Messina Monica, Piciocchi Alfonso, Ottone Tiziana, Paolini Stefania, Papayannidis Cristina, Lessi Federica, Fracchiolla Nicola Stefano, Forghieri Fabio, Candoni Anna, Mengarelli Andrea, Martelli Maria Paola, Venditti Adriano, Carella Angelo Michele, Albano Francesco, Mancini Valentina, Massimo Bernardi, Arena Valentina, Sargentini Valeria, Sciumè Mariarita, Pastore Domenico, Todisco Elisabetta, Roti Giovanni, Siragusa Sergio, Ladetto Marco, Pravato Stefano, De Bellis Eleonora, Simonetti Giorgia, Marconi Giovanni, Cerchione Claudio, Fazi Paola, Vignetti Marco, Amadori Sergio, Martinelli Giovanni, Voso Maria Teresa
GIMEMA Foundation, 00182 Roma, Italy.
Ematologia, Dipartimento di Biomedicina e Prevenzione, Università di Roma Tor Vergata, 00133 Roma, Italy.
Cancers (Basel). 2022 Jun 18;14(12):3012. doi: 10.3390/cancers14123012.
IDH1/2 mutations are common in acute myeloid leukemia (AML) and represent a therapeutic target. The GIMEMA AML1516 observational protocol was designed to study the prevalence of IDH1/2 mutations and associations with clinico-biological parameters in a cohort of Italian AML patients. We analyzed a cohort of 284 AML consecutive patients at diagnosis, 139 females and 145 males, of a median age of 65 years (range: 19−86). Of these, 38 (14%) harbored IDH1 and 51 (18%) IDH2 mutations. IDH1/2 mutations were significantly associated with WHO PS >2 (p < 0.001) and non-complex karyotype (p = 0.021) when compared to IDH1/2-WT. Furthermore, patients with IDH1 mutations were more frequently NPM1-mutated (p = 0.007) and had a higher platelet count (p = 0.036). At relapse, IDH1/2 mutations were detected in 6 (25%) patients. As per the outcome, 60.5% of IDH1/2-mutated patients achieved complete remission; overall survival and event-free survival at 2 years were 44.5% and 36.1%, respectively: these rates were similar to IDH1/2-WT. In IDH1/2-mutated patients, high WBC proved to be an independent prognostic factor for survival. In conclusion, the GIMEMA AML1516 confirms that IDH1/2 mutations are frequently detected at diagnosis and underlines the importance of recognizing IDH1/2-mutated cases up-front to offer the most appropriate therapeutic strategy, given the availability of IDH1/2 inhibitors.
异柠檬酸脱氢酶1/2(IDH1/2)突变在急性髓系白血病(AML)中很常见,是一个治疗靶点。GIMEMA AML1516观察性方案旨在研究意大利AML患者队列中IDH1/2突变的发生率及其与临床生物学参数的关联。我们分析了284例初诊的连续AML患者队列,其中139例女性,145例男性,中位年龄65岁(范围:19 - 86岁)。其中,38例(14%)携带IDH1突变,51例(18%)携带IDH2突变。与IDH1/2野生型相比,IDH1/2突变与世界卫生组织体能状态>2(p < 0.001)和非复杂核型(p = 0.021)显著相关。此外,携带IDH1突变的患者NPM1突变更为频繁(p = 0.007),血小板计数更高(p = 0.036)。复发时,在6例(25%)患者中检测到IDH1/2突变。就预后而言,60.5%的IDH1/2突变患者实现了完全缓解;2年总生存率和无事件生存率分别为44.5%和36.1%:这些比率与IDH1/2野生型相似。在IDH1/2突变患者中,高白细胞计数被证明是生存的独立预后因素。总之,GIMEMA AML1516证实,在诊断时经常检测到IDH1/2突变,并强调鉴于IDH1/2抑制剂的可用性,预先识别IDH1/2突变病例以提供最合适治疗策略的重要性。