Skip to main content
Erschienen in: Medical Oncology 4/2011

01.12.2011 | Original Paper

Investigation of the efficacy of 99 mTc-DTPA scintigraphic GFR measurement with Gates method in the detection of cisplatin-induced nephrotoxicity in comparison with plasma urea and creatinine measurement

verfasst von: Filiz Özülker, Tamer Özülker, Aysun Küçüköz Uzun, Tevfik Özpaçacı

Erschienen in: Medical Oncology | Ausgabe 4/2011

Einloggen, um Zugang zu erhalten

Abstract

In this study, we investigated the efficacy of 99mTc-DTPA scintigraphic analysis of GFR with the Gates method in comparison with the measurement of plasma urea and creatinine, in the detection of nephrotoxicity occurred in patients treated with cisplatin.Twenty-six male patients with a mean age of 26.73 ± 6.39 years (age range 15–42) who had seminomatous and nonseminomatous testicular carcinoma were included in our study. The patients received cisplatin with a dose of 20 mg/m2 per day for five consecutive days repeated every 21 days. Before starting chemotherapy, immediately after the end of four cycles of chemotherapy and 7 months after the beginning of chemotherapy, plasma urea and creatinine levels were measured and simultaneously scintigraphic GFR estimation using 99 mTc-DTPA with the Gates method was performed. In the measurements done immediately after the chemotherapy, in 18 of the 26 patients GFR levels decreased, in 4 of the 8 remaining patients GFR did not change, and in 4 patients there was an increase in the GFR levels. The changes in the averages of the plasma urea and creatinine levels between measurements done before and after the chemotherapy were not statistically significant. The decrease in the average of the GFR values immediately after chemotherapy, in comparison to the average of GFR values measured before chemotherapy, was found to be statistically significant with paired sample t test analysis (P < 0.009 with 95% CI). We concluded that scintigraphic GFR measurement using the Gates method with 99mTc-DTPA is a suitable method in the diagnosis of nephrotoxicity occuring due to cisplatine.
Literatur
1.
Zurück zum Zitat Skinner R, et al. Cisplatin dose rate as a risk factor for nephrotoxicity in children. Br J Cancer. 1998;77:1677–82.PubMedCrossRef Skinner R, et al. Cisplatin dose rate as a risk factor for nephrotoxicity in children. Br J Cancer. 1998;77:1677–82.PubMedCrossRef
2.
Zurück zum Zitat Brillet G, et al. Definitive end-stage chronic kidney failure after cisplatin treatment. Nephrologie. 1993;14:227–9.PubMed Brillet G, et al. Definitive end-stage chronic kidney failure after cisplatin treatment. Nephrologie. 1993;14:227–9.PubMed
3.
Zurück zum Zitat Cvitkovic E. Cumulative toxicities from cisplatin therapy and current cytoprotective measures. Cancer Treat Rev. 1998;24:265–81.PubMedCrossRef Cvitkovic E. Cumulative toxicities from cisplatin therapy and current cytoprotective measures. Cancer Treat Rev. 1998;24:265–81.PubMedCrossRef
4.
Zurück zum Zitat Daugaard G, et al. Renal tubular function in patients treated with high dose cisplatin. Clin Pharmacol Ther. 1988;44:164–72.PubMedCrossRef Daugaard G, et al. Renal tubular function in patients treated with high dose cisplatin. Clin Pharmacol Ther. 1988;44:164–72.PubMedCrossRef
5.
Zurück zum Zitat Lam M, Adelstein DJ. Hypomagnesemia and renal magnesium wasting in patients treated with cisplatin. Am J Kidney Dis. 1986;8:164–9.PubMed Lam M, Adelstein DJ. Hypomagnesemia and renal magnesium wasting in patients treated with cisplatin. Am J Kidney Dis. 1986;8:164–9.PubMed
6.
Zurück zum Zitat Guarino AM, et al. Platinate toxicity: past, present and prospect. Cancer Treat Rep. 1979;63:1475–83.PubMed Guarino AM, et al. Platinate toxicity: past, present and prospect. Cancer Treat Rep. 1979;63:1475–83.PubMed
7.
Zurück zum Zitat Sugiyama S, et al. Adverse effects of antitumor drug cisplatin on rat kidney mitochondria: disturbance in gluthatione peroxidase activity. Biochem Biophys Res Commun. 1989;59:1121–7.CrossRef Sugiyama S, et al. Adverse effects of antitumor drug cisplatin on rat kidney mitochondria: disturbance in gluthatione peroxidase activity. Biochem Biophys Res Commun. 1989;59:1121–7.CrossRef
8.
