Bilateral testicular germ cell tumors in patients treated for clinical stage I non-seminoma within two risk-adapted SWENOTECA protocols

Authors

  • Torgrim Tandstad The Cancer Clinic, St. Olavs University Hospital, Trondheim, Norway
  • Arne Solberg The Cancer Clinic, St. Olavs University Hospital, Trondheim, Norway
  • Ulf Håkansson Department of Urology, Malmö University Hospital, Malmö, Sweden
  • Olof Stahl Department of Oncology, Skåne University Hospital, Lund, Sweden
  • Hege Sagstuen Haugnes Institute of Clinical Medicine, University of Tromsø, Tromsø, Norway; University Hospital of North Norway, Tromsø, Norway
  • Jan Oldenburg Oslo University Hospital, Oslo, Norway
  • Olav Dahl Department of Clinical Science, Faculty of Medicine and Dentistry, University of Bergen, Bergen, Norway; Haukeland University Hospital, Bergen, Norway
  • Anders Kjellman Division of Urology, Karolinska University Hospital, Stockholm, Sweden
  • Anders Angelsen Department of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway; Department of Urological Surgery, St. Olavs University Hospital, Trondheim, Norway
  • Gabriella Cohn-Cedermark Department of Oncology-Pathology Karolinska Institute, Stockholm, Sweden; Karolinska University Hospital, Stockholm, Sweden

DOI:

https://doi.org/10.3109/0284186X.2014.953256

Abstract

Background. A contralateral tumor occurs in 3.5–5% of men diagnosed with testicular germ cell cancer (TGCC). Biopsy of the contralateral testis may detect intratubular germ cell neoplasia ITGCNU, a precursor of TGCC. Biopsy of the contralateral testis to detect ITGCNU is controversial. If adjuvant chemotherapy (ACT) protects against bilateral cancer is debated.

Material and methods. A total of 1003 patients with clinical stage I (CS I) non-seminomatous testicular germ cell cancer (NSGCT) were included in two prospective, population-based protocols. Fifteen patients were excluded. Treatment was either adjuvant chemotherapy (n = 494), or surveillance (n = 494). Contralateral testicular biopsy was recommended for all patients, but was performed only in 282 patients. In case of ITGCNU radiotherapy (RT) to 16 Gy was recommended.

Results. During a follow-up of 8.3 years, 31 (3.6%) patients developed contralateral TGCC. ITGCNU was detected in 3.2% (9/282) of biopsied patients. The incidence of bilateral TGCC was similar following ACT, 2.5% (11/494), and surveillance, 3.4% (13/494), p = 0.41. Young age was a risk factor for metachronous TGCC (HR 0.93; 95% CI 0.88–0.99, p = 0.02). In total 2.2% (6/273) of patients without ITGCNU in the biopsy developed contralateral TGCC. One irradiated patient developed contralateral cancer, and one developed contralateral tumor before RT was given.

Conclusion. ACT did not reduce the incidence of contralateral TGCC. Young patients had the highest risk of developing contralateral TGCC. The proportion of false negatives biopsies was higher than reported in earlier trials, but this may in part be related to patient selection, single biopsies and lack of mandatory immunohistochemistry.

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Published

2015-04-21

How to Cite

Tandstad, T., Solberg, A., Håkansson, U., Stahl, O., Sagstuen Haugnes, H., Oldenburg, J., … Cohn-Cedermark, G. (2015). Bilateral testicular germ cell tumors in patients treated for clinical stage I non-seminoma within two risk-adapted SWENOTECA protocols. Acta Oncologica, 54(4), 493–499. https://doi.org/10.3109/0284186X.2014.953256