Evidence map›Paper›PMID 39342135›Full record

Observational studyBMC neurology2024

Exploring clinical markers of Axon degeneration processes in Chemotherapy-induced peripheral neuropathy among young adults receiving vincristine or paclitaxel.

Robert Knoerl, Emanuele Mazzola, Maria Pazyra-Murphy, Birgitta Ryback, A Lindsay Frazier, Roy L Freeman, Marilyn Hammer, Ann LaCasce, Jennifer Ligibel, Marlise R Luskin and 2 more

Abstract readObservational Study
In one paragraph

Observational study in BMC neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. 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

12 authors.

Robert KnoerlPhyllis F. Cantor Center for Research in Nursing and Patient Care Services, Dana-Farber Cancer Institute, Boston, MA, USA. rjknoerl@med.umich.edu.ORCID http://orcid.org/0000-0002-6996-5068
Emanuele MazzolaDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA, USA.
Maria Pazyra-MurphyDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA, USA.
Birgitta RybackMetabolomics Core, Dana-Farber Cancer Institute, Boston, MA, USA.
A Lindsay FrazierDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Roy L FreemanDepartment of Neurology, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Marilyn HammerPhyllis F. Cantor Center for Research in Nursing and Patient Care Services, Dana-Farber Cancer Institute, Boston, MA, USA.
Ann LaCasceDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Jennifer LigibelDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Marlise R LuskinDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Donna L BerryBiobehavioral Nursing and Health Informatics, University of Washington, Seattle, WA, USA.
Rosalind A SegalDeparment of Neurobiology, Harvard Medical School, Boston, MA, USA.

Funding

Genetic Analysis and Manipulation Core (GAEC)P50HD105351 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI Hisashi Umemori · 2021 to 2026
$9.4M
(PQ9) The role of Bclw (bcl2l2) in preventing chemotherapy induced neuropathyR01CA205255 · NCI · DANA-FARBER CANCER INST · PI ROSALIND ANNE SEGAL · 2016 to 2026
$5.8M
Determining Mechanisms and Measures for the Design of Chemotherapy-Induced Peripheral Neuropathy Clinical Trials in Adolescents and Young Adults with CancerK23NR018689 · NINR · DANA-FARBER CANCER INST · PI KNOERL, ROBERT JAMES · 2020 to 2022
$341k
NCI NIH HHS R01 CA205255NCI NIH HHS R01CA205255NICHD NIH HHS P50 HD105351NINR NIH HHS K23 NR018689NINR NIH HHS K23NR018689
6 · The paper itself

Abstract

backgroundApproximately 70% of patients receiving neurotoxic chemotherapy (e.g., paclitaxel or vincristine) will develop chemotherapy-induced peripheral neuropathy. Despite the known negative effects of CIPN on physical functioning and chemotherapy dosing, little is known about how to prevent CIPN. The development of efficacious CIPN prevention interventions is hindered by the lack of knowledge surrounding CIPN mechanisms. Nicotinamide adenine dinucleotide (NAD

methodsYoung adults (18-39 years old) beginning vincristine or paclitaxel were recruited from Dana-Farber Cancer Institute. Young adults completed the QLQ-CIPN20 sensory and motor subscales and provided a blood sample prior to starting chemotherapy (T1) and at increasing cumulative vincristine (T2: 3-5 mg, T3: 7-9 mg) and paclitaxel (T2: 300-500 mg/m

resultsParticipants (N = 50) were mainly female (88%), white (80%), and receiving paclitaxel (78%). Sensory and motor CIPN severity increased from T1-T3 (p < 0.001). NAD

conclusionsTo our knowledge, this is the first study to measure plasma NAD

Indexed as

PaclitaxelPeripheral Nervous System DiseasesVincristineAdolescentAdultAntineoplastic Agents, PhytogenicAxonsBiomarkersFemaleHumansLongitudinal StudiesMaleNADNerve DegenerationYoung AdultAntineoplastic Agents, PhytogenicBiomarkersNADPaclitaxelVincristineChemotherapy-induced peripheral neuropathyNAD, human [Supplementary Concept]NeoplasmsYoung Adult

Identifiers

PMID39342135
PMCPMC11438373

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.