Zurück zum Zitat Bompart G. Cisplatin induced changes in cytochrome platin-450, lipid peroxidation and drug metabolising enzyme activities in rat kidney cortex. Toxicol Lett. 1989;48:193–9.PubMedCrossRef Bompart G. Cisplatin induced changes in cytochrome platin-450, lipid peroxidation and drug metabolising enzyme activities in rat kidney cortex. Toxicol Lett. 1989;48:193–9.PubMedCrossRef
9.
Zurück zum Zitat De Witt LM, Jones TW, Moore L. Stimulation of the renal endoplasmic reticulum calcium pump: a possible biomarker for platinum toxicity. Toxicol Appl Pharmacol. 1988;92:57–69. De Witt LM, Jones TW, Moore L. Stimulation of the renal endoplasmic reticulum calcium pump: a possible biomarker for platinum toxicity. Toxicol Appl Pharmacol. 1988;92:57–69.
10.
Zurück zum Zitat Mavichak V, et al. Renal magnesium wasting and hypocalciuria in chronic cisplatin nephropathy in man. Clin Sci. 1988;75:203–7.PubMed Mavichak V, et al. Renal magnesium wasting and hypocalciuria in chronic cisplatin nephropathy in man. Clin Sci. 1988;75:203–7.PubMed
11.
Zurück zum Zitat Guyton CA. Textbook of medical physiology, Chap. 28. 8th edn. Philadelphia: WB Saunders; 1991. p. 308–329. Guyton CA. Textbook of medical physiology, Chap. 28. 8th edn. Philadelphia: WB Saunders; 1991. p. 308–329.
12.
Zurück zum Zitat Schrier RW. editor. Manual of nephrology, Chap. 14, vol. 5. New York: Little Brown; 1990. p. 285–290. Schrier RW. editor. Manual of nephrology, Chap. 14, vol. 5. New York: Little Brown; 1990. p. 285–290.
13.
Zurück zum Zitat Dennis VW. Investigation of renal function. In Smith L, editor. Cecil textbook of medicine, Chap. 18, vol. 1. 18th edn. Philadelphia: WB Saunders; 1988. p. 520-8. Dennis VW. Investigation of renal function. In Smith L, editor. Cecil textbook of medicine, Chap. 18, vol. 1. 18th edn. Philadelphia: WB Saunders; 1988. p. 520-8.
14.
Zurück zum Zitat Mandal K, Anil Hebert, A Lee, editors. Renal diseases. Med Clinic North Am. 1990;74:859–1077. Mandal K, Anil Hebert, A Lee, editors. Renal diseases. Med Clinic North Am. 1990;74:859–1077.
15.
Zurück zum Zitat Stark JJ, Howell SB. Nephrotoxicity of cisplatin. Clin Pharmacol Ther. 1978;23:461–6.PubMed Stark JJ, Howell SB. Nephrotoxicity of cisplatin. Clin Pharmacol Ther. 1978;23:461–6.PubMed
16.
Zurück zum Zitat Brillet G, et al. Long-term renal effect of cisplatin in man. Am J Nephrol. 1994;14(2):81–4.PubMedCrossRef Brillet G, et al. Long-term renal effect of cisplatin in man. Am J Nephrol. 1994;14(2):81–4.PubMedCrossRef
17.
Zurück zum Zitat Schlegel JU, Hamway SA. Individual renal plasma flow determination in 2 minutes. J Urol. 1976;116:282–5.PubMed Schlegel JU, Hamway SA. Individual renal plasma flow determination in 2 minutes. J Urol. 1976;116:282–5.PubMed
18.
Zurück zum Zitat Gates GF. Glomerular filtration rate: Estimation from fractional accumulation of 99mTc-DTPA. Am J Roentgenol. 1982;3:565–70. Gates GF. Glomerular filtration rate: Estimation from fractional accumulation of 99mTc-DTPA. Am J Roentgenol. 1982;3:565–70.
19.
Zurück zum Zitat Wagner H, Szabo Z, Buchanan J. Principles of Nuclear Medicine. 2nd ed. Philadelphia: WB Saunders; 1995. p. 966–73. Wagner H, Szabo Z, Buchanan J. Principles of Nuclear Medicine. 2nd ed. Philadelphia: WB Saunders; 1995. p. 966–73.
20.
Zurück zum Zitat Petersen PM, Hansen SW. The course of long term toxicity in patients treated with cisplatin based chemotherapy for nonseminomatous germ cell cancer. Ann Oncol. 1999;12:1475–83.CrossRef Petersen PM, Hansen SW. The course of long term toxicity in patients treated with cisplatin based chemotherapy for nonseminomatous germ cell cancer. Ann Oncol. 1999;12:1475–83.CrossRef
Metadaten
Titel
Investigation of the efficacy of 99 mTc-DTPA scintigraphic GFR measurement with Gates method in the detection of cisplatin-induced nephrotoxicity in comparison with plasma urea and creatinine measurement
verfasst von
Filiz Özülker
Tamer Özülker
Aysun Küçüköz Uzun
Tevfik Özpaçacı
Publikationsdatum
01.12.2011
Verlag
Springer US
Erschienen in
Medical Oncology / Ausgabe 4/2011
Print ISSN: 1357-0560
Elektronische ISSN: 1559-131X
DOI
https://doi.org/10.1007/s12032-010-9565-5

Weitere Artikel der Ausgabe 4/2011

Medical Oncology 4/2011 Zur Ausgabe

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.