Kinoshita Taira, Konishi Masaru, Nakagohri Toshio, Inoue Kazuo, Oda Tatsuya, Takahashi Shinichiro, Boku Narikazu, Ohtsu Atsushi, Yoshida Shigeaki
Department of Surgical Oncology, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577, Japan.
Gastric Cancer. 2003;6 Suppl 1:40-4. doi: 10.1007/s10120-003-0220-0.
We conducted a pilot study using S-1 (TS-1), a novel oral derivative of 5-fluorouracil, as neoadjuvant chemotherapy for potentially resectable scirrhous gastric cancer. The neoadjuvant chemotherapy consisted of two courses (each, 4-week administration and 2-week withdrawal) of S-1 at 100-120 mg/body per day. Five patients were enrolled in this pilot study and underwent resection. The response rate for the neoadjuvant chemotherapy was 60% (three partial response [PR]; two stable disease [SD]). Three of the five patients received curative resection; the other two patients received noncurative resection because of localized peritoneal dissemination and positive results on cytological examination of the abdominal washing. No toxicity of grade 3 or more was exhibited during the two courses of chemotherapy. Pathological examination of the resected specimens revealed a marked reduction in the distribution of viable cancer cells in the stomach in the three patients with PR. In one of these patients, pathological findings suggestive of the possibility of disappearance of the cancer cells in the perigastric and paraaortic lymph nodes were noted. Because of the unexpectedly high response to S-1, we consider that the efficacy of S-1 as neoadjuvant chemotherapy for scirrhous gastric cancer should be verified by phase II and III trials.
我们开展了一项初步研究,使用新型口服5-氟尿嘧啶衍生物S-1(TS-1)作为潜在可切除的硬癌型胃癌的新辅助化疗药物。新辅助化疗由两个疗程的S-1组成(每个疗程为4周给药、2周停药),剂量为每日100 - 120 mg/体。五名患者参与了这项初步研究并接受了手术切除。新辅助化疗的有效率为60%(3例部分缓解[PR];2例病情稳定[SD])。五名患者中有三名接受了根治性切除;另外两名患者因局部腹膜播散和腹腔冲洗细胞学检查结果阳性而接受了非根治性切除。在两个化疗疗程中未出现3级或更高级别的毒性反应。对切除标本的病理检查显示,三名部分缓解患者的胃内存活癌细胞分布明显减少。在其中一名患者中,病理结果提示胃周和主动脉旁淋巴结中的癌细胞有可能消失。由于对S-1的反应出乎意料地高,我们认为S-1作为硬癌型胃癌新辅助化疗的疗效应通过II期和III期试验进行验证。