Martínez-Cuadrón David, Serrano Josefina, Mariz José, Gil Cristina, Tormo Mar, Martínez-Sánchez Pilar, Rodríguez-Arbolí Eduardo, García-Boyero Raimundo, Rodríguez-Medina Carlos, Martínez-Chamorro Carmen, Polo Marta, Bergua Juan, Aguiar Eliana, Amigo María L, Herrera Pilar, Alonso-Domínguez Juan M, Bernal Teresa, Espadana Ana, Sayas María J, Algarra Lorenzo, Vidriales María B, Vasconcelos Graça, Vives Susana, Pérez-Encinas Manuel M, López Aurelio, Noriega Víctor, García-Fortes María, Chillón María C, Rodríguez-Gutiérrez Juan I, Calasanz María J, Labrador Jorge, López Juan A, Boluda Blanca, Rodríguez-Veiga Rebeca, Martínez-López Joaquín, Barragán Eva, Sanz Miguel A, Montesinos Pau
Hospital Universitari i Politècnic La Fe, 46026 Valencia, Spain.
Hospital Universitario Reina Sofía and Instituto Maimónides de Investigación Biomédica Córdoba (IMIBIC), 14004 Córdoba, Spain.
Cancers (Basel). 2022 Jun 6;14(11):2817. doi: 10.3390/cancers14112817.
This retrospective study investigated outcomes of 404 patients with relapsed/refractory (R/R) FMS-like tyrosine kinase 3 (FLT3)-internal tandem duplication (ITD) acute myeloid leukemia (AML) enrolled in the PETHEMA registry, pre-approval of tyrosine kinase inhibitors. Most patients (63%) had received first-line intensive therapy with 3 + 7. Subsequently, patients received salvage with intensive therapy (n = 261), non-intensive therapy (n = 63) or supportive care only (n = 80). Active salvage therapy (i.e., intensive or non-intensive therapy) resulted in a complete remission (CR) or CR without hematological recovery (CRi) rate of 42%. More patients achieved a CR/CRi with intensive (48%) compared with non-intensive (19%) salvage therapy (p < 0.001). In the overall population, median overall survival (OS) was 5.5 months; 1- and 5-year OS rates were 25% and 7%. OS was significantly (p < 0.001) prolonged with intensive or non-intensive salvage therapy compared with supportive therapy, and in those achieving CR/CRi versus no responders. Of 280 evaluable patients, 61 (22%) had an allogeneic stem-cell transplant after they had achieved CR/CRi. In conclusion, in this large cohort study, salvage treatment approaches for patients with FLT3-ITD mutated R/R AML were heterogeneous. Median OS was poor with both non-intensive and intensive salvage therapy, with best long-term outcomes obtained in patients who achieved CR/CRi and subsequently underwent allogeneic stem-cell transplant.
这项回顾性研究调查了404例复发/难治性(R/R)FMS样酪氨酸激酶3(FLT3)-内部串联重复(ITD)急性髓系白血病(AML)患者的预后,这些患者已被纳入PETHEMA注册研究,该研究在酪氨酸激酶抑制剂获批之前进行。大多数患者(63%)接受了3 + 7方案的一线强化治疗。随后,患者接受了强化治疗(n = 261)、非强化治疗(n = 63)或仅接受支持性治疗(n = 80)进行挽救治疗。积极的挽救治疗(即强化或非强化治疗)导致完全缓解(CR)或无血液学恢复的完全缓解(CRi)率为42%。与非强化挽救治疗(19%)相比,更多患者通过强化挽救治疗(48%)实现了CR/CRi(p < 0.001)。在总体人群中,中位总生存期(OS)为5.5个月;1年和5年OS率分别为25%和7%。与支持性治疗相比,强化或非强化挽救治疗显著延长了OS(p < 0.001),在实现CR/CRi的患者与未缓解患者中也是如此。在280例可评估患者中,61例(22%)在实现CR/CRi后接受了异基因干细胞移植。总之,在这项大型队列研究中,FLT3-ITD突变的R/R AML患者的挽救治疗方法具有异质性。非强化和强化挽救治疗的中位OS均较差,在实现CR/CRi并随后接受异基因干细胞移植的患者中获得了最佳长期预后。