Sd. Fossa et al., CLINICAL AND BIOCHEMICAL LONG-TERM TOXICITY AFTER POSTOPERATIVE CISPLATIN-BASED CHEMOTHERAPY IN PATIENTS WITH LOW-STAGE TESTICULAR CANCER, Oncology, 52(4), 1995, pp. 300-305
In this case-control study the long-term chemotherapy-related morbidit
y was assessed in testicular cancer patients (greater than or equal to
5 years after treatment). The case group consisted of 47 patients wit
h nonseminomatous testicular cancer who had undergone retroperitoneal
surgery and 3-4 cycles of conventional-dose cisplatin-based chemothera
py (accumulated cisplatin dose: 300-400 mg/m(2)), also containing vinb
lastine and bleomycin. The results of the clinical and biochemical inv
estigations and the patients' responses to a questionnaire were compar
ed to similar observations from a control group comprising 47 patients
treated with surgery only. In the case group the serum magnesium valu
es and the levels of FVIIvWF were significantly lower (but within the
normal range) than in the control group. Serum cholesterol values were
distributed similarly in both groups. About 40% of the patients from
the chemotherapy group still suffered from Raynaud-like phenomena and/
or sensoric neurotoxicity as compared to 10% of the patients from the
control group. Chemotherapy resulted in a significant elevation of ser
um LH within the normal range, probably associated with a slight sucli
nical Leydig cell dysfunction. Serum FSH levels were similar in the ca
se and control groups, indicating an absence of long-term disturbance
of spermatogenesis after chemotherapy. No increased cardiovascular mor
bidity was observed as a result of chemotherapy. Raynaud-like phenomen
a and sensoric neurotoxicity represent the principal clinical long-ter
m side effects after 3-4 cycles of cisplatin-based chemotherapy contai
ning vinblastine and bleomycin. Serum LH is slightly elevated after ch
emotherapy, whereas long-term spermatogenesis seems to be unaffected.