Population-Based Study of Treatment Guided by Tumor Marker Decline in Patients With Metastatic Nonseminomatous Germ Cell Tumor: A Report From the Swedish-Norwegian Testicular Cancer Group

Author:

Olofsson Sven-Erik1,Tandstad Torgrim1,Jerkeman Mats1,Dahl Olav1,Ståhl Olof1,Klepp Olbjørn1,Bremnes Roy M.1,Cohn-Cedermark Gabriella1,Langberg Carl W.1,Laurell Anna1,Solberg Arne1,Stierner Ulrika1,Wahlqvist Rolf1,Wijkström Hans1,Anderson Harald1,Cavallin-Ståhl Eva1

Affiliation:

1. From Lund University Hospital, Lund University, Lund; Uppsala University Hospital, Uppsala; Sahlgrenska University Hospital, Göteborg; and Karolinska Institute and University Hospital, Stockholm, Sweden; St Olav University Hospital, Trondheim; University of Bergen and Haukeland University Hospital, Bergen; University of Tromsø and University Hospital of North Norway, Tromsø; and Ullevål University Hospital and Oslo University Hospital, Oslo, Norway.

Abstract

Purpose From 1995 to 2003, 603 adult patients from Sweden and Norway with metastatic testicular nonseminomatous germ cell tumor (NSGCT) were included prospectively in a population-based protocol with strict guidelines for staging, treatment, and follow-up. Patients with extragonadal primary tumor or previous treatment for contralateral testicular tumor were excluded. The basic strategy was to individualize treatment according to initial tumor marker response. Methods Initial treatment for all patients was two courses of standard bleomycin, etoposide, and cisplatin (BEP), with tumor markers analyzed weekly. Good response was defined as a half-life (t1/2) for α-fetoprotein (AFP) of ≤ 7 days and/or for β–human chorionic gonadotropin (β-HCG) of ≤ 3 days. Patients with prolonged marker t1/2 (ie, poor response) received intensification with addition of ifosfamide (BEP-if/PEI) in step 1. If poor response continued, the treatment was intensified with high-dose chemotherapy with stem-cell rescue as step 2. Results Overall, 99% of all patients with metastatic testicular NSGCT in the population were included in the protocol. Median follow-up was 8.2 years. Seventy-seven percent of the patients were treated with BEP alone; 18% received intensification step 1%, and 5% received intensification step 2. Grouped according to International Germ Cell Consensus Classification, 10-year overall survival was 94.7% in good-prognosis patients, 90.0% in intermediate-prognosis patients, and 67.4% in poor-prognosis patients. Conclusion With detailed treatment protocols and a dedicated collaborative group of specialists, treatment results comparable to those reported from large single institutions can be achieved at national level. With the treatment principles used in Swedish-Norwegian Testicular Cancer Group study SWENOTECA IV, the survival of intermediate-prognosis patients is remarkable and close to that of good-prognosis patients.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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