Cisplatin-based chemotherapy for advanced testicular cancer was associated with predominantly asymptomatic high tone hearing loss (77%) and peripheral nerve damage (50%) at 75 months median follow-up.
Cohort (n=30)
Does cisplatin-based combination chemotherapy cause late toxicity in men with advanced testicular cancer?
Cisplatin-based chemotherapy for advanced testicular cancer is associated with asymptomatic hearing and nerve abnormalities and elevated cholesterol, but is relatively free of major long-term side effects.
To date, the prevalence and nature of the late toxicity of cisplatin-based combination chemotherapy for advanced testicular cancer has been poorly documented. Thirty men with a median age of 35 years (range, 23 to 63), who had undergone such treatment were assessed with detailed investigation to determine the type and frequency of chronic toxicity. The median follow-up from the time of commencement of chemotherapy was 75 months (range, 48 to 126). The most common late toxic effects were high tone hearing loss in 23 men (77%) and electrophysiological evidence of peripheral nerve damage in 15 (50%). Both the hearing and nerve abnormalities were predominantly asymptomatic. In addition, elevation of serum cholesterol, noted in 20 patients (67%), was significant (P = .014) when compared with a control population. Hyperuricemia was present in nine patients (30%). Only one patient, with other risk factors (smoking, family history), had evidence of ischaemic heart disease while 20% (all with a smoking history) had a diminished single breath diffusing capacity for carbon monoxide (DLCO). Cisplatin-based chemotherapy is relatively free of major long-term side effects and should not be withheld for fear of late toxicity.
Boyer et al. (Mon,) conducted a cohort in metastatic testicular cancer (n=30). cisplatin-based combination chemotherapy vs. control population was evaluated on Type and frequency of chronic toxicity. Cisplatin-based chemotherapy for advanced testicular cancer was associated with predominantly asymptomatic high tone hearing loss (77%) and peripheral nerve damage (50%) at 75 months median follow-up.