Suppr超能文献

初诊急性早幼粒细胞白血病。

Newly diagnosed acute promyelocytic leukemia.

机构信息

Unità Operativa Complessa di Ematologia, Trapianto di cellule staminali, Medicina trasfusionale e Terapia cellulare. Università Campus Bio-Medico, Roma, Italy.

出版信息

Mediterr J Hematol Infect Dis. 2011;3(1):e2011064. doi: 10.4084/MJHID.2011.064. Epub 2011 Dec 20.

Abstract

Acute promyelocytic leukemia (APL) represents a medical emergency with a high rate of early mortality. As a consequence, as soon as the diagnosis is suspected based upon cytologic criteria, it is necessary to start all- trans retinoic acid (ATRA) treatment without delay. For patients with newly diagnosed APL, induction therapy with ATRA plus anthracycline based chemotherapy is recommended. At present the combination of arsenic trioxide plus ATRA should be considered for patients who are not candidates for anthracycline-based therapy. For pediatric and adult patients with APL aged < 60 years who achieve a CR with induction, I recommend 3 intensive courses of consolidation chemotherapy associated to ATRA, targeted on the basis of the risk group at diagnosis. In patients treated with a very intensive consolidation chemotherapy maintenance treatment can be omitted. However If a maintenance treatment has to be adopted I suggest the use of intermittent ATRA for 15 days every 3 months for a period of 2 years, rather than ATRA associated to chemotherapy. Moreover, taking into account the medical literature, a reduced dosage of ATRA ( 25 mg/m(2)) in pediatric patients and a consolidation chemotherapy of reduced intensity in elderly patients is recommended. Furthermore, in order to maximize survival, careful attention should be reserved to the coagulopathy and to the appearance of the differentiation syndrome. Finally, PCR for the PML/RARA fusion gene on a bone marrow specimen every three months for two years, and then every six months for additional three years are needed during the follow-up.

摘要

急性早幼粒细胞白血病(APL)是一种具有高早期死亡率的医学急症。因此,一旦根据细胞学标准怀疑诊断,就必须立即开始全反式维甲酸(ATRA)治疗。对于新诊断的 APL 患者,推荐使用 ATRA 加蒽环类药物化疗进行诱导治疗。目前,对于不适合蒽环类药物治疗的患者,应考虑使用三氧化二砷加 ATRA 的联合治疗。对于年龄 < 60 岁且诱导缓解后达到完全缓解的儿科和成人 APL 患者,我建议根据诊断时的风险组,进行 3 个强化巩固化疗联合 ATRA。对于接受非常强化巩固化疗的患者,可以省略维持治疗。然而,如果必须采用维持治疗,我建议每 3 个月使用 ATRA(15 天)进行间歇性治疗,持续 2 年,而不是 ATRA 联合化疗。此外,根据医学文献,建议在儿科患者中使用较低剂量的 ATRA(25mg/m²),并在老年患者中进行强度降低的巩固化疗。此外,为了最大限度地提高生存率,应仔细注意凝血功能障碍和分化综合征的出现。最后,在随访期间,需要每 3 个月对骨髓样本进行 PML/RARA 融合基因的 PCR 检测,持续 2 年,然后每 6 个月检测 3 年。

相似文献

1
Newly diagnosed acute promyelocytic leukemia.初诊急性早幼粒细胞白血病。
Mediterr J Hematol Infect Dis. 2011;3(1):e2011064. doi: 10.4084/MJHID.2011.064. Epub 2011 Dec 20.

本文引用的文献

7
How I treat acute promyelocytic leukemia.我如何治疗急性早幼粒细胞白血病。
Blood. 2009 Dec 10;114(25):5126-35. doi: 10.1182/blood-2009-07-216457.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验