Kasai M, Kiyama Y
Dept. of Internal Medicine, Sapporo Hokuyu Hospital.
Gan To Kagaku Ryoho. 1995 Oct;22(12):1749-55.
Germ cell tumor (GCT) is chemotherapy-sensitive, and with the development of a cisplatin combined regimen, the majority of patients can now be cured. Seventy percent to 80% of patients with advanced GCT have a lasting complete response to a cisplatin combined regimen, while 20 to 30% of these patients are refractory to the therapy. Refractory GCT patients need more effective and intense therapy. In order to overcome the conventional dose chemotherapy results, high-dose chemotherapy backed by autologous hematopoietic stem cell transplantation (AHSCT), has been applied to patients with GCT who have relapsed after achieving a complete response by first-line chemotherapy or to those in whom disease progression or the failure to achieve CR had occurred after initial and/or ifosfamide combined salvage therapy. The therapy with a high-dose combination of CBDCA (Carboplatin), VP-16 (Etoposide) and CPM (Cyclophosphamide) or IFM (Ifosfamide), supported with AHSCT is administered to the advanced GCT patients. The response rate (CR+PR) ranges from 40 to 78% by reported groups averaging about 50%, and disease-free survival is possible in about half the survivors thus far. Treatment related morbidity and mortality are observed, but are tolerable with the above dosage. Thanks to the technical development of collecting hematopoietic stem cells using either bone marrow or peripheral blood, and hematopoietic growth factor to lessen hematologic toxicities and obtain early hematological recovery, this method can be performed more safely. High-dose chemotherapy with AHSCT may well become more effective in patients with resistant GCT by a new combination of synergistic drugs or multicycle transplants.
生殖细胞肿瘤(GCT)对化疗敏感,随着顺铂联合方案的发展,现在大多数患者可以治愈。70%至80%的晚期GCT患者对顺铂联合方案有持久的完全缓解,而这些患者中有20%至30%对该疗法耐药。难治性GCT患者需要更有效、更强化的治疗。为了克服传统剂量化疗的结果,以自体造血干细胞移植(AHSCT)为支持的大剂量化疗已应用于一线化疗获得完全缓解后复发的GCT患者,或初始和/或异环磷酰胺联合挽救治疗后出现疾病进展或未达到完全缓解的患者。对晚期GCT患者采用大剂量联合卡铂(CBDCA)、依托泊苷(VP-16)和环磷酰胺(CPM)或异环磷酰胺(IFM)并辅以AHSCT进行治疗。据报道,缓解率(CR+PR)在40%至78%之间,平均约为50%,迄今为止,约一半的幸存者有可能实现无病生存。观察到有与治疗相关的发病率和死亡率,但上述剂量下是可耐受的。由于采用骨髓或外周血采集造血干细胞的技术发展,以及使用造血生长因子减轻血液学毒性并实现早期血液学恢复,这种方法可以更安全地进行。通过协同药物的新组合或多周期移植,大剂量化疗联合AHSCT可能对耐药GCT患者更有效。