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恶性淋巴瘤患者化疗后对新型合成胞壁酰二肽衍生物莫罗他辛的血液学反应。一项随机交叉试验。

Hematological response to the new synthetic muramyl dipeptide derivative muroctasin after chemotherapy in patients with malignant lymphoma. A randomized crossover trial.

作者信息

Hiraoka A, Masaoka T, Satoh T, Ota K, Oyama A, Horiuchi A, Hasegawa H, Nagai K, Kosaki M, Kanemaru A

机构信息

Fifth Department of Internal Medicine, Center for Adult Diseases, Osaka, Japan.

出版信息

Arzneimittelforschung. 1988 Oct;38(10):1499-501.

PMID:3058133
Abstract

A randomized crossover trial was performed in 20 patients receiving chemotherapy for malignant lymphoma. N2-[(N-acetylmuramoyl)-L-alanyl-D-isoglutaminyl]-N6-stearoyl-L-lysine (MDP-Lys(L18), muroctasin) at a dose of 200 micrograms was subcutaneously administered after one of two cycles of the same protocol. The administration was started on day 4 after the start of chemotherapy and continued for 10 days. The mean length from the start of chemotherapy to nadir of white blood cell (WBC) was not significantly different between the control and muroctasin cycles. The mean WBC and neutrophil counts at nadir of the control cycle were significantly lower than those at the same point of muroctasin cycle, respectively. A positive effect of muroctasin cycle, defined as WBC count at nadir being increased by 1,000/mm3, WBC count being increased by 1,000/mm3 on two points examined after nadir, or faster reach to nadir and faster recovery to normal range of WBC than in the control cycle, was observed in 7 (35%) of 20 patients. On the other hand, only one (5%) patient showed a superiority of the control cycle over the muroctasin cycle. Toxic effects of muroctasin were observed in 34.8% of patients, but were tolerable for most patients. These results show that muroctasin has a clinical efficacy in the restoration of leukopenia after chemotherapy.

摘要

对20例接受恶性淋巴瘤化疗的患者进行了一项随机交叉试验。在相同方案的两个周期中的一个周期后,皮下注射剂量为200微克的N2-[(N-乙酰胞壁酰)-L-丙氨酰-D-异谷氨酰胺基]-N6-硬脂酰-L-赖氨酸(MDP-Lys(L18),mur octasin)。给药在化疗开始后第4天开始,持续10天。从化疗开始到白细胞(WBC)最低点的平均时长在对照组和mur octasin周期之间无显著差异。对照组周期最低点时的平均WBC和中性粒细胞计数分别显著低于mur octasin周期相同时间点的计数。在20例患者中有7例(35%)观察到mur octasin周期的积极效果,定义为最低点时WBC计数增加1000/mm³、最低点后两个检测点WBC计数增加1000/mm³,或比对照组周期更快达到最低点并更快恢复到WBC正常范围。另一方面,只有1例(5%)患者显示对照组周期优于mur octasin周期。34.8%的患者观察到mur octasin的毒性作用,但大多数患者可以耐受。这些结果表明,mur octasin在化疗后白细胞减少的恢复方面具有临床疗效。

相似文献

1
Hematological response to the new synthetic muramyl dipeptide derivative muroctasin after chemotherapy in patients with malignant lymphoma. A randomized crossover trial.恶性淋巴瘤患者化疗后对新型合成胞壁酰二肽衍生物莫罗他辛的血液学反应。一项随机交叉试验。
Arzneimittelforschung. 1988 Oct;38(10):1499-501.
2
Restorative effect of muroctasin on leukopenia caused by anticancer chemotherapy in lung cancer. Comparative study by envelope method.多抗甲素对肺癌抗癌化疗所致白细胞减少症的恢复作用。采用随机信封法的对比研究。
Arzneimittelforschung. 1989 Jan;39(1):90-3.
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Restorative activity of muroctasin on leukopenia associated with anticancer treatment.鼠李糖对与抗癌治疗相关的白细胞减少症的恢复活性。
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[Restorative effect of muroctasin; MDP-Lys (L18) [DJ-7041] on leukopenia in urogenital cancer patients treated with chemotherapy].[uroctasin;MDP-Lys(L18)[DJ-7041]对接受化疗的泌尿生殖系统癌症患者白细胞减少症的恢复作用]
Hinyokika Kiyo. 1989 Mar;35(3):527-36.
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Activation of the cytokine network by muroctasin as a remedy for leukopenia and thrombopenia.用莫罗他辛激活细胞因子网络作为白细胞减少症和血小板减少症的一种治疗方法。
Arzneimittelforschung. 1989 Aug;39(8):915-7.
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[Restorative effect of muroctasin, MDP-Lys (L 18), on leukopenia caused by anticancer chemotherapy in lung cancer--comparative study by envelope method].[胞壁酰二肽赖氨酸(L18)对肺癌抗癌化疗所致白细胞减少的恢复作用——信封法比较研究]
Gan To Kagaku Ryoho. 1988 Nov;15(11):3095-101.
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Phase I study and clinical pharmacological study of muroctasin.穆罗他星的I期研究及临床药理学研究
Arzneimittelforschung. 1988 Jul;38(7A):1043-69.
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[Muroctasin, a muramyl dipeptide derivative].[胞壁酰二肽衍生物慕罗他辛]
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9
Local tolerance of muroctasin injection in rabbits.
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Beneficial effect of muroctasin on experimental leukopenia induced by cyclophosphamide or irradiation in mice.莫罗他辛对环磷酰胺或辐射诱导的小鼠实验性白细胞减少症的有益作用。
Arzneimittelforschung. 1988 Jul;38(7A):986-92.