Evidence map›Paper›PMID 31647151›Full record

ReviewJournal of the peripheral nervous system : JPNS2019

Platinum-induced peripheral neurotoxicity: From pathogenesis to treatment.

Nathan P Staff, Guido Cavaletti, Badrul Islam, Maryam Lustberg, Dimitri Psimaras, Stefano Tamburin

Open access · greenAbstract readReview
In one paragraph

Review in Journal of the peripheral nervous system : JPNS, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed, 2 pooled it
7.5field-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.

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

88 citing papers in PubMed, 2 syntheses or guidelines pooled it, 143 citations in OpenAlex.

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  14. Oxaliplatin-induced peripheral neuropathy: from pathogenesis to treatment.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Review
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28 more citing papers are in PubMed but not listed here.

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

6 authors at 6 institutions in 4 countries.

Nathan P StaffDepartment of Neurology, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0001-6760-3859
Guido CavalettiExperimental Neurology Unit, School of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.ORCID 0000-0003-4128-2406
Badrul IslamLaboratory Sciences and Services Division, The International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh.ORCID 0000-0001-7129-944X
Maryam LustbergDepartment of Internal Medicine, Division of Medical Oncology, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Dimitri PsimarasOncoNeuroTox Group, Center for Patients with Neurological Complications of Oncologic Treatments, Hôpitaux Universitaires Pitié-Salpetrière-Charles Foix et Hôpital Percy, Paris, France.ORCID 0000-0002-6641-288X
Stefano TamburinDepartment of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.ORCID 0000-0002-1561-2187
International Centre for Diarrhoeal Disease Research · BDMayo Clinic · USSorbonne Université · FRThe Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · USUniversity of Milano-Bicocca · ITUniversity of Verona · IT

Funding

Assessment of Chemotherapy-Induced Peripheral Neuropathy Susceptibility Using Patient-derived iPSC TechnologyR01CA211887 · NCI · MAYO CLINIC ROCHESTER · PI STAFF, NATHAN P · 2017 to 2021
$1.8M
NCI NIH HHS R01 CA211887
6 · The paper itself

Abstract

Platinum-induced peripheral neurotoxicity (PIPN) is a common side effect of platinum-based chemotherapy that may cause dose reduction and discontinuation, with oxaliplatin being more neurotoxic. PIPN includes acute neurotoxicity restricted to oxaliplatin, and chronic non-length-dependent sensory neuronopathy with positive and negative sensory symptoms and neuropathic pain in both upper and lower limbs. Chronic sensory axonal neuropathy manifesting as stocking-and-glove distribution is also frequent. Worsening of neuropathic symptoms after completing the last chemotherapy course may occur. Motor and autonomic involvement is uncommon. Ototoxicity is frequent in children and more commonly to cisplatin. Platinum-based compounds result in more prolonged neuropathic symptoms in comparison to other chemotherapy agents. Patient reported outcomes questionnaires, clinical evaluation and instrumental tools offer complementary information in PIPN. Electrodiagnostic features include diffusely reduced/abolished sensory action potentials, in keeping with a sensory neuronopathy. PIPN is dependent on cumulative dose but there is a large variability in its occurrence. The search for additional risk factors for PIPN has thus far yielded no consistent findings. There are currently no neuroprotective strategies to reduce the risk of PIPN, and symptomatic treatment is limited to duloxetine that was found effective in a single phase III intervention study. This review critically examines the pathogenesis, incidence, risk factors (both clinical and pharmacogenetic), clinical phenotype and management of PIPN.

Indexed as

Antineoplastic AgentsCisplatinDuloxetine HydrochlorideHumansNeurotoxicity SyndromesOrganoplatinum CompoundsOxaliplatinPeripheral Nervous System DiseasesSerotonin and Noradrenaline Reuptake InhibitorsTreatment OutcomeAntineoplastic AgentsCisplatinDuloxetine HydrochlorideOrganoplatinum CompoundsOxaliplatinSerotonin and Noradrenaline Reuptake Inhibitorsassessmentcarboplatinchemotherapycisplatindiagnosisneuropathyneurotoxicityoxaliplatinpreventiontreatment

Identifiers

PMID31647151
PMCPMC6818741
OpenAlexW2982135574

What OpenQuestion holds

Textmetadata
LicenceTDM
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.