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Risk Factors for Cisplatin-Induced Nephrotoxicity: A Multicenter Retrospective Study.
Miyoshi, Takanori; Uoi, Miyuki; Omura, Fuyuki; Tsumagari, Kyouichi; Maesaki, Sachi; Yokota, Chiaki.
Afiliação
  • Miyoshi T; Department of Pharmacy, National Hospital Organization Beppu Medical Center, Beppu, Japan, miyoshi.takanori.jv@mail.hosp.go.jp.
  • Uoi M; Department of Pharmacy, National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan.
  • Omura F; Department of Pharmacy, National Hospital Organization Kyushu Medical Center, Fukuoka, Japan.
  • Tsumagari K; Department of Pharmacy, National Hospital Organization Miyakonojo Medical Center, Miyakonojo, Japan.
  • Maesaki S; Department of Pharmacy, National Hospital Organization Kumamoto Saishun Medical Center, Koushi, Japan.
  • Yokota C; Department of Pharmacy, National Hospital Organization Kumamoto Medical Center, Kumamoto, Japan.
Oncology ; 99(2): 105-113, 2021.
Article em En | MEDLINE | ID: mdl-32966986
ABSTRACT

INTRODUCTION:

Cisplatin (CDDP)-induced nephrotoxicity is a concern in CDDP-based chemotherapy. The goal of this multicenter retrospective study was to identify potential risk factors for CDDP nephrotoxicity.

METHODS:

Clinical data were reviewed for 762 patients who underwent chemotherapy including CDDP ≥60 mg/m2 per day from Spring 2014 to September 2016. CDDP nephrotoxicity was defined according to the National Cancer Institute Common Terminology Criteria for Adverse Events for acute kidney injury. Univariate and multivariate logistic regression analyses were performed to identify risk factors for CDDP nephrotoxicity.

RESULTS:

CDDP nephrotoxicity was observed in 165 patients (21.7%). Multivariate analysis showed a significantly higher rate of CDDP nephrotoxicity in patients with cardiac disease (odds ratio [OR] 2.05, 95% confidence interval [CI] 1.07-3.93, p = 0.03), hypertension (OR 1.57, 95% CI 1.06-2.32, p = 0.02), and high-dose CDDP therapy (OR 2.15, 95% CI 1.50-3.07, p < 0.01). Magnesium (Mg) supplementation (OR 0.65, 95% CI 0.45-0.93, p = 0.02) and diuretic use (OR 0.22, 95% CI 0.08-0.63, p < 0.01) were also independent risk factors for CDDP nephrotoxicity.

CONCLUSIONS:

Our results suggest that high-dose CDDP and comorbidities of cardiac disease and hypertension are independent risk factors for CDDP nephrotoxicity. Therefore, close monitoring of serum creatinine values during CDDP treatment is recommended for patients with these risk factors. In addition, Mg supplementation and administration of diuretics might be effective for prevention of CDDP nephrotoxicity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cisplatino / Creatinina / Nefropatias / Antineoplásicos Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Oncology Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cisplatino / Creatinina / Nefropatias / Antineoplásicos Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Oncology Ano de publicação: 2021 Tipo de documento: Article