Nakao I, Ohashi Y, Ito K, Yokoyama T, Nishi I, Kanko T, Saito T
Cancer Institute Hospital.
Gan To Kagaku Ryoho. 1990 Feb;17(2):217-20.
Twenty-five courses (twenty-two pts) with NSCLC have been entered in the trial evaluating the combination of CDDP 20 mg/m2 i.v. day 1, 2, 3, 4, 5, CQ 7 mg/m2 i.v. day 1, and PS 30 mg/body per os day 1, 2, 3, 4, 5, repeated every 4 weeks. Except for 1 case of early death, judgement of efficacy was possible in 24 courses, including one case of squamous cell carcinoma and 23 cases of adenocarcinoma. CR was obtained in no cases and PR in 7 cases, all of which were adenocarcinoma, with an efficacy rate of 29%. Response for primary site was obtained in 4 of 22 cases (18%). Median survival time of the 22 cases was 11.5 months. Main side effects of PPQ Therapy were symptoms in digestive organs such as nausea and loss of appetite, and bone marrow inhibition. Renal dysfunction was controllable by measures to cope with diuresis.
已有25例非小细胞肺癌患者(22分)进入试验,该试验评估顺铂20mg/m²静脉滴注第1、2、3、4、5天、氯喹7mg/m²静脉滴注第1天、以及PS 30mg/体口服第1、2、3、4、5天的联合用药方案,每4周重复一次。除1例早期死亡外,24例患者可进行疗效判断,其中包括1例鳞状细胞癌和23例腺癌。无病例达到完全缓解,7例达到部分缓解,均为腺癌,有效率为29%。22例患者中4例(18%)原发部位有反应。22例患者的中位生存时间为11.5个月。PPQ疗法的主要副作用为消化系统症状,如恶心和食欲不振,以及骨髓抑制。肾功能障碍可通过利尿措施控制。