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氯法拉滨治疗成人急性髓系白血病的迟发效应。

Delayed-onset effect of clofarabine in the treatment of an adult patient with acute myeloid leukemia.

机构信息

Department of Pharmacy, West Virginia University Medicine, Morgantown, WV.

Osborn Hematopoietic Malignancy and Transplantation Program, West Virginia University, Morgantown, WV.

出版信息

Am J Health Syst Pharm. 2019 Feb 21;76(6):349-352. doi: 10.1093/ajhp/zxy055.

Abstract

PURPOSE

A delayed-onset effect of clofarabine in the treatment of an adult patient with acute myeloid leukemia (AML) is reported.

SUMMARY

A 44-year-old African-American man with pancytopenia was transferred to an academic medical center for evaluation. His medical history included bipolar depression, gynecomastia, and HIV infection (diagnosed 5 years prior) for which he was being treated with atazanavir, emtricitabine-tenofovir, and ritonavir. He was diagnosed with AML with 60% myeloblasts found during bone marrow biopsy. He had primary refractory disease after induction chemotherapy treatment. His disease was refractory to subsequent therapy with high-dose cytarabine and then etoposide and mitoxantrone. The patient then underwent treatment with granulocyte-colony stimulating factor-primed clofarabine and cytarabine (G-CLAC). At blood count recovery, he was diagnosed with refractory disease, with 17% blasts in peripheral blood and was subsequently discharged home on hospice 38 days after G-CLAC and 19 days after the last dose of filgrastim. He arrived at the outpatient clinic 79 days after G-CLAC chemotherapy with significantly improved blood counts. Two weeks later, a bone marrow biopsy confirmed complete remission with incomplete hematologic recovery.

CONCLUSION

A patient with relapsed AML achieved a delayed response to clofarabine at least 38 days after treatment.

摘要

目的

报告一例克拉屈滨治疗成人急性髓系白血病(AML)的迟发效应。

摘要

一名 44 岁的非裔美国男性因全血细胞减少症转入学术医疗中心进行评估。他的病史包括双相情感障碍、男性乳房发育症和 HIV 感染(5 年前确诊),他正在接受阿扎那韦、恩曲他滨替诺福韦和利托那韦治疗。他被诊断为 AML,骨髓活检中发现 60%的原始细胞。他在诱导化疗后患有原发性难治性疾病。随后,他接受了高剂量阿糖胞苷和依托泊苷及米托蒽醌治疗,但疾病仍有耐药性。然后,患者接受了粒细胞集落刺激因子预处理克拉屈滨和阿糖胞苷(G-CLAC)治疗。血液计数恢复时,他被诊断为难治性疾病,外周血中有 17%的原始细胞,随后在 G-CLAC 后 38 天和粒细胞集落刺激因子后 19 天因病情恶化在家中接受临终关怀。G-CLAC 化疗后 79 天,他的血液计数显著改善,来到了门诊。两周后,骨髓活检证实完全缓解,但血液学恢复不完全。

结论

一名复发性 AML 患者在接受克拉屈滨治疗至少 38 天后出现迟发反应。

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