首页> 外文期刊>Bone marrow transplantation >Intensive conditioning regimen of etoposide (VP-16), cyclophosphamide and carmustine (VCB) followed by autologous hematopoietic stem cell transplantation for relapsed and refractory Hodgkin's lymphoma.
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Intensive conditioning regimen of etoposide (VP-16), cyclophosphamide and carmustine (VCB) followed by autologous hematopoietic stem cell transplantation for relapsed and refractory Hodgkin's lymphoma.

机译:依托泊苷(VP-16),环磷酰胺和卡莫司汀(VCB)的强化调理方案,然后自体造血干细胞移植治疗复发性和难治性霍奇金淋巴瘤。

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Several high-dose therapy regimens are used for autologous hematopoietic stem cell transplantation (auto-HSCT) for relapsed and refractory Hodgkin's lymphoma (HL) with variable disease response. An intensified regimen of etoposide (VP-16) 2,400 mg/m(2), cyclophosphamide 7,200 mg/m(2) and carmustine (BCNU) 600 mg/m(2) (VCB) pre-auto-HSCT was developed to overcome disease recurrence. A total of 43 relapsed and refractory HL patients underwent auto-HSCT between January 1992 and December 2004. At day 100 there were 37 (86%) complete responses. A total of 40 patients survived beyond day 100, 14 of whom subsequently relapsed/progressed. At a median follow-up of 4.9 years (range 1.5-11.4 years), 26 patients (60%) are alive and disease free. Five-year actuarial event-free survival (EFS) was 53% (95% CI 35-70%) and median EFS was 5.9 years. Median progression-free and overall survivals have not been reached. EFS was reduced with an increasing number of prognostic factors (Karnofsky performance status, KPS <90, chemotherapy-resistant disease and >or=3 chemotherapy regimens prior to transplant or=2; P=0.049). Grade III-IV regimen-related toxicity was 9% (n=4). The 1-year cumulative incidence of interstitial pneumonitis (IP) was 36%, however only two patients died of IP complications. Disease progression was the most common cause of death (n=10, 23%). Intensive VCB is an effective and well-tolerated preparative regimen for relapsed and refractory HL auto-HSCT.
机译:几种大剂量治疗方案用于自体造血干细胞移植(auto-HSCT),以治疗具有可变疾病反应的复发性和难治性霍奇金淋巴瘤(HL)。依托泊苷(VP-16)2,400 mg / m(2),环磷酰胺7,200 mg / m(2)和卡莫司汀(BCNU)600 mg / m(2)(VCB)自动HSCT的强化治疗方案得以克服疾病复发。在1992年1月至2004年12月之间,共有43例复发性和难治性HL患者接受了自动HSCT。在第100天时,有37例(86%)完全缓解。共有40位患者在第100天后存活,其中14位患者随后复发/进展。中位随访时间为4.9年(范围1.5-11.4年),有26名患者(60%)存活并且没有疾病。五年精算无事件生存(EFS)为53%(95%CI 35-70%),中位EFS为5.9年。尚未达到中位无进展生存期和总生存期。 EFS随预后因素的增加而降低(Karnofsky行为状态,KPS <90,化疗耐药性疾病和>或= 3移植前化疗方案<或= 1 vs>或= 2; P = 0.049)。 III-IV级方案相关的毒性为9%(n = 4)。间质性肺炎(IP)的1年累积发生率是36%,但是只有2例患者死于IP并发症。疾病进展是最常见的死亡原因(n = 10,23%)。对于复发性和难治性HL auto-HSCT,强化VCB是一种有效且耐受性良好的制备方案。

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