Extragonadal germ cell tumors in Japan
Hiromichi Ebi
Division of Oncology/Hematology, Department of Medicine, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577
Department of Internal Medicine and Molecular Science, Nagoya City University Medical School, Mizuho-ku, Nagoya 467-8601
Search for more papers by this authorMasanobu Nakata
Division of Oncology/Hematology, Department of Medicine, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577
Search for more papers by this authorMakoto Tahara
Division of Oncology/Hematology, Department of Medicine, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577
Search for more papers by this authorTadahiko Igarashi
Division of Oncology/Hematology, Department of Medicine, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577
Search for more papers by this authorKenji Kawada
Division of Oncology/Hematology, Department of Medicine, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577
Search for more papers by this authorKuniaki Itoh
Division of Oncology/Hematology, Department of Medicine, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577
Search for more papers by this authorRyuzo Ueda
Department of Internal Medicine and Molecular Science, Nagoya City University Medical School, Mizuho-ku, Nagoya 467-8601
Search for more papers by this authorCorresponding Author
Hironobu Minami
Division of Oncology/Hematology, Department of Medicine, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577
To whom correspondence should be addressed. E-mail: [email protected]Search for more papers by this authorHiromichi Ebi
Division of Oncology/Hematology, Department of Medicine, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577
Department of Internal Medicine and Molecular Science, Nagoya City University Medical School, Mizuho-ku, Nagoya 467-8601
Search for more papers by this authorMasanobu Nakata
Division of Oncology/Hematology, Department of Medicine, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577
Search for more papers by this authorMakoto Tahara
Division of Oncology/Hematology, Department of Medicine, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577
Search for more papers by this authorTadahiko Igarashi
Division of Oncology/Hematology, Department of Medicine, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577
Search for more papers by this authorKenji Kawada
Division of Oncology/Hematology, Department of Medicine, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577
Search for more papers by this authorKuniaki Itoh
Division of Oncology/Hematology, Department of Medicine, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577
Search for more papers by this authorRyuzo Ueda
Department of Internal Medicine and Molecular Science, Nagoya City University Medical School, Mizuho-ku, Nagoya 467-8601
Search for more papers by this authorCorresponding Author
Hironobu Minami
Division of Oncology/Hematology, Department of Medicine, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577
To whom correspondence should be addressed. E-mail: [email protected]Search for more papers by this authorAbstract
Extragonadal germ cell tumors (EGCT) represent only 2–5% of adult germ cell malignancies. Some publications from Asia have reported inferior treatment outcomes compared to data from an international study group. To ascertain whether this is generally the case, here we analyze treatment outcomes for 30 Japanese patients with EGCT. The medical records of 30 patients (25 non-seminomas and 4 pure seminomas) treated from 1992 to 2002 were reviewed retrospectively. All patients with seminoma achieved long survival except one who died of chemotherapy-related sepsis. Ten and 11 patients with EGCT presented with mediastinal and retroperitoneal primary sites, respectively. The 5-year overall survival (OS) and progression-free survival (PFS) for non-seminoma was 71% and 42%, respectively. The 5-year OS and PFS was 60% and 44%, respectively, for 10 patients with mediastinal nonseminoma, and 91% and 48%, respectively, for patients with retroperitoneal nonseminoma. Tumor marker values on day 7 were available for 19 patients. Among the 19 patients in whom AFP or β-HCG were measured on day 7, the values had declined in 12 patients and were transiently elevated in 7 patients compared to pretreatment values. The transient elevations of tumor markers were significantly associated with poor OS (P=0.02) and PFS (P=0.008). The treatment outcome of Japanese patients with EGCT seemed to be comparable to that reported from international studies, suggesting no difference between ethnic groups. Transient tumor marker elevations on day 7 predict poor survival in EGCT patients and may be a useful parameter for identifying patients requiring more aggressive treatment.
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