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在某地区核医学科接受磷-32治疗的259例原发性增殖性红细胞增多症(PPP)和特发性血小板增多症(IT)患者的治疗结果——一项15年的回顾。

Outcome of 259 patients with primary proliferative polycythaemia (PPP) and idiopathic thrombocythaemia (IT) treated in a regional nuclear medicine department with phosphorus-32--a 15 year review.

作者信息

Balan K K, Critchley M

机构信息

Regional Department of Nuclear Medicine, Royal Liverpool University Hospital, UK.

出版信息

Br J Radiol. 1997 Nov;70(839):1169-73. doi: 10.1259/bjr.70.839.9536909.

Abstract

259 patients with primary proliferative polycythaemia (PPP) and idiopathic thrombocythaemia (IT) have been treated with 32P over the last 15 years. Complete follow-up data were obtained in 238 patients. PPP was the diagnosis in 183 patients and 76 patients had IT. The sex ratio in PPP was male/female 1.1:1 and in IT 1:1.4. Patients' ages ranged from 28 to 95 years (median 72 years). The number of 32P administrations per patient ranged from 1 to 13 (median 2) and the total administered activity per patient ranged from 81.4 to 4162 MBq (median 496 MBq). The outcome showed a normalization of the full blood count in 50% of patients after a single administration of 32P and in 73% after two treatments. 13 patients (5.5%) developed myelofibrosis; 18 (7.6%) developed leukaemia while other cancers arose in 19 patients (8%). 32P therapy proved to be of particular value in the elderly. 32P is easy to administer and is cost effective, compared with the alternative of chemotherapy where good compliance and frequent hospital visits are required.

摘要

在过去15年里,259例原发性增殖性红细胞增多症(PPP)和特发性血小板增多症(IT)患者接受了32P治疗。238例患者获得了完整的随访数据。其中183例诊断为PPP,76例为IT。PPP患者的男女比例为1.1:1,IT患者为1:1.4。患者年龄在28至95岁之间(中位数72岁)。每位患者接受32P治疗的次数为1至13次(中位数2次),每位患者接受的总活度为81.4至4162 MBq(中位数496 MBq)。结果显示,单次给予32P后,50%的患者全血细胞计数恢复正常,两次治疗后这一比例为73%。13例患者(5.5%)发生骨髓纤维化;18例(7.6%)发生白血病,19例患者(8%)发生其他癌症。32P治疗对老年人特别有价值。与需要良好依从性和频繁就诊的化疗相比,32P易于给药且具有成本效益。

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