International Journal of Molecular Sciences (Jan 2021)

Effect of Cilastatin on Cisplatin-Induced Nephrotoxicity in Patients Undergoing Hyperthermic Intraperitoneal Chemotherapy

  • Matilde Zaballos,
  • Mercedes Power,
  • María Iluminada Canal-Alonso,
  • María Ángeles González-Nicolás,
  • Wenceslao Vasquez-Jimenez,
  • Pablo Lozano-Lominchar,
  • Pilar Cabrerizo-Torrente,
  • Natividad Palencia-García,
  • Susana Gago-Quiroga,
  • María Dolores Ginel-Feito,
  • Consuelo Jiménez,
  • Alberto Lázaro,
  • Luis González-Bayón

DOI
https://doi.org/10.3390/ijms22031239
Journal volume & issue
Vol. 22, no. 3
p. 1239

Abstract

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Cisplatin is one of the most widely used chemotherapeutic agents in oncology, although its nephrotoxicity limits application and dosage. We present the results of a clinical study on prophylaxis of cisplatin-induced nephrotoxicity in patients with peritoneal carcinomatosis undergoing cytoreduction and hyperthermic intraperitoneal intraoperative chemotherapy (HIPEC-cisplatin). Prophylaxis was with imipenem/cilastatin. Cilastatin is a selective inhibitor of renal dehydropeptidase I in the proximal renal tubule cells that can reduce the nephrotoxicity of cisplatin. Unfortunately, cilastatin is not currently marketed alone, and can only be administered in combination with imipenem. The study has a retrospective part that serves as a control (n = 99 patients receiving standard surgical prophylaxis) and a prospective part with imipenem/cilastatin prophylaxis corresponding to the study group (n = 85 patients). In both groups, we collected specific data on preoperative risk factors of renal damage, fluid management, hemodynamic control, and urine volume during surgery (including the hyperthermic chemotherapy perfusion), as well as data on hemodynamic and renal function during the first seven days after surgery. The main finding of the study is that cilastatin may exert a nephroprotective effect in patients with peritoneal carcinomatosis undergoing cytoreduction and hyperthermic intraperitoneal cisplatin perfusion. Creatinine values remained lower than in the control group (ANOVA test, p = 0.037). This translates into easier management of these patients in the postoperative period, with significantly shorter intensive care unit (ICU) and hospital stay.

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