Kwon Ji Hyun, Koh Young-Il, Yoon Sung-Soo, Park Seonyang, Kim Inho
Department of Internal Medicine, Seoul National University Hospital, Seoul National University, College of Medicine, 101 Daehak-ro, Chongno-gu, Seoul, 110-744, Republic of Korea.
Department of Internal Medicine, ChungBuk National University Hospital, 776, 1 Sunhwan-ro, Seowon-gu, Cheongju, Chungchungbuk-do, Republic of Korea.
Int J Hematol. 2016 Nov;104(5):574-581. doi: 10.1007/s12185-016-2063-6. Epub 2016 Jul 18.
We investigated risk factors and outcome in acute myeloid leukemia (AML) patients with leptomeningeal involvement. Medical records of patients with non-promyelocytic AML at Seoul National University Hospital from January of 2000 to November of 2013 were reviewed. Leptomeningeal involvement was defined as the presence of atypical or malignant hematopoietic cells in the cerebrospinal fluid. Among 775 patients with AML, 141 patients (18.2 %) underwent cerebrospinal fluid examination. Leptomeningeal involvement of AML, confirmed in 38 patients (4.9 %), was associated with high white blood cell count and high level of lactic. There were seven patients in the favorable risk group (19.4 %), 21 in the intermediate risk group (58.3 %), and eight in the adverse risk group (22.2 %). Twenty-eight patients (85.7 %) developed leptomeningeal involvement during relapse status or refractory status. Thirty-one patients (81.6 %) received intrathecal chemotherapy, and whole-brain and/or craniospinal radiotherapy was conducted in 10 patients (27.0 %). The rate of complete remission after induction chemotherapy was 63.2 %. Median overall survival was 9.9 months. Radiotherapy and complete remission after the first induction chemotherapy were associated with longer overall survival. Leptomeningeal involvement in acute myeloid leukemia is rare, but relatively common in relapsed status or refractory status. Craniospinal radiotherapy and complete remission after induction chemotherapy were found to favorable prognostic factors.
我们调查了急性髓系白血病(AML)合并软脑膜受累患者的危险因素及预后情况。回顾了2000年1月至2013年11月在首尔国立大学医院就诊的非早幼粒细胞AML患者的病历。软脑膜受累定义为脑脊液中存在非典型或恶性造血细胞。在775例AML患者中,141例(18.2%)接受了脑脊液检查。38例(4.9%)确诊为AML合并软脑膜受累,其与高白细胞计数和高乳酸水平相关。有利风险组有7例患者(19.4%),中危组有21例(58.3%),高危组有8例(22.2%)。28例(85.7%)患者在复发状态或难治状态时出现软脑膜受累。31例(81.6%)患者接受了鞘内化疗,10例(27.0%)患者接受了全脑和/或全脊髓放疗。诱导化疗后的完全缓解率为63.2%。中位总生存期为9.9个月。放疗和首次诱导化疗后的完全缓解与更长的总生存期相关。急性髓系白血病合并软脑膜受累较为罕见,但在复发状态或难治状态时相对常见。发现全脊髓放疗和诱导化疗后的完全缓解是有利的预后因素。