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联合治疗在伴有中枢神经系统受累的成人急性髓系白血病中的价值。

The value of combination therapy in adult acute myeloid leukemia with central nervous system involvement.

作者信息

Castagnola C, Nozza A, Corso A, Bernasconi C

机构信息

Divisione di Ematologia, IRCCS Policlinico San Matteo di Pavia, Università degli Studi di Pavia, Italy.

出版信息

Haematologica. 1997 Sep-Oct;82(5):577-80.

PMID:9407724
Abstract

BACKGROUND AND OBJECTIVE

In adult patients with acute myeloid leukemia (AML), central nervous system (CNS) involvement is a rare event and treatment has not yet been defined. Because there are no definitive data as to the most appropriate therapeutic approach to CNS leukemia in AML, we retrospectively analyzed a cohort of AML patients with meningeal leukemia in order to increase our knowledge on this particular matter.

METHODS

Out of 410 patients with de novo AML observed at our Institute from 1986 to 1995, 9 (2.2%) showed CNS leukemia (CNSL) during the follow-up. CNSL was treated as follows: in a first group of 4 patients we combined systemic HD Ara-C 3 g/m2 (every 12 hours by 3-hour infusion, for 6 doses), cranial radiation therapy and intrathecal (IT) methotrexate (MTX); a second group of 4 patients was treated with HD Ara-C, IT MTX without cranial irradiation; HD Ara-C alone was administered in one patient.

RESULTS

All patients of the first group and 2 patients of the second who achieved a complete remission (CR) had a median survival of 10 months (range 5-25+) after CNS involvement, while for the non-remitters it was 2 months (range 1-5). The only patient still living underwent allogeneic bone marrow transplantation.

INTERPRETATION AND CONCLUSIONS

The combination treatment of HD Ara-C, IT MTX and cranial irradiation is well tolerated and seems to be an effective therapy for CNSL, presenting a high incidence of neurologic CR that correlates with a longer survival. As expected, the number of AML patients with CNSL was small, due to the fact that CNS in those patients is a rare complication. However, this study provides further information about the therapeutic possibilities in such restricted subsets of AML patients.

摘要

背景与目的

在成年急性髓系白血病(AML)患者中,中枢神经系统(CNS)受累是一种罕见事件,且治疗方法尚未明确。由于尚无关于AML中枢神经系统白血病最合适治疗方法的确切数据,我们对一组患有脑膜白血病的AML患者进行了回顾性分析,以增加我们对这一特殊问题的了解。

方法

1986年至1995年在我们研究所观察的410例初发AML患者中,9例(2.2%)在随访期间出现中枢神经系统白血病(CNSL)。CNSL的治疗如下:在第一组4例患者中,我们联合使用全身大剂量阿糖胞苷(HD Ara-C)3 g/m²(每12小时静脉滴注3小时,共6剂)、颅脑放射治疗和鞘内注射甲氨蝶呤(MTX);第二组4例患者接受HD Ara-C、鞘内注射MTX但未进行颅脑照射;仅1例患者接受了HD Ara-C单药治疗。

结果

第一组所有患者以及第二组中达到完全缓解(CR)的2例患者,在CNS受累后的中位生存期为10个月(范围5 - 25 +),而未缓解者的中位生存期为2个月(范围1 - 5)。唯一仍存活的患者接受了异基因骨髓移植。

解读与结论

HD Ara-C、鞘内注射MTX和颅脑照射的联合治疗耐受性良好,似乎是治疗CNSL的有效方法,神经学CR发生率高,且与较长生存期相关。正如预期的那样,由于CNSL在这些患者中是一种罕见并发症,患有CNSL的AML患者数量较少。然而,本研究提供了关于此类AML患者受限亚组治疗可能性的更多信息。

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