Kimura K, Yamada K, Uzuka Y, Masaoka T, Hirano M, Ohno R, Ogawa M
National Nagoya Hospital.
Gan To Kagaku Ryoho. 1989 Jan;16(1):123-30.
A total of 165 patients were entered into this study and 140 were evaluate for effects and 165 for toxicities. Of 39 patients with chronic myelogenous leukemia (CML) 21 achieved complete remission (CR), 6 achieved partial remission (PR) with a response rate of 69.2%. In MDS, of 11 patients with chronic myelomonocytic leukemia (CMMoL), one good partial response and 4 partial response were observed (CR + PR:45.5%); of 14 patients with RAEB, one complete response, 4 partial response (CR + PR: 35.7%); of 11 patients with RAEB in T, 3 partial response were observed (response rate: 27.3%). Of 13 patients with polycythemia vera, 4 excellent effect and 7 moderate effect (84.6%) were observed. Seven of 30 patients with acute myelocytic leukemia achieved partial response (23.3%). Mean dosages of SM-108 until remission were 400-500 mg/m2/day on CMMoL, RAEB in MDS, polycythemia vera and CML, and 600-800 mg/m2/day on RAEB in T and AML. In the analysis of adverse effects of SM-108, a subjective side effects including mainly gastrointestinal toxicities were observed in 38 cases (23.0%) of the patients : 26 patients (15.8%) showed objective side effects including liver dysfunction, but these symptoms were transient and not serious. Our study indicates that SM-108 is useful agent against MDS, especially CMMoL, RAEB, RAEB in T, polycythemia vera and CML.
共有165例患者进入本研究,其中140例评估疗效,165例评估毒性。在39例慢性粒细胞白血病(CML)患者中,21例达到完全缓解(CR),6例达到部分缓解(PR),缓解率为69.2%。在骨髓增生异常综合征(MDS)中,11例慢性粒单核细胞白血病(CMMoL)患者中,观察到1例良好部分缓解和4例部分缓解(CR+PR:45.5%);14例难治性贫血伴原始细胞增多(RAEB)患者中,1例完全缓解,4例部分缓解(CR+PR:35.7%);11例转化型难治性贫血伴原始细胞增多(RAEB-t)患者中,观察到3例部分缓解(缓解率:27.3%)。在13例真性红细胞增多症患者中,观察到4例显效和7例中效(84.6%)。30例急性髓细胞白血病患者中有7例达到部分缓解(23.3%)。CMMoL、MDS中的RAEB、真性红细胞增多症和CML患者达到缓解时SM-108的平均剂量为400-500mg/m²/天,RAEB-t和AML患者为600-800mg/m²/天。在对SM-108不良反应的分析中,38例(23.0%)患者出现了以胃肠道毒性为主的主观副作用;26例(15.8%)患者出现了包括肝功能障碍在内的客观副作用,但这些症状是短暂的,并不严重。我们的研究表明,SM-108是治疗MDS的有效药物,尤其是对CMMoL、RAEB、RAEB-t、真性红细胞增多症和CML。