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采用MACOP-B方案对艾滋病相关非霍奇金淋巴瘤进行强化治疗。

Intensive treatment of AIDS-related non-Hodgkin's lymphomas with the MACOP-B protocol.

作者信息

Schürmann D, Grünewald T, Weiss R, Jautzke G, Pohle H D, Ruf B

机构信息

Department of Infectious diseases, Rudolf Virchow University Hospital, Freie Universität Berlin, Germany.

出版信息

Eur J Haematol. 1995 Feb;54(2):73-7. doi: 10.1111/j.1600-0609.1995.tb01771.x.

Abstract

The usefulness of intensive chemotherapy with the MACOP-B protocol was evaluated in 8 patients with AIDS-related non-Hodgkin's lymphoma (NHL). Four patients had a prior AIDS diagnosis. The median CD4+ lymphocyte count was 0.079 cells x 10(9)/l (range 0.016-0.330). All patients responded to treatment. Four patients finished chemotherapy, all with complete remission, while another 3 patients deteriorated prior to finishing treatment and died. The median survival was 4 months (range 1 to 86 months). Major causes of the poor outcome were AIDS-related opportunistic infections and meningeal CNS involvement by NHL developing during or after chemotherapy. Patients with AIDS-related NHL usually do not appear to benefit from treatment with MACOP-B protocol. Advanced immunodeficiency is associated with poor tolerance to treatment and inability to finish this chemotherapy protocol. MACOP-B chemotherapy does not prevent meningeal spread of lymphoma in spite of using repeatedly systemic methotrexate crossing the blood-brain barrier. CNS prophylaxis with repeated application of intrathecal methotrexate may lower the risk of meningeal spread of lymphoma, which developed in 1 of 5 patients given CNS prophylaxis as compared to 2 of 3 patients without CNS prophylaxis.

摘要

采用MACOP - B方案的强化化疗对8例艾滋病相关非霍奇金淋巴瘤(NHL)患者的疗效进行了评估。4例患者先前已确诊患有艾滋病。CD4 +淋巴细胞计数中位数为0.079×10⁹个细胞/升(范围为0.016 - 0.330)。所有患者对治疗均有反应。4例患者完成化疗,均达到完全缓解,而另外3例患者在完成治疗前病情恶化并死亡。中位生存期为4个月(范围为1至86个月)。预后不良的主要原因是艾滋病相关的机会性感染以及化疗期间或化疗后NHL累及脑膜中枢神经系统。艾滋病相关NHL患者似乎通常无法从MACOP - B方案治疗中获益。严重免疫缺陷与对治疗耐受性差以及无法完成该化疗方案有关。尽管反复使用可透过血脑屏障的全身甲氨蝶呤,但MACOP - B化疗并不能预防淋巴瘤的脑膜播散。与3例未进行中枢神经系统预防的患者中有2例发生淋巴瘤脑膜播散相比,5例接受中枢神经系统预防的患者中有1例发生淋巴瘤脑膜播散,反复鞘内注射甲氨蝶呤进行中枢神经系统预防可能会降低淋巴瘤脑膜播散的风险。

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