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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
Olofsson, Sven-Erik
Tandstad, Torgrim
Jerkeman, Mats
Dahl, Olav
Ståhl, Olof
Klepp, Olbjörn
Bremnes, Roy M.
Cohn-Cedermark, Gabriella
Langberg, Carl W.
Laurell, Anna
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för radiologi, onkologi och strålningsvetenskap, Enheten för onkologi.
Solberg, Arne
Stierner, Ulrika
Wahlqvist, Rolf
Wijkström, Hans
Anderson, Harald
Cavallin-Ståhl, Eva
Vise andre og tillknytning
2011 (engelsk)
Inngår i:
Journal of Clinical Oncology, ISSN 0732-183X, E-ISSN 1527-7755, Vol. 29, nr 15, s. 2032-2039
Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]
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 (t(1/2)) for alpha-fetoprotein (AFP) of <= 7 days and/or for beta-human chorionic gonadotropin (beta-HCG) of <= 3 days. Patients with prolonged marker t(1/2) (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.
sted, utgiver, år, opplag, sider
2011. Vol. 29, nr 15, s. 2032-2039
HSV kategori
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URN:
urn:nbn:se:uu:diva-154544
DOI:
10.1200/JCO.2010.29.1278
ISI:
000290716900032
PubMedID:
21482994
OAI: oai:DiVA.org:uu-154544
DiVA, id:
diva2:420984
Tilgjengelig fra:
2011-06-07
Laget:
2011-06-07
Sist oppdatert:
2017-12-11
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