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Efficacy of etoposide, cyclophosphamide, and total body irradiation in allogeneic bone marrow transplantation for adult patients with hematological malignancies.

机译:依托泊苷,环磷酰胺和全身照射在成年血液系统恶性肿瘤患者异体骨髓移植中的疗效。

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Toubai T, Tanaka J, Mori A, Hashino S, Kobayashi S, Ota S, Miura Y, Kato N, Kahata K, Izumiyama K, Yonezumi M, Chiba K, Kondo T, Toyoshima N, Asaka M, Imamura M. Efficacy of etoposide, cyclophosphamide, and total body irradiation in allogeneic bone marrow transplantation for adult patients with hematological malignancies. Clin Transplant 2004 DOI: 10.1111/j.1399-0012.2004.00225.x Copyright Blackwell Munksgaard, 2004Abstract: Introduction: A combination of fractionated total body irradiation (TBI) with etoposide (VP-16) and cyclophosphamide (CY) as a preconditioning regimen (VP/CY/TBI) has been reported to be safe and effective for both adults and children undergoing allogeneic bone marrow transplantation (allo-BMT). However, the reported doses of VP-16 were different. We evaluated the efficacy and safety of a VP-16 (at less than the usual dose)/CY/TBI regimen for adults with hematological malignancies who are required to receive allo-BMT. Patients and methods: Thirty-eight patients received VP-16, CY and TBI (VP/CY/TBI) as a preconditioning regimen for allo-BMT. Twenty-one patients were in first complete remission (1CR), six patients were in second remission (2CR) and 11 patients were in non-remission status (non-CR) before allo-BMT. These patients received allo-BMT from related donors (n = 14) and unrelated donors (n = 24). The preconditioning regimen consisted of VP-16 (15 mg/kg/d for 2 d), CY (60 mg/kg/d for 2 d) and 12 Gy TBI in six fractions for 3 d. Results: Two patients died on day 30 after transplantation. The median follow-up period for all patients was 35.0 months (range 0.8-159.6 months). At the time of analysis, 10 patients had died. Seven of those 10 patients died because of relapse. The estimated 5-yr disease-free survival (DFS) rates for all cases and acute myelogenous leukemia and acute lymphoblastic leukemia cases were 73.6, 66.7 and 100%, respectively. The estimated 5-yr DFS rates for 1CR, 2CR and non-CR cases were 90.5, 83.3 and 40.9%, respectively (p < 0.05). Conclusion: Based on thesefindings, we suggest that a VP/CY/TBI regimen is effective and safe for adult patients with hematological malignancies in 1CR and 2CR.
机译:Toubai T,Tanaka J,Mori A,Hashino S,Kobayashi S,Ota S,Miura Y,Kato N,Kahata K,Izumiyama K,Yonezumi M,Chiba K,Kondo T,Toyoshima N,Asaka M,Imamura M.依托泊苷,环磷酰胺和异体骨髓移植对成年血液系统恶性肿瘤患者的全身照射。 Clin Transplant 2004 DOI:10.1111 / j.1399-0012.2004.00225.x版权所有Blackwell Munksgaard,2004摘要:简介:分次全身照射(TBI)与依托泊苷(VP-16)和环磷酰胺(CY)的组合作为预处理方案(VP / CY / TBI)(VP / CY / TBI)已被报道对于接受同种异体骨髓移植(allo-BMT)的成人和儿童都是安全有效的。但是,VP-16的报道剂量有所不同。我们评估了VP-16(以低于常规剂量的剂量)/ CY / TBI方案对需要接受异基因BMT的血液系统恶性肿瘤成人的疗效和安全性。患者和方法:38例患者接受了VP-16,CY和TBI(VP / CY / TBI)作为同种BMT的预处理方案。有21例患者首次完全缓解(1CR),6例患者达到第二缓解(2CR),11例患者在allo-BMT之前处于非缓解状态(non-CR)。这些患者从相关的供体(n = 14)和无关的供体(n = 24)接受了同种BMT。预处理方案由VP-16(15 mg / kg / d,持续2 d),CY(60 mg / kg / d,持续2 d)和12 Gy TBI六部分组成,持续3 d。结果:两名患者在移植后第30天死亡。所有患者的中位随访期为35.0个月(范围0.8-159.6个月)。在分析时,有10名患者死亡。这10名患者中有7名因复发而死亡。估计所有病例以及急性骨髓性白血病和急性淋巴细胞性白血病病例的5年无病生存率(DFS)分别为73.6、66.7和100%。估计1CR,2CR和非CR病例的5年DFS率分别为90.5%,83.3和40.9%(p <0.05)。结论:基于这些发现,我们建议VP / CY / TBI方案对于1CR和2CR的血液系统恶性肿瘤成年患者有效且安全。

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