Department of Urology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kamigyo-ku, Kyoto, Japan.
Int J Clin Oncol. 2009 Oct;14(5):436-41. doi: 10.1007/s10147-009-0899-y. Epub 2009 Oct 25.
We investigated the efficacy and toxicity of a regimen consisting of paclitaxel and gemcitabine plus nedaplatin, a derivative of cisplatin (TGN) in patients with heavily pretreated cisplatin-refractory germ cell tumors (GCTs).
Fifteen patients with advanced GCTs were treated with the TGN regimen. The combination chemotherapy consisted of paclitaxel (210 mg/m(2)) on day 1 and gemcitabine (1000 mg/m(2)) on days 1 and 8 in combination with nedaplatin (100 mg/m(2)) on day 2 every 3 weeks.
Patients enrolled in this study had been heavily pretreated with a median of 12 platinum-containing cycles (range, 7 to 26 cycles). Most of the regimens had included paclitaxel and ifosfamide plus cisplatin or nedaplatin (TIP/TIN) chemotherapy. The median follow-up period of the present study was 15 months. Patients received 2-11 cycles of the TGN combination chemotherapy. Six patients received the treatment combined with other therapeutic modalities; 2 patients received radiation therapy for retroperitoneal lymph node metastasis, 1 patient had cyber-knife radiosurgery for brain metastasis and 3 patients had radiofrequency ablation for liver and lung metastasis. Seven (46.7%) of the 15 patients achieved an objective response; 6 had marker-negative partial responses (PRs) and 1 had a marker-positive PR. Two (13%) of the 7 patients with PRs achieved a disease-free status after chemotherapy combined with RT and followed by surgical resection. However, 10 patients died of the disease and 3 patients are still alive with the disease.
The TGN regimen alone had limited efficacy in this patient population, with severe but manageable toxicities. However, TGN chemotherapy may offer a chance of cure for some heavily pretreated cisplatin-refractory (TIP/TIN-refractory) patients as part of multidisciplinary therapy.
我们研究了紫杉醇和吉西他滨联合奈达铂(顺铂的衍生物,TGN)治疗既往接受过多线铂类药物治疗且铂类药物耐药的生殖细胞肿瘤(GCT)患者的疗效和毒性。
15 例晚期 GCT 患者接受 TGN 方案治疗。该联合化疗方案包括紫杉醇(210mg/m²)于第 1 天,吉西他滨(1000mg/m²)于第 1 和 8 天,奈达铂(100mg/m²)于第 2 天,每 3 周 1 次。
本研究纳入的患者既往接受过多线铂类药物治疗,中位数为 12 个周期(范围为 7 至 26 个周期)。大多数方案均包含紫杉醇和异环磷酰胺联合顺铂或奈达铂(TIP/TIN)化疗。本研究的中位随访时间为 15 个月。患者接受了 2-11 个周期的 TGN 联合化疗。6 例患者接受了其他治疗方法的联合治疗;2 例患者接受了腹膜后淋巴结转移的放疗,1 例患者接受了脑部转移的 Cyber-knife 放射外科手术,3 例患者接受了肝和肺转移的射频消融治疗。15 例患者中,7 例(46.7%)达到了客观缓解;6 例为标志物阴性部分缓解(PR),1 例为标志物阳性 PR。7 例 PR 患者中有 2 例(13%)在化疗联合放疗后行手术切除达到无疾病状态。然而,10 例患者死于疾病,3 例患者仍患有疾病但存活。
TGN 方案单药治疗在该患者人群中疗效有限,但毒性严重但可管理。然而,TGN 化疗可能为某些既往接受过多线铂类药物治疗且铂类药物耐药(TIP/TIN 耐药)的患者提供治愈机会,作为多学科治疗的一部分。