环磷酰胺预处理在人食管癌肾下胶囊试验中的应用。

M Terashima, K Ikeda, S Kawamura, C Maesawa, K Ishida, M Sato, K Saito
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引用次数: 0

摘要

为了在肾下胶囊实验(SRCA)中抑制正常免疫活性小鼠的免疫反应,比较了环磷酰胺(CPM)预处理与环孢素A (CSA)处理的效果。CPM和CSA对宿主反应的抑制作用分别持续到第6天和第12天,但第6天的肿瘤组织学评价显示两组之间没有差异。测定小鼠血清中CPM对P388细胞的细胞毒性,评价CPM对移植肿瘤的残留活性。注射CPM后36小时血清中未见细胞毒性。在临床样本的组织学分析中,25例样本中只有4例观察到炎症浸润,28例样本中有27例发现肿瘤细胞保存。在富含肿瘤细胞的样品中发现了肿瘤细胞的持久性。在对照组中,33个肿瘤中有30个(91%)获得了足够的肿瘤生长,该试验的反应率与之前使用这些药物的临床经验相当。这些结果表明SRCA与CPM预处理作为食管癌化疗药物预测试验的可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The usefulness of cyclophosphamide pretreatment for subrenal capsule assay against human esophageal cancer.

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.

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