Kollmannsberger C, Beyer J, Liersch R, Schoeffski P, Metzner B, Hartmann J T, Rick O, Stengele K, Hohloch K, Spott C, Kanz L, Bokemeyer C
Department of Hematology/Oncology, University of Tuebingen Medical Center, Otfried-Mueller-Strasse 10, 72076 Tuebingen, Germany.
J Clin Oncol. 2004 Jan 1;22(1):108-14. doi: 10.1200/JCO.2004.06.068.
Long-term survival is rarely achieved in patients with cisplatin-refractory germ cell cancer (GCT). Both single-agent gemcitabine and oxaliplatin have shown activity in patients who experience relapse or are refractory to cisplatin treatment. This study investigates the activity of a gemcitabine plus oxaliplatin regimen in these patients.
Gemcitabine was administered at a dose of 1,000 mg/m(2) on days 1 and 8; oxaliplatin was administered at a dose of 130 mg/m(2) on day 1. Response was evaluated every 4 weeks.
Thirty-five patients with a median age of 37 years (range, 21 to 54 years) were enrolled onto the study. Primary tumor localization was gonadal, retroperitoneal, or mediastinal in 30, one, and four patients, respectively. Patients had been pretreated with a median of six platinum-containing cycles (range, four to 13 cycles) and 89% of patients previously had experienced treatment failure after high-dose chemotherapy with peripheral-blood stem-cell transplantation. Sixty-three percent of patients were considered absolutely cisplatin-refractory or cisplatin-refractory. A median of two cycles (range, 1 to 6 cycles) per patient were applied. Toxicity consisted mainly of myelosuppression, with Common Toxicity Criteria grade 3 occurring in 54% of patients. Only 9% of patients developed neutropenic fever. Three patients attained a complete remission (CR), two patients attained a marker-negative partial remission, and 11 patients attained a marker-positive partial remission, resulting in an overall response rate of 46% (95% CI, 30% to 64%). All three patients with CR and one patient with a marker-negative partial remission remained disease free at 16+, 12+, 4+, and 2+ months of follow-up. Seven (44%) of these 16 responses, including one CR, occurred in cisplatin-refractory patients.
Gemcitabine plus oxaliplatin demonstrates antitumor activity with acceptable toxicity in heavily pretreated patients with relapsed or cisplatin-refractory GCT, and may offer a chance of long-term survival for selected patients.
顺铂难治性生殖细胞癌(GCT)患者很少能实现长期生存。单药吉西他滨和奥沙利铂在复发或对顺铂治疗难治的患者中均已显示出活性。本研究调查吉西他滨加奥沙利铂方案在这些患者中的活性。
吉西他滨在第1天和第8天以1000mg/m²的剂量给药;奥沙利铂在第1天以130mg/m²的剂量给药。每4周评估一次反应。
35例患者入组本研究,中位年龄为37岁(范围21至54岁)。原发肿瘤定位分别为性腺、腹膜后或纵隔的患者有30例、1例和4例。患者接受含铂化疗的中位周期数为6个(范围4至13个周期),89%的患者此前在接受大剂量化疗及外周血干细胞移植后曾经历治疗失败。百分之六十三的患者被认为是绝对顺铂难治或顺铂难治的。每位患者应用的中位周期数为2个(范围1至6个周期)。毒性主要包括骨髓抑制,54%的患者出现3级常见毒性标准。仅9%的患者发生中性粒细胞减少性发热。3例患者达到完全缓解(CR),2例患者达到标志物阴性部分缓解,11例患者达到标志物阳性部分缓解,总缓解率为46%(95%CI,30%至64%)。所有3例CR患者和1例标志物阴性部分缓解患者在随访16+、12+、4+和2+个月时仍无疾病进展。这16例缓解中有7例(44%),包括1例CR,发生在顺铂难治性患者中。
吉西他滨加奥沙利铂在复发或顺铂难治的GCT的经过大量预处理的患者中显示出抗肿瘤活性且毒性可接受,并且可能为部分患者提供长期生存的机会。