Your browser doesn't support javascript.
loading
Incidence and risk factors for developing chemotherapy-induced neuropathic pain in 500 cancer patients: A file-based observational study.
Argyriou, Andreas A; Bruna, Jordi; Kalofonou, Foteini; Velasco, Roser; Litsardopoulos, Pantelis; Alemany, Montse; Anastopoulou, Garifallia G; Kalofonos, Haralabos P.
Afiliação
  • Argyriou AA; Neurological Department, "Agios Andreas" General Hospital of Patras, Patras, Greece.
  • Bruna J; Neuro-Oncology Unit, Hospital Universitari de Bellvitge-ICO L'Hospitalet, IDIBELL, Barcelona, Spain.
  • Kalofonou F; Department of Oncology, Guy's and St. Thomas' NHS Trust, London, UK.
  • Velasco R; Neuro-Oncology Unit, Hospital Universitari de Bellvitge-ICO L'Hospitalet, IDIBELL, Barcelona, Spain.
  • Litsardopoulos P; Neurological Department, "Agios Andreas" General Hospital of Patras, Patras, Greece.
  • Alemany M; Neuro-Oncology Unit, Hospital Universitari de Bellvitge-ICO L'Hospitalet, IDIBELL, Barcelona, Spain.
  • Anastopoulou GG; Department of Medicine, "Agios Andreas" General Hospital of Patras, Patras, Greece.
  • Kalofonos HP; Department of Medicine, Division of Oncology, University Hospital of Patras, Patras, Greece.
J Peripher Nerv Syst ; 29(1): 38-46, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38311337
ABSTRACT

OBJECTIVE:

To define the incidence and risk factors for developing chemotherapy-induced neuropathic pain (CINP).

METHODS:

Retrospective, file-based analysis on cancer patients who received any type of conventional chemotherapy and for whom neurological evaluation was asked to reveal the extent of chemotherapy-induced peripheral neurotoxicity (CIPN) with or without CINP. CINP was assessed by means of the PI-NRS and Douleur Neuropathique-4 questionnaire. The total neuropathy score-clinical version graded the severity of CIPN.

RESULTS:

The medical files of 500 chemotherapy-treated cancer patients were reviewed. Any grade chronic CIPN was disclosed in 343 (68.6%) patients and CINP in 127 (37%) of them, corresponding to an overall percentage of 25.4% among all 500 included patients. The logistic regression analysis identified as independent predictors for CINP development the presence of uncomplicated diabetes (OR 2.17; p = .039) and grade 2-3 chronic CIPN (OR 1.61; p < .001) as also the administration of combined paclitaxel plus cisplatin (reference variable), compared to oxaliplatin (OR 0.18; p = .001) and taxanes (OR 0.16; p < .001). The increased severity of acute OXAIPN was associated with CINP (OR 4.51; p < .001). OXA-treated patients with persistent CINP presented a worst likelihood to improve after chemotherapy discontinuation, than patients receiving combined paclitaxel plus cisplatin (OR 50; p < .001).

CONCLUSION:

The incidence of CINP in our cohort was comparable to previous reports, with severities fluctuating upwards during chemotherapy and declined post-chemotherapy. Uncomplicated diabetes, the combined paclitaxel plus cisplatin treatment and the increased severity of acute oxaliplatin neurotoxicity mostly increase the risk for developing CINP. OXA-treated patients present less possibilities to recover from CINP after chemotherapy discontinuation, than other chemotherapies.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Neurotóxicas / Diabetes Mellitus / Neoplasias / Neuralgia / Antineoplásicos Idioma: En Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Grécia

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Neurotóxicas / Diabetes Mellitus / Neoplasias / Neuralgia / Antineoplásicos Idioma: En Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Grécia