Wakisaka Naohiro, Kondo Satoru, Endo Kazuhira, Murono Shigeyuki, Yoshizaki Tomokazu
Division of Otolaryngology-Head and Neck Surgery, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan.
Ann Otol Rhinol Laryngol. 2012 Aug;121(8):555-62. doi: 10.1177/000348941212100810.
Radiation Therapy Oncology Group study 91-11 found that in resectable advanced laryngeal cancer, the locoregional control rate achieved with reduced intra-arterial cisplatin and concurrent radiotherapy (RADPLAT) was comparable to that of a concurrent chemoradiotherapy arm, with reduced toxicities. However, distant metastases were more frequent. Our study retrospectively evaluated the efficacy and feasibility of adjuvant chemotherapy with S-1, an oral fluoropyrimidine, for distant metastases following reduced RADPLAT.
We analyzed 61 patients who were treated with reduced RADPLAT and achieved a complete response at the primary site. After the use of reduced RADPLAT, 24 patients were administered S-1 for 2 weeks followed by 1 week of rest, and the cycle was repeated for 6 months (S-1+ group). Thirty-seven patients were not administered S-1 (S-1-group).
The hazard ratio for distant metastases in the S-1+ group was 0.114 (95% confidence interval, 0.015 to 0.881; p = 0.0374). There was a significant difference in disease-free survival in favor of the S-1+ group (p = 0.0455). Nineteen patients (79.2%) in the S-1+ group received S-1 according to the planned schedule and dose. Grade 3 toxicities were observed in 2 patients (8.3%), but there was no grade 4 event.
In resectable advanced laryngeal cancer, S-1 adjuvant chemotherapy is an effective and feasible treatment option to control distant metastases following reduced RADPLAT.
放射治疗肿瘤学组91 - 11研究发现,在可切除的晚期喉癌中,减少动脉内顺铂剂量并联合放疗(RADPLAT)所达到的局部区域控制率与同步放化疗组相当,且毒性降低。然而,远处转移更为常见。我们的研究回顾性评估了口服氟嘧啶S - 1辅助化疗对减少RADPLAT后远处转移的疗效和可行性。
我们分析了61例接受减少剂量RADPLAT治疗且原发部位达到完全缓解的患者。在使用减少剂量的RADPLAT后,24例患者给予S - 1治疗2周,随后休息1周,此周期重复6个月(S - 1 +组)。37例患者未给予S - 1(S - 1 -组)。
S - 1 +组远处转移的风险比为0.114(95%置信区间,0.015至0.881;p = 0.0374)。无病生存期在S - 1 +组有显著差异(p = 0.0455)。S - 1 +组19例患者(79.