Kusumoto H, Maehara Y, Kusumoto T, Anai H, Akazawa K, Sugimachi K
Cancer Centre of Kyushu University Hospital, Fukuoka, Japan.
Eur J Surg Oncol. 1988 Dec;14(6):685-9.
An in vitro chemosensitivity test, the succinate dehydrogenase inhibition (SDI) test, was used to examine 16 pairs of samples obtained simultaneously from primary and metastatic lesions of clinical gastric cancer. Concerning the metastases, 11 were in the lymph nodes and five in the liver. The chemosensitivities of metastatic lesions against six anti-tumour drugs, carboquone (CQ), adriamycin (ADM), mitomycin C (MMC), aclacinomycin A (ACR), and 5-fluorouracil (5-FU), differed from those in the primary lesions, and there were no correlations of chemosensitivities between the primary and the metastatic lesions against these drugs, except for DDP. The lymph nodes were more sensitive to CQ, ADM, MMC, DDP, ACR and 5-FU, while the liver was less sensitive than the primary lesions to CQ, ADM, MMC, DDP, and ACR. Our findings indicate that in patients with lymph node metastasis, there is a sensitivity to anti-tumour drugs, while in cases of liver metastasis, drug treatment may be less effective. We propose that chemosensitivity testing should be done when attempting to design anti-tumour drugs.
采用体外化学敏感性试验——琥珀酸脱氢酶抑制(SDI)试验,对16对同时取自临床胃癌原发灶和转移灶的样本进行检测。关于转移情况,11例转移至淋巴结,5例转移至肝脏。转移灶对卡波醌(CQ)、阿霉素(ADM)、丝裂霉素C(MMC)、阿克拉霉素A(ACR)和5-氟尿嘧啶(5-FU)这六种抗肿瘤药物的化学敏感性与原发灶不同,除顺铂(DDP)外,原发灶和转移灶对这些药物的化学敏感性无相关性。淋巴结对CQ、ADM、MMC、DDP、ACR和5-FU更敏感,而肝脏对CQ、ADM、MMC、DDP和ACR的敏感性低于原发灶。我们的研究结果表明,在有淋巴结转移的患者中,存在对抗肿瘤药物的敏感性,而在肝转移的病例中,药物治疗可能效果较差。我们建议在尝试设计抗肿瘤药物时应进行化学敏感性检测。