Sacchi S, Gugliotta L, Papineschi F, Liberati A M, Rupoli S, Delfini C, Ruggeri M, Cavanna L, Bucalossi A, Benedetti E, Ferrandina C, Vinci G, Morselli M, Torelli G
Dipartimento di Scienze Mediche, Radiologiche ed Oncologiche, Università di Modena, Italy.
Leukemia. 1998 Mar;12(3):289-94. doi: 10.1038/sj.leu.2400931.
The efficacy of alfa-interferon (alfa-IFN) in essential thrombocythemia (ET) patients has been reported by several authors. The aim of this study is to assess the magnitude of the effect of alfa-IFN on the neoplastic clone. As of December 1993, 11 ET patients received alfa-IFN at a dose of 3-6 MU/s.c./day for 6 months. Ten of 11 obtained complete hematological remission (CHR) and one achieved partial hematological remission. Megakaryocyte concentration was reduced in six cases. The spleen,which was enlarged in four patients, decreased in size in two patients. Seven of eight patients who were symptomatic at diagnosis obtained resolution of symptoms. In order to obtain indications about the structural modifications induced by alfa-IFN in ET megakaryocytes (Mks), Fourier-transform infra-red microspectroscopy analysis performed on 10 single Mks of each patient, was done in seven of 11 patients; the analysis showed a reduction of A1/A2 ratios (A1 integrated area of the band at 1080 cm(-1) due to the nucleic acids absorption; A2 integrated area of the band at 1540 cm(-1) due to proteic components absorption) in five cases, and in three of these five patients A1/A2 ratios achieved normal values. After alfa-IFN treatment we did not observe any change in the methylation pattern of DNA from the granulocyte fraction. Our results confirm the efficacy of alfa-IFN in ET patients, and the decrease of A1/A2 ratios in several patients is a demonstration of the depth of the effect of alfa-IFN on the neoplastic clone. The results of clonality studies showed the persistence of clonal hematopoiesis. Whether higher alfa-IFN dose and/or more prolonged alfa-IFN therapy may allow a restoration of polyclonal hematopoiesis remains to be determined and should be explored in future clinical trials.
几位作者报道了α-干扰素(α-IFN)对原发性血小板增多症(ET)患者的疗效。本研究的目的是评估α-IFN对肿瘤克隆的影响程度。截至1993年12月,11例ET患者接受α-IFN治疗,剂量为3 - 6 MU/皮下注射/天,共6个月。11例中有10例获得完全血液学缓解(CHR),1例获得部分血液学缓解。6例巨核细胞浓度降低。4例脾脏肿大的患者中,2例脾脏大小减小。8例诊断时有症状的患者中,7例症状得到缓解。为了了解α-IFN对ET巨核细胞(Mks)诱导的结构改变,对11例患者中的7例,对每位患者的10个单个Mks进行了傅里叶变换红外光谱分析;分析显示,5例患者的A1/A2比值(A1为1080 cm⁻¹处由于核酸吸收产生的谱带积分面积;A2为1540 cm⁻¹处由于蛋白质成分吸收产生的谱带积分面积)降低,这5例患者中有3例A1/A2比值达到正常水平。α-IFN治疗后,我们未观察到粒细胞部分DNA甲基化模式有任何变化。我们的结果证实了α-IFN对ET患者的疗效,部分患者A1/A2比值降低证明了α-IFN对肿瘤克隆的影响程度。克隆性研究结果显示克隆性造血持续存在。更高剂量的α-IFN和/或更长疗程的α-IFN治疗是否能恢复多克隆造血仍有待确定,应在未来的临床试验中进行探索。