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Chemotherapy with CDDP.

A Restaino1, V Traina, G Putignano

  • 1I Gynaecological Institute, University of Bari, Italy.

European Journal of Gynaecological Oncology
|January 1, 1988
PubMed
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This study on ovarian carcinoma patients found that monitoring kidney function (nephrologic monitoring) enables safer and more effective cisplatin chemotherapy. This approach improves the cost-benefit ratio of treatment.

Area of Science:

  • Oncology
  • Nephrology
  • Pharmacology

Background:

  • Ovarian carcinoma treatment often involves chemotherapy, with cisplatin (CDDP) being a common agent.
  • Chemotherapy can lead to kidney toxicity (tubulo-toxicity), necessitating careful monitoring.
  • Evaluating enzymuria is a reliable method for detecting both acute and chronic kidney damage.

Purpose of the Study:

  • To assess the efficacy and safety of different chemotherapy administration routes (parenteral and intraperitoneal) in ovarian carcinoma patients.
  • To investigate the role of nephrologic monitoring in managing cisplatin-induced tubulo-toxicity.
  • To determine the cost-benefit relationship of cisplatin chemotherapy with adequate renal function assessment.

Main Methods:

  • Retrospective analysis of 30 ovarian carcinoma patients treated with chemotherapy.

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  • 27 patients received parenteral chemotherapy (mono- or poly-chemotherapy with CDDP and alkylating agents).
  • 3 patients received low-dose intraperitoneal cisplatin. Enzymuria was measured pre- and post-therapy in 27 cases.
  • Main Results:

    • Chemotherapy regimens included cisplatin (CDDP) monotherapy and poly-chemotherapy (CDDP + alkylating agents).
    • Enzymuria evaluation served as a key indicator for assessing kidney tubule damage.
    • Nephrologic monitoring was found to facilitate more precise cisplatin usage.

    Conclusions:

    • Careful nephrologic monitoring is crucial for optimizing cisplatin chemotherapy in ovarian cancer.
    • This monitoring enhances treatment accuracy and improves the overall cost-benefit ratio.
    • Enzymuria is a valuable biomarker for detecting and managing cisplatin-related kidney toxicity.