Patient Characteristics Associated With Chemotherapy-Induced Peripheral Neuropathy Severity in a Phase II Clinical Trial: A Retrospective Analysis.


Journal

The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837

Informations de publication

Date de publication:
05 07 2023
Historique:
received: 29 11 2022
accepted: 09 02 2023
medline: 7 7 2023
pubmed: 28 3 2023
entrez: 27 3 2023
Statut: ppublish

Résumé

Chemotherapy-induced peripheral neuropathy (CIPN) can lead to chemotherapy dose reduction, delay, and discontinuation, and has limited effective prevention strategies. Our study aimed to identify patient characteristics associated with CIPN severity during weekly paclitaxel chemotherapy in people with early-stage breast cancer. We retrospectively collected baseline data including participants' age, gender, race, body mass index (BMI), hemoglobin (regular and A1C), thyroid stimulating hormone, Vitamins (B6, B12, and D), anxiety, and depression up to 4 months prior to their first paclitaxel treatment. We also collected CIPN severity by Common Terminology Criteria for Adverse Events (CTCAE) after chemotherapy, chemotherapy relative dose density (RDI), disease recurrence, and mortality rate at the time of the analysis. Logistic regression was used for statistical analysis. We extracted 105 participants' baseline characteristics from electronic medical records. Baseline BMI was associated with CIPN severity (Odds Ratio [OR] 1.08; 95% CI, 1.01-1.16, P = .024). No significant correlations were observed in other covariates. At median follow-up (61 months), there were 12 (9.5%) breast cancer recurrences and six (5.7%) breast cancer-related deaths. Higher chemotherapy RDI was associated with improved disease-free survival (DFS, OR 1.025; 95% CI, 1.00-1.05; P = .028). Baseline BMI may be a risk factor for CIPN and suboptimal chemotherapy delivery due to CIPN may negatively impact disease-free survival in patients with breast cancer. Further study is warranted to identify mitigating lifestyle factors to reduce incidences of CIPN during breast cancer treatment.

Identifiants

pubmed: 36972359
pii: 7087215
doi: 10.1093/oncolo/oyad062
pmc: PMC10322124
doi:

Substances chimiques

Paclitaxel P88XT4IS4D
Antineoplastic Agents 0

Types de publication

Clinical Trial, Phase II Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

604-608

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : R37 CA248563
Pays : United States

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press.

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Auteurs

Wanqing Iris Zhi (WI)

Breast Medicine Service, Solid Tumor Division, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Nechama Dreyfus (N)

Weill Department of Medicine Cornell Medicine, New York, NY, USA.

Alexie Lessing (A)

Department of Medicine, Renaissance School of Medicine, Stony Brook University, Stony Brook, NY, USA.

Marylou Galantino (M)

Department of Medicine, School of Health Sciences, Stockton University, Galloway, NJ, USA.

Lauren Piulson (L)

Integrative Medicine Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Kevin Liu Kot (KL)

Department of Medicine, Albert Einstein College of Medicine, Bronx, New York, NY, USA.

Susan Li (S)

Integrative Medicine Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Ting Bao (T)

Breast Medicine Service, Solid Tumor Division, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Integrative Medicine Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

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Classifications MeSH