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低级别非霍奇金淋巴瘤患者接受含BUCY或BEAC的大剂量化疗及未净化外周血干细胞输注。

High-dose chemotherapy with BUCY or BEAC and unpurged peripheral blood stem cell infusion in patients with low-grade non-Hodgkin's lymphoma.

作者信息

Weaver C H, Schwartzberg L, Rhinehart S, West J, Zhen B, West W H, Buckner C D

机构信息

Clinical Research Division of Response Oncology, Inc, Memphis, TN 98122, USA.

出版信息

Bone Marrow Transplant. 1998 Feb;21(4):383-9. doi: 10.1038/sj.bmt.1701101.

Abstract

Forty-nine patients with low-grade non-Hodgkin's lymphoma (NHL) received high-dose chemotherapy (HDC) with busulfan and cyclophosphamide (BUCY) or carmustine, etoposide, cytarabine and CY (BEAC) followed by unpurged autologous peripheral blood stem (PBSC) infusion. All patients had failed initial chemotherapy or progressed after an initial remission. Peripheral blood stem cells were mobilized with CY alone (n = 1), CY, etoposide (n = 19), or CY, etoposide and cisplatin (n = 29) followed by granulocyte colony-stimulating factor. Twenty-two patients received BU, 16 mg/kg, and CY, 120 mg/kg. Twenty-seven patients received carmustine 300 mg/m2, etoposide 600 mg/m2, cytarabine 600 mg/m2, and CY 140 mg/kg. Four patients (8%) died of non-relapse causes, two (9%) in the BUCY group and two (7%) in the BEAC group. Twenty-seven patients (55%) relapsed or progressed at a median of 9.4 months (2-38) from PBSC infusion. Ten patients who relapsed are alive a median of 31 months (range, 6-47) after relapse. The probabilities of relapse at 3.6 years for patients receiving BUCY or BEAC were 0.57 and 0.70, respectively (P = 0.92). Twenty-seven patients (55%) are alive at a median of 3.6 years (range, 1-5). The probabilities of survival at 3.6 years for patients receiving BUCY or BEAC were 0.58 and 0.55, respectively (P = 0.72). The probabilities of EFS at 3.6 years for patients receiving BUCY or BEAC were 0.36 and 0.28, respectively (P = 0.82). It was concluded that BUCY is an active regimen for the treatment of patients with low-grade NHL.

摘要

49例低度非霍奇金淋巴瘤(NHL)患者接受了白消安和环磷酰胺(BUCY)或卡莫司汀、依托泊苷、阿糖胞苷和环磷酰胺(BEAC)的大剂量化疗(HDC),随后进行未净化的自体外周血干细胞(PBSC)输注。所有患者初始化疗失败或在初始缓解后病情进展。外周血干细胞分别通过单独使用环磷酰胺(n = 1)、环磷酰胺联合依托泊苷(n = 19)或环磷酰胺联合依托泊苷和顺铂(n = 29)动员,随后使用粒细胞集落刺激因子。22例患者接受了16mg/kg的白消安和120mg/kg的环磷酰胺。27例患者接受了300mg/m²的卡莫司汀、600mg/m²的依托泊苷、600mg/m²的阿糖胞苷和140mg/kg的环磷酰胺。4例患者(8%)死于非复发原因,BUCY组2例(9%),BEAC组2例(7%)。27例患者(55%)在PBSC输注后中位9.4个月(2 - 38个月)复发或病情进展。10例复发患者复发后中位存活31个月(范围6 - 47个月)。接受BUCY或BEAC治疗的患者3.6年时的复发概率分别为0.57和0.70(P = 0.92)。27例患者(55%)存活,中位生存期3.6年(范围1 - 5年)。接受BUCY或BEAC治疗的患者3.6年时的生存概率分别为0.58和0.55(P = 0.72)。接受BUCY或BEAC治疗的患者3.6年时的无事件生存率分别为0.36和0.28(P = 0.82)。得出的结论是,BUCY是治疗低度NHL患者的有效方案。

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