Gochi A, Orita K, Fuchimoto S, Tanaka N, Ogawa N
First Department of Surgery, Okayama University Medical School 2-5-1, Shikata-cho, Okayama, Japan.
Br J Cancer. 2001 Feb;84(4):443-51. doi: 10.1054/bjoc.2000.1599.
To investigate, by a multi-institutional randomized trial, the prognostic significance of the augmentation of tumour-infiltrating lymphocytes (TILs) by preoperative intratumoral injection of OK-432 (OK-432 it), a bacterial biological response modifier, in patients with gastric cancer. The 10-year survival and disease-free survival were examined and analysis of the factors showing survival benefit was performed. 370 patients who had undergone curative resection of gastric cancer were enrolled in this study and followed up for 10 years postoperatively. Patients were randomized into either an OK-432 it group or a control group. Ten Klinishe Einheit (KE) of OK-432 was endoscopically injected at 1 to 2 weeks before the operation in the OK-432 it group. Both groups received the same adjuvant chemoimmunotherapy consisting of a bolus injection of mitomycin C (0.4 mg kg(-1) i.v.) and administration of tegafur and OK-432 from postoperative day 14 up to 1 year later. Tegafur (600 mg day(-1)) was given orally and OK-432 (5 KE/2 weeks) was injected intradermally for a maintenance therapy. The TILs grades in resected tumour specimens and presence of metastasis and metastatic pattern in dissected lymph nodes were examined. Multivariate analysis was performed to determine the efficacy of OK-432 it on prognostic factors. All patients were followed up for 10 years. The overall 5- and 10-year survival rates and disease-free survival rates of the OK-432 it group were not significantly higher than those of the control group. However, OK-432 it significantly increased the 5- and 10-year survival rates of patients with stage IIIA + IIIB, moderate lymph node metastasis (pN2), and positive TILs. OK-432 it was most effective at prolonging the survival of patients who had both positive TILs and lymph node metastasis. The OK-432 it group with positive TILs showed a significant decrease in metastatic lymph node frequency and in the number of lymph node micro- metastatic foci when compared to the control group. This study showed that only one time preoperative OK-432 it, particularly when it triggers TILs, is effective for reduction of regional lymph node metastasis. OK-432 it probably acts partly by eliminating micro-metastatic foci in lymph nodes. Preoperative intratumoral injection of OK-432 is technically very easy and has no serious adverse effects, so it is a promising form of neoadjuvant immunotherapy for advanced gastric cancer.
通过一项多机构随机试验,研究术前瘤内注射细菌生物反应调节剂OK - 432(OK - 432 it)增强胃癌患者肿瘤浸润淋巴细胞(TILs)的预后意义。检查10年生存率和无病生存率,并对显示生存获益的因素进行分析。370例行胃癌根治性切除术的患者纳入本研究,并在术后随访10年。患者被随机分为OK - 432 it组或对照组。OK - 432 it组在手术前1至2周经内镜注射10个临床单位(KE)的OK - 432。两组均接受相同的辅助化学免疫治疗,包括静脉推注丝裂霉素C(0.4 mg·kg⁻¹),并从术后第14天至1年后给予替加氟和OK - 432。替加氟(600 mg·d⁻¹)口服,OK - 432(5 KE/2周)皮内注射进行维持治疗。检查切除肿瘤标本中的TILs分级以及清扫淋巴结中的转移情况和转移模式。进行多因素分析以确定OK - 432 it对预后因素的疗效。所有患者随访10年。OK - 432 it组的总体5年和10年生存率及无病生存率均未显著高于对照组。然而,OK - 432 it显著提高了IIIA + IIIB期、中度淋巴结转移(pN2)且TILs阳性患者的5年和10年生存率。OK - 432 it对延长TILs阳性且有淋巴结转移患者的生存期最有效。与对照组相比,TILs阳性的OK - 432 it组转移淋巴结频率和淋巴结微转移灶数量显著减少。本研究表明,术前单次使用OK - 432 it,尤其是当它触发TILs时,对减少区域淋巴结转移有效。OK - 432 it可能部分通过消除淋巴结中的微转移灶起作用。术前瘤内注射OK - 432技术上非常简单且无严重不良反应,因此它是晚期胃癌有前景的新辅助免疫治疗形式。