Department of Pharmacy, West Virginia University Medicine, Morgantown, WV.
Osborn Hematopoietic Malignancy and Transplantation Program, West Virginia University, Morgantown, WV.
Am J Health Syst Pharm. 2019 Feb 21;76(6):349-352. doi: 10.1093/ajhp/zxy055.
A delayed-onset effect of clofarabine in the treatment of an adult patient with acute myeloid leukemia (AML) is reported.
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.
A patient with relapsed AML achieved a delayed response to clofarabine at least 38 days after treatment.
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。
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。
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。