WebFinal results indicate that the investigational chemotherapeutic analogs CBDCA (JM-8) and CHIP (JM-9) do not produce the ototoxicity and nephrotoxicity characteristic of cisplatin. Furthermore, these findings demonstrate 195mpt localization in the vestibular labyrinth and confirm previous platinum distribution studies in the organ of Corti and ... Web18/40 (45%) evidence of ototoxicity at audiometry. To date we have seen no neuro- or ototoxicity with carboplatin and 1/40 (2.5%) have developed WHO grade I renal toxicity. Myelo- ... Key words: Ovarian cancer; cisplatin, carboplatin, toxicity, efficacy, randomized study. Cisplatin is the most active drug in ovarian cancer ...
Mechanisms of Cisplatin-Induced Ototoxicity and …
WebSep 20, 2024 · The incidence of hearing loss was lower in the sodium thiosulfate and cisplatin arm (39%) compared with the cisplatin alone arm (68%); unadjusted relative risk 0.58 (95% CI: 0.40, 0.83). WebMar 29, 2024 · Platinum-based agents are a standard chemotherapy treatment for malignancies in both pediatric and adult populations. 1 However, mitigating and managing chemotherapy-associated adverse events remains a concern. 2 Ototoxicity is a well-documented side effect of these platinum-based agents, especially cisplatin. This … flightmike youtube
Serum platinum levels and cisplatin induced ototoxicity among …
WebMar 25, 2024 · The aim of this study is to evaluate the current state of ototoxicity monitoring for patients receiving cisplatin chemotherapy in an academic medical center with particular attention to how closely monitoring adheres to national ototoxicity guidelines. Case series including retrospective medical records review of patients (age > 18) treated … WebJan 1, 2024 · Regarding the frequency of ototoxicity of antineoplastic drugs and the dose required to trigger these effects, an important heterogeneity was observed. The frequency of ototoxicity caused by cisplatin ranged from 45% to 83.3% and, when used in combination with carboplatin, ranged from 16.6% to 75%. WebOtotoxicity of cisplatin as a single therapeutic agent is well documented. Less is known, however, about its interaction with other drugs and/or cranial irradiation. For example, ifosfamide, given as a single agent, is not known to be ototoxic but appears to potentiate the ototoxicity of cisplatin ( McHaney et al., 1992 ). chemist warehouse ciprofloxacin