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(32)P用于骨髓增殖性疾病的治疗。

(32)P in the treatment of myeloproliferative disorders.

作者信息

Lawless Sarah, McMullin Mary Frances, Cuthbert Robert, Houston Russell

机构信息

Department of Haematology, Belfast City Hospital, Belfast N. Ireland.

Department of Haematology, Belfast City Hospital, Belfast N. Ireland; Queen's University Belfast, N. Ireland; Centre for Cancer Research and Cell Biology, Queen's University, Belfast, N. Ireland.

出版信息

Ulster Med J. 2016 May;85(2):83-5.

Abstract

UNLABELLED

(32)P has been available for the treatment of myeloproliferative neoplasms (MPNs) for over seventy years. It was first used in 1938 by John H Lawrence in the treatment of polycythaemia and chronic leukaemias. With the introduction of agents such as hydroxycarbamide, interferon and anagrelide the role of (32)P has been diminished. Today, Polycythaemia Rubra Vera (PRV) and Essential Thrombocythaemia (ET) remain the only myeloproliferative conditions in which (32)P is indicated.

MATERIALS AND METHODS

We carried out a retrospective review of all patients who had received 32P in Northern Ireland over a 24 year period. The time to successful response, duration of response, and associated complications were reviewed.

RESULTS

(32)P was successful in inducing remission in 90% of patients. This remission was sustained following one dose without the need for further therapy in 37% of cases. 47% required repeated doses. 26% required recommencement of alternative therapies. No cases of thrombosis, myelofibrosis or acute leukaemia were observed.

DISCUSSION

We conclude that (32)P is a well-tolerated and efficacious treatment option in the elderly. We discuss our results compared with previous work in this area. (32)P will continue to be offered to elderly patients in our practice.

摘要

未标注

(32)P 可用于治疗骨髓增殖性肿瘤(MPN)已有七十多年历史。1938 年,约翰·H·劳伦斯首次将其用于治疗真性红细胞增多症和慢性白血病。随着羟基脲、干扰素和阿那格雷等药物的引入,(32)P 的作用有所减弱。如今,真性红细胞增多症(PRV)和原发性血小板增多症(ET)仍是仅有的适用(32)P 治疗的骨髓增殖性疾病。

材料与方法

我们对北爱尔兰 24 年间接受(32)P 治疗的所有患者进行了回顾性研究。回顾了达到成功缓解的时间、缓解持续时间及相关并发症。

结果

(32)P 在 90%的患者中成功诱导缓解。37%的病例单次给药后缓解持续,无需进一步治疗。47%的患者需要重复给药。26%的患者需要重新开始其他治疗。未观察到血栓形成、骨髓纤维化或急性白血病病例。

讨论

我们得出结论,(32)P 对老年患者是一种耐受性良好且有效的治疗选择。我们将我们的结果与该领域以前的研究进行了比较。在我们的实践中,(32)P 将继续用于老年患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dea/4920483/ad090ec828c8/umj0085-0083-f1.jpg

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