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Journal of Clinical Oncology, Vol 23, No 28 (October 1), 2005: pp. 6999-7004
© 2005 American Society of Clinical Oncology.
DOI: 10.1200/JCO.2005.21.956

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Incidence of Late-Relapse Germ Cell Tumor and Outcome to Salvage Chemotherapy

Ellen A. Ronnen, G. Varuni Kondagunta, Jennifer Bacik, Stephanie Marion, Dean F. Bajorin, Joel Sheinfeld, George J. Bosl, Robert J. Motzer

From the Departments of Medicine and Epidemiology and Biostatistics, Genitourinary Oncology Service, Division of Solid Tumor Oncology, Memorial Sloan-Kettering Cancer Center, New York; and the Department of Medicine, Joan and Sanford I. Weill Medical College of Cornell University, Ithaca, NY

Address reprint requests to Robert J. Motzer, MD, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021; e-mail: motzerr{at}mskcc.org

PURPOSE: To define the incidence, clinical features, and outcome to salvage chemotherapy in patients with late-relapse germ cell tumor (GCT) after a complete response to first-line chemotherapy.

PATIENTS AND METHODS: Two patient populations were examined. First, retrospective analysis of 246 patients treated on a clinical trial with salvage chemotherapy was performed; 29 patients with late-relapse GCT were identified and evaluated for treatment outcome and survival. Salvage regimens included paclitaxel, ifosfamide, and cisplatin, single agents, or a high-dose chemotherapy program. Second, the incidence of late relapse was assessed by retrospective analysis of 551 patients after a complete response (CR) to first-line chemotherapy.

RESULTS: Twenty-nine patients received salvage chemotherapy on a clinical trial for late relapse GCT. The median survival was 23.9 months. At a median follow-up of 50.6 months, there were nine survivors. The chemotherapy regimens varied, but the only CRs were observed in patients treated with paclitaxel, ifosfamide, and cisplatin. Seven (50%) of 14 patients treated with paclitaxel, ifosfamide, and cisplatin achieved a continuous CR. Among the second population of 551 patients who had previously achieved a CR to a first-line chemotherapy trial, 17 were identified as having a late relapse (3%). The median time to relapse for these 17 patients was 7.8 years.

CONCLUSION: Late-relapse GCT is uncommon and is associated with a poor prognosis resulting from a high degree of resistance to chemotherapy. Chemotherapy with paclitaxel, ifosfamide, and cisplatin followed by surgery may be effective in patients with late-relapse GCT who are not considered candidates for primary surgery.

Supported by the Craig D. Tifford Foundation.

Presented at the 41st Annual Meeting of the American Society of Clinical Oncology, Orlando, FL, May 12-17, 2005.

Authors’ disclosures of potential conflicts of interest are found at the end of this article.


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