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基于真性红细胞增多症研究组方案的真性红细胞增多症治疗建议。

Therapeutic recommendations in polycythemia vera based on Polycythemia Vera Study Group protocols.

作者信息

Berk P D, Goldberg J D, Donovan P B, Fruchtman S M, Berlin N I, Wasserman L R

出版信息

Semin Hematol. 1986 Apr;23(2):132-43.

PMID:3704665
Abstract

The PVSG was organized in 1967 to establish effective diagnostic criteria for polycythemia vera, to study the natural history of the disease and to define the optimal treatment. Although polycythemia vera and the other myeloproliferative diseases are relatively uncommon, the PVSG was able to accumulate well over 1,000 patients with these various disorders and to study them according to a total of 15 different protocols. PVSG-01, a long-term randomized controlled study of phlebotomy alone compared with the myelosuppressive agents, 32P or chlorambucil supplemented by phlebotomy, continues to receive follow-up data on 93% of surviving patients 18 years after initiation of the study. During its lifetime, PVSG has developed a widely accepted and highly effective set of criteria for the specific diagnosis of polycythemia vera as well as useful criteria for the diagnosis of essential thrombocythemia. It has gathered an enormous volume of data on the natural history of the myeloproliferative diseases and in particular on the nature of the prevalent complications, such as thrombotic events and hematologic and nonhematologic malignancies. With respect to the final question, the optimal treatment for polycythemia vera, it is apparent that the expectation of a single optimal therapy that would apply to all patients at all ages and stages of the disease was naive. Nevertheless considerable progress has been made. Moreover, the group has defined more precisely than ever before the nature of the complications of the disease and the association of the risks of specific complications with specific forms of therapy. It thus has made it possible to pose the next series of therapeutic questions that must be addressed in this disorder with a greater degree of sophistication than was previously possible.

摘要

真性红细胞增多症研究组(PVSG)于1967年成立,旨在确立真性红细胞增多症的有效诊断标准,研究该疾病的自然病程,并确定最佳治疗方法。尽管真性红细胞增多症和其他骨髓增殖性疾病相对不常见,但PVSG仍能够积累1000多名患有这些不同疾病的患者,并根据总共15种不同方案对他们进行研究。PVSG - 01是一项长期随机对照研究,比较单独放血疗法与骨髓抑制药物(32P或苯丁酸氮芥加放血疗法),在研究开始18年后,仍在收集93%存活患者的随访数据。在其存在期间,PVSG制定了一套广泛接受且高效的真性红细胞增多症特异性诊断标准以及原发性血小板增多症的有用诊断标准。它收集了大量关于骨髓增殖性疾病自然病程的数据,特别是关于常见并发症(如血栓形成事件以及血液学和非血液学恶性肿瘤)的性质的数据。关于最后一个问题,即真性红细胞增多症的最佳治疗方法,显然期望有一种适用于所有年龄和疾病阶段患者的单一最佳疗法是天真的。然而,已经取得了相当大的进展。此外,该研究组比以往任何时候都更精确地界定了该疾病并发症的性质以及特定并发症风险与特定治疗形式之间的关联。因此,使得提出下一系列必须在这种疾病中解决的治疗问题成为可能,且比以前更具复杂性。

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