Feldman Darren R, Hu James, Dorff Tanya B, Lim Kristina, Patil Sujata, Woo Kaitlin M, Carousso Maryann, Hughes Amanda, Sheinfeld Joel, Bains Manjit, Daneshmand Siamak, Ketchens Charlene, Bajorin Dean F, Bosl George J, Quinn David I, Motzer Robert J
Darren R. Feldman, Kristina Lim, Sujata Patil, Kaitlin M. Woo, Maryann Carousso, Amanda Hughes, Joel Sheinfeld, Manjit Bains, Dean F. Bajorin, George J. Bosl, and Robert J. Motzer, Memorial Sloan Kettering Cancer Center; Darren R. Feldman, Dean F. Bajorin, George J. Bosl, and Robert J. Motzer, Weill Medical College of Cornell University, New York, NY; and James Hu, Tanya B. Dorff, Siamak Daneshmand, Charlene Ketchens, and David I. Quinn, University of Southern California Norris Comprehensive Cancer Center, Los Angeles, CA.
J Clin Oncol. 2016 Jul 20;34(21):2478-83. doi: 10.1200/JCO.2016.66.7899. Epub 2016 May 16.
Paclitaxel, ifosfamide, and cisplatin (TIP) achieved complete responses (CRs) in two thirds of patients with advanced germ cell tumors (GCTs) who relapsed after first-line chemotherapy with cisplatin and etoposide with or without bleomycin. We tested the efficacy of first-line TIP in patients with intermediate- or poor-risk disease.
In this prospective, multicenter, single-arm phase II trial, previously untreated patients with International Germ Cell Cancer Collaborative Group poor-risk or modified intermediate-risk GCTs received four cycles of TIP (paclitaxel 240 mg/m(2) over 2 days, ifosfamide 6 g/m(2) over 5 days with mesna support, and cisplatin 100 mg/m(2) over 5 days) once every 3 weeks with granulocyte colony-stimulating factor support. The primary end point was the CR rate.
Of the first 41 evaluable patients, 28 (68%) achieved a CR, meeting the primary efficacy end point. After additional accrual on an extension phase, total enrollment was 60 patients, including 40 (67%) with poor risk and 20 (33%) with intermediate risk. Thirty-eight (68%) of 56 evaluable patients achieved a CR and seven (13%) achieved partial responses with negative markers (PR-negative) for a favorable response rate of 80%. Five of seven achieving PR-negative status had seminoma and therefore did not undergo postchemotherapy resection of residual masses. Estimated 3-year progression-free survival and overall survival rates were 72% (poor risk, 63%; intermediate risk, 90%) and 91% (poor risk, 87%; intermediate risk, 100%), respectively. Grade 3 to 4 toxicities consisted primarily of reversible hematologic or electrolyte abnormalities, including neutropenic fever in 18%.
TIP demonstrated efficacy as first-line therapy for intermediate- and poor-risk GCTs with an acceptable safety profile. Given higher rates of favorable response, progression-free survival, and overall survival compared with prior first-line studies, TIP warrants further study in this population.
紫杉醇、异环磷酰胺和顺铂(TIP方案)在三分之二一线接受顺铂、依托泊苷联合或不联合博来霉素化疗后复发的晚期生殖细胞肿瘤(GCT)患者中取得了完全缓解(CR)。我们测试了一线TIP方案治疗中危或低危疾病患者的疗效。
在这项前瞻性、多中心、单臂II期试验中,既往未接受过治疗的国际生殖细胞癌协作组低危或改良中危GCT患者每3周接受4个周期的TIP方案(紫杉醇240mg/m²,分2天给药;异环磷酰胺6g/m²,分5天给药并给予美司钠支持;顺铂100mg/m²,分5天给药),同时给予粒细胞集落刺激因子支持。主要终点是CR率。
在前41例可评估患者中,28例(68%)达到CR,达到主要疗效终点。在扩展期增加入组患者后,总入组人数为60例,其中40例(67%)为低危,20例(33%)为中危。56例可评估患者中有38例(68%)达到CR,7例(13%)达到部分缓解且标记物阴性(PR阴性),总有效率为80%。达到PR阴性状态的7例患者中有5例为精原细胞瘤,因此未进行化疗后残留肿块切除术。估计3年无进展生存率和总生存率分别为72%(低危,63%;中危,90%)和91%(低危,87%;中危,100%)。3至4级毒性主要包括可逆的血液学或电解质异常,其中18%的患者出现中性粒细胞减少性发热。
TIP方案作为中危和低危GCT的一线治疗方案显示出疗效,且安全性可接受。与既往一线研究相比,TIP方案具有更高的有效率、无进展生存率和总生存率,因此值得在该人群中进一步研究。