Evidence map›Paper›PMID 36326907›Full record

ReviewSupportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer2022

Management of adverse events related to first-generation tyrosine receptor kinase inhibitors in adults: a narrative review.

Christine Martineau, Maria-Kim Turcotte, Noémie Otis, Frédéric Provost, Ludovic Themens, Marie-Pascale Guay, Nathalie Letarte, Jean-Philippe Adam

Abstract readReview
PubMed Publisher
In one paragraph

Review in Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 11 citations in OpenAlex.

  1. Obstacles and Trials in Treating Primary Brain Tumors.International journal of molecular sciences · 2026
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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

8 authors at 4 institutions in 1 country.

Christine Martineau *Faculty of Pharmacy, Université de Montréal, Montréal, Canada.
Maria-Kim Turcotte *Faculty of Pharmacy, Université de Montréal, Montréal, Canada.
Noémie Otis *Faculty of Pharmacy, Université de Montréal, Montréal, Canada.
Frédéric Provost *Faculty of Pharmacy, Université de Montréal, Montréal, Canada.
Ludovic Themens *Faculty of Pharmacy, Université de Montréal, Montréal, Canada.
Marie-Pascale GuayDepartment of Pharmacy, CIUSSS West-Central Montreal, Montréal, Canada.
Nathalie LetarteFaculty of Pharmacy, Université de Montréal, Montréal, Canada.
Jean-Philippe AdamDepartment of Pharmacy, Centre hospitalier de l'Université de Montréal, 1050 Sanguinet, Montréal, H2X 0C1, Canada. jean-philippe.adam.chum@ssss.gouv.qc.ca.ORCID http://orcid.org/0000-0002-7938-0944
Université de Montréal · CACentre Hospitalier de l’Université de Montréal · CACentre Hospitalier Universitaire Sainte-Justine · CACentre Intégré Universitaire de Santé et de Services Sociaux du Centre-Sud-de-l'Île-de-Montréal · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe aim of this article is to conduct a literature review on first-generation TRK inhibitors (TRKi), namely entrectinib and larotrectinib, to describe the most common adverse events (AEs) and their management in adults.

methodsA search strategy was conducted in MEDLINE, EMBASE, and Google Scholar using a list of predetermined keywords. Peer-reviewed articles written in English and published through June 2021 were included. Articles covered included randomized clinical trials and expert recommendations, as well as patent and other types of reviews.

resultsThe discussed AEs include weight gain and withdrawal pain, as well as neuromuscular, central nervous system (dysesthesias and peripheral sensory neuropathies, dizziness and ataxia, and dysgeusia), gastrointestinal (nausea, vomiting, and diarrhea), and respiratory symptoms. Additionally, several AEs encountered with entrectinib specifically (cognitive and vision disorders, congestive heart failure, QTc elongation, and skeletal fractures) are discussed. First, an overall mechanism of action explaining these AEs is presented. Then, for each AE, incidence and severity are stated and followed by practical management recommendations. While nearly all AEs were reversible upon TRKi suspension, the proposed managements are mainly constituted of pharmacological and non-pharmacological interventions.

conclusionWith the estimated growth of gene sequencing in the coming years, it is foreseeable that TRKi will take a larger position in the oncologic therapeutic arsenal. Therefore, adequate management of AEs associated with TRKi in adults should be a prime focus.

Indexed as

Protein Kinase InhibitorsAdultBenzamidesHumansIndazolesReceptors, Amino AcidBenzamidesentrectinibIndazolesProtein Kinase InhibitorsReceptors, Amino Acidtyrosine receptorDizziness and ataxiaManagement of adverse eventsTRK inhibitorsWeight gainWithdrawal-associated pain

Identifiers

PMID36326907
OpenAlexW4307994288

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.