意大利FLT3突变AML患者(FLAM)队列研究的前期强化治疗分析:在现实生活中,FLT3抑制剂添加到标准化疗的影响

IF 5.1 2区 医学 Q1 ONCOLOGY
Cancer Pub Date : 2025-03-30 DOI:10.1002/cncr.35824
Jacopo Nanni MD, Irene Azzali PhD, Cristina Papayannidis MD, PhD, Antonino Mulè MD, Ernesta Audisio MD, Maria Paola Martelli MD, PhD, Barbara Scappini MD, Patrizia Chiusolo MD, PhD, Benedetta Cambò MD, PhD, Anna Candoni MD, Monia Lunghi MD, Francesco Albano MD, PhD, Attilio Olivieri MD, Nicola Fracchiolla MD, Massimo Bernardi MD, Claudio Romani MD, Gian Matteo Rigolin MD, PhD, Maria Benedetta Giannini MD, Monica Bocchia MD, Elisabetta Todisco MD, Daniela Cilloni MD, PhD, Maria Teresa Bochicchio MSc, Emanuela Ottaviani MSc, Agnese Mattei MD, Federica Zamagni MSS, Irene Valli M.Sc. in PVRA, MPharm, Roberta Volpi MPharm, Giovanni Marconi MD, PhD, Elisabetta Petracci PhD, FLAM Collaborative Group, Giovanni Martinelli MD, PhD
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引用次数: 0

摘要

在标准化疗中加入FLT3抑制剂(FLT3i)治疗适合新诊断(ND)的FLT3突变急性髓性白血病(AML)患者代表了临床试验结果的标准护理。然而,关于在常规临床实践中采用FLT3i的证据仍然很少。方法报告了394例flt3突变AML ND患者的临床数据,这些患者参加了flt3突变AML患者的回顾性观察性意大利队列研究,并接受了预先强化治疗(FLT3i组,n = 92)或不加FLT3i (CT组,n = 302)。结果中位随访时间为34.5个月,FLT3i联合治疗在总生存期(FLT3i组中位为34.9个月,而CT组中位为12.7个月,p <;.01)和无复发生存期(FLT3i组中位为18.9个月,而CT组中位为7.6个月,p = 0.01),综合完全缓解率更高(FLT3i组为75.4%,CT组为62.4%,p = 0.052)。FLT3i的益处似乎与移植率无关。总之,在一项大型现实队列研究中,FLT3i对新诊断的flt3突变AML患者进行前期强化治疗的益处得到了证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Upfront intensive treatment analysis of the Italian Cohort Study on FLT3-mutated AML patients (FLAM): The impact of a FLT3 inhibitor addition to standard chemotherapy in the real-life setting

Upfront intensive treatment analysis of the Italian Cohort Study on FLT3-mutated AML patients (FLAM): The impact of a FLT3 inhibitor addition to standard chemotherapy in the real-life setting

Background

The addition of a FLT3 inhibitor (FLT3i) to standard chemotherapy to treat fit newly diagnosed (ND) patients with FLT3-mutated acute myeloid leukemia (AML) represents the standard of care resulting from clinical trial results. However, evidence regarding FLT3i adoption in routine clinical practice is still scarce.

Methods

Clinical data are reported from 394 ND patients with FLT3-mutated AML enrolled in the retrospective observational Italian Cohort Study on FLT3-mutated patients with AML and treated with an upfront intensive regimen with (FLT3i group, n = 92) or without (CT group, n = 302) the addition of a FLT3i.

Results

With a median follow-up time of 34.5 months, an effectiveness benefit obtained by FLT3i incorporation both in terms of overall survival (median, 34.9 in the FLT3i vs 12.7 months in the CT group, p < .01) and relapse-free survival (median, 18.9 in the FLT3i vs 7.6 months in the CT group, p = .01) was documented, with a higher composite complete remission rate (75.4% in the FLT3i vs 62.4% in the CT group, p = .052). FLT3i benefit seemed to be independent from the transplant rate.

Conclusions

In conclusion, the benefit of FLT3i addition to upfront intensive treatment in newly diagnosed FLT3-mutated AML patients was confirmed in a large, real-life cohort study.

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来源期刊
Cancer
Cancer 医学-肿瘤学
CiteScore
13.10
自引率
3.20%
发文量
480
审稿时长
2-3 weeks
期刊介绍: The CANCER site is a full-text, electronic implementation of CANCER, an Interdisciplinary International Journal of the American Cancer Society, and CANCER CYTOPATHOLOGY, a Journal of the American Cancer Society. CANCER publishes interdisciplinary oncologic information according to, but not limited to, the following disease sites and disciplines: blood/bone marrow; breast disease; endocrine disorders; epidemiology; gastrointestinal tract; genitourinary disease; gynecologic oncology; head and neck disease; hepatobiliary tract; integrated medicine; lung disease; medical oncology; neuro-oncology; pathology radiation oncology; translational research
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