Browse > Article
http://dx.doi.org/10.7314/APJCP.2013.14.2.1111

Evaluation of Renal Function Using the Level of Neutrophil Gelatinase-Associated Lipocalin is Not Predictive of Nephrotoxicity Associated with Cisplatin-Based Chemotherapy  

Kos, F. Tugba (Department of Medical Oncology, Kahramanmaras Sutcu Imam University Faculty of Medicine)
Sendur, Mehmet Ali Nahit (Department of Medical Oncology, Ankara Numune Education and Research Hospital)
Aksoy, Sercan (Department of Medical Oncology, Hacettepe University Institute of Oncology)
Celik, Huseyin Tugrul (Department of Biochemistry, Fatih University Faculty of Medicine)
Sezer, Sevilay (Department of Biochemistry, Ankara Numune Education and Research Hospital)
Civelek, Burak (Department of Medical Oncology, Ankara Numune Education and Research Hospital)
Yaman, Sebnem (Department of Medical Oncology, Ankara Numune Education and Research Hospital)
Zengin, Nurullah (Department of Medical Oncology, Ankara Numune Education and Research Hospital)
Publication Information
Asian Pacific Journal of Cancer Prevention / v.14, no.2, 2013 , pp. 1111-1114 More about this Journal
Abstract
Background: For early detection of renal damage during the usage of cisplatin based chemotherapy, changes in renal function should be monitored carefully. In recent years, neutrophil gelatinase-associated lipocalin, a small polypeptide molecule, has shown promise as a marker of acute renal failure. The aim of this present study was to assess possible risk prediction of cisplatin-induced nephrotoxicity using serum NGAL. Materials and Methods: A total of 34 consecutive patients with documented serum creatinine at least 24 hours before every cycle of cisplatin-based chemotherapy were included in the study. Demographic and medical data including age, performance status, tumor characteristics and comorbid diseases were collected from medical charts. Renal function was evaluated at least 48 hours before the treatment and at the end of the treatment based on the Modification of Diet in Renal Disease (MDRD) formula. Before and after cisplatin infusion serum NGAL levels were measured for the first and 3rd cycles of chemotherapy. Results: The median age of the study population was 54 (32-70) years. Fifteen patients (41.1%) were treated on an adjuvant basis, whereas 19 patients (58.9%) were treated for metastatic disease. There was no correlation of serum NGAL levels with serum creatinine (r=0.20, p=0.26) and MDRD (r=-0.12, p=0.50) and creatinine clearance-Cockcroft-Gault (r=-0.22, p=0.22) after cisplatin infusion at the end of the 3rd cycle of chemotherapy. Conclusions: In our study, serum NGAL levels were not correlated with the cisplatin induced nephrotoxicity. Further prospective studies are needed to conclude that serum NGAL level is not a good surrogate marker to predict early cisplatin induced nephrotoxicity.
Keywords
Chemotherapy; cisplatin; neutrophil gelatinase-associated lipocalin;
Citations & Related Records
연도 인용수 순위
  • Reference
1 Asna N, Lewy H, Ashkenazi IE, et al (2005). Time dependent protection of amifostine from renal and hematopoietic cisplatin induced toxicity. Life Sci, 76, 1825-34.   DOI   ScienceOn
2 Gaspari F, Cravedi P, Mandala M, et al (2010). Predicting cisplatin-induced acute kidney injury by urinary neutrophil gelatinase-associated lipocalin excretion: a pilot prospective case-control study. Nephron Clin Pract, 115, 154-60.   DOI   ScienceOn
3 Hanigan MH, Devarajan P (2003). Cisplatin nephrotoxicity: molecular mechanisms. Cancer Ther, 1, 47-61.
4 Kjeldsen L, Bainton DF, Sengelov H, Borregaard No1994). Identification of neutrophil gelatinase-associated lipocalin as a novel matrix protein of specific granules in human neutrophils. Blood, 83, 799-807.
5 Kuwabara T, Mori K, Mukoyama M, et al (2009). Urinary neutrophil gelatinase- associated lipocalin levels reflect damage to glomeruli, proximal tubules, and distal nephrons. Kidney Int, 75, 285-94.   DOI   ScienceOn
6 Levey AS, Bosch JP, Lewis JB, et al (1999). A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation. Ann Intern Med, 130, 461-70.   DOI   ScienceOn
7 Ling W, Zhaohui N, Ben H, et al (2008). Urinary IL-18 and NGAL as early predictive biomarkers in contrast-induced nephropathy after coronary angiography. Nephron Clin Pract, 108, 176-81.   DOI   ScienceOn
8 Mishra J, Ma Q, Prada A, et al (2003). Identification of neutrophil gelatinase-associated lipocalin as a novel early urinary biomarker for ischemic renal injury. J Am Soc Nephrol, 14, 2534-43.   DOI   ScienceOn
9 Mishra J, Mori K, Ma Q, et al (2004). Neutrophil gelatinase-associated lipocalin: a novel early urinary biomarker for cisplatin nephrotoxicity. Am J Nephrol, 24, 307-15.   DOI   ScienceOn
10 Mohanram A, Toto R (2005). Measurement of kidney function. In 'Chronic Kidney Disease, Dialysis, and Transplantation. A Companion to Brenner and Rector's The Kidney'. Eds Pereira BJG, Sayegh MH, Blake PG. Philadelphia, Saunders pp.20-30.
11 Parikh CR, Jani A, Mishra J, et al (2006). Urine NGAL and IL-18 are predictive biomarkers for delayed graft function following kidney transplantation. Am J Transplant, 6, 1639-45.   DOI   ScienceOn
12 Perazella MA, Moeckel GW (2010). Nephrotoxicity from chemotherapeutic agents: clinical manifestations, pathobiology, and prevention/therapy. Semin Nephrol, 30, 570-81.   DOI   ScienceOn
13 Perrone RD, Madias NE, Levy AS (1992). Serum creatinine as an index of renal function: new insights into old concepts. Clin Chem, 38, 1933-53.
14 Shemesh O, Golbetz H, Kriss JP, Myers BD (1985). Limitations of creatinine as a filtration marker in glomerulopathic patients. Kidney Int, 28, 830-8.   DOI   ScienceOn
15 Townsend DM, Deng M, Zhang L, Lapus MG, Hanigan MH (2003). Metabolism of cisplatin to a nephrotoxin in proximal tubule cells. J Am Soc Nephrol, 14, 1-10.   DOI   ScienceOn
16 Wagener G, Jan M, Kim M, et al (2006). Association between increases in urinary neutrophil-associated lipocalin and acute renal dysfunction after adult cardiac surgery. Anesthesiology, 105, 485-91.   DOI   ScienceOn