Department of Hematology, Shinshu University School of Medicine, Matsumoto, Japan.
Cancer Sci. 2012 Jun;103(6):1079-83. doi: 10.1111/j.1349-7006.2012.02251.x. Epub 2012 Mar 23.
We conducted a retrospective Japan-Korea multicenter study to better elucidate the clinicopathologic features and therapeutic modalities for aggressive natural killer cell leukemia (ANKL). A total of 34 patients were analyzed. The median age of the patients was 40 years. Among the patients in the study, four had a history of Epstein-Barr virus-related disorders. Three types of ANKL cells were categorized according to their morphological features. Leukemic cells were below 20% in both peripheral blood and bone marrow of 11 patients. The clinical characteristics and prognoses of these 11 patients did not differ significantly from those of the others. As an initial therapy, l-asparaginase chemotherapy resulted in a better response. A total of six patients received allogeneic hematopoietic stem cell transplantation (HSCT) and two received autologous HSCT, with all in non-complete remission (CR). After HSCT, four with allogeneic and one with autologous HSCT reached CR. Median survival of all patients was 51 days. Median survival for the patients with and without HSCT were 266 and 36 days, respectively. A total of two patients with allogeneic HSCT were alive and in CR. All patients without HSCT died of ANKL. The use of L-asparaginase was indicated as a factor for longer survival (HR 0.33, 95% confidence interval; 0.13-0.83, P = 0.02). Early diagnosis of ANKL, l-asparaginase-based chemotherapy and allogeneic HSCT might lead to improved patient outcomes.
我们进行了一项日本-韩国多中心回顾性研究,以更好地阐明侵袭性自然杀伤细胞白血病(ANKL)的临床病理特征和治疗方式。共分析了 34 例患者。患者的中位年龄为 40 岁。在研究中的患者中,有 4 例有 EBV 相关疾病史。根据其形态特征将 3 种类型的 ANKL 细胞进行分类。11 例患者的外周血和骨髓中白血病细胞均低于 20%。这些 11 例患者的临床特征和预后与其他患者无显著差异。作为初始治疗,L-天冬酰胺酶化疗的反应更好。共有 6 例患者接受了异基因造血干细胞移植(HSCT),2 例接受了自体 HSCT,均未达到完全缓解(CR)。HSCT 后,4 例异基因和 1 例自体 HSCT 达到 CR。所有患者的中位总生存期为 51 天。接受和未接受 HSCT 的患者的中位生存期分别为 266 天和 36 天。2 例接受异基因 HSCT 的患者存活且处于 CR。所有未接受 HSCT 的患者均因 ANKL 死亡。使用 L-天冬酰胺酶被认为是延长生存期的一个因素(HR 0.33,95%置信区间;0.13-0.83,P = 0.02)。早期诊断 ANKL、基于 L-天冬酰胺酶的化疗和异基因 HSCT 可能会改善患者的预后。