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Journal of Clinical Oncology, Vol 24, No 35 (December 10), 2006: pp. 5503-5511
© 2006 American Society of Clinical Oncology.
DOI: 10.1200/JCO.2006.08.1836

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REVIEW ARTICLE

Late Relapses of Germ Cell Malignancies: Incidence, Management, and Prognosis

Jan Oldenburg, Jarad M. Martin, Sophie D. Fosså

From the Department of Clinical Cancer Research, University of Oslo, Rikshospitalet-Radiumhospitalet Medical Center, Oslo, Norway; Department of Radiation Oncology, Princess Margaret Hospital, Toronto, ON, Canada

Address reprint requests to Jan Oldenburg, MD, Department of Clinical Cancer Research, Rikshospitalet-Radiumhospitalet Medical Center, Oslo, Norway; e-mail: jan.oldenburg{at}medisin.uio.no

Late relapses of malignant germ cell tumors (MGCTs) are rare and occur, by definition, 2 years or later after successful treatment. They represent a major challenge of today's treatment of MGCTs. Because of the rarity and heterogeneity of late relapses, many aspects of their main characteristics remain obscure. We present relevant literature on relapsing MGCTs to highlight the following issues: incidence, impact of initial treatment on the subsequent risk of late relapse, treatment, and survival. In a pooled analysis, the incidence is 1.4% and 3.2% in seminoma and nonseminoma patients, respectively. The predominant site of relapse is the retroperitoneal space in both histologic types. The initial treatment appears to be important for the risk and localization of late relapses. The treatment of late relapses should be based on a representative presalvage biopsy and includes radical surgery and salvage chemotherapy in most cases. Five-year cancer-specific survival is above 50% in the recent large series and reaches 100% in case of single-site teratoma. Diagnosis and treatment of late-relapsing MGCT patients is challenging and should be performed in experienced centers only. Referral of late-relapsing patients to high-volume institutions ensures the best chances of cure and enables increasing understanding of tumor biology and the clinical course of these patients.

Supported by the Research Council of Norway, project No. 160619/V50.

Authors' disclosures of potential conflicts of interest and author contributions are found at the end of this article.


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