynton, Ira Anton Oliff, Mathias J Rummel, Anders Osterborg

Abstract readClinical Trial, Phase I
PubMed Publisher
In one paragraph

Article in Investigational new drugs, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Regulated cell death pathways in cardiomyopathy.Acta pharmacologica Sinica · 2023
    Review
  4. Abyssinone V-4' Methyl Ether, a Flavanone Isolated fromEvidence-based complementary and alternative medicine : eCAM · 2020
    Article
  5. Review
  6. Article
  7. Targeting Wnt pathways in disease.Cold Spring Harbor perspectives in biology · 2012
    Review
  8. Apoptosis in cancer: from pathogenesis to treatment.Journal of experimental & clinical cancer research : CR · 2011
    Review
  9. 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

9 authors at 7 institutions in 4 countries.

Markus JensenUniversity of Cologne, Kerpener Strasse 62, 50924, Cologne, Germany. Jensen@uni-koeln.de
Andreas Engert
Florian Weissinger
Wolfgang Knauf
Eva Kimby
Christopher Poynton
Ira Anton Oliff
Mathias J Rummel
Anders Osterborg
Karolinska University Hospital · SEGiessen School of Theology · DEMidwestern University · USPraxis für Hämatologie und Onkologie · DETH Köln - University of Applied Sciences · DEUniversity Hospital Cologne · DEUniversity Hospital of Wales · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

R-etodolac is a novel pro-apoptotic agent with potential antitumor activity against B-cell chronic lymphocytic leukemia (B-CLL). This phase I clinical trial was conducted to determine the tolerability, safety, and maximum tolerated dose (MTD) of R-etodolac, administered orally twice a day (BID), in patients with B-CLL. Secondary objectives included evaluating clinical response, pharmacodynamic activity (reduction of lymphocytes), and pharmacokinetic (PK) profile. Forty-three patients were enrolled in the study. The most frequently reported adverse events were diarrhea, rash, pruritus, and headache. Increases in alanine aminotransferase (ALT) were also observed. Adverse events were generally mild and self-limiting, although in an apparent dose-response relationship, grade 2 and 3 gastrointestinal toxicities and grade 3 skin toxicities were reported with the highest dose regimens (1,800 and 2,400 mg BID). Hematologic toxicity was rare. The MTD was determined to be 1,200 mg BID. PK results indicated that oral absorption of R-etodolac was rapid (time to maximum concentration ranged from 2 to 4 h), and the half-life ranged from 5 to 7 h. The increase in maximum concentration, however, was not proportional to the increase in dose. R-etodolac significantly reduced absolute lymphocyte count (ALC) in B-CLL patients in a dose-dependent manner up to 1,800 mg BID and caused partial responses in 2 patients. Further study of R-etodolac as a possible new maintenance therapy or as a part of combination therapy of B-CLL appears warranted.

Indexed as

Maximum Tolerated DoseAdministration, OralAdultAgedAlanine TransaminaseAntineoplastic AgentsApoptosisDose-Response Relationship, DrugEtodolacFemaleHalf-LifeHumansLeukemia, Lymphocytic, Chronic, B-CellLymphocytesMaleMiddle AgedAlanine TransaminaseAntineoplastic AgentsEtodolac

Identifiers

PMID18094935
OpenAlexW2089093684

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.