Jatoi Aminah, Martenson James, Mahoney Michelle R, Lair Bradley S, Brindle Jeffrey S, Nichols Frank, Caron Normand, Rowland Kendrith, Tschetter Loren, Alberts Steven
Mayo Clinic, Rochester, Minnesota, USA.
Int Semin Surg Oncol. 2004 Nov 8;1(1):9. doi: 10.1186/1477-7800-1-9.
An aggressive trimodality approach from the Minnie Pearl Cancer Research Network [carboplatin AUC = 6, days 1 and 22; 5-fluorouracil 225 mg/m2 continuous infusion, days 1-42, paclitaxel 200 mg/m2, days 1 and 22; 45 Gy] has resulted in remarkable pathologic response rates but notable toxicity. This trial was designed to mitigate this toxicity by starting with a lower carboplatin dose, AUC = 4, and by adding subcutaneous amifostine. METHODS: This phase II trial included patients with locally advanced, potentially resectable esophageal cancer. All were to receive the above regimen with modifications of carboplatin AUC = 4 and amifostine 500 mg subcutaneously before radiation. All were then to undergo an esophagectomy. A planned interim toxicity analysis after the first 10 patients was to determine whether the carboplatin dose should escalate to AUC = 6. RESULTS: Ten patients were enrolled, and all required dose reductions/omissions during neoadjuvant therapy. One patient died from paclitaxel anaphylaxis. Six patients manifested a complete pathologic response. CONCLUSION: With this regimen, carboplatin AUC = 4 for patients with locally advanced esophageal cancer is appropriate.
米妮·珀尔癌症研究网络采用的积极三联疗法(卡铂AUC = 6,第1天和第22天;5-氟尿嘧啶225 mg/m²持续输注,第1 - 42天,紫杉醇200 mg/m²,第1天和第22天;45 Gy)已取得显著的病理缓解率,但毒性显著。本试验旨在通过起始较低的卡铂剂量(AUC = 4)并添加皮下注射氨磷汀来减轻这种毒性。方法:这项II期试验纳入了局部晚期、潜在可切除食管癌患者。所有患者均接受上述方案,卡铂AUC调整为4,并在放疗前皮下注射氨磷汀500 mg。然后所有患者均接受食管切除术。在首批10例患者后进行计划中的中期毒性分析,以确定卡铂剂量是否应增至AUC = 6。结果:招募了10例患者,所有患者在新辅助治疗期间均需要降低剂量/遗漏用药。1例患者死于紫杉醇过敏反应。6例患者表现出完全病理缓解。结论:对于局部晚期食管癌患者,采用该方案,卡铂AUC = 4是合适的。