Fountzilas G, Papakostas P, Dafni U, Makatsoris T, Karina M, Kalogera-Fountzila A, Maniadakis N, Aravantinos G, Syrigos K, Bamias A, Christodoulou C, Economopoulos T, Kalofonos Hp, Nikolaou A, Angouridakis N, Stathopoulos G, Bafaloukos D, Pavlidis N, Daniilidis J
Department of Medical Oncology, Papageorgiou Hospital, Aristotle University of Thessaloniki School of Medicine, Thessaloniki, Macedonia, Greece.
Ann Oncol. 2006 Oct;17(10):1560-7. doi: 10.1093/annonc/mdl151. Epub 2006 Jun 21.
The prognosis of patients with recurrent and/or metastatic head and neck cancer (HNC) is poor. Median survival of these patients following chemotherapy is in the range of 6 to 9 months. In the present randomized phase III trial we compared two new combinations containing new drugs with proven activity in phase II studies with patients with HNC.
From November 1999 until November 2004, 166 eligible patients with HNC were enrolled in the study. They were treated with paclitaxel 175 mg/m(2) on day 1 and gemcitabine 1000 mg/m(2) on days 1 and 8 every 3 weeks (group A, 85 patients) or with paclitaxel, as in group A, and pegylated liposomal doxorubicin 40 mg/m(2) on day 1 every 4 weeks (group B, 81 patients).
There was no significant difference in response rate (20% versus 29%, P = 0.21), time to disease progression (median; 4.4 months versus 6.0 months, P = 0.09) and survival (median; 8.6 months versus 11.05 months, P = 0.25). Both regimens were generally well tolerated. The most frequently reported side effect, apart from alopecia, was neutropenia. Overall, there was no significant difference in severe toxicity between the two treatment arms.
The present study could not demonstrate a survival benefit with either regimen. Both treatments were well tolerated. Randomized studies comparing each of the two regimens with standard chemotherapy are warranted.
复发和/或转移性头颈癌(HNC)患者的预后较差。这些患者化疗后的中位生存期在6至9个月之间。在本项随机III期试验中,我们将两种含有在II期研究中已证实具有活性的新药的新联合方案与HNC患者进行了比较。
从1999年11月至2004年11月,166例符合条件的HNC患者入组本研究。他们接受如下治疗:每3周的第1天给予紫杉醇175mg/m²,第1天和第8天给予吉西他滨1000mg/m²(A组,85例患者);或如A组一样给予紫杉醇,每4周的第1天给予聚乙二醇脂质体阿霉素40mg/m²(B组,81例患者)。
在缓解率(20%对29%,P = 0.21)、疾病进展时间(中位值;4.4个月对6.0个月,P = 0.09)和生存期(中位值;8.6个月对11.05个月,P = 0.25)方面无显著差异。两种方案总体耐受性良好。除脱发外,最常报告的副作用是中性粒细胞减少。总体而言,两个治疗组之间的严重毒性无显著差异。
本研究未能证明两种方案中的任何一种对生存期有获益。两种治疗耐受性良好。有必要进行将这两种方案分别与标准化疗进行比较的随机研究。