Department of Medicine, University of Maryland School of Medicine and University of Maryland Greenebaum Cancer Center, Baltimore, MD 21201, USA.
Leuk Lymphoma. 2011 Jul;52(7):1211-4. doi: 10.3109/10428194.2011.566950. Epub 2011 May 3.
Imatinib mesylate and other tyrosine kinase inhibitors (TKIs) that inhibit BCR-ABL have had a favorable impact on the treatment of Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL). TKIs are generally well tolerated, but they can induce platelet dysfunction, which is of particular concern in the setting of thrombocytopenia in patients with acute leukemia. We present three patients with Ph+ ALL receiving imatinib mesylate in conjunction with systemic and intrathecal chemotherapy who developed subdural hematomas (SDHs). All three were thrombocytopenic and had undergone repeated lumbar punctures for prophylactic intrathecal chemotherapy, but they were not coagulopathic and did not have meningeal leukemia. SDHs occurred in three of a total of 10 adult patients with Ph+ ALL receiving imatinib mesylate in conjunction with systemic and intrathecal chemotherapy at our institution from 2007 to 2010, but in none of 22 adult patients with Ph- ALL receiving the same therapy without imatinib mesylate (p < 0.05). Patients with Ph+ ALL receiving imatinib mesylate, and likely also dasatinib, in conjunction with systemic and intrathecal chemotherapy may be at increased risk of SDH, and should be closely monitored for subtle manifestations of this complication.
甲磺酸伊马替尼和其他抑制 BCR-ABL 的酪氨酸激酶抑制剂(TKIs)对治疗费城染色体阳性(Ph+)急性淋巴细胞白血病(ALL)有良好的效果。TKIs 通常耐受性良好,但它们会引起血小板功能障碍,这在急性白血病血小板减少症患者中尤为重要。我们报告了 3 例接受甲磺酸伊马替尼联合全身和鞘内化疗的 Ph+ ALL 患者发生硬脑膜下血肿(SDH)。所有 3 例患者均血小板减少,并因预防性鞘内化疗而反复进行腰椎穿刺,但他们没有凝血功能障碍,也没有脑膜白血病。在我们机构 2007 年至 2010 年间,共收治 10 例接受甲磺酸伊马替尼联合全身和鞘内化疗的 Ph+ ALL 成年患者中,有 3 例发生 SDH,但在 22 例接受相同治疗但不使用甲磺酸伊马替尼的 Ph- ALL 成年患者中无一例发生(p<0.05)。接受甲磺酸伊马替尼联合全身和鞘内化疗的 Ph+ ALL 患者,可能还有达沙替尼,发生 SDH 的风险可能增加,应密切监测该并发症的细微表现。