Management Issues and Controversies in Low-Risk Patients with Essential Thrombocythemia and Polycythemia Vera.

IF 2.7 3区 医学 Q2 HEMATOLOGY
Current Hematologic Malignancy Reports Pub Date : 2021-10-01 Epub Date: 2021-09-03 DOI:10.1007/s11899-021-00649-x
Joan How, Gabriela Hobbs
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引用次数: 3

Abstract

Purpose of review: Essential thrombocythemia (ET) and polycythemia vera (PV) are the most common myeloproliferative neoplasms (MPNs). Treatment of ET and PV is based on the risk for subsequent thrombosis. High-risk patients, defined as older than 60, JAK2 V617F-positive patients, or patients with a history of prior thrombosis, merit cytoreduction to control blood counts, whereas a watchful waiting paradigm is utilized in low-risk patients. However, low-risk patients have a host of other specific management issues that arise during their disease course. This review will discuss the most common management issues specific to the care of low-risk patients, including anti-platelet therapy dosing, pregnancy, and indications for early cytoreduction.

Recent findings: Although low-dose aspirin is well established in PV, its indications and dosing regimens are less clear in ET. Recent evidence has supported twice daily low-dose aspirin in ET and observation alone in very low-risk ET patients. Pregnancy is not contraindicated in MPNs, and we recommend aspirin throughout pregnancy with consideration for prophylactic postpartum anticoagulation. High phlebotomy needs, symptom burden, and extreme thrombocytosis are common reasons for initiation of cytoreduction in low-risk patients, although we typically do not start cytoreduction for an isolated high platelet count alone. Recent data has also demonstrated a potential disease-modifying effect of interferons in MPNs, with some experts now advocating the early use of interferon in low-risk patients, although more mature data is needed before practice guidelines change. We evaluate the literature to inform clinical decision-making regarding these controversies, including most recent data that has challenged the "watchful waiting" paradigm. Our discussion provides guidance on common clinical scenarios seen in low-risk ET and PV patients, who face a myriad of complex management decisions in their care.

原发性血小板增多症和真性红细胞增多症低危患者的管理问题和争议。
综述目的:原发性血小板增多症(ET)和真性红细胞增多症(PV)是最常见的骨髓增生性肿瘤(mpn)。ET和PV的治疗是基于随后血栓形成的风险。高风险患者,定义为60岁以上,JAK2 v617f阳性患者,或既往有血栓病史的患者,需要减少细胞以控制血细胞计数,而低风险患者则采用观察等待模式。然而,低风险患者在其病程中有许多其他特定的管理问题。本综述将讨论低危患者护理中最常见的管理问题,包括抗血小板治疗剂量、妊娠和早期细胞减少的适应症。最近的发现:虽然小剂量阿司匹林在PV中已经确立,但其适应症和给药方案在ET中尚不明确。最近的证据支持ET患者每天两次小剂量阿司匹林和极低风险ET患者单独观察。妊娠不是mpn的禁忌症,我们建议在妊娠期间服用阿司匹林,同时考虑预防性产后抗凝。高放血需求、症状负担和严重的血小板增多是低风险患者开始细胞减少的常见原因,尽管我们通常不会仅仅因为孤立的高血小板计数而开始细胞减少。最近的数据也表明干扰素在mpn中具有潜在的疾病改善作用,一些专家现在提倡在低风险患者中早期使用干扰素,尽管在实践指南改变之前需要更成熟的数据。我们评估文献,为临床决策提供有关这些争议的信息,包括挑战“观察等待”范式的最新数据。我们的讨论为低风险ET和PV患者的常见临床情况提供了指导,这些患者在护理中面临着无数复杂的管理决策。
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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来源期刊
CiteScore
6.00
自引率
0.00%
发文量
28
审稿时长
>12 weeks
期刊介绍: his journal intends to provide clear, insightful, balanced contributions by international experts that review the most important, recently published clinical findings related to the diagnosis, treatment, management, and prevention of hematologic malignancy. We accomplish this aim by appointing international authorities to serve as Section Editors in key subject areas, such as leukemia, lymphoma, myeloma, and T-cell and other lymphoproliferative malignancies. Section Editors, in turn, select topics for which leading experts contribute comprehensive review articles that emphasize new developments and recently published papers of major importance, highlighted by annotated reference lists. An international Editorial Board reviews the annual table of contents, suggests articles of special interest to their country/region, and ensures that topics are current and include emerging research. Commentaries from well-known figures in the field are also provided.
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