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环孢素A与依托泊苷的相互作用。慢性髓性白血病急变期的临床及体外评估

Interaction of cyclosporin A and etoposide. Clinical and in vitro assessment in blast phase of chronic myeloid leukaemia.

作者信息

Maia R C, Noronha H, Vasconcelos F C, Rumjanek V M

机构信息

Serviço de Hematologia, Instituto Nacional de Câncer, INCA, Rio de Janeiro, Brasil.

出版信息

Clin Lab Haematol. 1997 Sep;19(3):215-7.

PMID:9352149
Abstract

Combination chemotherapy has had a low impact on survival of blast crises in chronic myelogeneous leukaemia (CML) which may be due to drug resistance. This work attempted to correlate the clinical response and some experimental evidence for the MDR phenotype. Blast cells were positive for P-glycoprotein using APAAP assay. In vitro tests showed that etoposide was partially toxic to blast cells when used alone but had its toxicity increased by nearly sixfold when combined with cyclosporin A (CSA). The patient responded poorly to treatment with etoposide combined with mitoxantrone and high-dose ara-c. However, when etoposide was associated with CSA, this patient returned to the chronic phase reinforcing our in vitro studies. Because no serious toxicity was seen clinically, we are inclined to consider the circumvention protocol an useful strategy to treat blast crises of CML.

摘要

联合化疗对慢性粒细胞白血病(CML)急变期患者的生存率影响较小,这可能是由于耐药性所致。本研究试图将临床反应与多药耐药(MDR)表型的一些实验证据联系起来。采用碱性磷酸酶抗碱性磷酸酶(APAAP)检测法,发现原始细胞P-糖蛋白呈阳性。体外试验表明,依托泊苷单独使用时对原始细胞有部分毒性,但与环孢素A(CSA)联合使用时,其毒性增加了近6倍。该患者接受依托泊苷联合米托蒽醌及大剂量阿糖胞苷治疗效果不佳。然而,当依托泊苷与CSA联合使用时,该患者恢复至慢性期,这进一步证实了我们的体外研究结果。由于临床上未观察到严重毒性反应,我们倾向于认为这种规避方案是治疗CML急变期的一种有效策略。

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