François Eric, Ychou Marc, Ducreux Michel, Bertheault-Cvitkovic Frédérique, Giovannini Marc, Conroy Thierry, Lemanski Claire, Thomas Olivier, Magnin Valérie
Department of Medical Oncology, Centre Antoine-Lacassagne, Avenue de Valombrose, 06189 Nice, Cedex 2, France.
Eur J Cancer. 2005 Dec;41(18):2861-7. doi: 10.1016/j.ejca.2005.08.029. Epub 2005 Nov 15.
The aim of this study was to determine the maximum-tolerated dose (MTD) of weekly oxaliplatin combined with 5-fluorouracil (5FU) continuous infusion administered concomitantly with fractionated radiotherapy in patients presenting advanced rectal cancer. Forty-three patients with rectal cancer (stage T3/T4 (n = 24), metastatic (n = 17) and 2 with local recurrence), were included. The radiotherapy dose delivered was 45 Gy over 5 weeks (1.8 Gy/fraction/day, 5 days per week). The initial weekly oxaliplatin dosage was 30 mg/m2 and the 5FU dosage 150 mg/m2/d. The oxaliplatin and 5FU doses were escalated. Eight dose levels were tested. At dose level 8 (oxaliplatin 80 mg/m2, 5FU 225 mg/m2/d), 2 patients out of 4 presented dose-limiting toxicity (severe diarrhoea with dehydration and fatal shock, rectovesical fistula). At dose level 7, 2 further patients presented with grade 3 diarrhoea. The main toxicity of the combination was diarrhoea. The hematological and neurological toxicities were not severe and were not dose-limiting. Out of the 30 patients undergoing surgery, 4 (13.3%) presented with pathological complete response and 4 (13.3%) only presented with microscopic residual disease. The results from this study enabled determination of the recommended weekly oxaliplatin dose (60 mg/m2) combined with 5FU continuous infusion (225 mg/m2) and fractionated radiotherapy (45 Gy) in the pre-operative treatment of advanced rectal cancer. The good safety profile of the regimen, associated with promising results in terms of histological response, suggest that the regimen could be developed in future phase II/III studies.
本研究的目的是确定在晚期直肠癌患者中,每周使用奥沙利铂联合5-氟尿嘧啶(5FU)持续输注并同步进行分次放疗的最大耐受剂量(MTD)。纳入了43例直肠癌患者(T3/T4期(n = 24)、转移性(n = 17)以及2例局部复发患者)。放疗剂量在5周内给予45 Gy(1.8 Gy/分次/天,每周5天)。初始每周奥沙利铂剂量为30 mg/m²,5FU剂量为150 mg/m²/天。奥沙利铂和5FU剂量逐步增加。共测试了8个剂量水平。在剂量水平8(奥沙利铂80 mg/m²,5FU 225 mg/m²/天)时,4例患者中有2例出现剂量限制性毒性(严重腹泻伴脱水和致命休克、直肠膀胱瘘)。在剂量水平7时,又有2例患者出现3级腹泻。联合治疗的主要毒性是腹泻。血液学和神经学毒性不严重,并非剂量限制性毒性。在接受手术的30例患者中,4例(13.3%)出现病理完全缓解,4例(13.3%)仅出现微小残留病灶。本研究结果确定了晚期直肠癌术前治疗中推荐的每周奥沙利铂剂量(60 mg/m²)联合5FU持续输注(225 mg/m²)和分次放疗(45 Gy)。该方案良好的安全性,以及在组织学反应方面的 promising results,表明该方案可在未来的II/III期研究中进一步开展。 (注:promising results这里直接保留英文,可能是原文有特定含义未明确给出准确中文对应词)