Terashima M, Ikeda K, Kawamura S, Maesawa C, Ishida K, Sato M, Saito K
First Department of Surgery, Iwate Medical University, School of Medicine, Japan.
Jpn J Surg. 1991 Mar;21(2):184-92. doi: 10.1007/BF02470907.
In order to suppress the host immune reaction in subrenal capsule assay (SRCA) using normal immunocompetent mice, the effects of cyclophosphamide (CPM) pretreatment were compared to those obtained after cyclosporine A (CSA) treatment. CPM and CSA suppressed the host reaction until day 6 and day 12, respectively, however, the histological evaluation of the tumors on day 6 revealed no differences between the two groups. The cytotoxicity of CPM in mouse serum against P388 cells was measured to evaluate the residual activity of CPM against the implanted tumor. No cytotoxicity was observed in the serum 36 hours after the CPM injection. In the histological analysis of clinical samples, inflammatory infiltration was observed in only 4 of 25 samples and tumor cell preservation recognized in 27 of 28 samples. A persistence of tumor cells was recognized in the samples rich in tumor cells. Adequate growth of the tumor in the control groups was obtained from 30 of 33 tumors (91 per cent), and the response rates of this assay were comparable to those of prior clinical experiences on each of these drugs. These results indicated the feasibility of SRCA with CPM pretreatment as a predictive test of chemotherapeutic agents for esophageal cancer.
为了在使用正常免疫活性小鼠的肾包膜下移植法(SRCA)中抑制宿主免疫反应,比较了环磷酰胺(CPM)预处理与环孢素A(CSA)处理后的效果。CPM和CSA分别在第6天和第12天之前抑制宿主反应,然而,第6天肿瘤的组织学评估显示两组之间无差异。测量了CPM在小鼠血清中对P388细胞的细胞毒性,以评估CPM对植入肿瘤的残留活性。CPM注射后36小时血清中未观察到细胞毒性。在临床样本的组织学分析中,25个样本中仅4个观察到炎性浸润,28个样本中27个识别出肿瘤细胞保存。在富含肿瘤细胞的样本中识别出肿瘤细胞的持续存在。对照组中33个肿瘤中有30个(91%)肿瘤生长良好,该试验的反应率与先前这些药物的临床经验相当。这些结果表明,CPM预处理的SRCA作为食管癌化疗药物预测试验的可行性。