Severe folate deficiency anemia associated with the use of a PARP inhibitor (olaparib) in a patient with fallopian tube cancer

B. Yohannan, K. McIntyre, M. Feldman
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引用次数: 2

Abstract

Treatment of cancer patients with olaparib (PARP inhibitor) is associated with an increased risk of anemia, which is seen in a majority of treated patients. However, symptomatic anemia requiring transfusion is rare. Olaparib-induced anemia can be secondary to bone marrow suppression, hemolysis or folate deficiency. We report a case of new onset severe folic acid deficiency anemia in a patient with breast and relapsed fallopian tube cancer being treated with olaparib. Complete blood count on admission showed a hemoglobin of 4.2 g/dl and serum folate was undetectable (< 1.6 ng/ml; reference range 7-31.4 ng/ml). This is the second report of olaparib-induced folate deficiency anemia. She received three units packed red cell transfusion and parenteral folic acid supplementation and improved symptomatically. This case highlights the importance of recognizing folate deficiency as a reversible cause of anemia with PARP inhibitor therapy.
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输卵管癌患者使用PARP抑制剂(奥拉帕尼)相关的严重叶酸缺乏性贫血
用奥拉帕尼(PARP抑制剂)治疗癌症患者与贫血风险增加相关,这在大多数接受治疗的患者中可见。然而,需要输血的症状性贫血是罕见的。奥拉帕尼诱发的贫血可继发于骨髓抑制、溶血或叶酸缺乏。我们报告一例新发严重叶酸缺乏性贫血患者与乳腺癌和复发输卵管癌正在接受奥拉帕尼治疗。入院时全血细胞计数显示血红蛋白为4.2 g/dl,血清叶酸未检出(< 1.6 ng/ml;参考范围7-31.4 ng/ml)。这是奥拉帕尼引起的叶酸缺乏性贫血的第二篇报道。她接受了3个单位的红细胞输血和静脉注射补充叶酸,症状得到改善。本病例强调了认识叶酸缺乏作为PARP抑制剂治疗贫血的可逆原因的重要性。
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