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自伊马替尼治疗问世以来慢性髓性白血病的生存率提高:单机构的历史经验。

Improved survival in chronic myeloid leukemia since the introduction of imatinib therapy: a single-institution historical experience.

机构信息

Department of Leukemia, M.D. Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030, USA.

出版信息

Blood. 2012 Mar 1;119(9):1981-7. doi: 10.1182/blood-2011-08-358135. Epub 2012 Jan 6.

DOI:10.1182/blood-2011-08-358135
PMID:22228624
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3311242/
Abstract

A total of 1569 patients with chronic myeloid leukemia (CML) referred to our institution within 1 month of diagnosis since 1965 were reviewed: 1148 chronic phase (CP), 175 accelerated phase (AP), and 246 blastic phase (BP). The median survival was 8.9 years in CP, 4.8 years in AP, and 6 months in BP. In CP, the 8-year survival was ≤ 15% before 1983, 42%-65% from 1983-2000, and 87% since 2001. Survival was worse in older patients (P = .004), but this was less significant since 2001 (P = .07). Survival by Sokal risk was significantly different before 2001 (P < .001), but not since 2001 (P = .4). In AP, survival improved over time (P < .001); the 8-year survival in patients treated since 2001 was 75%. Survival by age was not different in years < 2001 (P = .09), but was better since 2001 in patients ≤ 70 years of age (P = .004). In BP, the median survival improved over time (P < .001), although it has been only 7 months since 2001. In summary, survival in CML has significantly improved since 2001, particularly so in CP-AML and AP-CML. Imatinib therapy minimized the impact of known prognostic factors and Sokal risk in CP-CML and accentuated the impact of age in AP- and BP-CML.

摘要

共有 1569 例慢性髓性白血病(CML)患者于 1965 年以来确诊后 1 个月内被转诊至我院:1148 例处于慢性期(CP),175 例处于加速期(AP),246 例处于急变期(BP)。CP 期的中位生存期为 8.9 年,AP 期为 4.8 年,BP 期为 6 个月。CP 期患者中,1983 年之前的 8 年生存率≤15%,1983-2000 年为 42%-65%,2001 年以来为 87%。年龄较大的患者(P =.004)生存率较差,但 2001 年以来这一差异不显著(P =.07)。2001 年之前 Sokal 风险分组的生存率存在显著差异(P <.001),但之后无差异(P =.4)。AP 期患者的生存率随时间推移而改善(P <.001);2001 年以来接受治疗的患者的 8 年生存率为 75%。2001 年之前,年龄对生存率的影响无差异(P =.09),但 2001 年之后,≤70 岁患者的生存率较好(P =.004)。BP 期患者的中位生存期随时间推移而改善(P <.001),尽管 2001 年以来仅 7 个月。总之,2001 年以来 CML 的生存率显著提高,尤其是 CP-AML 和 AP-CML。伊马替尼治疗最小化了已知预后因素和 CP-CML 中 Sokal 风险的影响,并突出了 AP-和 BP-CML 中年龄的影响。

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本文引用的文献

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J Clin Oncol. 2011 Jun 20;29(18):2514-20. doi: 10.1200/JCO.2011.34.7146. Epub 2011 May 16.
2
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.
3
Results of dasatinib therapy in patients with early chronic-phase chronic myeloid leukemia.达沙替尼治疗慢性髓性白血病早期慢性期患者的疗效。
J Clin Oncol. 2010 Jan 20;28(3):398-404. doi: 10.1200/JCO.2009.25.4920. Epub 2009 Dec 14.
4
Recent trends in long-term survival of patients with chronic myelocytic leukemia: disclosing the impact of advances in therapy on the population level.慢性粒细胞白血病患者长期生存的近期趋势:揭示治疗进展对总体人群的影响。
Haematologica. 2008 Oct;93(10):1544-9. doi: 10.3324/haematol.13045. Epub 2008 Jul 18.
5
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7
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