Evidence map›Paper›PMID 9599702›Full record

ReviewEnvironmental health perspectives1998

Alternative testing systems for evaluating noncarcinogenic, hematologic toxicity.

R E Parchment

Abstract readReview
In one paragraph

Review in Environmental health perspectives, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

1 author.

R E ParchmentDivision of Hematology and Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, Michigan, USA. parchmen@med.wayne.edu

Funding

PHASE I TRIALS OF NEW ANTICANCER AGENTSU01CA062487 · NCI · WAYNE STATE UNIVERSITY · PI LORUSSO, PATRICIA M. · 1994 to 2013
$8.4M
THERAPEUTICS OF NEW SOLID TUMOR ANTICANCER AGENTSP01CA046560 · NCI · WAYNE STATE UNIVERSITY · PI CORBETT, THOMAS H · 1989 to 1998
–
PHASE II TRIAL OF BRYOSTATIN 1 AND 2-CDA IN RELAPSED CLLR03CA075283 · NCI · WAYNE STATE UNIVERSITY · PI AL-KATIB, AYAD M · 1997 to 1998
–
NCI NIH HHS CA46560NCI NIH HHS CA62487NCI NIH HHS CA75283
6 · The paper itself

Abstract

Hematopoietic tissues are the targets of numerous xenobiotics. Clinical hematotoxicity is either a decrease or an increase in peripheral blood cell counts in one or more cell lineages--a cytopenia or a cytosis, respectively--that carries a risk of an adverse clinical event. The purpose of in vitro hematotoxicology is the prediction of these adverse hematologic effects from the effects of the toxicants on human hematopoietic targets under controlled experimental conditions in the laboratory. Building on its important foundations in experimental hematology and the wealth of hematotoxicology data found in experimental oncology, this field of alternative toxicology has developed rapidly during the past decade. Although the colony-forming unit-granulocyte/monocyte neutrophil progenitor is most frequently evaluated, other defined progenitors and stem cells as well as cell types found in the marrow stroma can be evaluated in vitro. End points have been proposed for predicting toxicant exposure levels at the maximum tolerated dose and the no observable adverse effect level for the neutrophil lineage, and several clinical prediction models for neutropenia have developed to the point that they are ready for prospective evaluation and validation in both preclinical species and humans. Known predictive end points are the key to successful comparisons across species or across chemical structures when in vitro dose-response curves are nonparallel. Analytical chemistry support is critical for accurate interpretation of in vitro data and for relating the in vitro pharmacodynamics to the in vivo pharmacokinetics. In contrast to acute neutropenia, anemia and acute thrombocytopenia, as well as adverse effects from chronic toxicant exposure, are much more difficult to predict from in vitro data. Pharmacologic principles critical for clinical predictions from in vitro data very likely will apply to toxicities to other proliferative tissues, such as mucositis.

Indexed as

Animal Testing AlternativesAnemiaAnimalsDose-Response Relationship, DrugHematologyHumansIn Vitro TechniquesNeutropeniaPredictive Value of TestsThrombocytopeniaToxicity TestsXenobioticsXenobiotics

Identifiers

PMID9599702
PMCPMC1533375

What OpenQuestion holds

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Read underepoch 390

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.