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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.

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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