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采用BCOMM[1,3-双氯(2-氯乙基)-1-亚硝基脲(卡氮芥)、长春新碱、环磷酰胺、大剂量甲氨蝶呤和丙酮醛双缩氨基脲(MGBG)]治疗难治性骨髓性白血病患者。

Treatment of patients with refractory myelogenous leukemia with BCOMM[1,3-bis-chloro(2-chloroethyl)-1-nitrosourea (BCNU), oncovin (vincristine), cyclophosphamide, high-dose methotrexate and methyl-glyoxal bis-guanylhydrazone (MGBG)].

作者信息

Herman T S, Durie B G, Hutter J J

出版信息

Cancer Chemother Pharmacol. 1982;8(1):73-5. doi: 10.1007/BF00292874.

DOI:10.1007/BF00292874
PMID:6954016
Abstract

Ten patients with AML refractory to anthracyclines and cytosine arabinoside were treated with vincristine 1.4 mg/m2 and methotrexate (MTX) 2.5 gm/m2 by intravenous (IV) bolus on day 1 [citrovorum factor (CF) rescue began 24 h later], BCNU 80 mg/m2, and cyclophosphamide 900 mg/m2 IV 36 h after MTX and MGBG 300 mg/m2 IV over 1-2 h on days 3, 4, and 5. Bone marrow aplasia was achieved in all patients by day 12. Five patients (50%) achieved complete remission (CR). Two patients died of sepsis during induction. The median duration of remission was 24 weeks (range 8-38). Maintenance therapy was employed in three patients (high-dose MTX-CF in 2 and MGBG plus BCNU in 1), but did not appear to significantly increase the duration of remission. Nausea and vomiting occurred in eight patients. Five patients developed moderate stomatitis and one developed a moderately severe cutaneous reaction. This pilot experience demonstrates that patients with refractory AML can achieve CR after aggressive treatment with so-called second-line drugs. and may indicate that collateral sensitivity to MTX exists in cells which have become resistant to anthracyclines, a situation we previously described in an experimental cell line.

摘要

10例对蒽环类药物和阿糖胞苷难治的急性髓细胞白血病患者,于第1天接受静脉推注长春新碱1.4mg/m²和甲氨蝶呤(MTX)2.5g/m²(24小时后开始用亚叶酸钙(CF)解救),卡莫司汀80mg/m²,以及在MTX给药36小时后静脉注射环磷酰胺900mg/m²,并于第3、4和5天在1 - 2小时内静脉注射丙脒腙300mg/m²。到第12天所有患者均出现骨髓抑制。5例患者(50%)获得完全缓解(CR)。2例患者在诱导治疗期间死于败血症。缓解期的中位数为24周(范围8 - 38周)。3例患者接受了维持治疗(2例采用大剂量MTX - CF,1例采用丙脒腙加卡莫司汀),但似乎并未显著延长缓解期。8例患者出现恶心和呕吐。5例患者发生中度口腔炎,1例出现中度严重皮肤反应。这项初步经验表明,难治性急性髓细胞白血病患者在用所谓二线药物积极治疗后可获得CR,并且可能表明对蒽环类药物耐药的细胞对MTX存在旁敏感性,这是我们之前在一个实验细胞系中所描述的情况。

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Treatment of patients with refractory myelogenous leukemia with BCOMM[1,3-bis-chloro(2-chloroethyl)-1-nitrosourea (BCNU), oncovin (vincristine), cyclophosphamide, high-dose methotrexate and methyl-glyoxal bis-guanylhydrazone (MGBG)].采用BCOMM[1,3-双氯(2-氯乙基)-1-亚硝基脲(卡氮芥)、长春新碱、环磷酰胺、大剂量甲氨蝶呤和丙酮醛双缩氨基脲(MGBG)]治疗难治性骨髓性白血病患者。
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引用本文的文献

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本文引用的文献

1
Clinical experience with methylglyoxal bis (guanylhydrazone) dihydrochloride: a new agent with clinical activity in acute myelocytic leukemia and the lymphomas.盐酸甲脒亚磺酸的临床经验:一种对急性髓细胞白血病和淋巴瘤具有临床活性的新药。
Cancer Chemother Rep. 1963 Mar;27:15-26.
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4'-(9-Acridinylamino) methanesulfon-m-anisidide (AMSA): a new drug effective in the treatment of adult acute leukemia.
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Synergistic action of cyclophosphamide and 1,3-bis(2-chloroethyl)-1-nitrosourea on a transplanted murine lymphoma.
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4
Treatment of leukemia with large doses of methotrexate and folinic acid: clinical-biochemical correlates.大剂量甲氨蝶呤和亚叶酸治疗白血病:临床与生化相关性
J Clin Invest. 1969 Nov;48(11):2140-55. doi: 10.1172/JCI106181.
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Vincristine (NSC-67574) therapy for acute leukemia in children.长春新碱(NSC - 67574)治疗儿童急性白血病
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1,3-bis(2-chloroethyl)-1-nitrosourea (bcnu) and other nitrosoureas in cancer treatment: a review.
Adv Cancer Res. 1972;16:273-332. doi: 10.1016/s0065-230x(08)60343-7.
7
Refractory leukemia treated with cytosine arabinoside and cyclophosphamide.用阿糖胞苷和环磷酰胺治疗难治性白血病。
Cancer. 1973 Aug;32(2):294-7. doi: 10.1002/1097-0142(197308)32:2<294::aid-cncr2820320203>3.0.co;2-x.
8
New approaches to cancer chemotherapy with methotrexate.甲氨蝶呤用于癌症化疗的新方法。
N Engl J Med. 1975 Apr 17;292(16):846-51. doi: 10.1056/NEJM197504172921607.
9
Progress in the treatment of adults with acute leukemia: review of regimens containing cytarabine studied by the Southwest Oncology Group.成人急性白血病治疗进展:西南肿瘤协作组对含阿糖胞苷方案的研究综述
Arch Intern Med. 1976 Dec;136(12):1383-8.
10
The effect of vincristine on methotrexate uptake and inhibition of DNA synthesis by human lymphoblastoid cells.长春新碱对人淋巴母细胞样细胞摄取甲氨蝶呤及抑制DNA合成的影响。
Cancer Res. 1977 Sep;37(9):2993-7.