Department of Haematology, Peter MacCallum Cancer Centre and Royal Melbourne Hospital, Melbourne, VIC, Australia.
Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.
Blood. 2023 Dec 7;142(23):1960-1971. doi: 10.1182/blood.2023020301.
Sorafenib maintenance improves outcomes after hematopoietic cell transplant (HCT) for patients with FMS-like tyrosine kinase 3-internal tandem duplication (FLT3-ITD) acute myeloid leukemia (AML). Although promising outcomes have been reported for sorafenib plus intensive chemotherapy, randomized data are limited. This placebo-controlled, phase 2 study (ACTRN12611001112954) randomized 102 patients (aged 18-65 years) 2:1 to sorafenib vs placebo (days 4-10) combined with intensive induction: idarubicin 12 mg/m2 on days 1 to 3 plus either cytarabine 1.5 g/m2 twice daily on days 1, 3, 5, and 7 (18-55 years) or 100 mg/m2 on days 1 to 7 (56-65 years), followed by consolidation and maintenance therapy for 12 months (post-HCT excluded) in newly diagnosed patients with FLT3-ITD AML. Four patients were excluded in a modified intention-to-treat final analysis (3 not commencing therapy and 1 was FLT3-ITD negative). Rates of complete remission (CR)/CR with incomplete hematologic recovery were high in both arms (sorafenib, 78%/9%; placebo, 70%/24%). With 49.1-months median follow-up, the primary end point of event-free survival (EFS) was not improved by sorafenib (2-year EFS 47.9% vs 45.4%; hazard ratio [HR], 0.87; 95% confidence interval [CI], 0.51-1.51; P = .61). Two-year overall survival (OS) was 67% in the sorafenib arm and 58% in the placebo arm (HR, 0.76; 95% CI, 0.42-1.39). For patients who received HCT in first remission, the 2-year OS rates were 84% and 67% in the sorafenib and placebo arms, respectively (HR, 0.45; 95% CI, 0.18-1.12; P = .08). In exploratory analyses, FLT3-ITD measurable residual disease (MRD) negative status (<0.001%) after induction was associated with improved 2-year OS (83% vs 60%; HR, 0.4; 95% CI, 0.17-0.93; P = .028). In conclusion, routine use of pretransplant sorafenib plus chemotherapy in unselected patients with FLT3-ITD AML is not supported by this study.
索拉非尼维持治疗可改善 FMS 样酪氨酸激酶 3 内部串联重复(FLT3-ITD)急性髓系白血病(AML)患者造血细胞移植(HCT)后的疗效。尽管索拉非尼联合强化化疗的疗效令人鼓舞,但随机数据有限。这项安慰剂对照、2 期研究(ACTRN12611001112954)将 102 例年龄在 18-65 岁之间的患者以 2:1 的比例随机分为索拉非尼组和安慰剂组(第 4-10 天),联合强化诱导治疗:第 1-3 天给予伊达比星 12mg/m2,第 1、3、5 和 7 天给予阿糖胞苷 1.5g/m2 每日两次(18-55 岁)或第 1-7 天给予 100mg/m2(56-65 岁),随后进行 12 个月的巩固和维持治疗(HCT 后除外),用于新诊断的 FLT3-ITD AML 患者。在改良意向治疗的最终分析中,有 4 例患者被排除(3 例未开始治疗,1 例 FLT3-ITD 阴性)。两组完全缓解(CR)/不完全血液学恢复的完全缓解率均较高(索拉非尼组为 78%/9%,安慰剂组为 70%/24%)。中位随访 49.1 个月时,无事件生存(EFS)的主要终点未得到索拉非尼的改善(2 年 EFS 分别为 47.9%和 45.4%;风险比[HR],0.87;95%置信区间[CI],0.51-1.51;P=0.61)。索拉非尼组和安慰剂组的 2 年总生存率(OS)分别为 67%和 58%(HR,0.76;95%CI,0.42-1.39)。对于在首次缓解期接受 HCT 的患者,索拉非尼组和安慰剂组的 2 年 OS 率分别为 84%和 67%(HR,0.45;95%CI,0.18-1.12;P=0.08)。在探索性分析中,诱导后 FLT3-ITD 可测量残留疾病(MRD)阴性(<0.001%)与改善 2 年 OS 相关(83% vs 60%;HR,0.4;95%CI,0.17-0.93;P=0.028)。总之,这项研究不支持在未选择的 FLT3-ITD AML 患者中常规使用移植前索拉非尼联合化疗。