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在 ELN 有利风险的急性髓细胞白血病中,治疗结束时达到分子缓解是良好预后的必要目标:伦巴第血液学网络对 201 例患者的真实分析。

Molecular remission at the end of treatment is a necessary goal for a good outcome in ELN favorable-risk acute myeloid leukemia: a real-life analysis on 201 patients by the Rete Ematologica Lombarda network.

机构信息

Division of Hematology, Foundation IRCCS Policlinico San Matteo, University of Pavia, Pavia, Italy.

Department of Hematology, Niguarda Ca' Granda Hospital, Milan, Italy.

出版信息

Ann Hematol. 2018 Nov;97(11):2107-2115. doi: 10.1007/s00277-018-3424-4. Epub 2018 Jul 15.

DOI:10.1007/s00277-018-3424-4
PMID:30009341
Abstract

Favorable acute myeloid leukemia (AML) patients (pts.) demonstrate a relatively good outcome with standard induction; thus, pts. are generally not addressed to allogeneic transplant in first remission. However, it is not clear if also in a real-life setting, the outcome is homogeneous in the different favorable molecular groups and which are the parameters significantly associated to an increased relapse risk, useful to suggest the need of an intensified approach. In order to clarify this point, we collected clinical data on consecutive unselected AML pts. assigned to favorable category (modified ELN 2010 due to the inclusion of double-mutated CEBPA-positive cases), diagnosed and treated in six centers of the Italian network Rete Ematologica Lombarda (REL) from 2007 to 2015. We assessed response (CR, mCR), relapse rate (CIR), and outcome (OS, DFS) after first-line treatment. A total of 201 pts. was studied and the analysis was performed globally and in each molecular group: t(8;21)(q22;q22)/RUNX1-RUNX1T1 (30 pts., 14.9%), inv. (16)(p13q22) or t(16;16)(p13q22)/CBFB-MIH11 (35 pts., 17.4%), normal karyotype and mutated NPM1 and negative FLT3-ITD (116 pts., 57.7%) or double-mutated CEBPA (CEBPAdm) (20 pts., 10%). Complete remission (CR) was obtained in 188 pts. (93.5%), molecular CR (mCR) in 114 (67.5%); After a median follow-up of 2.4 years, cumulative incidence of relapse (CIR) was documented in 78 of 188 responding pts. (41%) after a median time of 11.3 months. CIR was higher in the CBFB-MIH11 group, in pts. achieving only a hematological response without mCR (72.1 vs 28.1%, p < 0.001), in older pts. and it resulted independently associated with a lower median cytarabine cumulative dose (CCD). Median OS was not reached: after 5 years it was 66.3%, and median DFS was 5.3 years, both without difference among groups. Molecular CR reached at any time, during or after the end of first-line treatment, was significantly associated with better DFS, and in particular, mCR assessed at the end of treatment was confirmed in multivariate analysis as an independent prognostic factor both for DFS and OS. In conclusion, the present study confirms in a real-life context the overall good prognosis of favorable-risk AML; the achievement of any molecular negativity during first-line treatment, particularly when assessed at the end of treatment, is associated with lower relapse and better survival. Increasing age at diagnosis has a negative prognostic impact, while CCD higher than 18 g/sqm is associated with better outcome.

摘要

有利的急性髓系白血病(AML)患者(pts.)在标准诱导下表现出相对较好的结果;因此,pts. 通常不会在首次缓解时被建议进行同种异体移植。然而,目前尚不清楚在实际情况下,不同有利分子组的结果是否具有同质性,以及哪些参数与复发风险增加显著相关,这有助于提示需要强化治疗。为了阐明这一点,我们收集了 2007 年至 2015 年期间意大利网络 Rete Ematologica Lombarda (REL) 的六个中心连续未经选择的 AML pts. 的临床数据,这些 pts. 被分配到有利类别(由于包括双突变 CEBPA 阳性病例,修改后的 ELN 2010)。我们评估了一线治疗后的反应(CR、mCR)、复发率(CIR)和结局(OS、DFS)。共研究了 201 例 pts.,并在全球和每个分子组中进行了分析:t(8;21)(q22;q22)/RUNX1-RUNX1T1(30 例,14.9%),inv. (16)(p13q22) 或 t(16;16)(p13q22)/CBFB-MIH11(35 例,17.4%),正常核型和突变 NPM1 和阴性 FLT3-ITD(116 例,57.7%)或双突变 CEBPA(CEBPAdm)(20 例,10%)。188 例 pts.(93.5%)获得完全缓解(CR),114 例(67.5%)获得分子 CR(mCR);中位随访 2.4 年后,记录了 188 例有反应 pts.(41%)中的 78 例(中位时间为 11.3 个月)的复发累积发生率(CIR)。在 CBFB-MIH11 组中,CIR 更高,在仅获得血液学反应而无 mCR 的 pts.(72.1%比 28.1%,p<0.001)中,在老年 pts.中,CIR 结果独立地与较低的中位阿糖胞苷累积剂量(CCD)相关。中位 OS 未达到:5 年后为 66.3%,中位 DFS 为 5.3 年,各组之间均无差异。在任何时间达到的分子 CR,无论是在一线治疗期间还是在治疗结束后,均与更好的 DFS 显著相关,特别是在治疗结束时评估的 mCR 在多变量分析中被证实为 DFS 和 OS 的独立预后因素。总之,本研究在真实环境中证实了有利风险 AML 的总体良好预后;在一线治疗期间达到任何分子阴性,特别是在治疗结束时评估时,与较低的复发和更好的生存相关。诊断时年龄较大具有负预后影响,而 CCD 高于 18 g/sqm 与更好的结局相关。

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