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[7;11染色体易位的治疗相关性急性非淋巴细胞白血病(M2型)经小剂量阿糖胞苷和磷酰阿糖胞苷治疗诱导完全缓解]

[Therapy-related acute non-lymphocytic leukemia (M2) with 7;11 chromosome translocation induced into complete remission by low dose cytosine arabinoside and cytarabine ocfosfate therapy].

作者信息

Shikoshi K, Shikoshi K, Niitsu N, Takada M, Umeda M

机构信息

First Department of Internal Medicine, Toho University School of Medicine.

出版信息

Nihon Ronen Igakkai Zasshi. 1994 Jun;31(6):468-71. doi: 10.3143/geriatrics.31.468.

Abstract

A case of therapy-related acute non-lymphocytic leukemia (t-ANLL) in a 70-year-old female patient is reported. An operation for lung cancer was performed in February 1991, and she was treated with etoposide (VP-16), a topoisomerase II inhibitor. Nineteen months after the start of chemotherapy, she complained of palpitations, and anemia and thrombocytopenia developed. The myelogram revealed 41.2% leukemic cells, and a diagnosis of t-ANLL induced by VP-16 was made. The karyotype of bone marrow cells showed 46, XX, t(7;11) (p13;p15), 16p+. She obtained complete remission (CR) by treatment with low dose cytosine arabinoside (Ara-C) and cytarabine ocfosfate (SPAC). Karyotype with t-ANLL induced by alkylate agents frequently shows unbalanced abnormalities. The difference of cytogenetic findings suggest the difference of mechanisms. Detailed chromosomal analysis make clear the oncogenesis of t-ANLL. It is reported that the prognosis of patients with t-ANLL treated by conventional chemotherapy is poor. Considering that elderly cases of acute leukemia have a lower probability of achieving CR than non-elderly cases, because of complications and side effects of chemotherapy such as bone marrow suppression, treatment with low dose Ara-C and SPAC is thought to be indicated in elderly patients with t-ANLL.

摘要

报告了一例70岁女性患者的治疗相关性急性非淋巴细胞白血病(t-ANLL)。1991年2月该患者因肺癌接受手术,并接受了拓扑异构酶II抑制剂依托泊苷(VP-16)治疗。化疗开始19个月后,她出现心悸,并发贫血和血小板减少。骨髓检查显示白血病细胞占41.2%,诊断为VP-16诱导的t-ANLL。骨髓细胞的核型显示为46, XX, t(7;11) (p13;p15), 16p+。她通过低剂量阿糖胞苷(Ara-C)和磷酰阿糖胞苷(SPAC)治疗获得完全缓解(CR)。烷化剂诱导的t-ANLL的核型常显示不平衡异常。细胞遗传学结果的差异提示机制不同。详细的染色体分析有助于明确t-ANLL的肿瘤发生机制。据报道,采用传统化疗治疗t-ANLL患者的预后较差。考虑到老年急性白血病患者由于化疗的并发症和副作用如骨髓抑制等,达到CR的概率低于非老年患者,因此对于老年t-ANLL患者,认为采用低剂量Ara-C和SPAC治疗是合适的。

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