de Manzoni Giovanni, Pedrazzani Corrado, Laterza Ernesto, Pasini Felice, Grandinetti Antonio, Bernini Marco, Ruzzenente Andrea, Zerman Germana, Tomezzoli Anna, Cordiano Claudio
First Department of General Surgery, University of Verona, Verona, Italy.
Ann Thorac Surg. 2005 Oct;80(4):1176-83. doi: 10.1016/j.athoracsur.2005.02.048.
This study analyzed the impact on long-term results of an increase in the dosage of an induction chemoradiotherapy protocol for squamous cell carcinoma (SCC) of the thoracic esophagus.
Two groups were considered among 177 patients who underwent preoperative chemoradiotherapy for SCC of the thoracic esophagus. Group A includes 111 patients (from 1987 to 1995) who were submitted to cisplatin and 5-fluorouracil (two cycles) and radiotherapy (3,000 cGy). Group B includes 66 patients (from 1995 to 2002) in which the doses were raised both in terms of chemotherapy (three cycles) and radiotherapy (5,000 cGy).
The induction treatment was completed in most of the patients (92.1%) with an acceptable treatment-related mortality (2.6%). Surgery was accomplished in 148 patients; 78.4% and 92.4% in groups A and B, respectively (p = 0.015). The postoperative in-hospital mortality was 8.8%. Tumor resection was possible in 91.8% with a better R0-resection rate for group B (83.9%; p = 0.004). Responders represented 34.9% of the patients with 20.1% of "complete" responses (29.5% in group B; p = 0.018). The overall 5-year survival rate was improved in group B (30.2%; p = 0.017), and when survival analysis was restricted to responders (70.1%; p = 0.027).
No differences in feasibility and complication rate were observed during the two study periods. A higher rate of R0-resections was achieved in group B. The increased dosage led to an increased rate of complete responses and to an improved overall 5-year survival.
本研究分析了增加胸段食管鳞状细胞癌诱导放化疗方案剂量对长期疗效的影响。
在177例行胸段食管鳞状细胞癌术前放化疗的患者中分为两组。A组包括111例患者(1987年至1995年),接受顺铂和5-氟尿嘧啶(两个周期)及放疗(3000 cGy)。B组包括66例患者(1995年至2002年),化疗周期增加至三个周期,放疗剂量提高至5000 cGy。
大多数患者(92.1%)完成了诱导治疗,治疗相关死亡率可接受(2.6%)。148例患者完成了手术;A组和B组的手术完成率分别为78.4%和92.4%(p = 0.015)。术后住院死亡率为8.8%。91.8%的患者可行肿瘤切除,B组的R0切除率更高(83.9%;p = 0.004)。缓解者占患者总数的34.9%,其中“完全”缓解者占20.1%(B组为29.5%;p = 0.018)。B组的总体5年生存率有所提高(30.2%;p = 0.017),当生存分析仅限于缓解者时也是如此(70.1%;p = 0.027)。
两个研究期间在可行性和并发症发生率方面未观察到差异。B组实现了更高的R0切除率。剂量增加导致完全缓解率提高和总体5年生存率改善。