Kp. Dieckmann et al., ADJUVANT CARBOPLATIN TREATMENT FOR SEMINOMA CLINICAL STAGE-I, Journal of cancer research and clinical oncology, 122(1), 1996, pp. 63-66
The traditional adjuvant therapy for seminoma stage I is abdominal rad
iotherapy. Although the relapse rate ranges below 5% this treatment is
challenged because concerns about adverse late effects are accumulati
ng. Carboplatin is effective in metastatic seminoma and two pilot stud
ies have indicated effectivity in the adjuvant setting also. As this d
rug is almost non-toxic in moderate doses it could be an ideal adjuvan
t treatment for seminoma stage I. A group of 82 patients, mean age 37.
5 years (range 22-73 years), with histologically pure seminoma stage I
, were given carboplatin 400 mg/m(2) after orchiectomy; 60 patients re
ceived only one course of carboplatin, and 22 patients received two co
urses. The median time of observation is 24 months, ranging from 2 to
48 months, and 66 patients have a minimum follow-up of 1 year. There i
s one relapse so far. Toxicity is rather mild with no severe nausea/em
esis. Mean platelet counts were 164/nl after 3 weeks and 208/nl after
4 weeks; thus, myelotoxicity was negligible. Gonadal toxicity was meas
ured by serial follicle-stimulating hormone levels. The mean level was
11.4 U/l before treatment, and 16.2 U/l after 5 weeks, 17.3 U/l after
4 months, 14.5 U/l after 8 months and 13.5 U/l after 12 months. Thus,
gonadal toxicity also appeared to be mild. In summary, the efficacies
of adjuvant carboplatin and of abdominal radiotherapy seem to be iden
tical. As carboplatin, in the dosage used, involves no severe acute si
de-effects and probably few late adverse effects, this regimen constit
utes a promising new treatment option in seminoma patients stage I tha
t deserves to be studied in randomized trials.