Kosmidis P, Mylonakis N, Dimopoulos A, Pavlidis N, Fountzilas G, Samantas E, Dimitriadis K, Kalophonos C, Tsavdaridis D, Skarlos D
Hygeia Hospital, Athens, Greece.
Semin Oncol. 2000 Feb;27(1 Suppl 2):3-8.
Gemcitabine plus paclitaxel and paclitaxel plus carboplatin are active and well tolerated in patients with advanced non-small cell lung cancer, showing similar rates of response and survival. The Hellenic Cooperative Oncology Group conducted a randomized phase III trial comparing gemcitabine plus paclitaxel with paclitaxel plus carboplatin. Patients were randomly assigned to two groups. Group A received paclitaxel 200 mg/m2 plus carboplatin (area under the curve = 6) on day I. Group B received paclitaxel in identical fashion to group A plus gemcitabine 1,000 mg/m2 on days I and 8 every 3 weeks. A minimum of two cycles and a maximum of six cycles was allowed. To date, 127 eligible patients (63 in group A and 64 in group B) have been randomized; the median follow-up time is 4.6 months. Preliminary results suggest that both combinations can be given in full doses and are well tolerated. Grade 3/4 neutropenia was mild but more prominent in group A (10% v 3%, respectively) while thrombocytopenia was not significant for either group. Moreover, severe neurotoxicity, hepatotoxicity, or cardiac toxicity has not been observed in the vast majority of patients in either group. Although patients in group B experienced higher response rates (37.5%) than those in group A (21.8%), the difference between the groups was not statistically significant. Definite conclusions about this study cannot be made until more data are available.
吉西他滨联合紫杉醇以及紫杉醇联合卡铂对于晚期非小细胞肺癌患者有效且耐受性良好,二者的缓解率和生存率相似。希腊肿瘤协作组开展了一项随机III期试验,比较吉西他滨联合紫杉醇与紫杉醇联合卡铂的疗效。患者被随机分为两组。A组在第1天接受紫杉醇200mg/m²加卡铂(曲线下面积=6)。B组以与A组相同的方式接受紫杉醇,并在每3周的第1天和第8天加用吉西他滨1000mg/m²。允许最少进行两个周期、最多进行六个周期的治疗。截至目前,已有127例符合条件的患者(A组63例,B组64例)被随机分组;中位随访时间为4.6个月。初步结果表明,两种联合方案均可给予全剂量且耐受性良好。3/4级中性粒细胞减少症较轻,但在A组中更明显(分别为10%和3%),而两组的血小板减少症均不显著。此外,两组绝大多数患者均未观察到严重的神经毒性、肝毒性或心脏毒性。虽然B组患者的缓解率(37.5%)高于A组(21.8%),但两组之间的差异无统计学意义。在获得更多数据之前,无法对该研究得出明确结论。