ADJUVANT CARBOPLATIN TREATMENT FOR SEMINOMA CLINICAL STAGE-I

Citation
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
Citations number
26
Categorie Soggetti
Oncology
ISSN journal
01715216
Volume
122
Issue
1
Year of publication
1996
Pages
63 - 66
Database
ISI
SICI code
0171-5216(1996)122:1<63:ACTFSC>2.0.ZU;2-7
Abstract
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.