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达卡巴嗪和福莫司汀治疗后人类外周血淋巴细胞中O6-烷基鸟嘌呤-DNA烷基转移酶的耗竭与再生

O6-alkylguanine-DNA alkyltransferase depletion and regeneration in human peripheral lymphocytes following dacarbazine and fotemustine.

作者信息

Lee S M, Thatcher N, Margison G P

机构信息

Department of Medical Oncology, Paterson Institute for Cancer Research, Christie Hospital, Manchester, United Kingdom.

出版信息

Cancer Res. 1991 Jan 15;51(2):619-23.

PMID:1824685
Abstract

O6-Alkylguanine-DNA alkyltransferase (ATase) levels were measured in peripheral blood lymphocytes of 13 patients with advanced malignant melanoma treated with sequential dacarbazine (DTIC) and fotemustine. Wide interindividual variation in the pretreatment levels and in depletion and regeneration of ATase activity was noted. Depletion of ATase was seen within the first h after DTIC administration with values ranging from 44 to 92% of pretreatment levels. In 10 patients, progressive depletion of ATase activity occurred with nadir activity occurring at about 4 to 6 h with values ranging from 0 to 67% of pretreatment activity; at 18 h after DTIC infusion. ATase activity varied from 6 to 81%. No significant difference was seen between the rates of ATase depletion or regeneration between the two groups of patients receiving either 500 or 800 mg/m2 of DTIC with the same dose of fotemustine (100 mg/m2). In one patient, maximum depletion occurred within 1 h and no ATase activity was detectable over the next 18 h. In another patient, maximum depletion occurred at 2 h after DTIC followed by recovery of ATase activity to 71% at 18 h. In 2 patients who returned for subsequent cycles of chemotherapy, an increase in pretreatment ATase activity was seen. Overall, the extent of depletion of ATase following DTIC/fotemustine was directly proportional to the initial ATase level.

摘要

在13例接受序贯达卡巴嗪(DTIC)和福莫司汀治疗的晚期恶性黑色素瘤患者的外周血淋巴细胞中,检测了O6-烷基鸟嘌呤-DNA烷基转移酶(ATase)水平。观察到预处理水平以及ATase活性的消耗和恢复存在广泛的个体间差异。在给予DTIC后的第1小时内可见ATase消耗,其值为预处理水平的44%至92%。在10例患者中,ATase活性逐渐消耗,最低点活性出现在约4至6小时,其值为预处理活性的0%至67%;在DTIC输注后18小时,ATase活性在6%至81%之间变化。接受相同剂量福莫司汀(100mg/m²)的两组患者,分别给予500或800mg/m² DTIC,其ATase消耗或恢复速率之间未见显著差异。在1例患者中,最大消耗在1小时内发生,在接下来的18小时内未检测到ATase活性。在另1例患者中,DTIC给药后2小时出现最大消耗,随后18小时ATase活性恢复至71%。在2例返回接受后续化疗周期的患者中,观察到预处理时ATase活性增加。总体而言,DTIC/福莫司汀治疗后ATase的消耗程度与初始ATase水平直接相关。

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