Interferon-alpha and interleukin-2 as treatment for leukemia relapse after allogeneic bone marrow transplantation.

Cytokines and molecular therapy Pub Date : 1995-06-01
S Giralt, S O'Brien, M Talpaz, K Van Besien, K W Chan, G Rondón, B Andersson, R Mehra, I Khouri, E Estey
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Abstract

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.

干扰素- α和白细胞介素-2治疗异基因骨髓移植后白血病复发。
我们用干扰素- α (ifn - α) ((2.5-5.0) × 10(6) IU/m2皮下注射,每周3次)和白细胞介素-2 (IL-2) ((1.8-3.6) × 10(6) IU/m2皮下注射,每周5次)联合治疗12例同种异体骨髓移植后白血病复发患者,以确定在这种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)。有九名女性和三名男性。BMT复发的中位时间为98天(范围:0-963天)。复发时,6例为AML, 4例为CML(2例为母细胞危象,2例为慢性期伴克隆进化),1例为淋巴母细胞淋巴瘤。联合细胞因子治疗开始于BMT后的中位108天(范围:37-2404)。由于毒性或GVHD(3例中枢神经系统疾病,2例GVHD, 1例高热,1例腹泻伴低血压,1例心包炎),接受较高剂量治疗的9例患者需要减少50%的剂量。在较低剂量水平下,10名患者中有2名因毒性或GVHD而停止治疗。6例患者在联合细胞因子治疗时出现与急性GVHD一致的临床表现。两名患者对联合细胞因子治疗有反应:一名CML患者和一名AML患者。细胞因子联合治疗在同种异体脑转移后复发是可行的。IL-2 1.8 × 10(6) IU/m2每周5次与IFN-2 2.5 × 10(6) U/m2每周3次的组合似乎是可以忍受的,值得在这种情况下进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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