Key result
Cisplatin plus ifosfamide shows no difference in nephrotoxicity versus cisplatin alone in pediatric cancer survivors.
Why the study?
The prevalence and risk factors of cisplatin-induced long-term nephrotoxicity in pediatric cancer survivors were not well characterized, especially comparing cisplatin alone versus combination with ifosfamide.
Does cisplatin and ifosfamide combination treatment increase the risk of nephrotoxicity compared to cisplatin alone in pediatric cancer survivors?
Observational (n=33)
Does cisplatin and ifosfamide combination treatment increase the risk of nephrotoxicity compared to cisplatin alone in pediatric cancer survivors?
p-value: p=>0.05
In pediatric cancer survivors, cumulative ifosfamide dose and younger age at treatment are independent risk factors for long-term cisplatin-induced nephrotoxicity.
No excess nephrotoxicity with combination versus cisplatin alone in survivors; leaves open independent roles of ifosfamide dose and younger age.
BACKGROUND: The aim of this study was to compare the nephrotoxicity risk of cisplatin (CPL) and ifosfamide (IFO) combination treatment (CT) with that of CPL alone and to evaluate the prevalence of CPL-induced long-term nephrotoxicity in pediatric cancer survivors (CS). METHODS: A total of 33 patients with pediatric solid tumors who have been cured of their disease were included in the study. They were divided into two groups based on the type of chemotherapeutics, either CPL (n = 21) or CT (n = 12), given during cancer treatment and were evaluated for glomerular and tubular function using the Skinner grading system. RESULTS: Nephrotoxicity was found in 15 CS (45.4%): seven (21.3%) of those had moderate, six (18.2%) had mild, and two (6.1%) had severe nephrotoxicity. Neither the rates of overall nephrotoxicity, glomerular toxicity and tubular toxicity, nor the mean overall, glomerular and tubular toxicity scores differed significantly among the CPL and CT groups (P > 0.05 for all parameters). Cumulative IFO dose and age at treatment were found to be independent risk factors for both development and severity of CPL-induced nephrotoxicity (P = 0.025 and P = 0.036 for development of nephrotoxicity; P = 0.004 and P = 0.050 for severity of nephrotoxicity, respectively). CONCLUSIONS: Although CPL-induced long-term nephrotoxicity was found in half of the pediatric CS of solid tumors, clinically significant nephrotoxicity was detected only in a minority of them. Both higher cumulative IFO dose and younger age at treatment were found to be independent risk factors for both development and severity of CPL-induced nephrotoxicity.
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Arga et al. (2014) conducted an observational in Pediatric solid tumors (n=33). Cisplatin and ifosfamide combination treatment vs. Cisplatin alone was evaluated on Overall nephrotoxicity, glomerular toxicity, and tubular toxicity (p=>0.05). Cisplatin and ifosfamide combination treatment did not significantly differ from cisplatin alone in rates of overall, glomerular, and tubular nephrotoxicity in pediatric cancer survivors (P>0.05).
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