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- O Rick, C Bokemeyer, S Weinknecht, J Schirren, T Pottek, J T Hartmann, T Braun, B Rachud, L Weissbach, M Hartmann, W Siegert, and J Beyer.
- Department of Hematology and Oncology, Charité, Germany.
- J. Clin. Oncol. 2004 Sep 15; 22 (18): 3713-9.
PurposeTo assess the role of residual tumor resection performed after high-dose chemotherapy (HDCT) in patients with relapsed or refractory germ cell tumors (GCT).Patients And MethodsBetween July 1987 and October 1999, postchemotherapy resections of residual tumors were performed in 57 patients who had been treated with HDCT for relapsed or refractory GCT and who had achieved a partial remission to this treatment.ResultsComplete resections of residual masses were achieved in 52 (91%) of 57 patients who were rendered disease free; in five (9%) of 57 patients, the resections were incomplete. Resection of a single site was performed in 39 (68%) of 57 patients, and the remaining 18 (32%) of 57 patients required interventions at two or more residual tumor sites. Necrosis was found in 22 (38%) of 57 patients, mature teratoma with or without necrosis was found in nine (16%) of 57 patients, and viable cancer with or without additional necrosis or mature teratoma was found in 26 (46%) of 57 patients. Viable cancer consisted either of residual germ cell or undifferentiated cancer in 22 (85%) of 26 patients, with additional non-GCT histologies in the remaining four patients. Patients with viable cancer had a significantly inferior outcome after surgery compared with patients with necrosis and/or mature teratoma even if all cancer was completely resected. Pulmonary lesions with a diameter of more than 2 cm were the only predictive variable for viable cancer in univariate analysis.ConclusionResections of all residual tumors should be attempted in patients with relapsed or refractory GCT and partial remissions after HDCT.
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