Evidence map›Paper›PMID 11030465›Full record

ReviewDrugs2000

Potential of substance P antagonists as antiemetics.

P Diemunsch, L Grélot

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Drugs, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02484911 (Aprepitant ,Olanzapine,Palonosetron and Dexamethasone for the Prevention of Chemotherapy-induced Nausea and Vomiting---A Randomized Single Center Phase III Trial), which is not on this map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
10.5field-weighted citation impact, top 2% 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.

NCT02484911 phase3completednot on this mapstarted 2015, after this paper: background citation

Aprepitant ,Olanzapine,Palonosetron and Dexamethasone for the Prevention of Chemotherapy-induced Nausea and Vomiting---A Randomized Single Center Phase III Trial

TypeinterventionalSponsorFirst Affiliated Hospital of Harbin Medical UniversityRan2015 to 2017Enrolled120ConditionsChemotherapy-induced Nausea and VomitingArmsOlanzapine, Aprepitant, Palonosetron, Dexamethasone
3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 189 citations in OpenAlex.

  1. Should palonosetron be a preferred 5-HTSupportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2018
    Pooled it
  2. Trial
  3. Trial
  4. Observational
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Suppression of Cisplatin-Induced Vomiting byFrontiers in pharmacology · 2018
    Article
  13. Gastroparesis: Medical and Therapeutic Advances.Digestive diseases and sciences · 2017
    Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. 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

2 authors at 2 institutions in 1 country.

P DiemunschDepartment of Anaesthesiology, IRCAD, Hôpitaux Universitaires de Strasbourg, France. pierre.diemunsch@ircad.u-strasbg.fr
L Grélot
Institut de Neurobiologie de la Méditerranée · FRInstitut de Recherche contre les Cancers de l’Appareil Digestif · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The introduction of serotonin 5-HT3 receptor antagonists into clinical practice allowed for a dramatic improvement in the management of nausea and vomiting. Despite this, postoperative and chemotherapy-induced emesis remains a significant, unresolved issue in many patients even when a combination of antiemetic drugs is used. Numerous neurotransmitters have been implicated in triggering emesis; however, the tachykinin substance P, by virtue of its localisation within both the gastrointestinal vagal afferent nerve fibres and brainstem emetic circuitry, and its ability to induce vomiting when administered intravenously, is thought to play a key role in emetic responses. Because substance P is the most likely endogenous ligand for the neurokinin-1 (NK1) receptor, the development of nonpeptide NK1 receptor antagonists led scientists to evaluate these compounds as antiemetics. The five NK1 receptor inhibitors that have been studied initially in humans are: vofopitant (GR-205171), CP-122721, ezlopitant (CJ-11974), MK-869 (L-754030) and its prodrug L-758298. Except for monotherapy in acute cisplatin-induced emesis, this new class of drugs has proven to be highly effective in the control of both chemotherapy-induced nausea and vomiting, and postoperative nausea and vomiting. No major adverse event was reported in the preliminary trials. Further investigation is mandatory in order to assess the optimal treatment regimen and to make sure the wide spectrum activity of the NK1 receptor inhibitors does not cause significant adverse effects in the context of the treatment of nausea and vomiting.

Indexed as

AntiemeticsClinical Trials as TopicHumansInfusions, IntravenousReceptors, Neurokinin-1Substance PVomitingAntiemeticsReceptors, Neurokinin-1Substance P

Identifiers

PMID11030465
OpenAlexW2119544301

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.