Gaziev D, Galimberti M, Polchi P, Angelucci E, Giardini C, Baronciani D, Andreani M, Persini B, Erer B, Sodani P, Manna M, Nicolini G, Visani G, Lucarelli G
Unità Operativa di Ematologia e Centro Trapianti di Midollo Osseo di Muraglia, Azienda Ospedaliera S, Salvatore di Pesaro, Italy.
Bone Marrow Transplant. 2002 Jan;29(1):1-8. doi: 10.1038/sj.bmt.1703323.
From April 1981 to February 2000, 105 patients with chronic myeloid leukemia (CML) underwent BMT from HLA-identical related donors at a single center. Eighty-eight patients were in chronic phase (CP), 11 patients in accelerated phase and six patients in blast crisis. Ten of these patients received a second BMT (BMT2). Comparison of BMT in CP with chemotherapy and/or alpha-IFN (n=70) was also made. Patients were given cyclophosphamide (CY) and single-dose TBI (CYTBI, n=38) or busulfan (BU) and CY (BUCY, n=67). Overall 54 patients are alive and 52 of them are disease-free with a median follow-up of 11.3 (range 1.1-19.4) years. Ten-year disease-free survival (DFS) in CP patients was better after BUCY, 61% (95% CI, 47-68%) than after CYTBI, 41% (95% CI, 23-61%) (P=0.07). For 88 patients who received a transplant in CP, results were significantly improved when BMT was performed within 1 year after diagnosis (P=0.02) or at an age < or = 25 years old (P=0.01). Ten-year survival in patients who received BMT in CP was better than in patients treated with chemotherapy (56% vs 10%; P=0.0001) or alpha-IFN-based treatment (33%; P=0.09) with survival curves crossing at 4.2 years and at 4 years, respectively. The probability of DFS after BMT2 was 60% (95% CI, 26-87%). CP patients who received BMT after CYTBI had a higher probability of relapse and transplant-related mortality than patients receiving BUCY (53% and 58% vs 9% and 34%; P=0.002 and P=0.08, respectively). All but six patients are currently on no medication and have resumed all activities without any limitation. These long-term results confirm that allogeneic BMT is the only curative approach for CML patients and should be offered to all patients with a suitable donor as soon after diagnosis as possible.
1981年4月至2000年2月,105例慢性髓性白血病(CML)患者在单一中心接受了来自人类白细胞抗原(HLA)相合同胞供者的骨髓移植(BMT)。88例患者处于慢性期(CP),11例处于加速期,6例处于急变期。其中10例患者接受了第二次BMT(BMT2)。还对CP期接受BMT的患者与化疗和/或α-干扰素治疗的患者(n = 70)进行了比较。患者接受了环磷酰胺(CY)和单次剂量全身照射(CYTBI,n = 38)或白消安(BU)和CY(BUCY,n = 67)。总体而言,54例患者存活,其中52例无病,中位随访时间为11.3年(范围1.1 - 19.4年)。CP期患者接受BUCY后的10年无病生存率(DFS)为61%(95%可信区间,47 - 68%),优于接受CYTBI后的41%(95%可信区间,23 - 61%)(P = 0.07)。对于88例在CP期接受移植的患者,在诊断后1年内进行BMT(P = 0.02)或年龄≤25岁时进行BMT(P = 0.01),结果有显著改善。CP期接受BMT的患者的10年生存率高于接受化疗的患者(56%对10%;P = 0.0001)或基于α-干扰素治疗的患者(33%;P = 0.09),生存曲线分别在4.2年和4年交叉。接受BMT2后的DFS概率为60%(95%可信区间,26 - 87%)。接受CYTBI后进行BMT的CP期患者比接受BUCY的患者有更高的复发概率和移植相关死亡率(分别为53%和58%对9%和34%;P = 0.002和P = 0.08)。除6例患者外,所有患者目前均未用药,已恢复所有活动且无任何限制。这些长期结果证实,异基因BMT是CML患者唯一的治愈方法,应在诊断后尽快为所有有合适供者的患者提供。