Kaneko H, Sekizawa Y, Ohashi A, Inuo T, Tsuchiya S
Gan To Kagaku Ryoho. 1982 Mar;9(3):496-502.
In 26 patients with cancer of the stomach, bone marrow function, cell mediated immunity and plasma CEA level were examined after administration of ACN-U. ACNU was given intravenously and intermittently with 5-FU given orally daily. Results 1) Delayed myelosuppression was observed in every cases and reached to the nadir in 2-7 weeks after ACNU administration. 2) Bone marrow suppression and recovery therefrom were observed earlier in platelet counts than in RBC and WBC counts. 3) Suppression of cell mediated immunity was not observed later than 4 weeks after ACNU administration. 4) Plasma CEA level decreased or stopped to increase after ACNU administration in 5 out of 8 patients having a high CEA level before treatment. 5) Regression of tumor size was observed in 4 out of 5 patients in whom a tumor was palpable. Conclusion ACNU has a strong antitumor activity and may be more effective if combined with antimetabolite agent, such as 5FU. Total dosage of ACNU given safely in one series was considered to be 150-200mg. Next series of ACNU administration should be started after restoration of platelet counts more than 100,000/mm3 was obtained.
对26例胃癌患者在给予嘧啶亚硝脲(ACN-U)后,检测其骨髓功能、细胞介导免疫及血浆癌胚抗原(CEA)水平。ACN-U静脉内间歇给药,同时每日口服氟尿嘧啶(5-FU)。结果:1)所有病例均观察到延迟性骨髓抑制,在给予ACN-U后2至7周达到最低点。2)血小板计数的骨髓抑制及恢复较红细胞和白细胞计数出现得更早。3)在给予ACN-U后4周内未观察到细胞介导免疫受抑制。4)在治疗前CEA水平高的8例患者中,5例在给予ACN-U后血浆CEA水平下降或停止升高。5)在5例可触及肿瘤的患者中,4例观察到肿瘤大小缩小。结论:ACN-U具有较强的抗肿瘤活性,若与抗代谢剂如5-FU联合使用可能更有效。一次安全给予ACN-U的总剂量被认为是150至200mg。在下一次给予ACN-U系列治疗前,应在血小板计数恢复至超过100,000/mm³后开始。