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[YNK01(1-β-D-阿拉伯呋喃糖基胞嘧啶-5'-硬脂酰磷酸酯)治疗血液系统恶性肿瘤的II期研究]

[Phase II study of YNK01 (1-beta-D-arabinofuranosylcytosine-5'-stearylphosphate) on hematological malignancies].

作者信息

Tatsumi N, Yamada K, Ohshima T, Nakamura T, Ohno R, Masaoka T, Kimura I, Kimura K

机构信息

Osaka City University, Medical School.

出版信息

Gan To Kagaku Ryoho. 1990 Dec;17(12):2387-95.

PMID:2260876
Abstract

Phase II study of YNK01 (1-beta-D-arabinofuranosylcytosine-5'-stearylphosphate), a derivative of cytosine arabinoside, on hematological malignancies was conducted by multi-institutional cooperative group. YNK01 was administered orally at dose of 100-300 mg/body/day for more than 2 weeks. The number of registered and evaluated patients were 211 and 156, respectively. Of 23 patients with acute myelogeneous leukemia (AML), 2 complete response (CR), one partial response (PR) were observed (CR + PR: 13.0%). Hypoplastic leukemia (1/4: 25%), acute unclassified leukemia (1/1: 100%). Of 45 patients with MDS, 2CRs, 6 good response (GR) and 5PRs were observed (CR + PR: 28.9%). AML developing after a prior history of MDS (5/17: 29.4%), CML-BC (2/9: 22.2%). Of 19 patients with CML, 9 achieved CR, 3 achieved PR (63.2%). Of 11 patients with polycythemia vera, 4 achieved CR, 5 achieved PR (81.8%). Of 6 patients with essential thrombocytosis, 2 achieved CR, one achieved PR (50%). The major adverse effects included gastrointestinal toxicities such as nausea, vomiting, anorexia, diarrhea, and elevation of GOT and GPT which were tolerable and reversible. This study indicates that YNK01 is a useful agent against acute leukemia and MDS, especially RAEB, RAEB in T, CMMoL.

摘要

多机构合作组开展了阿糖胞苷衍生物 YNK01(1-β-D-阿拉伯呋喃糖基胞嘧啶-5'-硬脂酰磷酸酯)治疗血液系统恶性肿瘤的 II 期研究。YNK01 以 100 - 300 mg/体/天的剂量口服给药超过 2 周。登记和评估的患者人数分别为 211 例和 156 例。在 23 例急性髓系白血病(AML)患者中,观察到 2 例完全缓解(CR)、1 例部分缓解(PR)(CR + PR:13.0%)。低增生性白血病(1/4:25%)、急性未分类白血病(1/1:100%)。在 45 例骨髓增生异常综合征(MDS)患者中,观察到 2 例 CR、6 例良好反应(GR)和 5 例 PR(CR + PR:28.9%)。既往有 MDS 病史后发生的 AML(5/17:29.4%)、慢性粒细胞白血病急变期(CML-BC)(2/9:22.2%)。在 19 例慢性粒细胞白血病(CML)患者中,9 例达到 CR,3 例达到 PR(63.2%)。在 11 例真性红细胞增多症患者中,4 例达到 CR,5 例达到 PR(81.8%)。在 6 例原发性血小板增多症患者中,2 例达到 CR,1 例达到 PR(50%)。主要不良反应包括胃肠道毒性,如恶心、呕吐、厌食、腹泻以及谷草转氨酶(GOT)和谷丙转氨酶(GPT)升高,这些不良反应是可耐受且可逆的。本研究表明,YNK01 是治疗急性白血病和 MDS,尤其是难治性贫血伴原始细胞增多(RAEB)、转化中的难治性贫血伴原始细胞增多(RAEB in T)、慢性粒-单核细胞白血病(CMMoL)的有效药物。

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