Giralt S, O'Brien S, Talpaz M, Van Besien K, Chan K W, Rondón G, Andersson B, Mehra R, Khouri I, Estey E
Department of Hematology, University of Texas MD Anderson Cancer Center, Houston 77030, USA.
Cytokines Mol Ther. 1995 Jun;1(2):115-22.
We treated 12 patients with leukemia relapse after allogenic bone marrow transplantation with a combination of interferon-alpha (IFN-alpha) ((2.5-5.0) x 10(6) u/m2 subcutaneously three times a week) and interleukin-2 (IL-2) ((1.8-3.6) x 10(6) IU/m2 subcutaneously five times a week) to determine the toxicity and efficacy of combination cytokine therapy in this setting. The median age of the patients was 39 years (range: 16-50). There were nine females and three males. The median time to relapse from BMT was 98 days (range: 0-963). At the time of relapse, six patients had AML, four patients had CML (two in blast crisis and two in chronic phase with clonal evolution), and one patient had lymphoblastic lymphoma. Combination cytokine therapy was started a median of 108 days post BMT (range: 37-2404). Nine patients treated at the higher dose level required a 50% dose reduction because of toxicity or GVHD (three CNS, two GVHD, one high fever, one diarrhoea with hypotension, and one pericarditis). At a lower dose level, 2 of 10 patients had their treatment discontinued because of toxicity or GVHD. Six patients developed clinical findings consistent with acute GVHD while on combination cytokine therapy. Two patients responded to combination cytokine therapy: one with CML and one with AML. Combination cytokine therapy is feasible in the setting of relapse post allogeneic BMT. The combination of IL-2 1.8 x 10(6) IU/m2 five times a week with IFN-2 2.5 x 10(6) U/m2 three times a week seems to be tolerable, and merits further study in this setting.
我们对12例异基因骨髓移植后白血病复发的患者采用α干扰素(IFN-α)(2.5 - 5.0×10⁶单位/平方米,皮下注射,每周3次)和白细胞介素-2(IL-2)(1.8 - 3.6×10⁶国际单位/平方米,皮下注射,每周5次)联合治疗,以确定在此情况下联合细胞因子治疗的毒性和疗效。患者的中位年龄为39岁(范围:16 - 50岁)。有9名女性和3名男性。从骨髓移植到复发的中位时间为98天(范围:0 - 963天)。复发时,6例患者患有急性髓系白血病(AML),4例患者患有慢性髓系白血病(CML)(2例处于急变期,2例处于慢性期伴克隆演变),1例患者患有淋巴细胞淋巴瘤。联合细胞因子治疗在骨髓移植后中位108天(范围:37 - 2404天)开始。9例接受较高剂量水平治疗的患者因毒性或移植物抗宿主病(GVHD)需要降低50%的剂量(3例中枢神经系统毒性,2例GVHD,1例高热,1例腹泻伴低血压,1例心包炎)。在较低剂量水平,10例患者中有2例因毒性或GVHD而停止治疗。6例患者在联合细胞因子治疗期间出现与急性GVHD一致的临床表现。2例患者对联合细胞因子治疗有反应:1例为CML,1例为AML。联合细胞因子治疗在异基因骨髓移植后复发的情况下是可行的。每周5次给予IL-2 1.8×10⁶国际单位/平方米,同时每周3次给予IFN-2 2.5×10⁶单位/平方米的联合方案似乎是可耐受的,值得在此情况下进一步研究。