Early taxane exposure and neurotoxicity in breast cancer patients.


Journal

Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer
ISSN: 1433-7339
Titre abrégé: Support Care Cancer
Pays: Germany
ID NLM: 9302957

Informations de publication

Date de publication:
08 Oct 2024
Historique:
received: 23 04 2024
accepted: 27 09 2024
medline: 8 10 2024
pubmed: 8 10 2024
entrez: 7 10 2024
Statut: epublish

Résumé

Breast cancer is the most diagnosed tumor and a leading cause of cancer death in women worldwide. Taxanes are the most used chemotherapeutic agents and are strictly connected to neurotoxicity. Taxane-induced neuropathy (TIN) significantly impacts patients' quality of life (QOL). Early identification and management of TIN could improve preventive strategies to preserve patients' QOL during and after breast cancer treatment. This prospective, observational study aimed to evaluate the taxane-induced neuropathy (TIN) in early breast cancer patients treated with weekly paclitaxel at an earlier stage and identify any correlation between TIN and QOL. Data from stage I-III breast cancer patients treated with taxane-based therapy between 2018 and 2022 were collected at the Medical Oncology Unit of the University Hospital of Cagliari. Peripheral neuropathy was evaluated using the NCI-CTCAE scale (National Cancer Institute, Common Terminology Criteria for Adverse Events) at every drug administration. In contrast, QOL was assessed using EORTC QLC-CIPN20 and FACT-Taxane questionnaire at baseline (T0), after 4 weeks (T1) and 12 (T2) weeks of treatment. Statistical analysis was performed to evaluate the correlation between neurotoxicity and QOL. Neurotoxicity incidence peaked at the third, fourth, and sixth week of treatment, with patients reporting grade 1 and 2 neurotoxicity. Simultaneously with increasing doses of paclitaxel, significant differences in QOL were observed in early treatment cycles relating to TIN presentation. Patients with higher neurotoxicity grades reported lower QOL scores. Despite the absence of effective treatments to prevent paclitaxel-induced neurotoxicity, symptoms are managed through dosage reduction, delay, or treatment interruption. Future research should focus on identifying neuroprotective measures to avoid an irreversible decline in the quality of life for breast cancer survivors.

Identifiants

pubmed: 39375221
doi: 10.1007/s00520-024-08908-2
pii: 10.1007/s00520-024-08908-2
doi:

Substances chimiques

Paclitaxel P88XT4IS4D
Taxoids 0
Antineoplastic Agents, Phytogenic 0
taxane 1605-68-1
Bridged-Ring Compounds 0

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

709

Informations de copyright

© 2024. The Author(s).

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Auteurs

Erika Cimbro (E)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042, Cagliari, Italy. erikacimbro@gmail.com.

Mariele Dessì (M)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042, Cagliari, Italy.

Pina Ziranu (P)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042, Cagliari, Italy.

Clelia Madeddu (C)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042, Cagliari, Italy.
Department of Medical Sciences and Public Health, University of Cagliari, 09042, Cagliari, Italy.

Francesco Atzori (F)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042, Cagliari, Italy.

Eleonora Lai (E)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042, Cagliari, Italy.

Andrea Pretta (A)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042, Cagliari, Italy.

Stefano Mariani (S)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042, Cagliari, Italy.

Clelia Donisi (C)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042, Cagliari, Italy.

Dario Spanu (D)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042, Cagliari, Italy.

Marta Pozzari (M)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042, Cagliari, Italy.

Sara Murgia (S)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042, Cagliari, Italy.

Giorgio Saba (G)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042, Cagliari, Italy.

Claudia Codipietro (C)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042, Cagliari, Italy.

Enrico Palmas (E)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042, Cagliari, Italy.

Giorgia Sanna (G)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042, Cagliari, Italy.

Francesca Semonella (F)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042, Cagliari, Italy.

Salvatore Sardo (S)

Department of Anesthesia, Resuscitation and Pain Therapy, University of Cagliari, 09042, Cagliari, Italy.

Gabriele Finco (G)

Department of Medical Sciences and Public Health, University of Cagliari, 09042, Cagliari, Italy.
Department of Anesthesia, Resuscitation and Pain Therapy, University of Cagliari, 09042, Cagliari, Italy.

Mario Scartozzi (M)

Medical Oncology Unit, University Hospital and University of Cagliari, 09042, Cagliari, Italy.
Department of Medical Sciences and Public Health, University of Cagliari, 09042, Cagliari, Italy.

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