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New developments in the treatment of chronic myeloid leukemia and Philadelphia-positive acute lymphoblastic leukemia.慢性髓性白血病和费城阳性急性淋巴细胞白血病治疗的新进展。
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2
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Introduction of the T315I gatekeeper mutation of BCR/ABL1 into a Philadelphia chromosome-positive lymphoid leukemia cell line using the CRISPR/Cas9 system.使用 CRISPR/Cas9 系统将 BCR/ABL1 的 T315I 守门员突变引入费城染色体阳性淋巴样白血病细胞系。
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Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2013 Jun;21(3):581-6. doi: 10.7534/j.issn.1009-2137.2013.03.009.
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Chronic myeloid leukemia 2011: successes, challenges, and strategies--proceedings of the 5th annual BCR-ABL1 positive and BCR-ABL1 negative myeloproliferative neoplasms workshop.慢性髓性白血病 2011:成就、挑战和策略——第五届 BCR-ABL1 阳性和 BCR-ABL1 阴性骨髓增殖性肿瘤研讨会会议记录。
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本文引用的文献

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Nilotinib in patients with Ph+ chronic myeloid leukemia in accelerated phase following imatinib resistance or intolerance: 24-month follow-up results.尼洛替尼治疗伊马替尼耐药或不耐受的 Ph+ 慢性髓性白血病加速期患者:24 个月随访结果。
Leukemia. 2012 Jun;26(6):1189-94. doi: 10.1038/leu.2011.323. Epub 2011 Nov 11.
2
Safety and efficacy of bosutinib (SKI-606) in chronic phase Philadelphia chromosome-positive chronic myeloid leukemia patients with resistance or intolerance to imatinib.博舒替尼(SKI-606)治疗对伊马替尼耐药或不耐受的慢性期费城染色体阳性慢性髓性白血病患者的安全性和疗效。
Blood. 2011 Oct 27;118(17):4567-76. doi: 10.1182/blood-2011-05-355594. Epub 2011 Aug 24.
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Dasatinib versus imatinib in newly diagnosed chronic-phase chronic myeloid leukemia.达沙替尼与伊马替尼治疗新诊断的慢性期慢性髓性白血病。
N Engl J Med. 2010 Jun 17;362(24):2260-70. doi: 10.1056/NEJMoa1002315. Epub 2010 Jun 5.
4
Nilotinib versus imatinib for newly diagnosed chronic myeloid leukemia.尼洛替尼与伊马替尼用于治疗新诊断的慢性髓性白血病。
N Engl J Med. 2010 Jun 17;362(24):2251-9. doi: 10.1056/NEJMoa0912614. Epub 2010 Jun 5.
5
Potent, transient inhibition of BCR-ABL with dasatinib 100 mg daily achieves rapid and durable cytogenetic responses and high transformation-free survival rates in chronic phase chronic myeloid leukemia patients with resistance, suboptimal response or intolerance to imatinib.达沙替尼 100mg 每日治疗可强效、短暂地抑制 BCR-ABL,对于对伊马替尼耐药、治疗反应欠佳或不耐受的慢性期慢性髓性白血病患者,可迅速并持久地获得细胞遗传学反应,且无进展生存率较高。
Haematologica. 2010 Feb;95(2):232-40. doi: 10.3324/haematol.2009.011452.
6
Dasatinib 140 mg once daily versus 70 mg twice daily in patients with Ph-positive acute lymphoblastic leukemia who failed imatinib: Results from a phase 3 study.达沙替尼 140 毫克每日一次与 70 毫克每日两次治疗伊马替尼治疗失败的费城染色体阳性急性淋巴细胞白血病患者:一项 3 期研究的结果。
Am J Hematol. 2010 Mar;85(3):164-70. doi: 10.1002/ajh.21615.
7
Phase III, randomized, open-label study of daily imatinib mesylate 400 mg versus 800 mg in patients with newly diagnosed, previously untreated chronic myeloid leukemia in chronic phase using molecular end points: tyrosine kinase inhibitor optimization and selectivity study.采用分子终点的新诊断、未经治疗的慢性期慢性髓性白血病患者每日甲磺酸伊马替尼 400mg 与 800mg 的随机、开放标签 III 期研究:酪氨酸激酶抑制剂优化和选择性研究。
J Clin Oncol. 2010 Jan 20;28(3):424-30. doi: 10.1200/JCO.2009.25.3724. Epub 2009 Dec 14.
8
Nilotinib as front-line treatment for patients with chronic myeloid leukemia in early chronic phase.尼罗替尼作为早期慢性期慢性髓性白血病患者的一线治疗药物。
J Clin Oncol. 2010 Jan 20;28(3):392-7. doi: 10.1200/JCO.2009.25.4896. Epub 2009 Dec 14.
9
Chronic myeloid leukemia: an update of concepts and management recommendations of European LeukemiaNet.慢性髓性白血病:欧洲白血病网络概念与管理建议的更新
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10
NCCN clinical practice guidelines in oncology: chronic myelogenous leukemia.美国国立综合癌症网络(NCCN)肿瘤学临床实践指南:慢性粒细胞白血病
J Natl Compr Canc Netw. 2009 Oct;7(9):984-1023. doi: 10.6004/jnccn.2009.0065.

慢性髓性白血病和费城阳性急性淋巴细胞白血病治疗的新进展。

New developments in the treatment of chronic myeloid leukemia and Philadelphia-positive acute lymphoblastic leukemia.

机构信息

M D Anderson Cancer Center, The University of Texas, Houston, TX 77030, USA.

出版信息

Leuk Lymphoma. 2011 Feb;52 Suppl 1(Suppl 1):81-91. doi: 10.3109/10428194.2010.546917.

DOI:10.3109/10428194.2010.546917
PMID:21299461
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5681224/
Abstract

Although imatinib revolutionized the management of chronic myeloid leukemia (CML), recent data indicate a transformation in the treatment approach likely in the near future. The superiority of second-generation tyrosine kinase inhibitors (TKIs) over imatinib in newly diagnosed disease has been recognized. Several investigational agents specific for those patients with the T315I mutation remain under evaluation. In Philadelphia-positive (Ph-positive) acute lymphoblastic leukemia (ALL), the addition of imatinib improved response rates. However, short remission durations with single agent therapy limit the benefit on survival. Early molecular remissions achieved with dasatinib will enable more patients to proceed to stem cell transplant (SCT), with increased likelihood of positive outcomes post-SCT.

摘要

虽然伊马替尼彻底改变了慢性髓性白血病(CML)的治疗方法,但最近的数据表明,这种治疗方法可能在不久的将来会发生转变。第二代酪氨酸激酶抑制剂(TKI)在新诊断疾病中的优越性已得到认可。几种针对 T315I 突变患者的研究药物仍在评估中。在费城染色体阳性(Ph 阳性)急性淋巴细胞白血病(ALL)中,加入伊马替尼可提高缓解率。然而,单一药物治疗的缓解时间较短,限制了对生存的益处。达沙替尼早期获得的分子缓解将使更多的患者能够进行干细胞移植(SCT),并且 SCT 后获得阳性结果的可能性增加。