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采用中剂量VP-16、环磷酰胺和全身照射预处理方案对成年急性淋巴细胞白血病患者进行异基因造血干细胞移植的良好疗效。

Excellent outcome of allogeneic hematopoietic stem cell transplantation using a conditioning regimen with medium-dose VP-16, cyclophosphamide and total-body irradiation for adult patients with acute lymphoblastic leukemia.

作者信息

Shigematsu Akio, Kondo Takeshi, Yamamoto Satoshi, Sugita Junichi, Onozawa Masahiro, Kahata Kaoru, Endo Tomoyuki, Shiratori Soichi, Ota Shuichi, Obara Masato, Wakasa Kentaro, Takahata Mutsumi, Takeda Yukari, Tanaka Junji, Hashino Satoshi, Nishio Mitsufumi, Koike Takao, Asaka Masahiro, Imamura Masahiro

机构信息

Department of Hematology and Oncology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.

出版信息

Biol Blood Marrow Transplant. 2008 May;14(5):568-75. doi: 10.1016/j.bbmt.2008.02.018.

Abstract

We retrospectively evaluated the outcomes of 37 adult patients with acute lymphoblastic leukemia (ALL) undergoing allogeneic hematopoietic stem cell transplantation (allo-SCT) conditioned with medium-dose VP-16 (VP, 30 mg/kg), cyclophosphamide (CY, 120 mg/kg), and fractionated total-body irradiation (TBI, 12 Gy) (medium-dose VP/CY/TBI). The median age of the patients was 26 years. Thirteen patients underwent transplantation from HLA-matched related donors (MRD), 18 patients underwent transplantation from HLA-matched unrelated donors (MUD), and 6 patients underwent transplantation from HLA-mismatched donors (MMD). Thirty-two patients received bone marrow and 4 patients received peripheral blood stem cells. Ten patients were Philadelphia chromosome-positive (Ph(+)) and 35 patients were in complete remission (CR) at transplantation. All of the patients achieved engraftment, and grade 3 organ toxicity before engraftment occurred in 27 patients. Grade II-III acute graft-versus-host disease (GVHD) and chronic GVHD (cGVHD) occurred in 15 and 18 patients, respectively. No patient developed grade IV acute GVHD (aGVHD) or died of GVHD. At median follow-up of 35.1 months, 32 patients were alive and all Ph(+) patients were alive. Three patients died of relapse and 2 died of transplant-related mortality (TRM). The actuarial 3-year overall survival (OS) rate, relapse rate, and TRM rate were 89.2%, 8.1%, and 5.4%, respectively. Non-CR at transplantation, MRD, and no aGVHD were significant adverse prognostic factors for survival. Medium-dose VP/CY/TBI for adult ALL patients was associated with lower relapse rate and no increase in toxicity, resulting in better survival.

摘要

我们回顾性评估了37例接受中剂量VP-16(VP,30mg/kg)、环磷酰胺(CY,120mg/kg)和分次全身照射(TBI,12Gy)(中剂量VP/CY/TBI)预处理的异基因造血干细胞移植(allo-SCT)的成年急性淋巴细胞白血病(ALL)患者的结局。患者的中位年龄为26岁。13例患者接受了来自HLA匹配的相关供者(MRD)的移植,18例患者接受了来自HLA匹配的无关供者(MUD)的移植,6例患者接受了来自HLA不匹配供者(MMD)的移植。32例患者接受了骨髓移植,4例患者接受了外周血干细胞移植。10例患者为费城染色体阳性(Ph(+)),35例患者在移植时处于完全缓解(CR)状态。所有患者均实现了造血重建,27例患者在造血重建前发生了3级器官毒性。15例和18例患者分别发生了II-III级急性移植物抗宿主病(GVHD)和慢性GVHD(cGVHD)。无患者发生IV级急性GVHD(aGVHD)或死于GVHD。在中位随访35.1个月时,32例患者存活,所有Ph(+)患者均存活。3例患者死于复发,2例死于移植相关死亡率(TRM)。3年总生存(OS)率、复发率和TRM率的精算值分别为89.2%、8.1%和5.4%。移植时未达到CR、MRD和无aGVHD是生存的显著不良预后因素。中剂量VP/CY/TBI用于成年ALL患者与较低的复发率相关,且毒性未增加,从而带来了更好的生存。

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